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        <title>Journal of Natural Medicines via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Journal of Natural Medicines' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Journal+of+Natural+Medicines&t=Journal+of+Natural+Medicines&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 14:04:19 +0100</lastBuildDate>
        <item>
            <title>Quantitative analysis of acylated oleanane-type triterpene saponins, chakasaponins I–III and floratheasaponins A–F, in the flower buds of Camellia sinensis from different regional origins</title>
            <link>http://www.medworm.com/index.php?rid=5667361&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3266705442411865%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A quantitative analytical method was developed for the determination of acylated oleanane-type triterpene saponins, chakasaponins
 I–III (1–3) and floratheasaponins A–F (4–9), found in Camellia sinensis (Theaceae). The practical conditions for separation and detection of these saponins were established on an ODS column with
 methanol containing 5&amp;nbsp;mM trifluoroacetic acid as a mobile phase, and the detection and quantitation limits of the method were
 estimated to be 1.1–3.8 and 3.5–12.5&amp;nbsp;ng, respectively. The relative standard deviation values of intra- and interday precision
 were lower than 2.35 and 6.12%, respectively, overall mean recoveries of all saponins being 94.7–108.8%, and the correlation
 coefficients of all the calibration curves showe...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5667361</comments>
            <pubDate>Fri, 03 Feb 2012 17:51:10 +0100</pubDate>
            <guid isPermaLink="false">5667361</guid>        </item>
        <item>
            <title>Honokiol suppresses the development of post-ischemic glucose intolerance and neuronal damage in mice</title>
            <link>http://www.medworm.com/index.php?rid=5620263&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fek6113366748786w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Honokiol, a constituent of Magnolia obovata, has various pharmacological effects, including protection against cerebral ischemia. However, few studies have been conducted
 to evaluate the possible neuroprotective effects of honokiol against cerebral ischemia. We recently reported that cerebral
 ischemic neuronal damage could be triggered by glucose intolerance that develops after the onset of ischemic stress (i.e.,
 post-ischemic glucose intolerance). In addition, suppression of post-ischemic glucose intolerance significantly ameliorated
 ischemic neuronal damage. Here, we investigated the effects of honokiol on the development of post-ischemic glucose intolerance
 and neuronal damage. Mice were subjected to middle cerebral artery occlusion (MCAO) for 2&amp;nbsp;h. The deve...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620263</comments>
            <pubDate>Fri, 20 Jan 2012 07:04:38 +0100</pubDate>
            <guid isPermaLink="false">5620263</guid>        </item>
        <item>
            <title>Effect of leaf extract of Capparis zeylanica Linn. on spatial learning and memory in rats</title>
            <link>http://www.medworm.com/index.php?rid=5620262&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnjw35377v02m6276%2F</link>
            <description>This study was designed to investigate the nootropic activity of Capparis zeylanica Linn. leaves in rats. The raw material of Capparis zeylanica leaves was successively extracted with petroleum ether and methanol using a Soxhlet apparatus and macerated to form an aqueous
 extract. The methanolic and aqueous extracts were evaluated for their effect on spatial learning and memory in rats using
 the Morris water maze task. Three doses (50, 100 and 150&amp;nbsp;mg/kg; p.o.) of methanolic and aqueous extracts of Capparis zeylanica were administered for 7 successive days to separate groups of animals. Results showed that both the extracts significantly
 enhanced memory, as shown by decrease in escape latency time. Furthermore, methanolic and aqueous extracts in all doses tested
 significantly increa...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620262</comments>
            <pubDate>Fri, 20 Jan 2012 07:04:38 +0100</pubDate>
            <guid isPermaLink="false">5620262</guid>        </item>
        <item>
            <title>Enzymatic fingerprints of polysaccharides of Dendrobium officinale and their application in identification of Dendrobium species</title>
            <link>http://www.medworm.com/index.php?rid=5620264&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw85843264155p6u2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Enzymatic fingerprinting of polysaccharides from Dendrobium officinale was studied and applied to authenticate Dendrobium species. Results showed that Dendrobium officinale species from Anhui province, Fujian province, Yunnan province, Guangdong province and Guangxi province of China, could be
 identified by polysaccharide analysis using carbohydrate gel electrophoresis (PACE). However, the fingerprints of Dendrobium officinale from Jiangxi province, Hu’nan province and Wenzhou, Yandangshan and Fuyang in Zhejiang province were very similar. As far
 as the fingerprints of different Dendrobium species were concerned, the differences between Dendrobium officinale, Dendrobium huoshanense, Dendrobium moniliforme, Dendrobium devonianum, Dendrobium aphyllum, Dendrobium wilso...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620264</comments>
            <pubDate>Fri, 20 Jan 2012 07:04:36 +0100</pubDate>
            <guid isPermaLink="false">5620264</guid>        </item>
        <item>
            <title>Anti-hyperlipidemic constituents from the bark of Shorea roxburghii</title>
            <link>http://www.medworm.com/index.php?rid=5620265&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd483162666564g48%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The methanol extract from the bark of Shorea roxburghii (Dipterocarpaceae, “Phayom” in Thai) was found to suppress plasma triglyceride elevation in olive oil-treated mice, and also
 to inhibit pancreatic lipase activity (IC50&amp;nbsp;=&amp;nbsp;31.6&amp;nbsp;μg/ml). From the extract, two new 3-acetyl-4-phenyl-3,4-dihydroisocoumarins, phayomphenols A1 (1) and A2 (2) were isolated, together with 22 known compounds. The structures of 1 and 2 were elucidated on the basis of chemical and spectroscopic evidence, including X-ray crystallographic analysis. Among the
 isolates, several oligostilbenoids, including (−)-hopeaphenol (3) and (+)-isohopeaphenol (4), showed inhibitory effects on plasma triglyceride elevation at a dose of 200&amp;nbsp;mg/kg p.o. and pancreatic lipase inhibitory...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620265</comments>
            <pubDate>Fri, 20 Jan 2012 07:04:34 +0100</pubDate>
            <guid isPermaLink="false">5620265</guid>        </item>
        <item>
            <title>Protective effect of Melothria maderaspatana leaf fraction on electrolytes, catecholamines, endothelial nitric oxide synthase and endothelin-1 peptide in uninephrectomized deoxycorticosterone acetate–salt hypertensive rats</title>
            <link>http://www.medworm.com/index.php?rid=5597944&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm82q164536069jn3%2F</link>
            <description>In conclusion, EAFM
 provides good blood pressure control by enhancing potassium and decreasing sodium levels, decreasing levels of epinephrine
 and norepinephrine, and preventing down-regulation of eNOS and significantly down-regulating ET-1 protein expression.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-9DOI 10.1007/s11418-011-0621-zAuthors
		Chinnadurai Veeramani, Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh, 11433 Saudi ArabiaKhalid S. Al-Numair, Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh, 11433 Saudi ArabiaGovindasamy Chandramohan, Department of Community Health Sciences, College of Applied Medical Sciences, K...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5597944</comments>
            <pubDate>Fri, 13 Jan 2012 17:19:27 +0100</pubDate>
            <guid isPermaLink="false">5597944</guid>        </item>
        <item>
            <title>Two new triterpenoid saponins from Caragana microphylla seeds</title>
            <link>http://www.medworm.com/index.php?rid=5597945&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv606622k386x4v8j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new triterpenoid saponins, caraganins A and B (1 and 2), structurally characterized by a 22-oxo group, were isolated from the seeds of Caragana microphylla Lam., together with their n-butyl esters as artifacts (1a and 2a). Their structures and configurations were elucidated by detailed spectroscopic analyses on the basis of NMR, IR, and MS
 data. Compounds 1a and 2a exhibited potent antibacterial activity against Staphylococcus aureus and Bacillus subtilis with minimum inhibitory concentration values ranging from 3.125 to 6.25&amp;nbsp;μg/ml.
 
 
	Content Type Journal ArticleCategory NotePages 1-6DOI 10.1007/s11418-011-0624-9Authors
		Cheng-Jian Zheng, Department of Pharmacognosy, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai, 200433 ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5597945</comments>
            <pubDate>Fri, 13 Jan 2012 17:19:26 +0100</pubDate>
            <guid isPermaLink="false">5597945</guid>        </item>
        <item>
            <title>Antiplasmodial decarboxyportentol acetate and 3,4-dehydrotheaspirone from Laumoniera bruceadelpha</title>
            <link>http://www.medworm.com/index.php?rid=5560355&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw732200445624605%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A new spiro heterocycle, decarboxyportentol acetate (1) was isolated from the barks of Laumoniera bruceadelpha Nooteboom (Simaroubaceae), together with 3,4-dehydrotheaspirone (2), and their structures were elucidated by 2D NMR analysis. 3,4-Dehydrotheaspirone (2) showed potent antiplasmodial activity against Plasmodium falciparum 3D7.
 
 
	Content Type Journal ArticleCategory NotePages 1-5DOI 10.1007/s11418-011-0618-7Authors
		Hiroshi Morita, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41 Shinagawa-ku, Tokyo, 142-8501 JapanReika Mori, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41 Shinagawa-ku, Tokyo, 142-8501 JapanJun Deguchi, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41 Shinagawa-ku, Tokyo, 142-8501 JapanSh...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5560355</comments>
            <pubDate>Mon, 02 Jan 2012 16:53:24 +0100</pubDate>
            <guid isPermaLink="false">5560355</guid>        </item>
        <item>
            <title>Ceramicines J–L, new limonoids from Chisocheton ceramicus</title>
            <link>http://www.medworm.com/index.php?rid=5505065&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp1w65p1417m06614%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three new limonoids, ceramicines J (1), K (2), and L (3), were isolated from the hexane layer of Chisocheton ceramicus bark extract. Their structures were elucidated from 1D and 2D NMR data. Ceramicines J–L (1–3) exhibited dose-dependent moderate cytotoxicity against the HL-60 cell line.
 
 
	Content Type Journal ArticleCategory NotePages 1-5DOI 10.1007/s11418-011-0616-9Authors
		Chin Piow Wong, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41 Shinagawa-ku, Tokyo, 142-8501 JapanMisae Shimada, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41 Shinagawa-ku, Tokyo, 142-8501 JapanAlfarius Eko Nugroho, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41 Shinagawa-ku, Tokyo, 142-8501 JapanYusuke Hirasawa, Faculty of Pharma...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5505065</comments>
            <pubDate>Mon, 12 Dec 2011 17:16:43 +0100</pubDate>
            <guid isPermaLink="false">5505065</guid>        </item>
        <item>
            <title>Medicinal plants of Thailand. II: chemical studies on the seed kernels of Entada rheedei Sprengel</title>
            <link>http://www.medworm.com/index.php?rid=5487017&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp57367720t3m6n61%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Chemical investigation of a methanolic extract of the seed kernels of Entada rheedei (Fabaceae), a Thai medicinal plant taken for stomachache, led to the isolation of five new compounds, 1-(3,4-dimethoxyphenyl)propan-9-ol
 O-(6″-O-α-l-arabinopyranosyl)-β-d-glucopyranoside, 1-(3,4,5-trimethoxyphenyl)prop-7-en-9-ol O-(6″-O-α-l-arabinopyranosyl)-β-d-glucopyranoside, and N-(2′-hydroxyethyl)-7-phenylacetamide 2′-O-β-d-glucopyranoside, and entadamide A 2′-O-(4″-O-β-d-glucopyranosyl)-β-d-glucopyranoside and 2′-O-(6″-O-β-d-glucopyranosyl)-β-d-glucopyranosides, together with one known compound, corchoionoside C. Their structures were elucidated on the basis of chemical
 and spectral evidence.
 
 
	Content Type Journal ArticleCategory NotePages 1-6DOI 10....</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5487017</comments>
            <pubDate>Tue, 06 Dec 2011 16:58:53 +0100</pubDate>
            <guid isPermaLink="false">5487017</guid>        </item>
        <item>
            <title>Phytochemical characterization and antinociceptive effect of Lippia gracilis Schauer</title>
            <link>http://www.medworm.com/index.php?rid=5487018&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F726354654l80r273%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Lippia gracilis Schauer is an aromatic plant widely found in Northeastern Brazil. The leaf infusions or decoctions and alcoholic macerate
 are used for some inflammatory diseases and headache. This paper reports the isolation of naringenin by semi-preparative liquid
 chromatography from the methanolic extract of L. gracilis (ELg) and the evaluation of the analgesic and anti-inflammatory activities of this extract by measuring nociception through
 acetic acid, formalin, and hot-plate tests in carrageenan-induced inflammation in mice. Following oral administration, ELg
 (100, 200, and 400&amp;nbsp;mg/kg) significantly reduced the number of writhes in the writhing test and the time of paw licks in both
 phases of the formalin test when compared to the control group animals. ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5487018</comments>
            <pubDate>Tue, 06 Dec 2011 16:58:52 +0100</pubDate>
            <guid isPermaLink="false">5487018</guid>        </item>
        <item>
            <title>Pharmacological explanation for the medicinal use of Juniperus excelsa in hyperactive gastrointestinal and respiratory disorders</title>
            <link>http://www.medworm.com/index.php?rid=5476729&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj3x3760t56630721%2F</link>
            <description>This study suggests that Juniperus excelsa possibly exhibits a combination of Ca2+ antagonist and phosphodiesterase inhibitory effects, which provides a pharmacological basis for its traditional use in disorders
 of gut and airways hyperactivity, such as diarrhoea, colic and asthma.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-10DOI 10.1007/s11418-011-0605-zAuthors
		Munasib Khan, Natural Products Research Unit, Department of Biological and Biomedical Sciences, Aga Khan University Medical College, Karachi, 74800 PakistanArif-ullah Khan, Institute of Pharmaceutical Sciences, Kohat University of Science and Technology, Kohat, 26000 KPK, PakistanNajeeb-ur-Rehman, Natural Products Research Unit, Department of Biological and Biomedical Sciences, Aga Khan University Medical Co...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476729</comments>
            <pubDate>Fri, 02 Dec 2011 06:48:26 +0100</pubDate>
            <guid isPermaLink="false">5476729</guid>        </item>
        <item>
            <title>Pyrenes and pyrendiones from Uvaria lucida</title>
            <link>http://www.medworm.com/index.php?rid=5469100&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd3u3432225168201%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A chemical investigation of the chloroform extract of the roots of Uvaria ludida Benth. (Annonaceae), an important African traditional medicine, led to the isolation of six new compounds; three pyrenes,
 2-hydroxy-1,8-dimethoxypyrene (1), 8-methoxy-1,2-methylenedioxypyrene (2), and 7-hydroxy-8-methoxy-1,2-methylenedioxypyrene (3), two pyrenediones, 2-hydroxy-1,8-pyrenedione (4) and 2-methoxy-1,8-pyrenedione (5), and a sesquiterpene, (−)-10-oxo-isodauc-3-en-15-oic acid (6), together with eight known compounds (7–14). The structural elucidation by spectroscopic studies of the compounds isolated is described. While pyrenes did not exhibit
 strong cytotoxicity against human promyelocytic leukemia HL-60 cells, pyrenediones showed strong cytotoxicity. The IC50 of 4 was 70...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5469100</comments>
            <pubDate>Wed, 30 Nov 2011 04:41:09 +0100</pubDate>
            <guid isPermaLink="false">5469100</guid>        </item>
        <item>
            <title>Difference in cultivation characteristics and genetic polymorphism between Chinese and Japanese strains of Wolfiporiacocos Ryvarden et Gilbertson (Poria cocos Wolf)</title>
            <link>http://www.medworm.com/index.php?rid=5469101&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk0l4t0h0h06m7466%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Poria, a dried sclerotium of Wolfiporia
 cocos Ryvarden et Gilbertson (Polyporaceae) has been used as a crude drug in both Chinese and Japanese (Kampo) traditional medicines.
 Recently, cultivated products of Chinese Poria strains have accounted for most of the market, while the cultivation of Japanese
 Poria strains has not been successful. Aiming to determine the relationship between the differences in cultivation characteristics
 and genetic polymorphism, we conducted a field cultivation experiment, a rot test, and rapid amplification of polymorphic
 DNA (RAPD) analysis of Poria strains collected from China and Japan: 3 Chinese and 7 Japanese strains. In field cultivation,
 although there was no marked inferiority of Japanese strains to Chinese ones in either myceliu...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5469101</comments>
            <pubDate>Wed, 30 Nov 2011 04:41:08 +0100</pubDate>
            <guid isPermaLink="false">5469101</guid>        </item>
        <item>
            <title>Three new secolignan glycosides from Urtica fissa E. Pritz</title>
            <link>http://www.medworm.com/index.php?rid=5457944&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft5tk73t534394wp0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three new secolignan glycosides {3,4-trans-4-[bis(3,4-dimethoxyphenyl)methyl]-2-oxotetrahydrafuran-3-yl}methyl-O-β-glucopyranoside (1), {3,4-trans-4-[(3-methoxy-4-hydroxyphenyl)(3,4-dimethoxyphenyl)methyl]-2-oxotetrahydrafuran-3-yl}methyl-O-β-glucopyranoside (2) and {3,4-cis-4-[(3-methoxy-4-hydroxyphenyl)(3,4-dimethoxyphenyl)methyl]-2-oxotetrahydrafuran-3-yl}methyl-O-β-glucopyranoside (3) were isolated from the roots of Urtica fissa E. Pritz. Their structures were identified by spectral methods including 1D NMR, 2D NMR and HR-EI-MS.
 
 
	Content Type Journal ArticleCategory NotePages 1-4DOI 10.1007/s11418-011-0615-xAuthors
		Bao-min Feng, School of Life Science and Biotechnology, Dalian University, Dalian, 116622 ChinaHai-hong Qin, Medical College, Dalian University,...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5457944</comments>
            <pubDate>Mon, 28 Nov 2011 16:59:34 +0100</pubDate>
            <guid isPermaLink="false">5457944</guid>        </item>
        <item>
            <title>Protective effect of herbomineral formulation (Dolabi) on early diabetic nephropathy in streptozotocin-induced diabetic rats</title>
            <link>http://www.medworm.com/index.php?rid=5449866&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0340qht176211n18%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The effect of a herbomineral formulation (HMF) on early diabetic nephropathy was investigated. Diabetes was induced in Wistar
 rats by administering streptozotocin (55&amp;nbsp;mg/kg, intraperitoneally). The occurrence of early diabetic nephropathy in rats was
 revealed by high plasma glucose and depleted liver glycogen, decreased glucose uptake by peripheral tissue, impaired renal
 function, increased antioxidants and lipid peroxidation in kidney. These changes were accompanied by elevated malondialdehyde,
 glutathione and superoxide dismutase activity in kidney. Furthermore, increased total urine volume, urinary albumin excretion
 rate, urinary albumin to creatinine ratio, increased relative kidney weight, decreased glomerular filtration rate (GFR) and
 urinary creatinine...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449866</comments>
            <pubDate>Thu, 24 Nov 2011 17:52:02 +0100</pubDate>
            <guid isPermaLink="false">5449866</guid>        </item>
        <item>
            <title>In vitro antitrypanosomal activity of some phenolic compounds from propolis and lactones from Fijian Kawa (Piper methysticum)</title>
            <link>http://www.medworm.com/index.php?rid=5449867&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp5tv86g36379x202%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During our search to discover new antitrypanosomal compounds, eight known plant compounds (three phenolic compounds and five
 kawa lactones) were evaluated for in vitro activity against Trypanosoma brucei brucei. Among them, we found two phenolic compounds and three kawa lactones possessing an α-pyrone influenced antitrypanosomal property.
 In particular, β-phenethyl caffeate, farnesyl caffeate and dihydrokawain exhibited high or moderate selective and potent antitrypanosomal
 activity in vitro. We detail here the antitrypanosomal activity and cytotoxicities of the compounds, in comparison with two
 commonly used antitrypanosomal drugs (eflornithine and suramin). Our findings represent the first report of the promising
 trypanocidal activity of these compounds.
 
 
	C...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449867</comments>
            <pubDate>Thu, 24 Nov 2011 17:52:00 +0100</pubDate>
            <guid isPermaLink="false">5449867</guid>        </item>
        <item>
            <title>Preventive effect of Terminalia bellirica on obesity and metabolic disorders in spontaneously obese type 2 diabetic model mice</title>
            <link>http://www.medworm.com/index.php?rid=5441194&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbm20218227n55716%2F</link>
            <description>In this study, we investigated the preventive effect of a hot water extract
 of T. bellirica fruit (TB) on obesity and various metabolic disorders, and explored its molecular mechanisms and active ingredients. TB treatment
 had a preventive effect on obesity, insulin resistance, and hyperlipidemia in spontaneously obese type 2 diabetic TSOD mice.
 To clarify the molecular mechanisms of TB in preventing obesity, we investigated the inhibitory effect on lipid absorption.
 TB suppressed absorption of triacylglycerol in an olive oil loading test (in vivo) and showed a strong inhibitory effect on
 pancreatic lipase activity (in vitro). Furthermore, a search for the active ingredients in TB revealed that gallic acid is
 the component primarily responsible for the inhibition of pancreatic lipase ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5441194</comments>
            <pubDate>Mon, 21 Nov 2011 18:08:32 +0100</pubDate>
            <guid isPermaLink="false">5441194</guid>        </item>
        <item>
            <title>Red ginseng and 20(S)-Rg3 control testosterone-induced prostate hyperplasia by deregulating androgen receptor signaling</title>
            <link>http://www.medworm.com/index.php?rid=5441196&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw8l8517183512324%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since prostate growth is governed by the androgen signaling pathway, blockade of the pathway is regarded as an appropriate
 strategy for the treatment of benign prostatic hyperplasia (BPH). Panax ginseng is known to have various pharmacological activities.
 Of several products of its root, red ginseng, having many bioactive ginsenosides, is most popularly used in Korea, and recently
 has been reported to control the proliferation of cancer cells. We here tested the effect of a water extract of Korean red
 ginseng (WKRG) on testosterone-induced prostate hyperplasia. WKRG (daily intraperitoneal injection) prevented prostate overgrowth
 and epithelial thickening induced by testosterone in rats, and suppressed a rat prostate kallikrein-S3. In human prostate
 cells, WKRG inh...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5441196</comments>
            <pubDate>Sat, 19 Nov 2011 16:52:18 +0100</pubDate>
            <guid isPermaLink="false">5441196</guid>        </item>
        <item>
            <title>New flav-3-en-3-ol glycosides, kaempferiaosides C and D, and acetophenone glycosides, kaempferiaosides E and F, from the rhizomes of Kaempferia parviflora</title>
            <link>http://www.medworm.com/index.php?rid=5441195&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F621h52651780k40k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new flav-3-en-3-ol glycosides, kaempferiaosides C (3) and D (4), and two new acetophenone glycosides, kaempferiaosides E (5) and F (6), were isolated from the Thai natural medicine Krachai Dum, the rhizomes of Kaempferia parviflora Wall. ex Baker. Their structures were established mainly on the basis of 1D and 2D NMR spectral data.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-7DOI 10.1007/s11418-011-0611-1Authors
		Saowanee Chaipech, Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, JapanToshio Morikawa, Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, JapanKiyofumi Ninomiya, Pharmaceutical Research and Technology Instit...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5441195</comments>
            <pubDate>Sat, 19 Nov 2011 16:52:18 +0100</pubDate>
            <guid isPermaLink="false">5441195</guid>        </item>
        <item>
            <title>Pharmacokinetics and organ distribution of diarylheptanoid phytoestrogens from Curcuma comosa in rats</title>
            <link>http://www.medworm.com/index.php?rid=5441198&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkg502516r4211475%2F</link>
            <description>This study provides the essential pharmacokinetic
 data for diarylheptanoid phytoestrogenic compounds of C. comosa extract which are required for clinical dose and dosage design.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-8DOI 10.1007/s11418-011-0607-xAuthors
		Jian Su, Center for Research and Development of Herbal Health Products, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40002 ThailandKittisak Sripanidkulchai, Department of Anatomy, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002 ThailandApichart Suksamrarn, Department of Chemistry, Faculty of Science, Ramkhamhaeng University, Bangkok, 10240 ThailandYing Hu, Center for Research and Development of Herbal Health Products, Faculty of Pharmaceutical Sciences, Khon Kaen University, K...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5441198</comments>
            <pubDate>Sat, 19 Nov 2011 06:51:20 +0100</pubDate>
            <guid isPermaLink="false">5441198</guid>        </item>
        <item>
            <title>Chemical and pharmacological studies of Oplopanax horridus, a North American botanical</title>
            <link>http://www.medworm.com/index.php?rid=5441197&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu252138673760u35%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Oplopanax horridus (OH), or Devil’s club, is an ethnobotanical used by the indigenous people native to the Pacific Northwest of North America.
 There are three species in the genus Oplopanax, and OH is the only species that is distributed in North America. Compared with the extensive research on OH’s “cousin,”
 American ginseng, there is comparatively little reported about the chemical makeup and pharmacological effects of OH. Nevertheless,
 there has been some research over the past few years that shows promise for the future usage perspectives of OH. To date,
 17 compounds were isolated and elucidated, including polyynes, glycosides, lignans, and polyenes, with most of the attention
 being paid to the polyynes. Gas chromatography (GC) and high-performance li...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5441197</comments>
            <pubDate>Sat, 19 Nov 2011 06:51:20 +0100</pubDate>
            <guid isPermaLink="false">5441197</guid>        </item>
        <item>
            <title>Anti-inflammatory and anti-nociceptive effects of the ethanolic extracts of Alkanna frigida and Alkanna orientalis</title>
            <link>http://www.medworm.com/index.php?rid=5422300&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F48u82662x69063xv%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Alkanna species are used in Iranian traditional medicine for treatment of rheumatoid arthritis and other inflammatory diseases. This
 study was designed to evaluate the anti-inflammatory and anti-nociceptive effects of Alkanna frigida and Alkanna orientalis ethanolic extracts via the carrageenan-induced paw edema test and formalin test in rat and mouse, respectively. Ethanolic
 extracts of plant root were prepared and were injected intraperitoneally 60&amp;nbsp;min before carrageenan-induced inflammation or
 formalin-induced nociception at 100, 200 and 400&amp;nbsp;mg/kg. Anti-inflammatory effects of plants were monitored for 3&amp;nbsp;h after carrageenan
 injection and anti-nociceptive effects were evaluated during the first hour after formalin injection. Diclofenac, a well-kno...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5422300</comments>
            <pubDate>Tue, 15 Nov 2011 16:48:06 +0100</pubDate>
            <guid isPermaLink="false">5422300</guid>        </item>
        <item>
            <title>Quantitative determination of four compounds and fingerprint analysis in the rhizomes of Drynaria fortunei (Kunze) J. Sm.</title>
            <link>http://www.medworm.com/index.php?rid=5422302&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk6g1n12657n14034%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A rapid, sensitive, and accurate reversed-phase high-performance liquid chromatography with photodiode array detection method
 was developed for both quantitative determination of four compounds (caffeic acid-4-O-β-d-glucopyranoside, 5,7-dihydroxychromone-7-O-rutinoside, neoeriocitrin and naringin) and fingerprint analysis of the rhizomes of Drynaria fortunei (Kunze) J. Sm. The chromatographic separation was accomplished on an MZ-C18 column (4.6&amp;nbsp;×&amp;nbsp;250&amp;nbsp;mm, 5&amp;nbsp;μm) using gradient elution
 with acetonitrile and 0.02% aqueous acetic acid, at a flow rate of 1.0&amp;nbsp;mL&amp;nbsp;min−1, an operating temperature of 25°C, and a wavelength of 260&amp;nbsp;nm. The four compounds showed good regression relationship (R
 2&amp;nbsp;&amp;gt;&amp;nbsp;0.9990) within linear ranges, ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5422302</comments>
            <pubDate>Tue, 15 Nov 2011 16:48:05 +0100</pubDate>
            <guid isPermaLink="false">5422302</guid>        </item>
        <item>
            <title>Withania somnifera extract attenuates stem cell factor-stimulated pigmentation in human epidermal equivalents through interruption of ERK phosphorylation within melanocytes</title>
            <link>http://www.medworm.com/index.php?rid=5422301&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu5154263r01r2jx4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We previously demonstrated that mitogen-activated protein kinase (MAPK) signaling, including microphthalmia-associated transcription
 factor (MITF) and cAMP response element-binding protein (CREB) phosphorylation, is a major pathway involved in up-regulating
 melanogenesis within human melanocytes in several hyperpigmentary disorders such as UVB melanosis and lentigo senilis. Recently,
 a redox imbalance was shown to be closely linked to a variety of altered cellular responses in which the precise balance between
 levels of oxidizing and reducing equivalents that reflect the intracellular redox condition profoundly affects intracellular
 signaling pathways, especially the MAPK pathway. To elucidate the effects of redox balance regulation on epidermal pigmentation,
 we u...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5422301</comments>
            <pubDate>Tue, 15 Nov 2011 16:48:05 +0100</pubDate>
            <guid isPermaLink="false">5422301</guid>        </item>
        <item>
            <title>Vasorelaxant effect of isoquinoline derivatives from two species of Popowia perakensis and Phaeanthus crassipetalus on rat aortic artery</title>
            <link>http://www.medworm.com/index.php?rid=5360533&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw24r2m4045583234%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Five bisbenzyl isoquinolines (1–5), three benzyl isoquinolines (6–8), four isoquinoline alkaloids (9–12), and two unclassified compounds (13 and 14) from Popowia perakensis and Phaeanthus crassipetalus were evaluated for their vasorelaxant effect on rat aortic arteries. In aortic rings pre-contracted with phenylephrine (PE,
 0.3&amp;nbsp;μM), some of the bisbenzyl isoquinoline alkaloids, benzyl isoquinoline alkaloids, and isoquinoline alkaloids showed clearly
 vasorelaxant effects at 30&amp;nbsp;μM. The action of (−)-limacine (4) was deduced to be mediated through the increased release of NO from endothelial cells, and that of pecrassipine A (7) and backebergine (12) partly mediated by NO release. Further, the action of pecrassipine A (7) and backebergine (12) may be ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5360533</comments>
            <pubDate>Fri, 28 Oct 2011 06:04:40 +0100</pubDate>
            <guid isPermaLink="false">5360533</guid>        </item>
        <item>
            <title>Nondestructive prediction of oren extract powder, a herbal medicine, in suppositories by chemometric near-infrared spectroscopy</title>
            <link>http://www.medworm.com/index.php?rid=5336062&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0h1254162ng40723%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Near-infrared (NIR) spectroscopy combined with chemometrics has been utilized in predictions of natural medicine content without
 destroying samples. Suppositories (oren powdered extract content 0, 0.5, 1.0, 2.5, 10, 12.5, and 15%) were produced by mixing
 oren powdered extract with macrogol mixture consisting of 1 part macrogol 1500 and 2.5 parts macrogol 4000 at 54°C, and pouring
 the melt mixture into a plastic container. NIR spectra of the 10 prepared samples were recorded 10 times, and a total of 100
 spectra were randomly divided into two data sets, one for calibration and the other for validation. The calibration model
 for the oren content of the suppository was calculated based on NIR spectra using a partial least-squares regression analysis
 after pre-treatme...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5336062</comments>
            <pubDate>Mon, 17 Oct 2011 16:03:42 +0100</pubDate>
            <guid isPermaLink="false">5336062</guid>        </item>
        <item>
            <title>Pharmacological and histological effects of Centaurea bruguierana ssp. belangerana on indomethacin-induced peptic ulcer in rats</title>
            <link>http://www.medworm.com/index.php?rid=5324156&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F363vn1x154223816%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The species Centaurea bruguierana (DC.) Hand.-Mazz. ssp. belangerana (DC.) Bornm. (CBB) (Asteraceae), known as “Baad-Avard” in Borazjan, Bushehr Province, southern Iran, is used in folk medicine
 as a hypoglycemic herb in diabetes and as a remedy for peptic ulcer disorders. Total 80% EtOH extract and petroleum ether,
 CHCl3, EtOAc, n-BuOH, and remaining fractions obtained by solvent–solvent fractionation of dried aerial flowering parts of the plant were
 investigated for anti-ulcer activity against indomethacin-induced ulcerogenesis in rats. Anti-ulcer activity was evaluated
 by measuring the ulcer index (UI) and ulcer inhibition. The UI was significantly reduced in all treated animals. A dramatic
 decrease in the UI was observed following the administration of to...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5324156</comments>
            <pubDate>Thu, 13 Oct 2011 05:47:24 +0100</pubDate>
            <guid isPermaLink="false">5324156</guid>        </item>
        <item>
            <title>Curcuminoid analogs inhibit nitric oxide production from LPS-activated microglial cells</title>
            <link>http://www.medworm.com/index.php?rid=5324155&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk49841128k5k1427%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The chemically modified analogs, the demethylated analogs 4–6, the tetrahydro analogs 7–9 and the hexahydro analogs 10–12, of curcumin (1), demethoxycurcumin (2) and bisdemethoxycurcumin (3) were evaluated for their inhibitory activity on lipopolysaccharide activated nitric oxide (NO) production in HAPI microglial
 cells. Di-O-demethylcurcumin (5) and O-demethyldemethoxycurcumin (6) are the two most potent compounds that inhibited NO production. The analogs 5 and 6 were twofold and almost twofold more active than the parent curcuminoids 1 and 2, respectively. Moreover, the mRNA expression level of inducible NO synthase was inhibited by these two compounds. The strong
 neuroprotective activity of analogs 5 and 6 provide potential alternative compounds to be develop...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5324155</comments>
            <pubDate>Thu, 13 Oct 2011 05:47:24 +0100</pubDate>
            <guid isPermaLink="false">5324155</guid>        </item>
        <item>
            <title>Two new acetylated flavonoid glycosides from Centaurium spicatum L</title>
            <link>http://www.medworm.com/index.php?rid=5314691&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4843n124220872g1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new acetylated flavonol glycosides, quercetin 3-O-[(2,4-diacetyl-α-l-rhamnopyranosyl)-(1→6)]-2,4-diacetyl-β-d-galactopyranoside (1) and quercetin 3-O-[(2,4-diacetyl-α-l-rhamnopyranosyl)-(1→6)]-3,4-diacetyl-β-d-galactopyranoside (2), in addition to two known acetylated quercetin glycosides quercetin 3-O-[(2,3,4-triacetyl-α-l-rhamnopyranosyl)-(1→6)-β-d-galactopyranoside (3) and quercetin 3-O-[(2,3,4-triacetyl-α-l-rhamnopyranosyl)-(1→6)-3-acetyl-β-d-galactopyranoside (4), were isolated from the aerial part of Centaurium spicatum (L.) Fritsch (Gentianaceae). Structure elucidation, especially the localization of the acetyl groups, and complete 1H and 13C NMR assignments of these biologically active compounds were carried out using one- and two-dimensional...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314691</comments>
            <pubDate>Wed, 12 Oct 2011 05:42:22 +0100</pubDate>
            <guid isPermaLink="false">5314691</guid>        </item>
        <item>
            <title>Antiobesity effect of Tamarindus indica L. pulp aqueous extract in high-fat diet-induced obese rats</title>
            <link>http://www.medworm.com/index.php?rid=5314693&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7176131008j676p5%2F</link>
            <description>In conclusion, TIE improved obesity-related parameters in
 blood, liver, and adipose tissue in a rat model and suppressed obesity induced by a high-fat diet, possibly by regulating
 lipid metabolism and lowering plasma leptin and FAS levels. A dose-dependant effect of TIE is detected, where TIE at 50&amp;nbsp;mg/kg
 showed the most prominent effect, followed by TIE at 25&amp;nbsp;mg/kg and, subsequently, 5&amp;nbsp;mg/kg.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-10DOI 10.1007/s11418-011-0597-8Authors
		Khairunnuur Fairuz Azman, Phytomedicine Research Group, Department of Human Anatomy, Division of Physiology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, UPM, 43400 Serdang, Selangor, MalaysiaZulkhairi Amom, Phytomedicine Research Group, Department of Human ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314693</comments>
            <pubDate>Tue, 11 Oct 2011 15:53:25 +0100</pubDate>
            <guid isPermaLink="false">5314693</guid>        </item>
        <item>
            <title>Hypoglycemic effects of clove (Syzygium aromaticum flower buds) on genetically diabetic KK-Ay mice and identification of the active ingredients</title>
            <link>http://www.medworm.com/index.php?rid=5314695&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe61v6m58443r71x9%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clove (Syzygium aromaticum flower buds) EtOH extract significantly suppressed an increase in blood glucose level in type 2 diabetic KK-Ay mice. In-vitro evaluation showed the extract had human peroxisome proliferator-activated receptor (PPAR)-γ ligand-binding
 activity in a GAL4-PPAR-γ chimera assay. Bioassay-guided fractionation of the EtOH extract resulted in the isolation of eight
 compounds, of which dehydrodieugenol (2) and dehydrodieugenol B (3) had potent PPAR-γ ligand-binding activities, whereas oleanolic acid (4), a major constituent in the EtOH extract, had moderate activity. Furthermore, 2 and 3 were shown to stimulate 3T3-L1 preadipocyte differentiation through PPAR-γ activation. These results indicate that clove
 has potential as a functional food ingre...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314695</comments>
            <pubDate>Tue, 11 Oct 2011 05:47:29 +0100</pubDate>
            <guid isPermaLink="false">5314695</guid>        </item>
        <item>
            <title>Entadosides A–D, triterpene saponins and a glucoside of the sulphur-containing amide from the kernel nuts of Entada phaseoloides (L.) Merrill</title>
            <link>http://www.medworm.com/index.php?rid=5314696&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk083655161857450%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;From a MeOH extract of kernel nuts of Entada phaseoloides (L.) Merrill, one new and one known sulphur-containing glucoside were isolated. From the 1-BuOH-soluble fraction of a H2O extract, four new triterpene saponins containing N-acetylglucosamine in their sugar chains were isolated. The antiproliferative activities of the triterpene saponins were assayed.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-8DOI 10.1007/s11418-011-0591-1Authors
		Yoshihiro Iwamoto, Department of Pharmacognosy, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanSachiko Sugimoto, Department of Pharmacognosy, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 Ja...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314696</comments>
            <pubDate>Sat, 08 Oct 2011 05:47:46 +0100</pubDate>
            <guid isPermaLink="false">5314696</guid>        </item>
        <item>
            <title>San-Huang-Xie-Xin-Tang protects cardiomyocytes against hypoxia/reoxygenation injury via inhibition of oxidative stress-induced apoptosis</title>
            <link>http://www.medworm.com/index.php?rid=5304592&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu03737u416572q23%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Oxidative stress has been widely implicated in the pathogenesis of hypoxia/reoxygenation (H/R) injury. San-Huang-Xie-Xin-Tang
 (SHXT), a widely used traditional Chinese medication, has been shown to possess antioxidant effects. Here, we investigated
 whether SHXT and its main component baicalin can attenuate oxidative stress induced by H/R injury. H9c2 rat ventricular cells
 were exposed to SHXT or baicalin followed by hypoxia for 24&amp;nbsp;h and/or reoxygenation for 8&amp;nbsp;h. Pretreatment with SHXT and baicalin
 both significantly prevented cell death and production of reactive oxygen species induced by hypoxia or H/R in H9c2 cardiomyoctes.
 In addition, SHXT and baicalin also inhibited hypoxia- or H/R-induced apoptosis, with associated decreased Bax protein, increased
 ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304592</comments>
            <pubDate>Fri, 07 Oct 2011 05:49:01 +0100</pubDate>
            <guid isPermaLink="false">5304592</guid>        </item>
        <item>
            <title>Antihypertensive effect of Melothria maderaspatana leaf fractions on DOCA-salt-induced hypertensive rats and identification of compounds by GC–MS analysis</title>
            <link>http://www.medworm.com/index.php?rid=5297163&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F738343862m140556%2F</link>
            <description>In conclusion, the EAFM controls blood
 pressure in DOCA-salt hypertensive rats and reverts the metabolic alterations in magnesium, copper and zinc.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s11418-011-0590-2Authors
		Chinnadurai Veeramani, Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh, 11433 Saudi ArabiaKhalid S. Al-Numair, Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh, 11433 Saudi ArabiaGovindasamy Chandramohan, Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh, 11433 Saudi ArabiaMohammed A. Alsaif, Department of Community Healt...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5297163</comments>
            <pubDate>Sat, 01 Oct 2011 06:46:38 +0100</pubDate>
            <guid isPermaLink="false">5297163</guid>        </item>
        <item>
            <title>In vitro cytotoxic screening of selected Saudi medicinal plants</title>
            <link>http://www.medworm.com/index.php?rid=5274078&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd54k505227426k71%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Many natural products from plants have been identified to exert anticancer activity. It might be expected to be a challenge
 to look at the Saudi plants in order to discover new sources for new molecules which may have anticancer activity. The methanolic
 extracts of forty species of plants traditionally used in Saudi Arabia for the treatment of a variety of diseases were tested
 in vitro for their potential anticancer activity on different human cancer cell lines. The cytotoxic activity of the methanolic
 extracts of the tested plants were determined using three human cancer cell lines, namely, breast cancer (MCF7), hepatocellular
 carcinoma (HEPG2), and cervix cancer (HELA) cells. In addition, human normal melanocyte (HFB4) was used as normal nonmalignant
 cells. Sulf...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5274078</comments>
            <pubDate>Wed, 28 Sep 2011 05:48:14 +0100</pubDate>
            <guid isPermaLink="false">5274078</guid>        </item>
        <item>
            <title>Growth and asiaticoside production in multiple shoot cultures of a medicinal herb, Centella asiatica (L.) Urban, under the influence of nutrient manipulations</title>
            <link>http://www.medworm.com/index.php?rid=5260973&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr16mq81m3w8n6380%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Growth and in vitro asiaticoside accumulation in multiple shoot cultures of Centella asiatica (L.) Urban was studied as a function of nutrient manipulations in the culture media. Shoot cultures raised in liquid Murashige
 and Skoog medium supplemented with 2.5&amp;nbsp;mg/l kinetin attained a growth index (GI) of 6.06 along with the highest asiaticoside
 content of 3.8&amp;nbsp;mg/g dry weight on the 35th day of the culture cycle. The shoot growth and asiaticoside accumulation were found
 to be influenced by the relative proportions of NH4
 +-N:NO3
 −-N or Cu2+ concentration in the medium. Asiaticoside content in shoots increased from 5.3 to 8.9 and 8.7&amp;nbsp;mg/g dry weight when total
 nitrogen concentration of 60&amp;nbsp;mM in the control medium was reduced to 50 and 40&amp;nbsp;mM...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260973</comments>
            <pubDate>Fri, 23 Sep 2011 05:56:10 +0100</pubDate>
            <guid isPermaLink="false">5260973</guid>        </item>
        <item>
            <title>Production of lignans in calluses of Schisandra chinensis</title>
            <link>http://www.medworm.com/index.php?rid=5225963&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2255436w677p1593%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Calluses were induced from leaves of Schisandra chinensis Baillon (Schisandraceae). Murashige–Skoog (MS) and Woody Plant (WP) media were used for the induction, in full and half strength
 (1/2 MS or 1/2 WP) salt formulations. Test media were solidified with 0.25% gelrite and supplemented with 2% sucrose and various
 concentrations and combinations of 2,4-dichlorophenoxyacetic acid (2,4-D), kinetin (Kin), 3-indolebutyric acid (IBA), and
 6-benzylaminopurine (BAP). Optimal conditions for callus induction and growth were found to be 1/2 MS medium containing 0.02&amp;nbsp;mg/l
 Kin and 0.2&amp;nbsp;mg/l 2,4-D. Chloroform extracts of all induced calluses contained gomisin A and F as major components. Gomisin
 A and F contents of calluses that were cultured under the optimal condit...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225963</comments>
            <pubDate>Fri, 16 Sep 2011 16:43:43 +0100</pubDate>
            <guid isPermaLink="false">5225963</guid>        </item>
        <item>
            <title>In vitro antitrypanosomal activity of bis(bibenzyls)s and bibenzyls from liverworts against Trypanosoma brucei</title>
            <link>http://www.medworm.com/index.php?rid=5225964&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm1n4534gwl08184t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During the course of our screening program to discover new antitrypanosomal compounds, 17 known plant aromatic compounds [12
 bis(bibenzyls)s and 5 bibenzyls] were evaluated for in vitro activity against Trypanosoma brucei brucei. Sixteen compounds were found to exhibit antitrypanosomal activity. In particular, three compounds, marchantin A (1), plagiochin A (5) and 2(R)-2-isopropenyl-6,7-dihydroxy-4-(2-phenylethyl)dihydrobenzofuran (16) demonstrated moderate selective and potent antitrypanosomal activities in vitro. We detail here the antitrypanosomal properties
 and cytotoxicities of the compounds in comparison with two commonly used therapeutic drugs, eflornithine and suramin. Our
 finding represents the first report of the promising trypanocidal activity of these co...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225964</comments>
            <pubDate>Thu, 15 Sep 2011 15:51:11 +0100</pubDate>
            <guid isPermaLink="false">5225964</guid>        </item>
        <item>
            <title>Protective effects of flavonoids and extract from Vellozia kolbekii Alves against oxidative stress induced by hydrogen peroxide in yeast</title>
            <link>http://www.medworm.com/index.php?rid=5225965&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F64130452772t7856%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two flavonoids 3,5,7,3′,4′-pentahydroxy-6-prenylflavonol (1) and 3,5,7,3′,4′-pentahydroxy-8-methyl-6-prenylflavonol (2) were isolated from the ethyl acetate extract of sheaths of Vellozia kolbekii Alves (Velloziaceae). This is the first time that compound 2 has been described. The crude extract and flavonoids were found to be active as 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical
 scavengers and were able to the increase tolerance of the eukaryotic microorganism Saccharomyces cerevisiae to oxidative stress generated by H2O2. The protective effect was correlated with a reduction in the oxidation of proteins and lipids. In addition, flavonoids isolated
 from Velloziaceae showed an inhibitory effect on mutations in p53, which is mutated and nonfunctional in more th...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225965</comments>
            <pubDate>Tue, 13 Sep 2011 15:43:21 +0100</pubDate>
            <guid isPermaLink="false">5225965</guid>        </item>
        <item>
            <title>Low-molecular-weight lignin-rich fraction in the extract of cultured Lentinula edodes mycelia attenuates carbon tetrachloride-induced toxicity in primary cultures of rat hepatocytes</title>
            <link>http://www.medworm.com/index.php?rid=5209088&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm92311182t621132%2F</link>
            <description>In this study, we fractionated the LEM extract
 to explore novel active compounds related to hepatoprotection by using primary cultures of rat hepatocytes exposed to carbon
 tetrachloride (CCl4). The LEM extract and the fractions markedly inhibited the release of alanine aminotransferase (ALT) from hepatocytes damaged
 by CCl4 into the culture medium. The strongest hepatocyte-protective activity was seen in a fraction (Fr. 2) in which a 50% ethanol
 extract was further eluted with 50% methanol and separated using reverse-phase HPLC. Fr. 2 had an average molecular weight
 of 2753, and the main components are lignin (49%) and saccharides (36%, of which xylose comprises 41%). Therefore, Fr. 2 was
 presumed to be a low-molecular-weight compound consisting mainly of lignin and xylan-like polysa...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5209088</comments>
            <pubDate>Fri, 09 Sep 2011 05:48:25 +0100</pubDate>
            <guid isPermaLink="false">5209088</guid>        </item>
        <item>
            <title>Solalyratins A and B, new anti-inflammatory metabolites from Solanum lyratum</title>
            <link>http://www.medworm.com/index.php?rid=5209089&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F860247401p770863%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A new coumestan (solalyratin A, 1) and a novel cyclic eight-membered α,β-unsaturated ketone (solalyratin B, 3), together with three known compounds, puerariafuran (2), coumestrol (4) and 9-hydroxy-2′,2′-dimethylpyrano[5′,6′:2,3]-coumestan (5), were isolated from the whole plant of Solanum lyratum. Their structures were elucidated on the basis of spectroscopic analyses. In vitro, compounds 1–5 showed anti-inflammatory activities, with IC50 values in the range 6.3–9.1&amp;nbsp;μM.
 
 
	Content Type Journal ArticleCategory NotePages 1-5DOI 10.1007/s11418-011-0581-3Authors
		De-Wu Zhang, School of Pharmaceutical Science, Yantai University, 264005 Yantai, People’s Republic of ChinaYan Yang, Institute of Materia Medica, Chinese Academy of Medical Sciences, Peking...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5209089</comments>
            <pubDate>Tue, 06 Sep 2011 15:48:25 +0100</pubDate>
            <guid isPermaLink="false">5209089</guid>        </item>
        <item>
            <title>Three new megastigmanes from the leaves of Annona muricata</title>
            <link>http://www.medworm.com/index.php?rid=5209090&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4027x862876r2063%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three new megastigmanes (1–3), named annoionols A and B (1, 2) and annoionoside (3), were isolated from the leaves of Annona muricata L. (Annonaceae) together with 14 known compounds (4–17). Among the known compounds, annoionol C (4) was isolated from a natural source for the first time. The structures of all compounds were elucidated by spectroscopic
 and chemical analyses.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-8DOI 10.1007/s11418-011-0583-1Authors
		Ayano Matsushige, Department of Xenobiotic Metabolism and Molecular Toxicology, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanKatsuyoshi Matsunami, Department of Pharmacognosy, Graduate School of Biomedical Sciences, Hiroshima U...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5209090</comments>
            <pubDate>Sun, 04 Sep 2011 10:45:50 +0100</pubDate>
            <guid isPermaLink="false">5209090</guid>        </item>
        <item>
            <title>Apoptosis of HL-60 leukemia cells induced by carbazole alkaloids isolated from Murraya euchrestifolia</title>
            <link>http://www.medworm.com/index.php?rid=5184206&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc36353n126267677%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We carried out primary screening of 13 carbazole alkaloids isolated from the plant species Murraya euchrestifolia (Rutaceae) on cell growth inhibition of the human leukemia cell line HL-60. Among them, murrayafoline-A (1) and murrayazolinine (7) exhibited significant growth suppression due to apoptosis mediated by the activation of the caspase-9/caspase-3 pathway.
 
 
	Content Type Journal ArticleCategory NotePages 1-5DOI 10.1007/s11418-011-0584-0Authors
		Chihiro Ito, Department of Medicinal Chemistry, Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tempaku-ku, Nagoya, 468-8503 JapanMasataka Itoigawa, Faculty of Human Wellness, Tokai Gakuen University, 21-233 Nishinohora, Ukigai, Miyoshi, Aichi 470-0207, JapanKeisuke Nakao, Department of Medicinal Chemistry, Fac...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184206</comments>
            <pubDate>Tue, 30 Aug 2011 15:59:18 +0100</pubDate>
            <guid isPermaLink="false">5184206</guid>        </item>
        <item>
            <title>Gambogenic acid-induced time- and dose-dependent growth inhibition and apoptosis involving Akt pathway inactivation in U251 glioblastoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5184207&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fut81078760376886%2F</link>
            <description>In this study, we found that gambogenic acid (GNA), a polyprenylated xanthone isolated from the traditional
 medicine gamboge, efficiently arrested the cell cycle at the G0/G1 phase by specifically repressing the expression of cyclin D1 and cyclin E, suppressed cell proliferation, colony formation
 and cell migration, and induced caspase-dependent apoptosis in U251 glioblastoma cells in a time- and dose-dependent manner.
 The pro-apoptotic effect of GNA on U251 cells was shown to be mediated through inactivation of the Akt pathway, because GNA
 efficiently suppressed the expression level of EGFR and reduced the phosphorylation of Akt (T308) and GSK3β (S9). Furthermore,
 the combined treatment with LY294002, a specific inhibitor of the PI3K/Akt kinase pathway, and GNA showed a synergistic ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5184207</comments>
            <pubDate>Tue, 30 Aug 2011 15:59:17 +0100</pubDate>
            <guid isPermaLink="false">5184207</guid>        </item>
        <item>
            <title>A rapid one-step immunochromatographic assay for the detection of asiaticoside</title>
            <link>http://www.medworm.com/index.php?rid=5175948&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frph275860031g800%2F</link>
            <description>In this study, an immunochromatographic strip test has been developed for
 the detection of asiaticoside in plant samples that uses a monoclonal antibody against asiaticoside. The limit of detection
 for the strip test was 12.5&amp;nbsp;μg/ml. Immunoassay using monoclonal antibodies could be useful for the determination of small
 quantities of asiaticoside in plant extracts.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-5DOI 10.1007/s11418-011-0582-2Authors
		Boonchoo Sritularak, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, 10330 ThailandThaweesak Juengwatanatrakul, Faculty of Pharmaceutical Sciences, Ubon Ratchathani University, Ubon Ratchathani, 34190 ThailandWaraporn Putalun, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175948</comments>
            <pubDate>Sat, 27 Aug 2011 15:48:50 +0100</pubDate>
            <guid isPermaLink="false">5175948</guid>        </item>
        <item>
            <title>The inductive effects of Centella asiatica on rat spermatogenic cell apoptosis in vivo</title>
            <link>http://www.medworm.com/index.php?rid=5170493&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq53h74571330vp22%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Centella asiatica (L.) Urban has been traditionally used for the treatment of various disease and as a food for thousands of years in various
 parts of the world including eastern Asia, China and India. The goal of this study was to investigate the effects of Centella asiatica aqueous leaf extract on the induction of spermatogenic cell apoptosis in male rats. After lethal dose (LD50) assessment of plant extract, rats were divided in five groups. The experimental groups received orally 10, 50, 80 and 100&amp;nbsp;mg/kg
 aqueous leaf extract daily for 60&amp;nbsp;days and the control group received just water. After 60&amp;nbsp;days, body and testis weight were
 measured and blood samples were taken from the heart. To evaluate apoptosis and histological changes, tissue samples obta...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5170493</comments>
            <pubDate>Fri, 26 Aug 2011 05:49:25 +0100</pubDate>
            <guid isPermaLink="false">5170493</guid>        </item>
        <item>
            <title>Davallialactone protects against adriamycin-induced cardiotoxicity in vitro and in vivo</title>
            <link>http://www.medworm.com/index.php?rid=5161989&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7423454543626330%2F</link>
            <description>In this study, we investigated whether
 DAVA has protective effects against ADR-induced free radical accumulation and apoptosis in cardiac muscle cells and compared
 the effects of DAVA with N-acetylcysteine, a potent antioxidant. We evaluated the effect of DAVA on ADR-induced cytotoxicity by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium
 bromide) assay and crystal violet staining, the reactive oxygen species (ROS) production by flow cytometry, and the expression
 of stress-related proteins like Cu/Zn superoxide dismutase (SOD), Mn-SOD, and the involvement of mitogen-activated protein
 kinase pathway by Western blot analysis. Apoptosis was assessed by nuclear condensation and the expression levels of pro-apoptotic
 proteins, such as caspase-3 and polyadenosine diphosphate-ribos...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161989</comments>
            <pubDate>Sat, 20 Aug 2011 15:50:27 +0100</pubDate>
            <guid isPermaLink="false">5161989</guid>        </item>
        <item>
            <title>Antibacterial activity of Capsicum annuum extract and synthetic capsaicinoid derivatives against Streptococcus mutans</title>
            <link>http://www.medworm.com/index.php?rid=5161990&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F267293w461842v42%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The inhibitory effects of the ethyl acetate extract and capsaicin (1) and dihydrocapsaicin (2) isolated from fruits of Capsicum annuum chili pepper type, and synthetic capsaicinoid derivatives (N-(4-hydroxyphenylethyl)decamide (3), (E)-N-(4-hydroxy-3-methoxybenzyl)-3,7-dimethylocta-2,6-dienamide (4), 4-hydroxy-3-methoxy-N-((E)-3,7-dimethylocta-2,6-dienyl)benzamide (5) and N-(4-hydroxy-3-methoxybenzyl)decamide (6) at different concentrations were evaluated against Streptococcus mutans. The minimum inhibitory concentration at which the ethyl acetate extract prevented the growth of S. mutans was 2.5&amp;nbsp;mg/mL; those of the isolated compounds 1 and 2 were 1.25&amp;nbsp;μg/mL, while 3 was 5.0&amp;nbsp;μg/mL, and 4, 5 and 6 were 2.5&amp;nbsp;μg/mL, respectively.
 
 
	Content Type Jou...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161990</comments>
            <pubDate>Sat, 20 Aug 2011 05:42:36 +0100</pubDate>
            <guid isPermaLink="false">5161990</guid>        </item>
        <item>
            <title>Genetic diversity of Centella asiatica in China analyzed by inter-simple sequence repeat (ISSR) markers: combination analysis with chemical diversity</title>
            <link>http://www.medworm.com/index.php?rid=5161991&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5168518q838jv03n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Centella asiatica is an important plant species used in traditional Chinese medicine. To help the efficient use and conservation of this species,
 the genetic diversity of C. asiatica populations in China was investigated using inter-simple sequence repeat (ISSR) markers. Fourteen natural populations comprising
 162 individuals were included to estimate genetic diversity. At the species level, genetic diversity was relatively high (P&amp;nbsp;=&amp;nbsp;66.33%, H&amp;nbsp;=&amp;nbsp;0.2183, I&amp;nbsp;=&amp;nbsp;0.3305). At the population level, the genetic diversity of JH (Jinhua, Zhejiang Province, China) and JJ (Jiujiang, Jiangxi
 Province, China) populations was relatively high (P&amp;nbsp;=&amp;nbsp;43.88%, 38.78%, H&amp;nbsp;=&amp;nbsp;0.1610, 0.1301, I&amp;nbsp;=&amp;nbsp;0.2376, 0.1957, respectively), where...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161991</comments>
            <pubDate>Fri, 19 Aug 2011 06:42:46 +0100</pubDate>
            <guid isPermaLink="false">5161991</guid>        </item>
        <item>
            <title>Tanshinone IIA activates calcium-dependent apoptosis signaling pathway in human hepatoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5161992&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F408848h67176718h%2F</link>
            <description>In conclusion, these results
 indicate that Tan IIA-induced cancer cell apoptosis acts via activation of calcium-dependent apoptosis signaling pathways
 and upregulation of MT 1A expression.
 
 
	Content Type Journal ArticleCategory Original PaperPages 1-10DOI 10.1007/s11418-011-0576-0Authors
		Zhi-Kai Dai, Department of Pharmacology, Pharmaceutical Institute of Guilin Medical University, 541004 Guilin, ChinaJiang-Ke Qin, Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources of State Education Ministry, College of Chemistry and Chemical Engineering, Guangxi Normal University, 541004 Guilin, ChinaJiao-E Huang, Department of Pharmacology, Pharmaceutical Institute of Guilin Medical University, 541004 Guilin, ChinaYong Luo, Department of Neurology, Aerospace Hospita...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161992</comments>
            <pubDate>Fri, 19 Aug 2011 06:42:45 +0100</pubDate>
            <guid isPermaLink="false">5161992</guid>        </item>
        <item>
            <title>Micropropagation of a Thai medicinal plant for women’s health, Curcuma comosa Roxb., via shoot and microrhizome inductions</title>
            <link>http://www.medworm.com/index.php?rid=5161993&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp3377341072l7808%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We studied the effects of explant types, plant growth regulators, and sucrose concentrations on shoot and microrhizome inductions
 of Curcuma
 comosa Roxb., an important Thai medicinal plant for women’s health. Explant types significantly affected shoot induction of the
 plant. The maximum shoot multiplication rate of 11.82&amp;nbsp;±&amp;nbsp;1.03&amp;nbsp;shoots/responding explant was obtained when culturing terminal
 bud explants on semi-solid Murashige and Skoog (MS) medium supplemented with 18.16&amp;nbsp;μM thidiazuron for 8&amp;nbsp;weeks. Subsequently,
 they were transferred to a semi-solid MS medium without plant growth regulators for 4&amp;nbsp;weeks. The regenerated shoots produced
 roots spontaneously. Rooted plantlets were successfully transferred to the soil. Microrhizome ind...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161993</comments>
            <pubDate>Thu, 18 Aug 2011 05:48:12 +0100</pubDate>
            <guid isPermaLink="false">5161993</guid>        </item>
        <item>
            <title>Labisia pumila extract down-regulates hydroxysteroid (11-beta) dehydrogenase 1 expression and corticosterone levels in ovariectomized rats</title>
            <link>http://www.medworm.com/index.php?rid=5132296&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F89115mn077142042%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We evaluated the effects of a standardized Labisia pumila var. alata (LPva) extract on body weight change, hydroxysteroid (11-beta) dehydrogenase 1 (HSD11B1) expressions and corticosterone (CORT)
 level in ovariectomized (OVX) rats. The decoction of LPva has been used for generations among Malay women in Malaysia to maintain
 a healthy reproductive system.Thirty-six Sprague–Dawley OVX rats were treated orally with LPva extract (10, 20 or 50&amp;nbsp;mg/kg/day)
 or estrogen replacement (ERT) for 30&amp;nbsp;days. Sham operated rats were used as controls. Compared to untreated OVX rats, LPva-treated
 rats showed less weight gain and had significantly down-regulated HSD11B1 mRNA in liver tissues. HSD11B1 mRNA in adipose tissues increased by 55% (p&amp;nbsp;&amp;lt;&amp;nbsp;0.05) in OVX rat...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5132296</comments>
            <pubDate>Thu, 11 Aug 2011 06:02:01 +0100</pubDate>
            <guid isPermaLink="false">5132296</guid>        </item>
        <item>
            <title>Herbal formula HMC05 prevents human aortic smooth muscle cell migration and proliferation by inhibiting the ERK1/2 MAPK signaling cascade</title>
            <link>http://www.medworm.com/index.php?rid=5132297&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff15440272j6v3r10%2F</link>
            <description>In this study, we investigated the influence
 of HMC05 regulation on the MAPK/extracellular signal-regulated kinase (ERK) 1/2 signaling cascade in the inhibition of the
 migration and proliferation of human aortic smooth muscle cells (HASMCs). The inhibitory effects of HMC05 (25, 50, and 100&amp;nbsp;μg/ml)
 on tumor necrosis factor-alpha (TNF-α; 0 or 100&amp;nbsp;ng/ml)-induced HASMC migration and proliferation were investigated by wound
 migration and proliferation assays, Western blotting and reverse transcription-polymerase chain reaction. HMC05 completely
 inhibited TNF-α-induced HASMC migration and proliferation. HMC05 prevented TNF-α receptor 1-mediated phosphorylation of signal
 transduction molecules involved in MAPK signaling cascades such as MEK1/2, ERK1/2, Elk-1 transcription facto...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5132297</comments>
            <pubDate>Thu, 11 Aug 2011 06:02:00 +0100</pubDate>
            <guid isPermaLink="false">5132297</guid>        </item>
        <item>
            <title>Curcumin-like diarylpentanoid analogues as melanogenesis inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=5126472&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fml6072358842j675%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Anti-melanogenesis screening of 47 synthesized curcumin-like diarylpentanoid analogues was performed to show that some had
 a potent inhibitory effect on the melanogenesis in B16 melanoma cells. Their actions were considered to be mostly due to tyrosinase
 inhibition, tyrosinase expression inhibition, and melanin pigment degradation. The structure–activity relationships of those
 curcumin-like diarylpentanoid analogues which inhibited the melanogenesis and tyrosinase activity were also discussed. Of
 those compounds assayed, (2E,6E)-2,6-bis(2,5-dimethoxybenzylidene)cyclohexanone showed the most potent anti-melanogenesis effect, the mechanism of which
 is considered to be the degradation of the melanin pigment in B16 melanoma cells, affecting neither the tyrosinase act...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126472</comments>
            <pubDate>Wed, 10 Aug 2011 15:45:44 +0100</pubDate>
            <guid isPermaLink="false">5126472</guid>        </item>
        <item>
            <title>Antiplasmodial indole alkaloids from Leuconotis griffithii</title>
            <link>http://www.medworm.com/index.php?rid=5126473&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc888187383845kj1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A new indole alkaloid, leucoridine A N-oxide (1), consisting of two units of a strychnan type of skeleton, was isolated from the leaves of Leuconotis griffithii. Its structure was elucidated by various spectroscopic means such as NMR and MS, and also by chemical means. Antiplasmodial
 activity against Plasmodium falciparum 3D7 of indole alkaloids isolated from L. griffithii was investigated.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s11418-011-0574-2Authors
		Alfarius E. Nugroho, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-ku, Tokyo, 142-8501 JapanYusuke Hirasawa, Faculty of Pharmaceutical Sciences, Hoshi University, Ebara 2-4-41, Shinagawa-ku, Tokyo, 142-8501 JapanWong Chin Piow, Faculty of Pharmaceutical Sciences, Hoshi Un...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126473</comments>
            <pubDate>Wed, 10 Aug 2011 15:45:43 +0100</pubDate>
            <guid isPermaLink="false">5126473</guid>        </item>
        <item>
            <title>Aqueous-methanolic extract of sweet flag (Acorus calamus) possesses cardiac depressant and endothelial-derived hyperpolarizing factor-mediated coronary vasodilator effects</title>
            <link>http://www.medworm.com/index.php?rid=5126474&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0747683051680077%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This investigation was aimed to probe the pharmacological base of medicinal use of Acorus calamus in ischemic heart diseases. Effect on heart parameters was studied in isolated rabbit heart while coronary vasodilator effect
 was studied in isolated bovine coronary arterial rings, suspended in tissue baths filled with Krebs solution, maintained at
 37°C, aerated with carbogen and responses were measured on PowerLab data acquisition system. In Langendorrf’s perfused rabbit
 heart, the crude extract of Acorus calamus (Ac.Cr) at 0.01–10&amp;nbsp;mg/mL partially suppressed force of ventricular contractions (FVC), heart rate (HR) and coronary flow
 (CF). The ethylacetate fraction completely suppressed FVC, partially suppressed HR and CF, while the nHexane fraction exhibited ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126474</comments>
            <pubDate>Tue, 09 Aug 2011 05:43:28 +0100</pubDate>
            <guid isPermaLink="false">5126474</guid>        </item>
        <item>
            <title>Inhibitory activities of Puerariae Flos against testosterone 5α-reductase and its hair growth promotion activities</title>
            <link>http://www.medworm.com/index.php?rid=5109642&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd78224148482p523%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Crude drugs expected to have an estrogenic effect were screened for their inhibitory activity on testosterone 5α-reductase.
 Testosterone 5α-reductase is an enzyme catalyzing the conversion of testosterone to dihydrotestosterone, which possesses high
 affinity for the androgen receptor. Among the crude drugs tested, we focused on Puerariae Flos (the flowers of Pueraria thomsonii) due to its potent inhibitory activity and suitability for commercial use. The 50% ethanolic extract of Puerariae Flos (PF-ext)
 showed inhibitory activity of 60.2% at 500&amp;nbsp;μg/ml against testosterone 5α-reductase. Interestingly, it was more potent than
 that of Puerariae Radix (roots of Pueraria lobata). PF-ext also showed in vivo anti-androgenic activity using a hair growth assay in tes...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109642</comments>
            <pubDate>Sat, 06 Aug 2011 05:59:39 +0100</pubDate>
            <guid isPermaLink="false">5109642</guid>        </item>
        <item>
            <title>A new iridoid glycoside and NO production inhibitory activity of compounds isolated from Russelia equisetiformis</title>
            <link>http://www.medworm.com/index.php?rid=5109641&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw022l338j82g2521%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;From the 1-BuOH-soluble fraction of a MeOH extract of the leaves of Russelia equisetiformis, one new iridoid glucoside was isolated along with 24 known compounds, comprising iridoids and iridoid glucosides, phenyl
 propane glucosides, phenyl ethanoids, lignan glucosides, and flavonoid glucosides. The structure of the new compound was elucidated
 to be 10-O-cinnamoyl sinuatol. Of the 25 compounds isolated, rehmaglutin B exhibited moderate inhibitory activity toward NO production,
 which was not associated with cytotoxicity.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s11418-011-0569-zAuthors
		Madoka Ochi, Department of Pharmacognosy, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanKatsuyoshi Matsu...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109641</comments>
            <pubDate>Sat, 06 Aug 2011 05:59:39 +0100</pubDate>
            <guid isPermaLink="false">5109641</guid>        </item>
        <item>
            <title>Antitrypanosomal activities of acetylated bruceines A and C; a structure–activity relationship study</title>
            <link>http://www.medworm.com/index.php?rid=5109640&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe6g530668162u34k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The crude extract of Brucea javanica showed strong in vitro inhibitory activity against Trypanosoma evansi. Among the isolated quassinoids, bruceines A, C, and bruceantinol were found to be the most potent compounds against T. evansi. To gain a deeper understanding of the relationship between the free hydroxyl groups and the activity, several O-acetylated derivatives of bruceines A and C were synthesized and their in vitro antitrypanosomal activities against trypomastigotes
 of T. evansi were examined and compared with those of the original compounds. The following structure–activity relationships were observed:
 (1) the free hydroxyl groups at positions C-3, C-11, and C-12 are essential for antitrypanosomal activity; (2) the C-11 and
 C-12 hydroxyl groups are more im...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109640</comments>
            <pubDate>Sat, 06 Aug 2011 05:59:39 +0100</pubDate>
            <guid isPermaLink="false">5109640</guid>        </item>
        <item>
            <title>Two new indole alkaloids, 2-(3,3-dimethylprop-1-ene)-costaclavine and 2-(3,3-dimethylprop-1-ene)-epicostaclavine, from the marine-derived fungus Aspergillus fumigatus</title>
            <link>http://www.medworm.com/index.php?rid=5079674&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr7pm831381487676%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new indole alkaloids, 2-(3,3-dimethylprop-1-ene)-costaclavine (1) and 2-(3,3-dimethylprop-1-ene)-epicostaclavine (2), together with the known compounds costaclavine (3), fumgaclavine A (4) and C (5), were isolated from the marine-derived fungus Aspergillus fumigatus. The planar structures of the two new compounds were elucidated on the basis of chemical and physicochemical evidence including
 MS, UV, IR and NMR spectra. Their stereochemistry was studied by NOESY, 1H–1H coupling constant and CD spectra. The compounds 1, 2, 3 and 5 showed weak cytotoxicity against a mouse leukemia cell line (P388).
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s11418-011-0565-3Authors
		Dahai Zhang, Department of Chemistry, School of Science, The University of Tokyo, 7-3-1 H...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5079674</comments>
            <pubDate>Wed, 27 Jul 2011 05:49:48 +0100</pubDate>
            <guid isPermaLink="false">5079674</guid>        </item>
        <item>
            <title>Insights into mechanisms underlying the gut and airways modulatory effects of Swertia chirata</title>
            <link>http://www.medworm.com/index.php?rid=5079675&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F10708uq307408204%2F</link>
            <description>This study was carried out in order
 to provide a pharmacological basis for its medicinal use in gastrointestinal and respiratory disorders. Crude extract of Swertia chirata (Sc.Cr) and its fractions were studied using rabbit isolated tissue preparations. In jejunum, Sc.Cr, which tested positive
 for alkaloids, flavonoids, saponins, tannins, and terpenes, caused stimulation at concentrations of 0.01–1.0&amp;nbsp;mg/mL, followed
 by a relaxant effect at higher concentrations. In the presence of atropine, the contractile effect was blocked and only relaxation
 occurred. Sc.Cr inhibited high K+ (80&amp;nbsp;mM)-induced contractions at 0.01–10&amp;nbsp;mg/mL and shifted Ca2+ concentration–response curves to the right, similar to that caused by verapamil. In trachea, Sc.Cr relaxed the carbachol
 (1&amp;n...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5079675</comments>
            <pubDate>Wed, 27 Jul 2011 05:49:47 +0100</pubDate>
            <guid isPermaLink="false">5079675</guid>        </item>
        <item>
            <title>New α-glucosides of caffeoyl quinic acid from the leaves of Moringa oleifera Lam.</title>
            <link>http://www.medworm.com/index.php?rid=5030614&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw506n854670tm6u2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new caffeoyl quinic acid α-glucosides, together with three known caffeoyl quinic acids and five known flavonoid glucosides,
 were isolated from the leaves of Moringa oleifera Lam. The structures of the new compounds were elucidated as 4-O-(4′-O-α-d-glucopyranosyl)-caffeoyl quinic acid (1) and 4-O-(3′-O-α-d-glucopyranosyl)-caffeoyl quinic acid (2) by spectroscopic analyses.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s11418-011-0563-5Authors
		Yoshiki Kashiwada, Graduate School of Pharmaceutical Sciences, University of Tokushima, Shomochi 1-78, Tokushima, 770-8505 JapanFakhruddin Ali Ahmed, Graduate School of Pharmaceutical Sciences, University of Tokushima, Shomochi 1-78, Tokushima, 770-8505 JapanShin-ichiro Kurimoto, Graduate School of Pharmaceutic...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030614</comments>
            <pubDate>Tue, 12 Jul 2011 06:10:41 +0100</pubDate>
            <guid isPermaLink="false">5030614</guid>        </item>
        <item>
            <title>Phenolic lipid ingredients from cashew nuts</title>
            <link>http://www.medworm.com/index.php?rid=5020958&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F276w5120434p1554%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Five new phenolic lipids, 2-(8″Z-eicosenoyl)-6-(8′Z-pentadecenyl) salicylic acid (3), 2-(9″Z-hexadecenoyl)-6-(8′Z, 11′Z-pentadecadienyl) methyl salicylate (5), 2-(10″Z, 13″Z-nonadecadienoyl)-6-(8′Z, 11′Z-pentadecadienyl) salicylic acid (6), 2-(16″Z-pentacosenoyl)-6-(8′Z-pentadecenyl) salicylic acid (7) and 2-(9″Z-octadecenoyl)-6-(8′Z, 11′Z-pentadecadienyl) methyl salicylate (8), and three known compounds, cardols (1), anacardic acid (2) and cardanols (4), were isolated from the nuts of the cashew, Anacardium occidentale L. The structures were established on the basis of detailed MS and NMR spectroscopic analyses. Compound 1 highly enhanced both Th-1 (IL-2, IFN-γ) and Th-2 (IL-4, IL-5) cytokine production, and compounds 7 and 8 highly increas...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020958</comments>
            <pubDate>Thu, 07 Jul 2011 05:44:41 +0100</pubDate>
            <guid isPermaLink="false">5020958</guid>        </item>
        <item>
            <title>Antipsychotic property of aqueous and ethanolic extracts of Lonchocarpus cyanescens (Schumach and Thonn.) Benth. (Fabaceae) in rodents</title>
            <link>http://www.medworm.com/index.php?rid=4999371&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh2h1p10048n82613%2F</link>
            <description>This study was designed to examine whether the aqueous and ethanolic extracts of LC possess antipsychotic property
 in rats. The antipsychotic effects of the extracts were assessed using the amphetamine animal model of psychosis in rats.
 The effect of the extracts on spontaneous motor activity was also studied in the open field test in mice. The extrapyramidal
 side effect of catalepsy was tested based on the ability of the extracts to alter the duration of akinesia in mice placed
 on a vertical wrapped string. Aqueous and ethanolic extracts of LC (25–400&amp;nbsp;mg/kg, i.p.) significantly (p&amp;nbsp;&amp;lt;&amp;nbsp;0.05) suppressed stereotyped behaviour induced by amphetamine (10.0&amp;nbsp;mg/kg, i.p.) in rats, which suggest antipsychotic activity.
 The extracts (25–400&amp;nbsp;mg/kg, i.p.) further pr...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4999371</comments>
            <pubDate>Thu, 30 Jun 2011 06:10:07 +0100</pubDate>
            <guid isPermaLink="false">4999371</guid>        </item>
        <item>
            <title>Protective effect of Pueraria tuberosa DC. embedded biscuit on cisplatin-induced nephrotoxicity in mice</title>
            <link>http://www.medworm.com/index.php?rid=4999370&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F22mg124640pg7v25%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recently, the nephroprotective property of Pueraria tuberosa DC. tuber (PT) has been reported by our group. Here, PT-embedded biscuits were prepared and tested on cisplatin-induced nephrotoxicity
 in Swiss albino mice. The PT powder was characterized by RAPD (random amplified polymorphic DNA) to ascertain its authenticity
 and PT biscuits were prepared in different concentrations (1, 2, or 4&amp;nbsp;g of PT powder). These biscuits were given as diet for
 a total of 10&amp;nbsp;days, but on the 7th&amp;nbsp;day cisplatin injection (8&amp;nbsp;mg/kg bw, i.p.) was given. On the 10th&amp;nbsp;day animals were killed
 to collect kidneys for assessment of antioxidant status. Blood samples were collected on both the 7th and 10th&amp;nbsp;days for assessment
 of liver and kidney functions. In mice, P...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4999370</comments>
            <pubDate>Thu, 30 Jun 2011 06:10:07 +0100</pubDate>
            <guid isPermaLink="false">4999370</guid>        </item>
        <item>
            <title>Studies on chemical fingerprints of Siraitia grosvenorii fruits (Luo Han Guo) by HPLC</title>
            <link>http://www.medworm.com/index.php?rid=4993751&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn6u0158135020774%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A novel, efficient, and accurate fingerprinting method using high performance liquid chromatography–photodiode array detection
 has been developed and optimized for the investigation and demonstration of the variance in chemical properties among Siraitia grosvenorii fruits from different origins. The effects of growth stages, cultivated varieties, collection locations, and fruit portions
 of the herb on chromatographic fingerprints were examined. Eleven compounds were identified on chromatograms by comparing
 the retention time and UV spectrum of each peak separately with those of external references. The results revealed that chromatographic
 fingerprints, combining similarity or hierarchical clustering analysis along with reference compounds, could efficiently ident...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993751</comments>
            <pubDate>Wed, 29 Jun 2011 10:50:57 +0100</pubDate>
            <guid isPermaLink="false">4993751</guid>        </item>
        <item>
            <title>Inhibition of cyclooxygenase-2 and inducible nitric oxide synthase by silymarin in proliferating mesenchymal stem cells: comparison with glutathione modifiers</title>
            <link>http://www.medworm.com/index.php?rid=4993752&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1360731504483752%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Silymarin, a mixture of flavonolignans, is extracted from milk thistle (Silybum marianum) and has a strong antioxidant activity and exhibits anticarcinogenic, anti-inflammatory, and cytoprotective effects. In this
 study we attempted to determine whether silymarin and the glutathione modifiers, buthionine sulfoxamine (BSO) and N-acetylcysteine (NAC), are involved in regulation of cyclooxygenase (COX)-2 and inducible nitric oxide synthase (iNOS) in
 proliferating mesenchymal stem cells (MSCs). Cellular glutathione was manipulated during a 14-day culture using BSO, NAC and
 silymarin. At intervals of 2, 7 and 14&amp;nbsp;days, cells were collected and COX-2 and iNOS levels were measured. In parallel, generation
 of cellular H2O2 and glutathione were measured. Supplementation ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993752</comments>
            <pubDate>Tue, 28 Jun 2011 05:56:54 +0100</pubDate>
            <guid isPermaLink="false">4993752</guid>        </item>
        <item>
            <title>New advanced glycation end-products inhibitors from Dichrostachys cinerea Wight &amp; Arn.</title>
            <link>http://www.medworm.com/index.php?rid=4970509&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8607873rv3m27322%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Free radical scavenging and advanced glycation end-product (AGE) inhibitory potential were evaluated in the crude methanol
 extract of Dichrostachys cinerea. Bioassay-guided isolation led to the identification of four flavan-3-ols, namely (−)-mesquitol (1), oritin (2), (−)-festidinol (3) and (−)-epicatechin (4). Analysis of structure–activity relationships revealed that the presence of 7,8-dihydroxyl groups in the A-ring of flavan-3-ols
 in conjunction with 3′,4′-dihydroxyls in the B-ring (1) is an important criterion for displaying potent AGE inhibitory activity along with free radical scavenging properties. (−)-Mesquitol
 (1), oritin (2), and (−)-festidinol (3) were found to be new natural AGE inhibitors. (−)-Mesquitol (1) displayed the most potent A...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4970509</comments>
            <pubDate>Fri, 24 Jun 2011 16:14:59 +0100</pubDate>
            <guid isPermaLink="false">4970509</guid>        </item>
        <item>
            <title>Qualitative and quantitative determination of ten iridoids and secoiridoids in Gentiana straminea Maxim. by LC-UV-ESI-MS</title>
            <link>http://www.medworm.com/index.php?rid=4970510&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft437x05105784h16%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A simple and accurate HPLC-UV/MS method was developed for the simultaneous determination of ten iridoids and secoiridoids
 in the roots of Gentiana straminea Maxim. Separations were performed on a Kromasil-C18 column by gradient elution using methanol and water containing phosphoric
 acid. Analytes were identified by HPLC coupled with ESI-MS experiments. The chromatographic method was validated for selectivity,
 linearity, precision, limit of detection, limit of quantification, accuracy, and stability. The developed assay could be considered
 as a suitable quality control method for G. straminea and other “Qinjiao” herbs.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s11418-011-0560-8Authors
		Shihu Wei, College of Life Science and Technology, Beijing Univer...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4970510</comments>
            <pubDate>Thu, 23 Jun 2011 05:58:00 +0100</pubDate>
            <guid isPermaLink="false">4970510</guid>        </item>
        <item>
            <title>Pretreatment with morin, a flavonoid, ameliorates adenosine triphosphatases and glycoproteins in isoproterenol-induced myocardial infarction in rats</title>
            <link>http://www.medworm.com/index.php?rid=4970511&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa02t15664641q3l8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this investigation was to evaluate the preventive role of morin, a flavonoid, on cardiac marker enzymes such as
 aspartate transaminase, lactate dehydrogenase, creatine kinase and creatine kinase-MB, membrane-bound enzymes such as sodium
 potassium-dependent adenosine triphosphatase, calcium-dependent adenosine triphosphatase and magnesium-dependent adenosine
 triphosphatase, and glycoproteins such as hexose, hexosamine, fucose and sialic acid in isoproterenol (ISO)-induced myocardial
 infarction (MI) in rats. Male albino Wistar rats were pretreated with morin (20, 40 and 80&amp;nbsp;mg/kg) daily for a period of 30&amp;nbsp;days.
 After the treatment period, ISO (85&amp;nbsp;mg/kg) was subcutaneously injected into the rats at an interval of 24&amp;nbsp;h for 2&amp;nbsp;days. ISO...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4970511</comments>
            <pubDate>Thu, 23 Jun 2011 05:57:59 +0100</pubDate>
            <guid isPermaLink="false">4970511</guid>        </item>
        <item>
            <title>Growth inhibition and apoptotic effect of alpha-eleostearic acid on human breast cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=4970512&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq4724566301535v6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Alpha-eleostearic acid (α-ESA) is a natural and biologically active compound which possesses potent antioxidant and anti-tumor
 activity. The purpose of this study was to confirm the anticancer activity of α-ESA against human breast cancer cells and
 to further elucidate its mechanism of activity. Human breast cancer cells and normal liver cells were used for in-vitro tests
 of the anticancer activity of α-ESA, including cytotoxicity, colony formation inhibition, EdU incorporation, AO/EB staining
 of apoptotic cells, cell cycle distribution through flow cytometry, and PPARγ, p21, Bax, p53, and caspase-3 mRNA expressions
 through RT-PCR. After α-ESA treatment, the proliferation, colony formation, and EdU labeling indices of cancer cells decreased
 (p&amp;nbsp;&amp;lt;&amp;nbsp;...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4970512</comments>
            <pubDate>Tue, 21 Jun 2011 18:34:17 +0100</pubDate>
            <guid isPermaLink="false">4970512</guid>        </item>
        <item>
            <title>Hypolipidemic activity of Symplocos cochinchinensis S. Moore leaves in hyperlipidemic rats</title>
            <link>http://www.medworm.com/index.php?rid=4946655&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq7061pj2110365gw%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The hypolipidemic activity of Symplocos cochinchinensis S. Moore leaves was studied in Triton WR-1339- and high fat diet-induced hyperlipidemic rats. In Triton WR-1339-induced hyperlipidemic
 rats, the hexane extract (250 and 500&amp;nbsp;mg/kg) exerted a significant (P&amp;nbsp;&amp;lt;&amp;nbsp;0.01) lipid-lowering effect compared to ethyl acetate and methanol extracts, as assessed by the reversal of the plasma
 levels of total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein
 cholesterol (LDL-C). In high fat diet-fed hyperlipidemic rats, the hexane extract (250 and 500&amp;nbsp;mg/kg) caused the lowering
 of lipid levels in the plasma and liver. The hypolipidemic activity of S. cochinchinensis leaves was compared with fenofi...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946655</comments>
            <pubDate>Fri, 17 Jun 2011 12:00:50 +0100</pubDate>
            <guid isPermaLink="false">4946655</guid>        </item>
        <item>
            <title>Three new flavonoid glycosides from Oxytropis myriophylla</title>
            <link>http://www.medworm.com/index.php?rid=4946656&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn263529256r45v54%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three new flavonoids, myriophylloside I, II and III, were isolated from Oxytropis myriophylla (Leguminosae), together with four known flavonoid glycosides: isorhamnetin-3-O-β-d-glucoside, isorhamnetin-3-O-α-l-arabinosyl(1→6)-β-d-glucoside, quercetin and rutin. The structural elucidations of all the compounds were based on extensive spectroscopic methods,
 including HRESIMS and 2D-NMR experiments (HSQC, HMBC, 1H–1H COSY and HSQC-TOCSY), UV, IR and chemical evidence, together with comparison with reference values.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s11418-011-0551-9Authors
		Gaimei She, School of Chinese Pharmacy, Beijing University of Chinese Medicine, No. 6, Zhonghuan South Road, Wangjing District, Beijing, 100102 People’s Republic of ChinaFa...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946656</comments>
            <pubDate>Wed, 15 Jun 2011 05:49:51 +0100</pubDate>
            <guid isPermaLink="false">4946656</guid>        </item>
        <item>
            <title>Patchouli alcohol: in vitro direct anti-influenza virus sesquiterpene in Pogostemon cablin Benth.</title>
            <link>http://www.medworm.com/index.php?rid=4946657&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8472268002112260%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During the screening of anti-influenza virus substances from traditional herbal medicines, the methanol extract from the leaves
 of Pogostemon cablin Benth. showed potent in vitro antiviral activity (99.8% inhibition at a concentration of 10&amp;nbsp;μg/mL) against influenza virus
 A/PR/8/34 (H1N1). The anti-influenza virus principle was isolated from the hexane-soluble fraction, through solvent fractionation,
 repeated silica gel column chromatography, and reversed-phase HPLC. The major active principle was a volatile substance that
 was identified as a sesquiterpene, patchouli alcohol (1), on the basis of its spectral analyses. When anti-influenza virus activity against A/PR/8/34 was evaluated by the plaque
 forming assay, patchouli alcohol reduced the number of plaques ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946657</comments>
            <pubDate>Tue, 14 Jun 2011 06:01:28 +0100</pubDate>
            <guid isPermaLink="false">4946657</guid>        </item>
        <item>
            <title>Coptisine inhibits RANKL-induced NF-κB phosphorylation in osteoclast precursors and suppresses function through the regulation of RANKL and OPG gene expression in osteoblastic cells</title>
            <link>http://www.medworm.com/index.php?rid=4937251&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq0023q356m042170%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Excessive receptor activator of NF-κB ligand (RANKL) signaling causes enhanced osteoclast formation and bone resorption. The
 downregulation of RANKL expression and its downstream signals may be an effective therapeutic approach to the treatment of
 bone loss diseases such as osteoporosis. Here, we found that coptisine, one of the isoquinoline alkaloids from Coptidis Rhizoma, exhibited inhibitory effects on osteoclastogenesis in vitro. Although coptisine has been studied for its antipyretic, antiphotooxidative,
 dampness dispelling, antidote, antinociceptive, and anti-inflammatory activities in vitro and in vivo, its effects on osteoclastogenesis
 have not been investigated. Therefore, we evaluated the effects of coptisine on osteoblastic cells as well as osteoclast pr...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4937251</comments>
            <pubDate>Thu, 09 Jun 2011 05:48:19 +0100</pubDate>
            <guid isPermaLink="false">4937251</guid>        </item>
        <item>
            <title>Phellinus baumii ethyl acetate extract inhibits lipopolysaccharide-induced iNOS, COX-2, and proinflammatory cytokine expression in RAW264.7 cells</title>
            <link>http://www.medworm.com/index.php?rid=4937250&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9t223w4351815j72%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Mushrooms are valuable sources of biologically active compounds possessing anticancer, antiplatelet, and anti-inflammatory
 properties. Phellinus baumii is a mushroom used in folk medicine for a variety of human diseases. However, its potential anti-inflammatory effect has
 remained unclear. Therefore, we studied the effect of P. baumii ethyl acetate extract (PBEAE) on inflammatory mediator and proinflammatory cytokine protein and/or mRNA expression levels
 using the nitric oxide (NO) assay, enzyme immunoassay (EIA), western blot, and reverse transcription polymerase chain reaction
 (RT–PCR) in lipopolysaccharide (LPS)-stimulated macrophage like RAW264.7 cells. PBEAE markedly inhibited NO generation and
 prostaglandin E2 (PGE2) synthesis in a concentration-dependent p...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4937250</comments>
            <pubDate>Thu, 09 Jun 2011 05:48:19 +0100</pubDate>
            <guid isPermaLink="false">4937250</guid>        </item>
        <item>
            <title>Promoting the effect of chemical constituents from the flowers of Poacynumhendersonii on adipogenesis in 3T3-L1 cells</title>
            <link>http://www.medworm.com/index.php?rid=4913839&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8p1q275533r56770%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A novel sugar ester poacynose (1) was isolated from the flowers of Poacynum
 hendersonii together with 31 known compounds. The structure of 1 was established mainly on the basis of 1D and 2D NMR spectral data. Among the isolates, several constituents, such as kaempferol
 3-O-sophoroside (5), picein (16), and 4-hydroxybenzoic acid 4-O-β-d-glucopyranoside (17) moderately promoted adipogenesis of 3T3-L1 cells. In addition, simultaneous quantitative analysis of eight flavonoid constituents
 from the flower and leaf parts of P.
 hendersonii was developed.
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s11418-011-0549-3Authors
		Toshio Morikawa, Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, JapanKats...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913839</comments>
            <pubDate>Mon, 06 Jun 2011 14:57:53 +0100</pubDate>
            <guid isPermaLink="false">4913839</guid>        </item>
        <item>
            <title>Triterpenes involved in the anti-inflammatory effect of ethanolic extract of Pterodon emarginatus Vogel stem bark</title>
            <link>http://www.medworm.com/index.php?rid=4913840&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr720k2jj6248p130%2F</link>
            <description>In conclusion, EtEx has antinociceptive
 effects arising from anti-inflammatory activity; this activity could be due to the presence of lupeol and betulin.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s11418-011-0547-5Authors
		Weuller F. de Moraes, Laboratório de Pesquisa em Produtos Naturais, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia, GO, BrazilPablinny Moreira Galdino, Laboratório de Farmacologia de Produtos Naturais, Instituto de Ciências Biológicas, Universidade Federal de Goiás, Sala 216, ICB 2, CP 131, Goiânia, GO 74001-970, BrazilMarcus Vinícius M. Nascimento, Laboratório de Farmacologia de Produtos Naturais, Instituto de Ciências Biológicas, Universidade Federal de Goiás, Sala 216, ICB 2, CP 131, Goiânia, GO 74001-970, BrazilFrederico Ar...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913840</comments>
            <pubDate>Sat, 04 Jun 2011 06:06:15 +0100</pubDate>
            <guid isPermaLink="false">4913840</guid>        </item>
        <item>
            <title>Factors affecting podophyllotoxin yield in the ex situ grown Podophyllum hexandrum, an endangered alpine native of the western Himalayas</title>
            <link>http://www.medworm.com/index.php?rid=4904286&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F62h561851q865422%2F</link>
            <description>This study reports an appreciable yield of podophyllotoxin (PDT) in P. hexandrum plants grown ex situ under polyhouse conditions of a temperate locale. The PDT content of below-ground parts was affected
 by both plant age and growth period. However, only the effect of plant age on PDT content was significant. Thus, the highest
 amounts of PDT were recorded in the below-ground parts of 2-year-old plants harvested during the late-growth period (LGP).
 High total soluble sugars in the below-ground parts during the early growth period (EGP) and the highest nitrate and nitrate
 reductase in the leaves of 2-year-old plants during the peak-growth period (PGP) indicated higher mobilization and assimilation
 of starch and nitrate. Probably the surplus carbon and nitrogen gained during the PGP were ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4904286</comments>
            <pubDate>Mon, 30 May 2011 17:09:53 +0100</pubDate>
            <guid isPermaLink="false">4904286</guid>        </item>
        <item>
            <title>Neuroprotective effect of ginkgolide K against acute ischemic stroke on middle cerebral ischemia occlusion in rats</title>
            <link>http://www.medworm.com/index.php?rid=4904287&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuk13734674111835%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ginkgolide K, a natural platelet-activating factor receptor antagonist, was isolated from the leaves of Ginkgo biloba. However, little is known about its neuroprotective effect in ischemia–reperfusion (I/R)-induced cerebral injury. Hence,
 the present study was carried out to investigate the effect of ginkgolide K on neuroprotection and the potential mechanisms
 in the rat I/R model induced by middle cerebral artery occlusion (MCAO). The rats were pretreated with ginkgolide K 2, 4 and
 8&amp;nbsp;mg/kg (i.v.) once a day for 5&amp;nbsp;days before MCAO. Neurological deficit score (NDS), brain water content, 2,3,5-triphenyltetrazolium
 chloride (TTC) staining and pathology of brain tissue, as well as indexes of oxidative stress [superoxide dismutase (SOD),
 malondialdehyde (MDA...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4904287</comments>
            <pubDate>Wed, 25 May 2011 06:17:24 +0100</pubDate>
            <guid isPermaLink="false">4904287</guid>        </item>
        <item>
            <title>Vascular relaxation induced by aqueous extract of Lespedeza cuneata via the NO-cGMP pathway</title>
            <link>http://www.medworm.com/index.php?rid=4904288&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa76m61482w4p323p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aqueous extract of Lespedeza cuneata G. Don. (ALC) induced vasorelaxation of phenylephrine precontracted aorta in a dose-dependent manner. This effect disappeared
 in the absence of functional endothelium. Pretreatment of the aortic tissues with NG-nitro-l-arginine methyl ester (l-NAME), or 1H-[1,2,4]-oxadiazole-[4,3-α]-quinoxalin-1-one (ODQ) blocked ALC-induced vascular relaxation. Incubation of endothelium-intact
 thoracic aortic rings with ALC increased cGMP production. ALC-induced cGMP production was blocked by pretreatment with l-NAME or ODQ. ALC-induced vascular relaxation was also markedly attenuated by addition of verapamil or diltiazem, but was
 not blocked by pretreatment with indomethacine, glibenclamide, tetraethylammonium, atropine, or propranolol. The...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4904288</comments>
            <pubDate>Tue, 24 May 2011 05:53:55 +0100</pubDate>
            <guid isPermaLink="false">4904288</guid>        </item>
        <item>
            <title>Pharmacological effect of carvacrol on d-galactosamine-induced mitochondrial enzymes and DNA damage by single-cell gel electrophoresis</title>
            <link>http://www.medworm.com/index.php?rid=4904289&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk760401m1771l262%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The present study aimed at investigating the effect of carvacrol on hepatic mitochondrial enzyme activities and DNA damage
 in d-galactosamine (d-GalN)-induced hepatotoxicity in male albino Wistar rats. The activities of hepatic mitochondrial enzymes such as isocitrate
 dehydrogenase, α-ketoglutarate dehydrogenase, succinate dehydrogenase, malate dehydrogenase, NADPH dehydrogenase and cytochrome
 c oxidase significantly decreased in d-GalN-hepatotoxic rats, and administration of carvacrol brought these parameters towards normality. In d-GalN-hepatotoxic rats, the hepatic mitochondrial concentration of thiobarbituric acid reactive substances significantly increased,
 and administration of carvacrol significantly reduced them towards normality. Furthermore, the activitie...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4904289</comments>
            <pubDate>Sat, 21 May 2011 23:22:19 +0100</pubDate>
            <guid isPermaLink="false">4904289</guid>        </item>
        <item>
            <title>Screening of promising chemotherapeutic candidates against human adult T-cell leukemia/lymphoma from plants: active principles from Physalis pruinosa and structure–activity relationships with withanolides</title>
            <link>http://www.medworm.com/index.php?rid=4831818&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy57386566m643851%2F</link>
            <description>In this study,
 214 extracts from 162 plants belonging to 65 families were screened for the purpose of elucidating the anti-proliferative
 effect against HTLV-1-infected T-cell lines. Extracts from aerial parts of Physalis pruinosa showed potent inhibitory effect. We isolated five withanolides from the extracts by activity-guided fractionation and examined
 the structure–activity relationships. The presence of a 5β,6β-epoxy function is suggested to be essential for the activity,
 and the most active principle showed selective toxicity to HTLV-1-infected T-cell lines.
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s11418-011-0543-9Authors
		Daisuke Nakano, Faculty of Pharmaceutical Sciences, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180 JapanKenji Ishitsuka, Di...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4831818</comments>
            <pubDate>Sat, 14 May 2011 05:47:21 +0100</pubDate>
            <guid isPermaLink="false">4831818</guid>        </item>
        <item>
            <title>In vitro screening for antihyperlipidemic activities in foodstuffs by evaluating lipoprotein profiles secreted from human hepatoma cells</title>
            <link>http://www.medworm.com/index.php?rid=4831819&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn12112uj57mlk666%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We screened the antihyperlipidemic effects of seven edible plants by evaluation of the triglyceride (TG) and cholesterol profiles
 secreted from HepG2 cells. We found that the water- and ethanol-extracts of Brasenia schreberi at 100&amp;nbsp;μg/ml exhibited strong inhibitory activities against TG and cholesterol secretions from HepG2 cells stimulated with
 sodium oleate. Real-time RT-PCR analysis demonstrated that ethanol extract of B. schreberi (BSET) attenuated the expression of the sterol regulatory element binding protein-1c and -2, fatty acid synthase and HMG
 CoA synthase-1 genes, which are involved in lipid synthesis in hepatocyte/hepatoma cells. Furthermore, we studied the action
 of BSET on adipose tissue accumulation and serum parameters in mice fed a high-fat di...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4831819</comments>
            <pubDate>Thu, 12 May 2011 18:54:16 +0100</pubDate>
            <guid isPermaLink="false">4831819</guid>        </item>
        <item>
            <title>Hypotensive effect of the water extract of the leaves of Pseuderanthemum palatiferum</title>
            <link>http://www.medworm.com/index.php?rid=4822198&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb723475202678j06%2F</link>
            <description>In conclusion, the water extract from fresh leaves of P. palatiferum possessed hypotensive and bradycardic effects. The vasorelaxant effect of the extract was dependent partly on the vascular
 endothelium but was not dependent on the synthesis of nitric oxide and did not act through activation of the muscarinic receptor.
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s11418-011-0540-zAuthors
		Parirat Khonsung, Department of Pharmacology, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200 ThailandA. Panthong, Department of Pharmacology, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200 ThailandN. Chiranthanut, Department of Pharmacology, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200 ThailandS. Intahphuak, McCormick Faculty of Nursing, Payap Uni...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4822198</comments>
            <pubDate>Tue, 10 May 2011 05:55:24 +0100</pubDate>
            <guid isPermaLink="false">4822198</guid>        </item>
        <item>
            <title>Glycyrrhiza glabra (Linn.) and Lavandula officinalis (L.) cell suspension cultures-based biotransformation of β-artemether</title>
            <link>http://www.medworm.com/index.php?rid=4806126&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F233x7l62545k604q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The biotransformation of β-artemether (1) by cell suspension cultures of Glycyrrhiza glabra and Lavandula officinalis is reported here for the first time. The major biotransformed product appeared as a grayish-blue color spot on thin-layer
 chromatography (TLC) with transparent crystal-like texture. Based on its infrared (IR) and 1H nuclear magnetic resonance (NMR) spectra, the product was characterized as a tetrahydrofuran (THF)–acetate derivative (2). The highest conversion efficiencies of 57 and 60% were obtained when 8–9-day-old cell suspensions of G. glabra and L. officinalis were respectively fed with 4–7&amp;nbsp;mg of compound 1 in 40&amp;nbsp;ml of medium per culture and the cells were harvested after 2–5&amp;nbsp;days of incubation. The addition of compound 1 at ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4806126</comments>
            <pubDate>Thu, 05 May 2011 05:45:16 +0100</pubDate>
            <guid isPermaLink="false">4806126</guid>        </item>
        <item>
            <title>Tinospora cordifolia attenuates oxidative stress and distorted carbohydrate metabolism in experimentally induced type 2 diabetes in rats</title>
            <link>http://www.medworm.com/index.php?rid=4790399&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr761628v11p10x60%2F</link>
            <description>In conclusion, the traditional
 plant Tinospora cordifolia mediates its anti-diabetic potential through mitigating oxidative stress, promoting insulin secretion and also by inhibiting
 gluconeogenesis and glycogenolysis, thereby regulating blood glucose.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s11418-011-0538-6Authors
		Marimuthu Kannan Sangeetha, Herbal and Indian Medicine Research Laboratory, Department of Biochemistry, Sri Ramachandra University, Chennai, 600116 IndiaHanumantha Rao Balaji Raghavendran, Herbal and Indian Medicine Research Laboratory, Department of Biochemistry, Sri Ramachandra University, Chennai, 600116 IndiaVeeraraghavan Gayathri, Herbal and Indian Medicine Research Laboratory, Department of Biochemistry, Sri Ramachandra University, Chennai, 600116 IndiaH...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4790399</comments>
            <pubDate>Tue, 03 May 2011 05:45:33 +0100</pubDate>
            <guid isPermaLink="false">4790399</guid>        </item>
        <item>
            <title>Genetic variation of Croton stellatopilosus Ohba based on non-coding DNA sequences of ITS, trnK and trnL-F regions</title>
            <link>http://www.medworm.com/index.php?rid=4745143&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa7853m1h96g27k50%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Croton stellatopilosus Ohba (Plau-noi), a well-known Thai medicinal plant, was investigated for its genetic variation by analyzing three DNA regions,
 one nuclear internal transcribed spacer (ITS) region and two chloroplast trnL-F intergenic spacer and trnK intron regions. The results of ITS sequencing from 30 leaf samples showed that there were two major genotypes of C. stellatopilosus which were designated as STEL Type A and B. In addition, various nucleotide additive sequences which had presumably arisen
 from these two groups were also found. These so-called “putative hybrids”, interestingly, displayed trnK intron sequences identical to the STEL Type B but different from the Type A. For the trnL-F region, all the 30 samples showed identical sequences. Thus, it...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4745143</comments>
            <pubDate>Sat, 16 Apr 2011 05:56:41 +0100</pubDate>
            <guid isPermaLink="false">4745143</guid>        </item>
        <item>
            <title>Evaluation of systemic administration of Boswellia papyrifera extracts on spatial memory retention in male rats</title>
            <link>http://www.medworm.com/index.php?rid=4710329&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx0n1756vu3l7q076%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Time-dependent effects of ethanolic extract of Boswellia papyrifera, administered systemically, on spatial memory retention in the Morris water maze were investigated in male rats. A total
 extract of Boswellia papyrifera (300&amp;nbsp;mg/kg) was administered every eight hours to three groups of rats by gavage for 1, 2 and 4&amp;nbsp;weeks. In a separate set
 of experiments, three doses of a fraction of the extract, called the boswellic acids (100, 200 and 300&amp;nbsp;mg/kg) were administered
 by gavage to three groups of rats three times a day for 2&amp;nbsp;weeks. Following these applications, animals were trained for 4&amp;nbsp;days.
 Behavioral testing for evaluation of spatial memory retention was performed 48&amp;nbsp;h after completion of training. Boswellia papyrifera extracts and bos...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4710329</comments>
            <pubDate>Sun, 10 Apr 2011 15:42:23 +0100</pubDate>
            <guid isPermaLink="false">4710329</guid>        </item>
        <item>
            <title>Adaptogenic potential of curcumin in experimental chronic stress and chronic unpredictable stress-induced memory deficits and alterations in functional homeostasis</title>
            <link>http://www.medworm.com/index.php?rid=4710330&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe538630w574pn537%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The present study was designed to investigate the role of curcumin in chronic stress and chronic unpredictable stress-induced
 memory deficits and alteration of functional homeostasis in mice. Chronic stress was induced by immobilizing the animal for
 2&amp;nbsp;h daily for 10&amp;nbsp;days, whereas chronic unpredictable stress was induced by employing a battery of stressors of variable magnitude
 and time for 10&amp;nbsp;days. Curcumin was administered to drug-treated mice prior to induction of stress. Body weight, adrenal gland
 weight, ulcer index and biochemical levels of glucose, creatine kinase, cholesterol, corticosterone, thiobarbituric acid reactive
 substances (TBARS) and reduced glutathione (GSH) were evaluated to assess stress-induced functional changes. Memory deficits...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4710330</comments>
            <pubDate>Sun, 10 Apr 2011 15:42:22 +0100</pubDate>
            <guid isPermaLink="false">4710330</guid>        </item>
        <item>
            <title>Possible attenuation of nitric oxide expression in anti-inflammatory effect of Ziziphus jujuba in rat</title>
            <link>http://www.medworm.com/index.php?rid=4710331&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg26ll45265805246%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The hydroalcoholic extract of fruits of Ziziphus jujuba (ZJ) was investigated for its anti-inflammatory effect using acute and chronic models of inflammation in rat. Wistar albino
 rats of either sex were employed in the present study (n&amp;nbsp;=&amp;nbsp;6). Acute inflammation was induced by subplantar administration of carrageenan (1%) in rat hind paw. Chronic inflammation
 was induced by interscapular implantation of a sterile cotton pellet (50&amp;nbsp;mg). ZJ extract as test drug and indomethacin (10&amp;nbsp;mg/kg)
 as standard were used. Serum nitrite/nitrate was also estimated to determine the expression of nitric oxide. In the acute
 study, carrageenan (1%) administration caused marked paw edema. Pretreatment with ZJ extract exhibited marked dose-dependent
 attenuation in ed...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4710331</comments>
            <pubDate>Sun, 10 Apr 2011 05:52:08 +0100</pubDate>
            <guid isPermaLink="false">4710331</guid>        </item>
        <item>
            <title>Preventive effects of the extract of kinka-cha, a folk tea, on a rat model of metabolic syndrome</title>
            <link>http://www.medworm.com/index.php?rid=4710332&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu0380g710r5hg33k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Kinka-cha (dried leaf of Camellia nitidissima) is used as a folk tea for detoxication, diuresis and antihypertension. In the present study, we evaluated the extract of
 kinka-cha on metabolic, vascular and oxidative stress parameters in a model of metabolic syndrome, SHR/NDmcr-cp/cp (SHR/cp)
 rats that manifest hypertension, obesity, glucose intolerance and hyperlipidemia. Treatment with the extract of kinka-cha
 alleviated the increase in blood pressure, decrease in tail blood flow and elevated serum oxidative stress marker levels including
 lipid peroxides, 8-hydroxy-2′-deoxyguanosine, 3-nitrotyrosine and 3-chlorotyrosine. However, kinka-cha did not affect weight
 gain, hyperglycemia and hyperlipidemia, nor the relaxation responses of the aorta mesenteric artery, th...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4710332</comments>
            <pubDate>Sat, 09 Apr 2011 15:49:13 +0100</pubDate>
            <guid isPermaLink="false">4710332</guid>        </item>
        <item>
            <title>Genomic organization of δ-guaiene synthase genes in Aquilaria crassna and its possible use for the identification of Aquilaria species</title>
            <link>http://www.medworm.com/index.php?rid=4698575&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd83867vt8611641v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The resinous portions of Aquilaria plants, called agarwood, have been used as medicines and incenses. Agarwood contains a great variety of sesquiterpenes, and
 a study using cultured cells of Aquilaria crassna showed that the production of sesquiterpenes (α-guaiene, α-humulene, and δ-guaiene) was induced by treatment with methyl
 jasmonate, which led to the cloning of δ-guaiene synthases. In the present study, analyses of genomic organization and Southern
 blotting of δ-guaiene synthase in A. crassna were performed in order to examine the genomic background of δ-guaiene synthases in Aquilaria plants. Genomic cloning and sequencing revealed five types of sequence in putative δ-guaiene synthases sharing more than
 96% identity in exon regions, and that these enzyme...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4698575</comments>
            <pubDate>Thu, 07 Apr 2011 06:01:37 +0100</pubDate>
            <guid isPermaLink="false">4698575</guid>        </item>
        <item>
            <title>Methanol extract from mycelium of endophytic fungus Rhizoctonia sp. induces antinociceptive and anti-inflammatory activities in mice</title>
            <link>http://www.medworm.com/index.php?rid=4693854&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhm710650h4371395%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The present study aimed to elucidate the antinociceptive and anti-inflammatory properties of the methanol extract from the
 mycelium of the endophytic fungus Rhizoctonia sp. (MEMRh) in mice. The antinociceptive activity was assessed using the abdominal constriction, hot plate, and formalin tests.
 The anti-inflammatory activity was assessed using a murine model of paw edema. Intraperitoneal administration of MEMRh (0.1,
 1, 10 and 100&amp;nbsp;mg/kg, i.p.) produced an inhibition of acetic acid-induced writhing in mice for at least 8&amp;nbsp;h. In addition, all
 doses tested of the methanol extract were able to prevent thermal nociception in the hot-plate test. Furthermore, treatment
 with MEMRh (10&amp;nbsp;mg/kg, i.p.) inhibited both the early and late phases of formalin-induced ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4693854</comments>
            <pubDate>Wed, 06 Apr 2011 06:45:20 +0100</pubDate>
            <guid isPermaLink="false">4693854</guid>        </item>
        <item>
            <title>Free radical scavenging and hepatoprotective potential of Ficus microcarpa L. fil. bark extracts</title>
            <link>http://www.medworm.com/index.php?rid=4693853&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F28q3p02217585235%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Successive extracts of Ficus microcarpa L. fil. bark (FMB) were tested for antioxidant and hepatoprotective activity against carbon tetrachloride- and paracetamol-induced
 hepatotoxicities in rats. The ethyl acetate extract of FMB exhibited significant antioxidant and hepatoprotective activity
 by reducing carbon tetrachloride- and paracetamol-induced changes in biochemical parameters as evidenced by enzymatic and
 histological examination. Pretreatment with ethyl acetate extract of FMB significantly shortened the duration of pentobarbitone-induced
 necrosis in mice, indicating its hepatoprotective potential. Phytochemical studies confirmed the presence of the phenolic
 compound, catechin, in FMB, which may interfere with free-radical formation and may account for its s...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4693853</comments>
            <pubDate>Wed, 06 Apr 2011 06:45:20 +0100</pubDate>
            <guid isPermaLink="false">4693853</guid>        </item>
        <item>
            <title>Acoschimperoside P, 2′-acetate: a Hedgehog signaling inhibitory constituent from Vallaris glabra</title>
            <link>http://www.medworm.com/index.php?rid=4686590&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe629180j646p53l5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Complete 1H and 13C NMR assignments of acoschimperoside P, 2′-acetate (1) and a new cardiac glycoside (2), isolated from the leaves of Vallaris glabra, are described. Compound 1 was active in the assay for Hedgehog signaling inhibition. In further experiments, this compound showed a strong cytotoxicity
 against human pancreatic (PANC1) and human prostate (DU145) cancer cells. The expression of GLI-related proteins (PTCH and
 BCL-2) in a dose-dependent manner was also inhibited by 1.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s11418-011-0530-1Authors
		Yusnita Rifai, Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba, 263-8522 JapanMidori A. Arai, Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Ya...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4686590</comments>
            <pubDate>Tue, 05 Apr 2011 16:53:52 +0100</pubDate>
            <guid isPermaLink="false">4686590</guid>        </item>
        <item>
            <title>Comparison of contents of five ephedrine alkaloids in three official origins of Ephedra Herb in China by high-performance liquid chromatography</title>
            <link>http://www.medworm.com/index.php?rid=4686591&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flk6k8n68142132u1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the present paper, a fast and economical HPLC method [on a Phenomenex Polar-RP column with a solution of (phosphoric acid:triethylamine:dibutylamine:water&amp;nbsp;=&amp;nbsp;0.40:0.1:0.2:499.3)
 and methanol] is developed, and applied for the determination of norephedrine, norpseudoephedrine, ephedrine (E), pseudoephedrine
 (PE) and methylephedrine (ME) in 64 samples of three species from main habitats in China. Quantitation data showed that total
 alkaloid content in Ephedra equisetina Bge. (2.708&amp;nbsp;±&amp;nbsp;0.642%) is higher than that in E. sinica Stapf. (1.365&amp;nbsp;±&amp;nbsp;0.624%) and E. intermedia Schrenk et C. A. Mey. (1.537&amp;nbsp;±&amp;nbsp;0.746%), but the range of total alkaloid content in each species is so wide that the ranges
 of the three species greatly overlap. ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4686591</comments>
            <pubDate>Tue, 05 Apr 2011 09:47:28 +0100</pubDate>
            <guid isPermaLink="false">4686591</guid>        </item>
        <item>
            <title>Increased galectin-1 expression in muscle of Astragalus polysaccharide-treated Type 1 diabetic mice</title>
            <link>http://www.medworm.com/index.php?rid=4623299&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8767ll3542143360%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In order to investigate the immunopharmacological function of Astragalus polysaccharide (APS) in Type 1 diabetes mellitus
 (T1DM), multiple low-dose streptozotocin-induced diabetic mice and normal mice were administered either APS or saline intraperitoneally
 once daily. The changes in galectin-1 expression in different organs of the mice were detected by ELISA, Real-time fluorescence
 quantitative RT-PCR and Western blot. The percentages of apoptotic CD8+ T cells from spleens of APS-treated diabetic mice were measured by flow cytometry. We found that the expression of galectin-1
 was increased in serum of APS-treated diabetic mice compared to the non-treated diabetic mice (*p&amp;nbsp;&amp;lt;&amp;nbsp;0.05). Increased galectin-1 was mainly expressed in the muscle of APS-treated m...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4623299</comments>
            <pubDate>Sat, 19 Mar 2011 16:55:25 +0100</pubDate>
            <guid isPermaLink="false">4623299</guid>        </item>
        <item>
            <title>Camalexin induces apoptosis in T-leukemia Jurkat cells by increased concentration of reactive oxygen species and activation of caspase-8 and caspase-9</title>
            <link>http://www.medworm.com/index.php?rid=4623300&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj21352p113h41m77%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Camalexin, a major indole phytoalexin of Arabidopsis thaliana, accumulates in various cruciferous plants in response to environmental stress and reportedly displays antimicrobial activities
 against various plant pathogens. However, its cytotoxicity against eukaryotic cells and potential as a prospective drug for
 human diseases has been examined only in a limited context. Our data demonstrate the time- and concentration-dependent cytotoxicity
 of camalexin on human T-leukemia Jurkat cells in the micromolar range, and the lower potency of cytotoxic effects on human
 lymphoblasts and primary fibroblasts. Cytotoxicity of camalexin is enhanced by the glutathione-depleting agent buthionine
 sulfoximine and completely blocked by pan-caspase inhibitor Z-VAD-FMK. Treatment of ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4623300</comments>
            <pubDate>Sat, 19 Mar 2011 06:36:51 +0100</pubDate>
            <guid isPermaLink="false">4623300</guid>        </item>
        <item>
            <title>Antioxidant and antiglycating activities of Salvia sahendica and its protective effect against oxidative stress in neuron-like PC12 cells</title>
            <link>http://www.medworm.com/index.php?rid=4623301&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj55698743q460w41%2F</link>
            <description>This study raises the possibility of developing S. sahendica as a potential neuroprotective agent.
 
 
	Content Type Journal ArticlePages 1-11DOI 10.1007/s11418-011-0519-9Authors
		Fatemeh Shaerzadeh, Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranAbolhassan Ahmadiani, Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranMohammad Ali Esmaeili, Department of Biology, Medicinal Plants and Drugs Research Institute, Shahid Beheshti University, GC, Tehran, IranNiloufar Ansari, Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranSareh Asadi, Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IranSolaleh Khoramian Tusi, Neuroscience Research Cent...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4623301</comments>
            <pubDate>Sat, 19 Mar 2011 02:52:27 +0100</pubDate>
            <guid isPermaLink="false">4623301</guid>        </item>
        <item>
            <title>Protective effect of Justicia gendarussa Burm.f. on carrageenan-induced inflammation</title>
            <link>http://www.medworm.com/index.php?rid=4616846&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F775745763g3760um%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The present study focuses on the anti-inflammatory activity of Justicia gendarussa Burm.f. on an acute model of inflammation: the carrageenan-induced paw edema assay. Methanolic extract of J. gendarussa (JRM) roots at a dose of 100&amp;nbsp;mg/kg significantly inhibited edema formation 5 h after carrageenan induction. JRM inhibited
 carrageenan-elicited total cycloxygenase activity, 5-lipoxygenase and 15-lipoxygenase activities in blood mononuclear cells
 of rats, decreased neutrophil infiltration in paw tissue as shown by low myeloperoxidase activity, and also caused a 53% inhibition
 in cyclooxygenase-2 activity in paw tissue. Purification of JRM by liquid–liquid partitioning yielded an ethyl acetate fraction
 of JRM that showed interleukin-6 downregulation potential an...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4616846</comments>
            <pubDate>Thu, 17 Mar 2011 19:22:22 +0100</pubDate>
            <guid isPermaLink="false">4616846</guid>        </item>
        <item>
            <title>Attenuating effect of hydroalcoholic extract of Acorus calamus in vincristine-induced painful neuropathy in rats</title>
            <link>http://www.medworm.com/index.php?rid=4611511&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff47680l4j760v635%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The present study was designed to investigate the attenuating potential of hydroalcoholic extract of Acorus calamus in vincristine-induced neuropathic pain in rats. Vincristine (50&amp;nbsp;μg/kg, i.p. for 10 consecutive days) was administered to
 induce neuropathic pain in rats. Hot plate, plantar, Randall–Selitto and von Frey hair tests were performed to assess the
 degree of thermal and mechanical hyperalgesia and mechanical allodynia, respectively, at different time intervals, viz., 0,
 1, 3, 6, 9, 12, 15, 18 and 21 days. Tissue myeloperoxidase, superoxide anion and total calcium levels were determined after
 day 21to assess biochemical alterations. Histopathological evaluations were also performed. Hydroalcoholic extract of Acorus calamus (HAE-AC, 100 and 200&amp;nbsp;m...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4611511</comments>
            <pubDate>Tue, 15 Mar 2011 05:49:25 +0100</pubDate>
            <guid isPermaLink="false">4611511</guid>        </item>
        <item>
            <title>Anti-inflammatory and gastromucosal protective effects of Calotropis procera (Asclepiadaceae) stem bark</title>
            <link>http://www.medworm.com/index.php?rid=4601668&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy572g30498556q41%2F</link>
            <description>This study was aimed at evaluating the anti-inflammatory and gastromucosal protective effect of chloroform extract (CH) and
 hydroalcoholic extract (HE) of the stem bark of Calotropis procera obtained successively by cold maceration. The anti-inflammatory effect of the CH and HE extracts of the stem bark of Calotropis procera against carrageenan-induced paw oedema and also its gastromucosal protective effect has been studied by using two acute models:
 aspirin (100&amp;nbsp;mg/kg, p.o.) and ethanol (96%) in albino rats. CH and HE extracts showed significant anti-inflammatory activity
 at 200 and 400&amp;nbsp;mg/kg, while CH extract at 400&amp;nbsp;mg/kg was also found to have a significant gastromucosal protective effect.
 As part of investigations to obtain compounds with anti-inflammatory and gastro...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4601668</comments>
            <pubDate>Mon, 14 Mar 2011 06:40:20 +0100</pubDate>
            <guid isPermaLink="false">4601668</guid>        </item>
        <item>
            <title>Bioactive metabolites of Diaporthe sp. P133, an endophytic fungus isolated from Pandanus amaryllifolius</title>
            <link>http://www.medworm.com/index.php?rid=4581855&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj48030372103n047%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new benzopyranones, diaportheone A (1) and B (2), were obtained via bioassay-guided isolation of the secondary metabolites from the endophytic fungus Diaporthe sp. P133 isolated from Pandanus amaryllifolius leaves. Their structures were determined from spectral analysis including mass spectrometry, 1D and 2D nuclear magnetic resonance.
 Both 1 and 2 inhibited the growth of the virulent strain of Mycobacterium tuberculosis H37Rv with minimum inhibitory concentrations of 100.9 and 3.5&amp;nbsp;μM, respectively.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s11418-011-0518-xAuthors
		Melfei E. Bungihan, The Graduate School, Research Center for the Natural and Applied Sciences, University of Santo Tomas, España, 1015 Manila, PhilippinesMario A. Tan, The Graduate S...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4581855</comments>
            <pubDate>Fri, 11 Mar 2011 06:53:41 +0100</pubDate>
            <guid isPermaLink="false">4581855</guid>        </item>
        <item>
            <title>Antinociceptive effects of methyl jasmonate in experimental animals</title>
            <link>http://www.medworm.com/index.php?rid=4578494&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd2345212865v3237%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Methyl jasmonate (MJ) is a chemical compound that has been postulated to play a role in plant wound and pathogen responses.
 While the anti-inflammatory property of MJ has been reported in literature, no studies have been carried out to describe its
 role in the modulation of pain. Thus, this present investigation sought to evaluate the antinociceptive activity of MJ in
 animal models of pain. The antinociceptive activity of MJ (10–50&amp;nbsp;mg/kg) administered intraperitoneally (i.p.) was screened
 using the acetic acid-induced writhing, tail immersion, formalin-induced paw licking and Randall–Selitto paw pressure tests
 in rodents. MJ demonstrated inhibitory activity against acetic acid-induced abdominal constrictions in mice. It further produced
 a significant supp...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4578494</comments>
            <pubDate>Tue, 08 Mar 2011 17:04:48 +0100</pubDate>
            <guid isPermaLink="false">4578494</guid>        </item>
        <item>
            <title>Gallates of isoorientin and (2S)-1,2-propanediol glucoside from the leaves of Schoepfiajasminodora</title>
            <link>http://www.medworm.com/index.php?rid=4567141&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa23836p015715824%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;From the 1-BuOH-soluble fraction of a MeOH extract of the leaves of Schoepfia jasminodora collected from Okinawa Island, two new galloyl esters and 15 known compounds were isolated. The structures of the new compounds
 were elucidated by spectroscopic analysis to be isoorientin 4″-O-gallate and (2S)-1,2-propanediol 1-O-β-d-glucopyranoside 6′-O-gallate. The compounds possessing galloyl or cathechol moieties showed equal radical scavenging activity.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s11418-011-0521-2Authors
		Yoshiko Tsuboi, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanTakashi Doi, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4567141</comments>
            <pubDate>Mon, 07 Mar 2011 17:04:57 +0100</pubDate>
            <guid isPermaLink="false">4567141</guid>        </item>
        <item>
            <title>Anti-HIV activity of Indian medicinal plants</title>
            <link>http://www.medworm.com/index.php?rid=4550299&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F05u52471tr33h486%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Acquired immunodeficiency syndrome patients face great socio-economic difficulties in obtaining treatment. There is an urgent
 need for new, safe, and cheap anti-HIV agents. Traditional medicinal plants are a valuable source of novel anti-HIV agents
 and may offer alternatives to expensive medicines in future. Various medicinal plants or plant-derived natural products have
 shown strong anti-HIV activity and are under various stages of clinical development in different parts of the world. The present
 study was directed towards assessment of anti-HIV activity of various extracts prepared from Indian medicinal plants. The
 plants were chosen on the basis of similarity of chemical constituents with reported anti-HIV compounds or on the basis of
 their traditional usage as...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4550299</comments>
            <pubDate>Wed, 02 Mar 2011 07:49:52 +0100</pubDate>
            <guid isPermaLink="false">4550299</guid>        </item>
        <item>
            <title>In vitro determination of the effect of Andrographis paniculata extracts and andrographolide on human hepatic cytochrome P450 activities</title>
            <link>http://www.medworm.com/index.php?rid=4550300&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy8745541307q2385%2F</link>
            <description>In conclusion, data
 presented in this study suggest that AP extracts have the potential to inhibit CYP isoforms in vitro. There was, however,
 variation in the potency of inhibition depending on the extracts and the isoforms investigated.
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s11418-011-0516-zAuthors
		Yan Pan, School of Pharmacy and Health Sciences, International Medical University, 126, Jalan 19/155B, Bukit Jalil, 57000 Kuala Lumpur, MalaysiaBadrul Amini Abd-Rashid, Herbal Medicine Research Centre, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, MalaysiaZakiah Ismail, Herbal Medicine Research Centre, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, MalaysiaRusli Ismail, Pharmacogenetics Research Group, Institute for Research in Molecula...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4550300</comments>
            <pubDate>Wed, 02 Mar 2011 07:49:51 +0100</pubDate>
            <guid isPermaLink="false">4550300</guid>        </item>
        <item>
            <title>Effect of altitude on picroside content in core collections of Picrorhiza kurrooa from the north western Himalayas</title>
            <link>http://www.medworm.com/index.php?rid=4541561&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj542849w13850411%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Picrorhiza kurrooa Royle ex Benth (Scrophulariaceae), commonly known as Kutki, is a major ingredient of many ayurvedic preparations prescribed
 in the treatment of various diseases. Picrosides I and II are the active agents responsible for the medicinal effects of Kutki,
 and the variation in content of these compounds in plants at different altitudes is a major question to be addressed. The
 picroside I and II content in various plant parts of P. kurrooa collected from different altitudes, viz. Sonemarg (2,740&amp;nbsp;m a.s.l.), Tangmarg (2,690&amp;nbsp;m a.s.l.), and Pulwama (1,630&amp;nbsp;m a.s.l.)
 in the north-western Kashmir Himalayas was analyzed by HPLC. A considerable degree of variation in picroside content was observed.
 Picroside I and II was highest in populations ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4541561</comments>
            <pubDate>Wed, 23 Feb 2011 23:36:14 +0100</pubDate>
            <guid isPermaLink="false">4541561</guid>        </item>
        <item>
            <title>Antinociceptive effect of Lafoensia pacari A. St.-Hil. independent of anti-inflammatory activity of ellagic acid</title>
            <link>http://www.medworm.com/index.php?rid=4513536&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkq46h63r0x5w5k02%2F</link>
            <description>This study was performed to determine the antinociceptive and anti-inflammatory activities of ethanolic extract of Lafoensia pacari A. St.-Hil. (PEtExt) stem bark and its fractions using various animal models such as acetic acid-induced abdominal writhing,
 formalin-induced pain and croton oil-induced ear edema tests. The PEtExt inhibited the acetic acid-induced abdominal writhing,
 reduced the pain reaction time on both phases of the formalin test and decreased the edema in a dose-dependent manner. Pre-treatment
 with naloxone did not reverse the antinociceptive effect. Only the ethyl acetate fraction showed antinociceptive and anti-inflammatory
 effects. Our results also showed that this extract contains compounds with analgesic action independent of anti-inflammatory
 activity.
 
 
	Con...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4513536</comments>
            <pubDate>Mon, 21 Feb 2011 17:07:29 +0100</pubDate>
            <guid isPermaLink="false">4513536</guid>        </item>
        <item>
            <title>New phenolic compounds from Camellia sinensis L. leaves fermented with Aspergillus sp.</title>
            <link>http://www.medworm.com/index.php?rid=4496033&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fft65w0x765v44353%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new phenolic compounds, teadenol A (1) and teadenol B (2), were isolated from tea (Camellia sinensis L.) leaves fermented with Aspergillus sp. (PK-1, FARM AP-21280). The chemical structures of 1 and 2 were elucidated based on the analyses of their spectroscopic data. The absolute configurations of the structures of 1 and 2 were also certified by their biosynthetic preparation in the treatment of tea catechins with Aspergillus sp.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s11418-011-0515-0Authors
		Rani Agustina Wulandari, Department of Applied Biological Sciences, Faculty of Agriculture, Saga University, 1 Honjo, Saga, 840-8502 JapanMasami Amano, Department of Applied Biological Sciences, Faculty of Agriculture, Saga University, 1 Honjo, Saga, 840-8502 J...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4496033</comments>
            <pubDate>Wed, 16 Feb 2011 07:03:51 +0100</pubDate>
            <guid isPermaLink="false">4496033</guid>        </item>
        <item>
            <title>Ferrearin C induces apoptosis via heme oxygenase-1 (HO-1) induction in neuroblastoma</title>
            <link>http://www.medworm.com/index.php?rid=4496034&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fng6370476166t8j6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We investigated the cytotoxicity of six neolignans (1–6), which are similar in structure to furanocyclohexenone with an angular allyl group, in human neuroblastoma cell lines (IMR-32,
 LA-N-1, NB-39, SK-N-SH) and normal cells [human umbilical vein endothelial cells (HUVEC) and human dermal fibroblasts (HDF)]
 using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Two neolignans, ferrearin C (1) and 2, showed significant cytotoxicity in neuroblastoma cells. Typical morphologic features of apoptosis were observed for the
 ferrearin-type neolignans using Hoechst 33342, and apoptotic cytoplasmic membrane inversion was also induced by ferrearin-type
 neolignans in IMR-32. Furthermore, a Proteome Profiler Array showed that the ferrearin-type neoli...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4496034</comments>
            <pubDate>Wed, 16 Feb 2011 07:03:50 +0100</pubDate>
            <guid isPermaLink="false">4496034</guid>        </item>
        <item>
            <title>Psychopharmacological properties of an aqueous extract of Tetracarpidium conophorum Hutch. &amp; Dalziel in mice</title>
            <link>http://www.medworm.com/index.php?rid=4496036&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm837775172w23678%2F</link>
            <description>This study describes the psychopharmacological properties of the aqueous extract
 of the nut of TC in mice. The spectrum of activities studied were the effects of TC on the duration of immobility in the forced
 swim test of the behavioural despair model of depression; prolongation of the duration of sleep produced by thiopentone; amphetamine-induced
 stereotyped behaviour; and on pain episodes produced by acetic acid and by formalin. Orally administered TC (50–200&amp;nbsp;mg/kg)
 produced a significant and dose-related decrease in the duration of immobility in the forced swim test in mice. TC also exhibited
 analgesic property, as shown by its ability to reduce the frequency of abdominal constrictions induced by acetic acid and
 to inhibit the nociceptive responses produced by formalin. How...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4496036</comments>
            <pubDate>Wed, 16 Feb 2011 07:03:49 +0100</pubDate>
            <guid isPermaLink="false">4496036</guid>        </item>
        <item>
            <title>Honokiol enhances adipocyte differentiation by potentiating insulin signaling in 3T3-L1 preadipocytes</title>
            <link>http://www.medworm.com/index.php?rid=4496035&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw171583g012554p3%2F</link>
            <description>In this study, we found that honokiol, an ingredient of Magnolia officinalis used in traditional Chinese and Japanese medicines, enhanced adipocyte differentiation in 3T3-L1 preadipocytes. Oil Red O
 staining showed that treatment with honokiol in the presence of insulin dose-dependently increased lipid accumulation in 3T3-L1
 preadipoyctes although its activity was weak compared with rosiglitazone. During adipocyte differentiation, the expression
 of peroxisome proliferator-activated receptor γ2 (PPARγ2) mRNA and PPARγ target genes such as adipocyte protein 2 (aP2), adiponectin,
 and GLUT4 was induced by treatment with 10&amp;nbsp;μM honokiol. However, honokiol failed to show direct binding to the PPARγ ligand-binding
 domain in vitro. In preadipocytes, treatment with honokiol in the pre...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4496035</comments>
            <pubDate>Wed, 16 Feb 2011 07:03:49 +0100</pubDate>
            <guid isPermaLink="false">4496035</guid>        </item>
        <item>
            <title>Active components from Siberian ginseng (Eleutherococcus senticosus) for protection of amyloid β(25–35)-induced neuritic atrophy in cultured rat cortical neurons</title>
            <link>http://www.medworm.com/index.php?rid=4461050&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn562476781h18620%2F</link>
            <description>In this study, a comprehensive evaluation of constituents
 was conducted to explore active components from Siberian ginseng which can protect against neuritic atrophy induced by Aβ(25–35) in cultured rat cortical neurons. The ethyl acetate, n-butanol and water fractions from the methanol extract of Siberian ginseng showed protective effects against Aβ-induced neuritic atrophy. Twelve compounds were isolated from the active fractions and identified. Among them, eleutheroside
 B, eleutheroside E and isofraxidin showed obvious protective effects against Aβ(25–35)-induced atrophies of axons and dendrites at 1 and 10&amp;nbsp;μM.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s11418-011-0509-yAuthors
		Yanjing Bai, Division of Pharmacognosy, Institute of Natural Medicine, University ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4461050</comments>
            <pubDate>Mon, 07 Feb 2011 23:07:50 +0100</pubDate>
            <guid isPermaLink="false">4461050</guid>        </item>
        <item>
            <title>Production of monoclonal antibodies against antitumor cyclohexapeptide RA-VII from Rubia cordifolia and their characterization</title>
            <link>http://www.medworm.com/index.php?rid=4461051&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm351633356216m81%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An immunoassay system was established for the estimation of the quantity of an antitumor cyclic hexapeptide RA-VII (1) from Rubia cordifolia L. and R. akane Nakai (Rubiaceae). First, 1 was converted into its hapten, which was then conjugated with a carrier protein to be used as an effective antigen to obtain
 its monoclonal antibody (MAb). In the resulting conjugate, the molecular ratio between 1 and the carrier protein as assayed by matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF
 MS) was about 5:1. Then, the splenocytes from the mouse immunized with the conjugate were fused with mouse myeloma cells to
 produce hybridoma, secreting MAb against 1. Two clones were isolated, one producing MAb IgG1 and the other IgM, both having a κ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4461051</comments>
            <pubDate>Mon, 07 Feb 2011 23:07:42 +0100</pubDate>
            <guid isPermaLink="false">4461051</guid>        </item>
        <item>
            <title>Toxic metal contamination in Artemisia annua L. herbal preparations from different commercial sources in China</title>
            <link>http://www.medworm.com/index.php?rid=4442860&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff57027t485wg3622%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Toxic metal contamination was investigated in Artemisia annua L. herbal preparations from different commercial sources in China. Measurable amounts of copper (Cu), lead (Pb), arsenic
 (As), mercury (Hg), cadmium (Cd), chromium (Cr), manganese (Mn), nickel (Ni) and aluminium (Al) were detected in commercial
 dried Artemisia annua L., Massa Medicata Fermentata (Shenqu), Semen Sojae Praeparatum, medicated leaven (Jianqu) and an oral dose of Zhongganling-pian by inductively coupled plasma optical emission spectrometry
 (ICP-OES) and atomic fluorescence spectrometry (AFS). A total of 69 samples were collected from different sources in the Chinese
 market. Toxic metals contents in the investigated samples were found at different levels. Results showed that 94.20, 100,
 97.10,...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4442860</comments>
            <pubDate>Fri, 04 Feb 2011 09:23:50 +0100</pubDate>
            <guid isPermaLink="false">4442860</guid>        </item>
        <item>
            <title>Inhibition of proliferation by agricultural plant extracts in seven human adult T-cell leukaemia (ATL)-related cell lines</title>
            <link>http://www.medworm.com/index.php?rid=4442861&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc579245u6282314j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adult T-cell leukaemia (ATL) is caused by human T-cell leukaemia virus type I (HTLV-I) infection and is resistant to conventional
 chemotherapy. We evaluated the inhibitory effects of agricultural plants on the proliferation of seven ATL-related human leukaemia
 cells, using three ATL cell lines (ED, Su9T01 and S1T), two human T-cell lines transformed by HTLV-I infection (HUT-102 and
 MT-2) and two HTLV-I-negative human T-cell acute lymphoblastic leukaemia cell lines (Jurkat and MOLT-4). A total of 52 samples
 of 80% ethanol extracts obtained from 30 types of agricultural plants were examined. On the basis of IC50 values, we selected samples with greater activity than genistein, which was used as a positive control. The highest inhibitory
 effect was observed with extra...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4442861</comments>
            <pubDate>Fri, 04 Feb 2011 03:36:13 +0100</pubDate>
            <guid isPermaLink="false">4442861</guid>        </item>
        <item>
            <title>Sedative effects of vapor inhalation of the essential oil of Microtoena patchoulii and its related compounds</title>
            <link>http://www.medworm.com/index.php?rid=4442862&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy8152vr81m34hg81%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Microtoena patchoulii (Labiatae) is a perennial herb that grows in southern China. In the present study, the sedative activity of the essential oil of the
 leaves was evaluated using mice when the volatile oil was administered by inhalation. The inhalation of the oil by mice significantly
 reduced the spontaneous motor activity. Fractionation of the oil revealed that the main constituents in the oil were 1-octen-3-ol,
 terpinolene, patchouli alcohol, and methyl salicylate. Each 1-octen-3-ol, terpinolene, or patchouli alcohol significantly
 reduce the locomotor activity when it was administered singly. However, the essential oil fraction containing both patchouli
 alcohol and methyl salicylate did not exhibit any effects. It is suggested that methyl salicylate might ne...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4442862</comments>
            <pubDate>Thu, 03 Feb 2011 21:06:24 +0100</pubDate>
            <guid isPermaLink="false">4442862</guid>        </item>
        <item>
            <title>Compounds isolated from Curcuma aromatica Salisb. inhibit human P450 enzymes</title>
            <link>http://www.medworm.com/index.php?rid=4442863&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F75112881338j6p41%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Curcuma species (Zingiberaceae) are used as both food and medicine in Asia. Ten sesquiterpenes (1–10) and two curcuminoids (11 and 12) were isolated from the rhizomes of Curcuma aromatica Salisb. and identified. The compounds were evaluated for their ability to inhibit cytochrome P450 (CYP). Among them, the
 sesquiterpene (4S,5S)-(+)-germacrone-4,5-epoxide (7) inhibited certain subtypes of CYP more potently than or at levels comparable to the curcuminoids curcumin (11) and demethoxycurcumin (12); 7 (IC50&amp;nbsp;=&amp;nbsp;1.0&amp;nbsp;±&amp;nbsp;0.2&amp;nbsp;μM)&amp;nbsp;&amp;gt;&amp;nbsp;12 (IC50&amp;nbsp;=&amp;nbsp;7.0&amp;nbsp;±&amp;nbsp;1.7&amp;nbsp;μM)&amp;nbsp;&amp;gt;&amp;nbsp;11 (IC50&amp;nbsp;=&amp;nbsp;14.9&amp;nbsp;±&amp;nbsp;1.4&amp;nbsp;μM) for CYP3A4 inhibition; 12 (IC50&amp;nbsp;=&amp;nbsp;1.4&amp;nbsp;±&amp;nbsp;0.2&amp;nbsp;μM)&amp;nbsp;&amp;gt;&amp;nbs...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4442863</comments>
            <pubDate>Thu, 03 Feb 2011 21:06:19 +0100</pubDate>
            <guid isPermaLink="false">4442863</guid>        </item>
        <item>
            <title>Evaluation of anti-inflammatory and antinociceptive effects of D-002 (beeswax alcohols)</title>
            <link>http://www.medworm.com/index.php?rid=4400981&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh612k6142q61uhl2%2F</link>
            <description>This study confirmed the anti-inflammatory
 effects of D-002 and demonstrated its analgesic effects on the acetic acid-induced writhing, but not on the hot plate response,
 which suggests that the antinociceptive effects of D-002 could be related to its anti-inflammatory activity.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s11418-010-0496-4Authors
		Yazmin Ravelo, Pharmacology Department, Centre of Natural Products, National Centre for Scientific Research, 198 Ave Between 19 and 21 sts., Atabey, Playa, Havana, CubaVivian Molina, Pharmacology Department, Centre of Natural Products, National Centre for Scientific Research, 198 Ave Between 19 and 21 sts., Atabey, Playa, Havana, CubaDaisy Carbajal, Pharmacology Department, Centre of Natural Products, National Centre for Scientific R...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4400981</comments>
            <pubDate>Fri, 21 Jan 2011 20:30:32 +0100</pubDate>
            <guid isPermaLink="false">4400981</guid>        </item>
        <item>
            <title>Laevigatbenzoate from Croton laevigatus Vahl.</title>
            <link>http://www.medworm.com/index.php?rid=4400982&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk96h36494010t5m1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A new trans-clerodane diterpenoid, laevigatbenzoate (1), was isolated from the leaves of Croton laevigatus Vahl. Its structure was established on the basis of spectroscopic analysis, and the absolute configuration was determined
 by application of the CD excitation chirality method. This compound showed weak cytotoxicity against HeLa cells, with an IC50 value of 45.4&amp;nbsp;μM.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s11418-010-0503-9Authors
		Guo-An Zou, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193 People’s Republic of ChinaHong-Wu Zhang, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100193 People...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4400982</comments>
            <pubDate>Fri, 21 Jan 2011 15:37:28 +0100</pubDate>
            <guid isPermaLink="false">4400982</guid>        </item>
        <item>
            <title>Methyl galbanate, a novel inhibitor of nitric oxide production in mouse macrophage RAW264.7 cells</title>
            <link>http://www.medworm.com/index.php?rid=4383463&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv156832x13403507%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It is well known that inflammation is associated with various neurodegenerative diseases, such as Parkinson’s disease and
 Alzheimer’s disease. An inflammatory mediator, nitric oxide (NO), is produced by inducible NO synthase (iNOS) in microglia
 and seems to be one of the possible causes of neurodegeneration. Several natural and synthetic compounds which exert anti-inflammatory
 effects by inhibiting NO production have been reported to date. The aim of this work was to investigate whether any of the
 6 terpenoid coumarins (methyl galbanate, galbanic acid, farnesiferol A, badrakemone, umbelliprenin, and aurapten) isolated
 from Ferula szowitsiana DC. have inhibitory activity against NO production in RAW264.7 mouse macrophage cells stimulated with lipopolysaccharide
...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4383463</comments>
            <pubDate>Tue, 18 Jan 2011 19:37:56 +0100</pubDate>
            <guid isPermaLink="false">4383463</guid>        </item>
        <item>
            <title>Constituents of cultivated Agaricus blazei</title>
            <link>http://www.medworm.com/index.php?rid=4373627&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F92jj07567t348333%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two phenylhexane derivatives (1, 2), benzoylergostane (3), N-benzoyl-l-leucine methyl ester (4), two known ergostanes, and highly degraded incisterol were isolated from fruit bodies of Agaricus blazei. Compound 3 exhibited strong cytotoxicity toward HepG2 cells (IC50&amp;nbsp;=&amp;nbsp;6.0&amp;nbsp;±&amp;nbsp;0.33&amp;nbsp;μM).
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s11418-010-0495-5Authors
		Yumi Ueguchi, Department of Pharmacognosy, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanKatsuyoshi Matsunami, Department of Pharmacognosy, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanHideaki Otsuka, Department of Pharmacognosy, Graduate School of Biom...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4373627</comments>
            <pubDate>Mon, 17 Jan 2011 06:47:58 +0100</pubDate>
            <guid isPermaLink="false">4373627</guid>        </item>
        <item>
            <title>Red ginseng deregulates hypoxia-induced genes by dissociating the HIF-1 dimer</title>
            <link>http://www.medworm.com/index.php?rid=4373629&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F03q8913855x5713j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Water extract of Korean red ginseng (KRGW) contains numerous bioactive ginsenosides and is very popular as a multi-purpose
 medicine for health improvement. KRGW has been in the limelight because of its clinical benefit in cancer control. A growing
 body of evidence suggests that hypoxia-inducible factor-1 (HIF-1) plays critical roles in tumor promotion under hypoxia and
 that it is a compelling target for cancer therapy. In this paper we investigated the effect of KRGW on HIF-1-mediated adaptation
 to hypoxia. In both Hep3B cancer and HEK293 immortalized normal cell lines, KRGW attenuated the expression of hypoxia-induced
 genes without apparent cytotoxicity. Mechanistically, KRGW did not affect the synthesis, degradation, and translocation of
 HIF-1 in hypoxia. Intere...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4373629</comments>
            <pubDate>Mon, 17 Jan 2011 06:47:56 +0100</pubDate>
            <guid isPermaLink="false">4373629</guid>        </item>
        <item>
            <title>New phenolic compounds from Meehania urticifolia</title>
            <link>http://www.medworm.com/index.php?rid=4373628&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0328121p3152v044%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A new phenylethanoid glycoside, rashomoside A (1), a new phenolic glucoside, rashomoside B (2), and a new shikimic acid derivative (3) were isolated from Meehania urticifolia together with 12 known flavones (4–15), three known phenylethanoid glycosides (16–18), and 13 other compounds (19–31). The structure of each of these compounds was elucidated based on the results of spectroscopic analysis.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s11418-010-0501-yAuthors
		Toshihiro Murata, Department of Pharmacognosy, Tohoku Pharmaceutical University, 4-1 Komatsushima 4-chome Aoba-ku, Sendai, 981-8558 JapanToshio Miyase, School of Pharmaceutical Sciences, University of Shizuoka, 52-1, Yada, Suruga-ku, Shizuoka, 422-8526 JapanFumihiko Yoshizaki, Department of Pha...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4373628</comments>
            <pubDate>Mon, 17 Jan 2011 06:47:56 +0100</pubDate>
            <guid isPermaLink="false">4373628</guid>        </item>
        <item>
            <title>Chemical studies on the roots of Uvaria welwitschii</title>
            <link>http://www.medworm.com/index.php?rid=4356531&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb2k3p052k3x3n8j7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A chemical investigation of the chloroform extract of the roots of Uvaria welwitschii (Annonaceae), an African traditional medicine taken for stomach ache, led to the isolation of eight new compounds, named
 welwitschins A–H (1–8), together with five known compounds (9–13). The structural elucidation by spectroscopic studies of the compounds isolated is described. All new compounds were flavonoids
 having a 2-hydroxy-3,4,6-trimethoxyphenyl moiety in the A-ring, and unsubstituted phenyl in the B-ring. Four of them (1–4) were monomeric flavonoids while the others (5–8) were dimeric flavonoids. The cytotoxicity of the isolated compounds against human promyelocytic leukemia HL-60 cells was
 investigated.
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s11418...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4356531</comments>
            <pubDate>Fri, 14 Jan 2011 14:28:59 +0100</pubDate>
            <guid isPermaLink="false">4356531</guid>        </item>
        <item>
            <title>Fast pesticide multiresidue analysis in American ginseng (Panax quinquefolium L.) by gas chromatography with electron capture detection</title>
            <link>http://www.medworm.com/index.php?rid=4327405&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3532w73215717t71%2F</link>
            <description>This study indicates that the proposed method is useful for analyzing OCPs in American ginseng.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s11418-010-0500-zAuthors
		Jianwei Wu, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, 100193 Beijing, ChinaYougang Liu, Tianjin University of Traditional Chinese Medicine, 300193 Tianjin, ChinaRunhuai Zhao, Technology Development Center, China National Group Corporation of Traditional and Herbal Medicine, 102600 Beijing, ChinaRong Xu, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, 100193 Beijing, China
	

	
		Journal Journal of Natural MedicinesOnline ISSN 1861-0293Print ISSN 1340-3443 (Source: Journal of Natural Medicin...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4327405</comments>
            <pubDate>Fri, 07 Jan 2011 06:50:46 +0100</pubDate>
            <guid isPermaLink="false">4327405</guid>        </item>
        <item>
            <title>Trichodermanin A, a novel diterpenoid from endophytic fungus culture</title>
            <link>http://www.medworm.com/index.php?rid=4327404&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb701871rm08u4605%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Trichodermanin A, a structurally unique diterpenoid with skeletal carbons arranged compactly in a fused 6-5-6-6 ring system,
 has been isolated from cultures of Trichoderma atroviride (strain no. S361), an endophytic fungus isolate in Cephalotaxus fortunei. The structure of this compound was elucidated based on extensive spectroscopic methods and confirmed by X-ray diffraction
 analysis.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s11418-010-0499-1Authors
		Pei-Xin Sun, Department of Pharmacognosy, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai, 200433 People’s Republic of ChinaCheng-Jian Zheng, Department of Pharmacognosy, School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai, 200433 People’s Re...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4327404</comments>
            <pubDate>Fri, 07 Jan 2011 06:50:46 +0100</pubDate>
            <guid isPermaLink="false">4327404</guid>        </item>
        <item>
            <title>The antioxidant effects of Joongpoongtang 05 on brain injury after transient focal cerebral ischemia in rats</title>
            <link>http://www.medworm.com/index.php?rid=4327406&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft650412665h381u1%2F</link>
            <description>In this study, the antioxidant effects of Joongpoongtang 05 (JP05) were evaluated in rat middle
 cerebral artery occlusion (MCAO). Male Sprague–Dawley rats treated with JP05 (100 and 200&amp;nbsp;mg/kg body weight, p.o.) for 5&amp;nbsp;days
 showed a reduction in infarct sizes and a decrease in oxidants after MCAO. Furthermore, a significant inhibition of enzymatic
 antioxidants in the ischemic cerebral cortex was observed. Treatment with JP05 reversed the inhibition to normal levels. In
 the glutathione system, the reduced glutathione (GSH) level was decreased while oxidized glutathione (GSSG) was increased
 in MCAO rats. Treatment with JP05 increased the GSH/GSSG ratio and redox index by enhancing the synthesis of GSH from GSSG.
 Moreover, in vitro studies showed that JP05 has strong antioxida...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4327406</comments>
            <pubDate>Fri, 07 Jan 2011 06:50:45 +0100</pubDate>
            <guid isPermaLink="false">4327406</guid>        </item>
        <item>
            <title>Simultaneous quantification of marker components in Ojeok-san by HPLC–DAD</title>
            <link>http://www.medworm.com/index.php?rid=4301065&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv51448171w213383%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A systematic high-performance liquid chromatography–diode array detection (HPLC–DAD) method was developed for the rapid, accurate,
 and simultaneous quantification of eight marker compounds, paeoniflorin, 6-gingerol, decursin, glycyrrhizin, cinnamic acid,
 hesperidin, poncirin and magnolol, in Ojeok-san, a traditional Korean herbal medicine. These compounds were separated in less
 than 50&amp;nbsp;min using a Dionex C18 column with a gradient elution system of water and methanol at a flow rate of 1&amp;nbsp;ml/min. All calibration curve of standard
 components showed excellent linearity (R
 2&amp;nbsp;&amp;gt;&amp;nbsp;0.9922). Limits of detection (LOD) and limits of quantification (LOQ) ranged from 0.01 to 0.11&amp;nbsp;μg/ml and 0.03 to 0.34&amp;nbsp;μg/ml,
 respectively. The relative stan...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4301065</comments>
            <pubDate>Tue, 28 Dec 2010 15:14:03 +0100</pubDate>
            <guid isPermaLink="false">4301065</guid>        </item>
        <item>
            <title>Ameliorative effects of Eriobotrya japonica seed extract on cellular aging in cultured rat fibroblasts</title>
            <link>http://www.medworm.com/index.php?rid=4301067&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F319083892059400h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To investigate the effects of Eriobotrya japonica seed extract (ESE) on cellular aging, intracellular calcium homeostasis in young and senescent cells was analyzed using a
 rat fibroblast culture as an in vitro model system and a calcium imaging technique. The application of bradykinin (BK) transiently
 elicited intracellular calcium ion (Ca2+) increased in most of the young fibroblasts, whereas these responses were scarcely observed or were significantly attenuated
 in senescent cells. However, the long-term treatment of senescent cells with ESE (for 7&amp;nbsp;days) dose-dependently increased the
 amplitude of BK-induced responses and the percentage of BK-responding cells. In particular, most senescent cells could respond
 to BK with long-term treatment with ESE (1.0% or ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4301067</comments>
            <pubDate>Tue, 28 Dec 2010 15:14:00 +0100</pubDate>
            <guid isPermaLink="false">4301067</guid>        </item>
        <item>
            <title>Application of 1H-NMR spectroscopy to validation of berberine alkaloid reagents and to chemical evaluation of Coptidis Rhizoma</title>
            <link>http://www.medworm.com/index.php?rid=4301066&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb3711880w3653w7j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Berberine, palmatine, and coptisine are major pharmacologically active protoberberine alkaloids in Coptidis Rhizoma, and have
 been used as indices for chemical evaluation of the crude drug. 1H-NMR spectroscopy was applied to determination of purities of commercial reagents of protoberberine alkaloids. The purities
 of the alkaloids were calculated from the ratios of the intensities of the H-13 singlet signal at about δ 8.7&amp;nbsp;ppm of target
 protoberberine alkaloids to integration of a hexamethyldisilane (HMD) signal at 0&amp;nbsp;ppm. The concentration of HMD was corrected
 with SI traceability using potassium hydrogen phthalate of certified reference material (CRM) grade. The purity of the reagent
 estimated by the 1H-NMR was, in general, lower than that claimed by the...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4301066</comments>
            <pubDate>Tue, 28 Dec 2010 15:14:00 +0100</pubDate>
            <guid isPermaLink="false">4301066</guid>        </item>
        <item>
            <title>Five new phenylpropanoid glycosides from Paraboea glutinosa (Gesneriaceae)</title>
            <link>http://www.medworm.com/index.php?rid=4301068&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frk144062m6771837%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Five new phenylpropanoid glycosides, paraboside A, paraboside B, paraboside I, paraboside II and paraboside III along with
 the three known phenylethanoids, nuomioside A, caleolarioside B, isonuomioside A have been isolated from the whole plants
 of Paraboea glutinosa. The structures of the new compounds have been elucidated on the basis of spectroscopic data.
 
 
	Content Type Journal ArticleDOI 10.1007/s11418-010-0493-7Authors
		Xiaoqin Wang, Beijing University of Chinese Medicine, Beijing, 100102 People’s Republic of ChinaLi Li, Beijing University of Chinese Medicine, Beijing, 100102 People’s Republic of ChinaZhenfang Bai, Beijing University of Chinese Medicine, Beijing, 100102 People’s Republic of ChinaYong Peng, Institute of Medicinal Plant Development, Chine...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4301068</comments>
            <pubDate>Tue, 28 Dec 2010 15:13:58 +0100</pubDate>
            <guid isPermaLink="false">4301068</guid>        </item>
        <item>
            <title>Inhibition of chemiluminescence and chemotactic activity of phagocytes in vitro by the extracts of selected medicinal plants</title>
            <link>http://www.medworm.com/index.php?rid=4295985&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb617k317x56h67q2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The methanol extracts of 20 selected medicinal plants were investigated for their effects on the respiratory burst of human
 whole blood, isolated human polymorphonuclear leukocytes (PMNs) and isolated mice macrophages using a luminol/lucigenin-based
 chemiluminescence assay. We also tested the effect of the extracts on chemotactic migration of PMNs using the Boyden chamber
 technique. The extracts of Curcuma domestica L., Phyllanthus amarus Schum &amp; Thonn and C. xanthorrhiza Roxb. were the samples producing the strongest oxidative burst of PMNs with luminol-based chemiluminescence, with IC50 values ranging from 0.5 to 0.7&amp;nbsp;μg/ml. For macrophage cells, the extracts which showed strong suppressive activity for luminol-based
 chemiluminescence were C. xanthorrhiza and...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4295985</comments>
            <pubDate>Fri, 24 Dec 2010 07:02:08 +0100</pubDate>
            <guid isPermaLink="false">4295985</guid>        </item>
        <item>
            <title>Five condensed furanocoumarins from the root of Heracleum candicans Wall.</title>
            <link>http://www.medworm.com/index.php?rid=4289174&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg2832l33233l41x5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Three new spirotrifuranocoumarins, canditririns C–E (1–3), a new spirotetrafuranocoumarin, canditetrarin A (4), and a new tetrafuranocoumarin, canditetrarin B (5), were isolated from the roots of Heracleum candicans Wall. Their structures were established using spectral methods.
 
 
	Content Type Journal ArticleDOI 10.1007/s11418-010-0488-4Authors
		Masahiko Taniguchi, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, JapanAtsuko Inoue, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, JapanMakio Shibano, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, JapanNian-He Wang, Institute of Botany, Jiangsu Province and Academia Sinica, Nanjing, 20014 China...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4289174</comments>
            <pubDate>Wed, 22 Dec 2010 20:21:48 +0100</pubDate>
            <guid isPermaLink="false">4289174</guid>        </item>
        <item>
            <title>Evaluation of the taste of crude drug and Kampo formula by a taste-sensing system (4): taste of Processed Aconite Root</title>
            <link>http://www.medworm.com/index.php?rid=4254241&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F06rt84175370h153%2F</link>
            <description>In this study, we revealed the objective taste of
 PAR by using a taste-sensing system. The PAR samples examined were classified into four types by how the samples were processed:
 PAR1 processed by autoclaving; PAR2-a processed by autoclaving after rinsing in salt (sodium chloride) solution; PAR2-h processed
 by heating after rinsing in calcium chloride solution; PAR3 processed by treating with hydrated lime after rinsing in salt
 solution. The most characteristic taste factor of PAR is an aftertaste of cationic bitterness, which was detected in all PAR
 sample solutions, even at the concentration of 0.1&amp;nbsp;mg/ml. In addition, anionic bitterness and saltiness were detected in all
 sample solutions at 1&amp;nbsp;mg/ml. Furthermore, umami was detected in the PAR1, PAR2-a, and PAR3 sample solu...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4254241</comments>
            <pubDate>Fri, 10 Dec 2010 18:18:04 +0100</pubDate>
            <guid isPermaLink="false">4254241</guid>        </item>
        <item>
            <title>Effect of hydroalcoholic extract of Acorus calamus on tibial and sural nerve transection-induced painful neuropathy in rats</title>
            <link>http://www.medworm.com/index.php?rid=4254242&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl41711kj3003003t%2F</link>
            <description>This study was designed to investigate the therapeutic potential of hydroalcoholic extracts of Acorus calamus (AC) in tibial and sural nerve transection (TST)-induced neuropathic pain in rats. The hot plate, paw heat allodynia, acetone
 drop, and pinprick tests were performed to assess the degree of heat hyperalgesia, heat and cold allodynia, and mechanical
 hyperalgesia, respectively, at different time intervals, i.e., day 0, 1, 3, 6, 9, 12, 15, 18, and 21. The tissue superoxide
 anion and total calcium were measured as markers of oxidative stress. Tissue myeloperoxidase activity was measured as a specific
 marker of inflammation. Histopathological evaluation was also performed in the nervous tissue to assess the axonal degeneration.
 Pregabalin served as positive control in this study. T...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4254242</comments>
            <pubDate>Thu, 09 Dec 2010 17:53:02 +0100</pubDate>
            <guid isPermaLink="false">4254242</guid>        </item>
        <item>
            <title>Effects of yokukansan on anxiety-like behavior in a rat model of cerebrovascular dementia</title>
            <link>http://www.medworm.com/index.php?rid=4249762&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn42342807g551835%2F</link>
            <description>This study revealed that yokukansan shows anxiolytic effects not only in normal animals but also in cerebrovascular
 model rats.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s11418-010-0487-5Authors
		Ai Nogami, Department of Neuropharmacology, Faculty of Pharmaceutical Science, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180 JapanYuri Sakata, Department of Neuropharmacology, Faculty of Pharmaceutical Science, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180 JapanNaoki Uchida, Department of Psychiatry, Fukuoka University School of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180 JapanKazuko Yamaguchi, Department of Neuropharmacology, Faculty of Pharmaceutical Science, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka,...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4249762</comments>
            <pubDate>Wed, 08 Dec 2010 18:14:28 +0100</pubDate>
            <guid isPermaLink="false">4249762</guid>        </item>
        <item>
            <title>Antifibrotic activity of coumarins from Cnidium monnieri fruits in HSC-T6 hepatic stellate cells</title>
            <link>http://www.medworm.com/index.php?rid=4180134&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuj881g010mt00287%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The CHCl3 fraction of Cnidium monnieri fruits significantly inhibited the proliferation of hepatic stellate cells in an in-vitro assay system employing HSC-T6 hepatic
 stellate cell lines. Activity-guided fractionation of the CHCl3 fraction of C. monnieri led to the isolation of ten coumarins: osthol (1), meranzin (2), auraptenol (3), meranzin hydrate (4), 7-hydroxy-8-methoxy coumarin (5), imperatorin (6), xanthotoxol (7), xanthotoxin (8), bergapten (9) and isopimpinellin (10). Of these, compounds 1 and 6 significantly inhibited proliferation of HSCs in a time- and concentration-dependent manner. In addition, compounds 1 and 6 significantly reduced collagen content in HSC-T6 cells.
 
 
	Content Type Journal ArticleDOI 10.1007/s11418-010-0485-7Authors
		Eunjin Shin, Coll...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4180134</comments>
            <pubDate>Tue, 16 Nov 2010 19:30:45 +0100</pubDate>
            <guid isPermaLink="false">4180134</guid>        </item>
        <item>
            <title>Rubus suavissimus S. Lee extract increases early adipogenesis in 3T3-L1 preadipocytes</title>
            <link>http://www.medworm.com/index.php?rid=4180135&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft45738377p0632t4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Leaves of Rubus suavissimus S. Lee (Rosaceae) are used to prepare tiencha or sweet tea, which is helpful for body weight control by restricting calorie
 intake in obese patients. Obesity is a risk factor for metabolic syndrome, and a possible approach to treatment is to promote
 early adipogenesis in adipose tissue, thereby leading to replacement of enlarged adipocytes that secrete inflammatory factors
 with small adipocytes.We therefore investigated the effect of extract of tiencha leaves on early adipogenesis by using 3T3-L1
 preadipocytes as a model. Tiencha extract significantly and concentration-dependently increased adipogenesis measured in terms
 of lipid accumulation by means of Oil Red O assay and increased the expression of adiponectin and leptin. In the early...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4180135</comments>
            <pubDate>Tue, 16 Nov 2010 19:30:43 +0100</pubDate>
            <guid isPermaLink="false">4180135</guid>        </item>
        <item>
            <title>Rapid determination of atropine and scopolamine content in scopolia extract powder by HPLC</title>
            <link>http://www.medworm.com/index.php?rid=4176325&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff0wn673574552740%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A rapid method that does not require a complicated preparation was developed for determining by HPLC the content of atropine
 (At) and scopolamine (Sc) in a sample of scopolia extract powder. The sample solution for HPLC was extracted using 0.1&amp;nbsp;mol/L
 HCl/methanol (8:2). At and Sc were separated using a pentafluorophenylpropyl column and detected at a wavelength of 210&amp;nbsp;nm.
 Acetonitrile–10&amp;nbsp;mmol/L ammonium acetate adjusted to pH 5.0 (8:2, v/v) was used as the mobile phase. The linearity was good
 in the 5.0–500&amp;nbsp;μg/mL range for At and 0.5–500&amp;nbsp;μg/mL range for Sc. The specificity for both At and Sc was satisfactory. The
 quantitation limits were 5.0&amp;nbsp;μg/mL for At and 0.5&amp;nbsp;μg/mL for Sc. The quantitative values of total alkaloid calc...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4176325</comments>
            <pubDate>Sat, 13 Nov 2010 06:47:39 +0100</pubDate>
            <guid isPermaLink="false">4176325</guid>        </item>
        <item>
            <title>Flavonol glycosides from the leaves of Indigofera zollingeriana</title>
            <link>http://www.medworm.com/index.php?rid=4176328&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6220420l243270x6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Two new flavonol glycosides were isolated from the 1-butanol (1-BuOH)-soluble fraction of a methanol (MeOH) extract of the
 leaves of Indigofera
 zollingeriana, along with four flavonol glycosides and three known megastigmane glucosides. The structures of the new compounds were elucidated
 by spectroscopic analyses as kaempferol 3-O-β-d-(2″-O-β-d-apiofuranosyl)glucopyranoside 7-O-α-l-rhamnopyranoside and 3-O-β-d-(2″-O-β-d-apiofuranosyl, 6″-O-α-l-rhamnopyranosyl)glucopyranoside 7-O-α-l-rhamnopyranoside.
 
 
	Content Type Journal ArticleDOI 10.1007/s11418-010-0482-xAuthors
		Aya Hisaeda, Department of Pharmacognosy, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanKatsuyoshi Matsunami, Department ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4176328</comments>
            <pubDate>Sat, 13 Nov 2010 06:47:38 +0100</pubDate>
            <guid isPermaLink="false">4176328</guid>        </item>
        <item>
            <title>Beneficial effect of Sparassis crispa on stroke through activation of Akt/eNOS pathway in brain of SHRSP</title>
            <link>http://www.medworm.com/index.php?rid=4176327&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn64442lm77ju53h7%2F</link>
            <description>In conclusion, S. crispa could ameliorate cerebrovascular endothelial dysfunction by promoting recovery of Akt-dependent eNOS phosphorylation and
 increasing NO production in the cerebral cortex. S. crispa may be useful for preventing stroke and hypertension.
 
 
	Content Type Journal ArticleDOI 10.1007/s11418-010-0475-9Authors
		Hisae Yoshitomi, School of Pharmaceutical Sciences, Mukogawa Women’s University, 11-68 Koshien Kyuban-cho, Nishinomiya, Hyogo 663-8179, JapanEmiko Iwaoka, School of Pharmaceutical Sciences, Hyogo University of Health Science, Hyogo, JapanMasahide Kubo, Katsuragi Industry Co. Ltd, Wakayama, JapanMasaru Shibata, Suzuka University of Medical Science, Mie, JapanMing Gao, School of Pharmaceutical Sciences, Mukogawa Women’s University, 11-68 Koshien Kyuban-cho, Nish...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4176327</comments>
            <pubDate>Sat, 13 Nov 2010 06:47:38 +0100</pubDate>
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        <item>
            <title>A glycerol α-d-glucuronide and a megastigmane glycoside from the leaves of Guettardaspeciosa L.</title>
            <link>http://www.medworm.com/index.php?rid=4176326&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn51p00542w801242%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;From the 1-BuOH-soluble fraction of a MeOH extract of the leaves of Guettarda speciosa L., two new compounds (1, 2) were isolated together with six known compounds. Spectroscopic analysis of 1 and 2 established their structures to be derivatives of a glycerol α-glucuronide and a megastigmane glycoside, respectively. HPLC
 analysis of the hydrolyzate of 1 confirmed the presence of d-glucuronic acid in the structure, and the modified Mosher’s method established the absolute structure of 2.
 
 
	Content Type Journal ArticleDOI 10.1007/s11418-010-0484-8Authors
		Wen-Hu Cai, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8553 JapanKatsuyoshi Matsunami, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4176326</comments>
            <pubDate>Sat, 13 Nov 2010 06:47:38 +0100</pubDate>
            <guid isPermaLink="false">4176326</guid>        </item>
        <item>
            <title>Inhibitory effect of Iboga-type indole alkaloids on capsaicin-induced contraction in isolated mouse rectum</title>
            <link>http://www.medworm.com/index.php?rid=4135673&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6131g2765pj7702k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Voacanga africana (Apocynaceae) is used as an anti-diarrheal medicine in West Africa. In the present study, we investigated the effect of an
 extract of V. africana and its constituents on smooth muscle contraction induced by capsaicin in mouse rectum, where transient receptor potential
 vanilloid type 1 (TRPV1)-immunoreactive fibers are abundant. Methanol and alkaloid extracts of the root bark of V. africana were found to inhibit capsaicin-induced contraction in a dose-dependent manner (30–300&amp;nbsp;μg/ml). Major constituents isolated
 from the alkaloid extract were then studied for their effects on the capsaicin-induced contraction. The main active constituents
 were found to be Iboga-type alkaloids, including voacangine (1), 3-oxovoacangine (2), voacristine (3), ...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135673</comments>
            <pubDate>Mon, 01 Nov 2010 17:59:12 +0100</pubDate>
            <guid isPermaLink="false">4135673</guid>        </item>
        <item>
            <title>Anti-angiogenic effect of triterpenoidal saponins from Polygala senega</title>
            <link>http://www.medworm.com/index.php?rid=4135674&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5624jn5t3654u827%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Senegasaponins [senegin II (1), senegin III (2), senegin IV (3), senegasaponin a (4), and senegasaponin b (5)] from Polygala senega were re-discovered as selective anti-proliferative substances against human umbilical vein endothelial cells (HUVECs). Senegasaponins
 (1–5) showed anti-proliferative activity against HUVECs with IC50 values in the range 0.6–6.2&amp;nbsp;μM, and the selective index was 7–100-fold in comparison with those for several cancer cell lines,
 while the desacyl mixture of senegasaponins (6) and tenuifolin (7) lost anti-proliferative activity, indicating that the 28-O-glycoside moiety and methoxycinnamoyl group were essential for the HUVEC-selective growth inhibition of senegasaponins. Senegin
 III (2) inhibited the vascular endothelial growth fa...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135674</comments>
            <pubDate>Mon, 01 Nov 2010 17:59:10 +0100</pubDate>
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        <item>
            <title>Cytotoxic and EGFR tyrosine kinase inhibitory activities of aglycone derivatives obtained by enzymatic hydrolysis of oleoside-type secoiridoid glucosides, oleuropein and ligustroside</title>
            <link>http://www.medworm.com/index.php?rid=4135675&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvj1553q675757140%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hydrolysis of oleoside-type secoiridoid glucosides, oleuropein (1) and ligustroside (2), in the presence of β-glucosidase provided their aglycones, named (5S,8R,9S)-7-3,4-dihydroxyphenethyl elenolate (3) and (5S,8R,9S)-7-4-hydroxyphenethyl elenolate (4), respectively. The structures of 3 and 4 were identified by spectroscopic means and optical rotation measurements. Evaluation of the cytotoxic and epidermal growth
 factor receptor (EGFR) tyrosine kinase inhibitory activities of compounds 1–4 showed that compounds 3 and 4 exhibited moderate cytotoxicity against a disease-oriented panel of 39 human cancer cell lines in vitro, whereas compound
 3 inhibited the enzyme.
 
 
	Content Type Journal ArticleDOI 10.1007/s11418-010-0476-8Authors
		Masafumi Kikuchi, Department of...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4135675</comments>
            <pubDate>Mon, 01 Nov 2010 17:59:09 +0100</pubDate>
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        <item>
            <title>Quantitative analysis of neosalacinol and neokotalanol, another two potent α-glucosidase inhibitors from Salacia species, by LC-MS with ion pair chromatography</title>
            <link>http://www.medworm.com/index.php?rid=4120553&amp;cid=s_33359_13_f&amp;fid=33359&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn6577m63847m6441%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A quantitative analytical method for the highly polar sulfonium pseudo-sugar constituents neosalacinol (3) and neokotalanol (4), another two potent α-glucosidase inhibitors isolated from Ayurvedic traditional medicine Salacia species, was developed by employing an ion pair reagent upon chromatographic separation. The optimum conditions for separation
 and detection of these two constituents were achieved on an ODS column (3-µm particle size, 2.1-mm i.d.&amp;nbsp;×&amp;nbsp;100&amp;nbsp;mm) with 5&amp;nbsp;mM
 undecafluorohexanoic acid–MeOH (99:1, v/v) as the mobile phase and using MS equipped with an electrospray ionization source.
 More than ten samples of Salacia from different origins were analyzed, and the results indicated that the assay was reproducible and precise and could...</description>
            <author>Journal of Natural Medicines</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4120553</comments>
            <pubDate>Wed, 27 Oct 2010 16:16:32 +0100</pubDate>
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