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        <title>Cell Biochemistry and Function 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 'Cell Biochemistry and Function' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Cell+Biochemistry+and+Function&t=Cell+Biochemistry+and+Function&s=Search&f=source]]></link>
        <lastBuildDate>Sat, 20 Mar 2010 16:01:06 +0100</lastBuildDate>
        <item>
            <title>Proton leak modulation in testicular mitochondria affects reactive oxygen species production and lipid peroxidation</title>
            <link>http://www.medworm.com/index.php?rid=3373578&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1644</link>
            <description>Mitochondrial proton leak can account for almost 20% of oxygen consumption and it is generally accepted that this process contributes to basal metabolism. In order to clarify the role of basal proton leak in testicular mitochondria, we performed a comparative study with kidney and liver mitochondrial fractions. Proton leak stimulated by linoleic acid and inhibited by guanosine diphosphate (GDP) was detected, in a manner that was correlated with protein levels for uncoupling protein 2 (UCP2) in the three fractions. Modulation of proton leak had an effect on reactive oxygen species production as well as on lipid peroxidation, and this effect was also tissue-dependent. However, a possible role for the adenine nucleotide transporter (ANT) in testicular mitochondria proton leak could not be exc...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3373578</comments>
            <pubDate>Wed, 17 Mar 2010 00:00:00 +0100</pubDate>
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        <item>
            <title>New volatile anesthetic, desflurane, reduces vitamin E level in blood of operative patients via oxidative stress</title>
            <link>http://www.medworm.com/index.php?rid=3369594&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1641</link>
            <description>In conclusion, we observed that desflurane produced oxidative stress by decreasing [alpha]-tocopherol levels. Use of vitamin E may be possible to reduce the oxidative effect of desflurane. Copyright © 2010 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3369594</comments>
            <pubDate>Tue, 16 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3369594</guid>        </item>
        <item>
            <title>Vascular redox imbalance in rats submitted to chronic exercise</title>
            <link>http://www.medworm.com/index.php?rid=3369593&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1640</link>
            <description>Exercise training has been used for treatment/prevention of many cardiovascular diseases, but the mechanisms need to be clarified. Thus, our aim was to compare oxidative stress parameters between rats submitted to a swimming training and sedentary rats (control). Twelve male rats were divided into two groups: control and exercise training. The exercise training had daily 1 h swimming sessions for 8 weeks and a load (5% of its body mass) was placed in rat's tail. Thereafter the animals were killed, aorta and heart were surgically removed and blood was collected. Body mass gain, thiobarbituric acid reactive species (TBARS), carbonyl content, total reactive antioxidant potential (TRAP), total antioxidant reactivity (TAR), superoxide dismutase (SOD) activity and catalase (CAT) activity were ev...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3369593</comments>
            <pubDate>Tue, 16 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3369593</guid>        </item>
        <item>
            <title>Pluripotent plasticity of stem cells and liver repopulation</title>
            <link>http://www.medworm.com/index.php?rid=3369592&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1630</link>
            <description>Different types of stem cells have a role in liver regeneration or fibrous repair during and after several liver diseases. Otherwise, the origin of hepatic and/or extra-hepatic stem cells in reactive liver repopulation is under controversy. The ability of the human body to self-repair and replace the cells and tissues of some organs is often evident. It has been estimated that complete renewal of liver tissue takes place in about a year. Replacement of lost liver tissues is accomplished by proliferation of mature hepatocytes, hepatic oval stem cells differentiation, and sinusoidal cells as support. Hepatic oval cells display a distinct phenotype and have been shown to be a bipotential progenitor of two types of epithelial cells found in the liver, hepatocytes, and bile ductular cells. In g...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3369592</comments>
            <pubDate>Tue, 16 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3369592</guid>        </item>
        <item>
            <title>Erythropoietin induces nuclear translocation of Nrf2 and heme oxygenase-1 expression in SH-SY5Y cells</title>
            <link>http://www.medworm.com/index.php?rid=3365693&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1639</link>
            <description>Erythropoietin (Epo) exerts neuroprotective, glioprotective, and vascular protective effects in the nervous system. However, the mechanisms of the cytoprotective effect of Epo have not been fully clarified. Here, we investigated whether Epo affects the transcription and activation of nuclear factor erythroid 2-related factor 2 (Nrf2), which is a key transcription factor of the cellular anti-oxidant defense system, and mRNA expression of its target genes including heme oxygenase-1 (HO-1). Epo was added to SH-SY5Y cells at 1 U mL-1 and cultures were incubated for 24 h and then mRNA expression of Nrf2 target genes were analyzed with real-time PCR. SH-SY5Y cells were incubated with Epo at different time points and the nuclear and cytoplasmic levels of Nrf2 protein expression were examined by W...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3365693</comments>
            <pubDate>Mon, 15 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3365693</guid>        </item>
        <item>
            <title>Preventive role of PD-1 on MPTP-induced dopamine depletion in mice</title>
            <link>http://www.medworm.com/index.php?rid=3301462&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1642</link>
            <description>This study was designed to investigate the effect of PD-1 extract in the Parkinson's model of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) lesioned mice. The MPTP administration caused the dopamine neuron loss in the striatum and substantia nigra pars compacta (SNpc), which was demonstrated by a depletion of tyrosine hydroxylase (TH). In addition, a reduction of bcl-2 expression with elevation of bax expression, caspase-3 activation, and release of cytochrome c into cytosol in dopaminergic neurons of SNpc were noted. Oral administration of PD-1 extract (50 and 100 mg kg-1) attenuated the MPTP-induced depletion of TH proteins in the striatum and SNpc and prevented the apoptotic effects. These results indicate that PD-1 extract is able to protect dopaminergic neurons from MPTP-induced...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3301462</comments>
            <pubDate>Wed, 24 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3301462</guid>        </item>
        <item>
            <title>The pharmacological role of nucleotidases in snake venoms</title>
            <link>http://www.medworm.com/index.php?rid=3301463&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1637</link>
            <description>Several hydrolytic enzymes of snake venom have evolved to interfere in various physiological processes, which are well defined. However, hydrolytic enzymes such as nucleotidases (5[prime]nucleotidase, ATPase, and ADPase) are less studied and their pharmacological role in venoms is not clearly defined. Very few studies have shown the pharmacological importance of these endogenous purine release related enzymes in venoms. The near-ubiquitous distribution of these enzymes in venoms, suggests a significant role for these enzymes in envenomation. It is suggested that their major function is in the generation of purines (mainly adenosine) - a multitoxin. Therefore, it appears that these enzymes play a central role in liberating adenosine and through the action of adenosine help in prey immobiliz...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3301463</comments>
            <pubDate>Tue, 23 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3301463</guid>        </item>
        <item>
            <title>Erratum</title>
            <link>http://www.medworm.com/index.php?rid=3279388&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1651</link>
            <description>John D. Currey, Paul D. Baxter and Jonathan W. Pitchford (2009) Significance and importance: some common misapprehensions about statistics. Cell Biochemistry &amp; Function 2009; 27: 499-502. DOI: (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3279388</comments>
            <pubDate>Tue, 16 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3279388</guid>        </item>
        <item>
            <title>Regulation of cardiovascular cell function by hydrogen sulfide (H2S)</title>
            <link>http://www.medworm.com/index.php?rid=3211613&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1618</link>
            <description>Since the discovery of endogenously-produced hydrogen sulfide (H2S) in various tissues, there has been an explosion of interest in H2S as a biological mediator alongside other gaseous mediators, nitric oxide and carbon monoxide. The identification of enzyme-regulated H2S synthetic pathways in the cardiovascular system has led to a number of studies examining specific regulatory actions of H2S. We review evidence showing that endogenously-generated and exogenously-administered H2S exerts a wide range of actions in vascular and myocardial cells including vasodilator/vasoconstrictor effects via modification of the smooth muscle tone, induction of apoptosis and anti-proliferative responses in the smooth muscle cells, angiogenic actions, effects relevant to inflammation and shock, and cytoprote...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3211613</comments>
            <pubDate>Wed, 27 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3211613</guid>        </item>
        <item>
            <title>Erythroid 5-aminolevulinate synthase mediates the upregulation of membrane band 3 protein expression by iron</title>
            <link>http://www.medworm.com/index.php?rid=3184849&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1629</link>
            <description>In this study, we investigated the effect of short hairpin RNA (shRNA) mediated silencing of eALAS on the expression of band 3 protein induced by iron. By real-time RT-PCR and Western blot we showed that at mRNA and protein level iron-induced expression of band 3 protein was lower in eALAS-shRNA transfected K562 cells than in control cells. Of note, the lowest expression was detected in K562 cells cultured in iron deficiency condition (p &lt; 0.01). Thus either iron deficiency or depletion of eALAS could suppress the expression of erythroid band 3 protein. These results demonstrated for the first time that iron and the iron-regulatory system regulate the expression of the erythrocyte membrane proteins. Copyright © 2010 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184849</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184849</guid>        </item>
        <item>
            <title>Different neuronal Na+/K+-ATPase isoforms are involved in diverse signaling pathways</title>
            <link>http://www.medworm.com/index.php?rid=3184848&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1632</link>
            <description>Inhibition of rat neuronal Na+/K+-ATPase [alpha]3 isoform at low (100 nM) ouabain concentration led to activation of MAP kinase cascade via PKC and PIP3 kinase. In contrast to ouabain-sensitive [alpha]3 isoform of Na+/K+-ATPase, an ouabain-resistant [alpha]1 isoform (inhibition with 1 mM of ouabain) of Na+/K+-ATPase regulates MAP kinase via Src kinase dependent reactions. Using of Annexin V-FITC apoptotic test to determine the cells with early apoptotic features allows to conclude that [alpha]3 isoform stimulates and [alpha]1 suppresses apoptotic process in cerebellum neurons. These data are the first demonstration showing participation of ouabain-resistant ([alpha]1) and ouabain-sensitive ([alpha]3) Na+/K+-ATPase isoforms in diverse signaling pathways in neuronal cells. Copyright © 2010 ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184848</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184848</guid>        </item>
        <item>
            <title>Thiol redox status critically influences mitochondrial response to thyroid hormone-induced hepatic oxidative injury: A temporal analysis</title>
            <link>http://www.medworm.com/index.php?rid=3184847&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1631</link>
            <description>The objective of the present study was to investigate temporal regulation of mitochondrial glutathione and protein-bound thiol redox status in hyperthyroid liver. Mitochondria were isolated from control and hyperthyroid rat liver tissues at different time intervals, i.e., 24, 72, and 120 h following treatment, and sub-fractionated into sub-mitochondrial particles (SMPs) and matrix fractions. Increased prooxidant levels were indicative of oxidative stress in hyperthyroid mitochondria. Sensitivity to membrane lipid peroxidation (LPx) was maximal after 24 h, which subsided with time. Oxidative damage to proteins was evident as high carbonylation after 72 h; thiol residue damage was an early phenomenon. Reduced and oxidized glutathione (GSH and GSSG) pools of mitochondria were progressively de...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184847</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184847</guid>        </item>
        <item>
            <title>Soybean and sunflower oil-induced insulin resistance correlates with impaired GLUT4 protein expression and translocation specifically in white adipose tissue</title>
            <link>http://www.medworm.com/index.php?rid=3184846&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1628</link>
            <description>Free fatty acids are known for playing a crucial role in the development of insulin resistance. High fat intake is known for impairing insulin sensitivity; however, the effect of vegetable-oil injections have never been investigated. The present study investigated the effects of daily subcutaneous injections (100 µL) of soybean (SB) and sunflower (SF) oils, during 7 days. Both treated groups developed insulin resistance as assessed by insulin tolerance test. The mechanism underlying the SB- and SF-induced insulin resistance was shown to involve GLUT4. In SB- and SF-treated animals, the GLUT4 protein expression was reduced [sim]20% and 10 min after an acute in vivo stimulus with insulin, the plasma membrane GLUT4 content was [sim]60% lower in white adipose tissue (WAT). No effects were obs...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184846</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184846</guid>        </item>
        <item>
            <title>Protective effects of antioxidant combination against D-galactosamine-induced kidney injury in rats</title>
            <link>http://www.medworm.com/index.php?rid=3184845&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1625</link>
            <description>In conclusion, it seems reasonable to conclude that the treatment of the antioxidant combination has a protective effect on D-GaIN-induced kidney injury of rats. Copyright © 2010 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184845</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184845</guid>        </item>
        <item>
            <title>Effects of ammonia and allopurinol on rat hippocampal NMDA receptors</title>
            <link>http://www.medworm.com/index.php?rid=3184844&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1636</link>
            <description>Ammonia is considered to be the main agent responsible for hepatic encephalopathy which progressively leads to altered mental status. N-methyl-D-aspartate (NMDA) is an ionotropic glutamate receptor, which is involved in synaptogenesis, memory and neurotoxicity. The aim of this study was to investigate the effects of ammonia intoxication and allopurinol, a xanthine oxidase (XO) inhibitor, on NMDA receptor subunits, NR2A and NR2B, in the hippocampus of rats. Thirty-six male rats were divided into three groups (n = 12/group) as follows: (1)control group (phosphate buffered saline (PBS) solution); (2)ammonia group (ammonium acetate, 2.5 mmol/kg), (3)ammonia + allopurinol group (ammonium acetate, 2.5 mmol/kg, allopurinol, 50 mg/kg). Each rat received intraperitoneal injection for 28 days. Weste...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184844</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184844</guid>        </item>
        <item>
            <title>Iron metabolism markers and haptoglobin phenotypes in susceptibility to HSV-1 or/and HSV-2 lesion relapses</title>
            <link>http://www.medworm.com/index.php?rid=3184843&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1633</link>
            <description>Different haptoglobin (Hp) phenotypes play a role in several pathologic processes including infectious diseases. In order to evaluate the role of iron storage and metabolism in susceptibility to herpetic manifestations, we studied the frequency of the Hp phenotypes and iron metabolism in patients affected by H. Simplex virus 1 or 2 (HSV-1 or HSV-2), compared with controls. Hp phenotype and iron metabolism were determined in 100 patients with recurrent HSV-1 or HSV-2 manifestations during the relapses, and in 110 healthy subjects. The frequencies of the three Hp phenotypes in the patient group compared to the control group were 18% versus 14.5% p = NS for Hp 1.1, 25% versus 40% p = 0.03 for Hp 2.2 and 57% versus 45.5% p = NS for Hp 2.1. All iron metabolism parameters tested showed significa...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184843</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184843</guid>        </item>
        <item>
            <title>Bacoside A downregulates matrix metalloproteinases 2 and 9 in DEN-induced hepatocellular carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=3184842&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1638</link>
            <description>Cancer metastasis is a complex multi-step process, responsible for a majority of cancer-related deaths by affecting the critical organs and causing complications in therapies. Hepatocellular carcinoma is a multi-factorial disease and is the third most common cause of cancer related mortality worldwide. Clinical and experimental studies have shown that MMP-2 and MMP-9 are involved in tumor invasion and metastases and their elevated expression has been associated with poor prognosis. Our recent studies showed a strong anti-oxidant and hepatoprotective effects of bacoside A (BA) against carcinogen. Nevertheless the effect of BA on the activities and expression of MMP-2 and MMP-9 during hepatocellular carcinoma is not yet recognized. Therefore, the present study was designed to assess the same...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184842</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184842</guid>        </item>
        <item>
            <title>The actions of fisetin on glucose metabolism in the rat liver</title>
            <link>http://www.medworm.com/index.php?rid=3184841&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1635</link>
            <description>Fisetin is a flavonoid dietary ingredient found in the smoke tree (Cotinus coggyria) and in several fruits and vegetables. The effects of fisetin on glucose metabolism in the isolated perfused rat liver and some glucose-regulating enzymatic activities were investigated. Fisetin inhibited glucose, lactate, and pyruvate release from endogenous glycogen. Maximal inhibitions of glycogenolysis (49%) and glycolysis (59%) were obtained with the concentration of 200 µM. The glycogenolytic effects of glucagon and dinitrophenol were suppressed by fisetin 300 µM. No significant changes in the cellular contents of AMP, ADP, and ATP were found. Fisetin increased the cellular content of glucose 6-phosphate and inhibited the glucose 6-phosphatase activity. Gluconeogenesis from lactate and pyruvate or f...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184841</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184841</guid>        </item>
        <item>
            <title>Decrease of adenosine deaminase activity and increase of the lipid peroxidation after acute methotrexate treatment in young rats: protective effects of grape seed extract</title>
            <link>http://www.medworm.com/index.php?rid=3114427&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1627</link>
            <description>The methotrexate (MTX) is an anti-folate used to treat cancer and some inflammatory diseases. The efficacy of MTX is often limited by its severe toxicity. The present study was undertaken to determine whether Grape seed (Cabernet Sauvignon) extract (GSE) could ameliorate the MTX-induced oxidative injury and the effect on adenosine deaminase activity (ADA) in rats. The rats were pretreated with 50 mg/kg of GSE, i.p., prior to MTX administration (10 mg/kg, i.p.) with a second dose given 4 h and a third dose 16 h after MTX administration. Biochemical parameters were investigated 48 h after the last MTX administration. The administration of MTX increased thiobarbituric acid reactive species (TBARS) levels in hippocampus, kidney and liver, whereas induced a significant decreased in the ADA acti...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3114427</comments>
            <pubDate>Tue, 22 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3114427</guid>        </item>
        <item>
            <title>The effects of Nigella sativa on bile duct ligation induced-liver injury in rats</title>
            <link>http://www.medworm.com/index.php?rid=3114426&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1624</link>
            <description>Nigella sativa (NS) has been shown to have antioxidant and antiinflammatory activities in different conditions. The goal of this study was to evaluate the effects of NS on cholestatic liver injury in rats. Thirty rats were recruited in the study as follows: Group 1, Bile duct ligation (BDL) (n = 10); Group 2, BDL plus NS (n = 10); and Group 3, Sham (n = 10). Bile duct ligated group received 0.2 mL kg-1 dose of NS intraperitoneally daily throughout 14 days. Liver damage and cholestasis were determined by the biochemical and the pathologic examination. Data showed a decrease in gamma glutamyl transferase (GGT), alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and lactate dehydrogenase (LDH) activities of the NS treated rats when compared with BDL ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3114426</comments>
            <pubDate>Tue, 22 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3114426</guid>        </item>
        <item>
            <title>Dose-dependent actions of curcumin in experimentally induced myocardial necrosis: a biochemical, histopathological, and electron microscopic evidence</title>
            <link>http://www.medworm.com/index.php?rid=3114425&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1623</link>
            <description>Curcumin, an active component of turmeric, is a well-known antioxidant due to its reactive oxygen species (ROS) scavenging property. However, some in vitro studies have suggested that curcumin induces generation of ROS at higher doses and thus exerts pro-oxidant effect. We demonstrate, for the first time, the dose-dependent effects of curcumin in isoprenaline-induced model of myocardial necrosis in rats. The animals were assigned to control, isoprenaline and three curcumin treatment groups. Curcumin (100, 200, and 400 mg/kg) and vehicle (dimethyl sulfoxide) were administrated orally for 15 days and isoprenaline (85 mg/kg, s.c.) was given to curcumin treated and isoprenaline group on 13th and 14th day, respectively. Thereafter, on 15th day, the animals were sacrificed for biochemical analys...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3114425</comments>
            <pubDate>Tue, 22 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3114425</guid>        </item>
        <item>
            <title>Protein disulfide isomerase chaperone ERP-57 decreases plasma membrane expression of the human GnRH receptor</title>
            <link>http://www.medworm.com/index.php?rid=3114424&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1622</link>
            <description>Retention of misfolded proteins by the endoplasmic reticulum (ER) is a quality control mechanism involving the participation of endogenous chaperones such as calnexin (CANX). CANX interacts with and restricts plasma membrane expression (PME) of the gonadotropin releasing hormone receptor (GnRHR), a G protein-coupled receptor. CANX also interacts with ERP-57 a thiol oxidoreductase chaperone present in the ER. CANX along with ERP-57 promotes the formation of disulfide bond bridges in nascent proteins. The human GnRH receptor (hGnRHR) is stabilized by two disulfide bond bridges (C14-C200 and C114-C196), that, when broken, lead to a decrease in receptor expression at the plasma membrane. To determine if the presence of chaperones CANX and ERP-57 exerts an influence over membrane routing and se...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3114424</comments>
            <pubDate>Tue, 22 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3114424</guid>        </item>
        <item>
            <title>The inhibitory effects of rosiglitazone on cardiac hypertrophy through modulating the renin-angiotensin system in diet-induced hypercholesterolemic rats</title>
            <link>http://www.medworm.com/index.php?rid=3114423&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1621</link>
            <description>Cardiac hypertrophy is not only an adaptational state before heart failure but also is an independent risk factor for ischemia, arrhythmia, and sudden death. However, the direct effects of hypercholesterolemia on the myocardium and mechanisms are not completely understood. It has been demonstrated that peroxisome proliferator-activated receptor-[gamma] (PPAR[gamma]) ligand agonists attenuate cardiac hypertrophy through anti-inflammatory effects. The present study investigated the effects of PPAR[gamma] agonists on hypercholesterolemia-dependent, renin-angiotensin-system-related cardiac hypertrophy. The findings showed that left ventricular hypertrophy, eminent cardiomyocyte hypertrophy, and lipid deposits in myocardium were observed in the rats fed a cholesterol-rich diet for 6 months, whi...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3114423</comments>
            <pubDate>Tue, 22 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3114423</guid>        </item>
        <item>
            <title>The novel ruthenium - [gamma]-linolenic complex [Ru2(aGLA)4Cl] inhibits C6 rat glioma cell proliferation and induces changes in mitochondrial membrane potential, increased reactive oxygen species generation and apoptosis in vitro</title>
            <link>http://www.medworm.com/index.php?rid=3011635&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1626</link>
            <description>The present study reports the synthesis of a novel compound with the formula [Ru2(aGLA)4Cl] according to elemental analyses data, referred to as Ru2GLA. The electronic spectra of Ru2GLA is typical of a mixed valent diruthenium(II,III) carboxylate. Ru2GLA was synthesized with the aim of combining and possibly improving the anti-tumour properties of the two active components ruthenium and [gamma]-linolenic acid (GLA). The properties of Ru2GLA were tested in C6 rat glioma cells by analysing cell number, viability, lipid droplet formation, apoptosis, cell cycle distribution, mitochondrial membrane potential and reactive oxygen species. Ru2GLA inhibited cell proliferation in a time and concentration dependent manner. Nile Red staining suggested that Ru2GLA enters the cells and ICP-AES elemental...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3011635</comments>
            <pubDate>Thu, 19 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3011635</guid>        </item>
        <item>
            <title>Age-related effects of DHEA on peripheral markers of oxidative stress</title>
            <link>http://www.medworm.com/index.php?rid=3003155&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1619</link>
            <description>Ageing is an inevitable biological process characterized by a general decline in various physiological functions. DHEA and DHEAS levels are maximal between the second and third life decades, then start to decline 2% per year, leaving a residual of 10-20% of the peak production by the eighth decade. Erythrocytes are exposed to frequent oxidative stress due to the oxygen radicals continuously generated by haemoglobin auto-oxidation. We investigated DHEA chronic (10 mg/kg, subcutaneously, for 5 weeks) effects over oxidative stress markers in erythrocytes of male Wistar rats of 3, 13 and 18 month-old. In the 13 month-old group, we found increased lipid peroxidation (LPO), superoxide dismutase (SOD), glutathione-S-transferase and catalase activities when compared to the other age groups. DHEA p...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3003155</comments>
            <pubDate>Wed, 18 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3003155</guid>        </item>
        <item>
            <title>p63 and its isoforms as markers of rat oral mucosa epidermal stem cells in vitro</title>
            <link>http://www.medworm.com/index.php?rid=2995210&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1612</link>
            <description>Although techniques for purifying epidermal stem cells (ESCs) have been established, enriching a pure population of viable ESCs is still a challenging task. One approach toward enhancing the purity and viability of ESCs involves cell markers. While evidence suggests that p63 plays a role in maintaining the population of ESCs, whether p63 can function as a specific marker for ESCs is unclear. We isolated and cultured oral ESCs and illustrated the expression of p63 and its isoforms in rat oral mucosa tissues and stem cells before and after differentiation. Semi-reverse transcription PCR detected the TA, [Delta]N, [alpha] and [beta] isoforms when cells were cultured for 2 days, but only TA and [gamma] were detected after 14 days. We also found that p63 is expressed in basal and suprabasal epi...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2995210</comments>
            <pubDate>Mon, 16 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2995210</guid>        </item>
        <item>
            <title>Differential responses to oxidative stress and calcium influx on expression of the transforming growth factor-[beta] family in myoblasts and myotubes</title>
            <link>http://www.medworm.com/index.php?rid=2995209&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1614</link>
            <description>Changes in gene expression of TGF-[beta] family members and their receptors in response to treatment with H2O2 and a calcium ionophore, A23187, were examined in C2C12 myoblasts and myotubes. The expression of Myf5, an initial regulator of myogenesis, was increased by A23187, and H2O2 inhibited the up-regulation of Myf5. Treatment with H2O2 decreased the expression of MHC IIb, a protein component of the myofibrils, irrespective of the presence of A23187, suggesting an inhibitory role of oxidative stress for myogenesis. Expression of ligands and receptors for the TGF-[beta] family was modulated in response to H2O2 and A23187. Treatment with H2O2 decreased expression of TGF-[beta]3, BMP-4, ALK4, ALK5, and ActRIIB, and increased expression of inhibin [alpha] and inhibin [beta]A in either the m...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2995209</comments>
            <pubDate>Mon, 16 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2995209</guid>        </item>
        <item>
            <title>Apoptosis-inducing effects of Morinda citrifolia L. and doxorubicin on the Ehrlich ascites tumor in Balb-c mice</title>
            <link>http://www.medworm.com/index.php?rid=2980537&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1604</link>
            <description>Morinda citrifolia L. (Noni) is a herbal remedy with promising anti-cancer properties. However, its effects on various cancers are to be investigated to make a firm conclusion before implementing it into the clinical practice. Therefore, we investigated the cytotoxic potential of noni on Ehrlich ascites tumor grown in female Balb-c mice and also combined it with a potent anti-cancer agent, doxorubicin. One group received noni only (n = 8), another one doxorubicin (n = 8), and the other one noni + doxorubicin (n = 8) for 14 days after the inoculation of cells. The control group (n = 7) received 0.9% NaCl only. We found that short and long diameters of the tumor tissues were about 40-50% smaller, compared to those in control group. This anti-growth effect resulted from the induction of apopt...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2980537</comments>
            <pubDate>Wed, 11 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2980537</guid>        </item>
        <item>
            <title>Analysis of paraoxonase 1 (PON1) genetic polymorphisms and activities as risk factors for ischemic stroke in Turkish population</title>
            <link>http://www.medworm.com/index.php?rid=2976732&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1607</link>
            <description>In this study, we aimed to determine the importance of -107T/C, 192Q/R and 55L/M polymorphisms of PON1 gene and three PON1 activities (diazoxonase, paraoxonase, arylesterase) as risk factors for ischemic stroke.Study population was comprised of 172 unrelated adult Caucasian patients with acute hemispheric ischemic stroke and 105 symptom-free controls. Genotypes were attained by PCR followed by restriction enzyme digestion and phenotypes were determined by spectrophotometric assays.This is the first study analyzing diazoxonase activity as a risk factor for ischemic stroke. Nevertheless, diazoxonase, paraoxonase and arylesterase activities were almost the same in stroke patients and controls. The -107TT genotype was associated with a 1.97 times increased risk for stroke in elderly (age &gt; 59)...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2976732</comments>
            <pubDate>Tue, 10 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2976732</guid>        </item>
        <item>
            <title>Effects of supplementation with free glutamine and the dipeptide alanyl-glutamine on parameters of muscle damage and inflammation in rats submitted to prolonged exercise</title>
            <link>http://www.medworm.com/index.php?rid=2953886&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1611</link>
            <description>In this study, we investigated the effect of the supplementation with the dipeptide L-alanyl-L-glutamine (DIP) and a solution containing L-glutamine and L-alanine on plasma levels markers of muscle damage and levels of pro-inflammatory cytokines and glutamine metabolism in rats submitted to prolonged exercise. Rats were submitted to sessions of swim training for 6 weeks. Twenty-one days prior to euthanasia, the animals were supplemented with DIP (n = 8) (1.5 g.kg-1), a solution of free L-glutamine (1 g.kg-1) and free L-alanine (0.61 g.kg-1) (G&amp;A, n = 8) or water (control (CON), n = 8). Animals were killed at rest before (R), after prolonged exercise (PE - 2 h of exercise). Plasma concentrations of glutamine, glutamate, tumour necrosis factor-[alpha] (TNF-[alpha]), prostaglandin E2 (PGE2) a...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2953886</comments>
            <pubDate>Tue, 03 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2953886</guid>        </item>
        <item>
            <title>Transcriptional regulation of IER3IP1 gene by tumor necrosis factor-[alpha] and Sp family proteins</title>
            <link>http://www.medworm.com/index.php?rid=2953888&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1613</link>
            <description>In this report, we investigated the molecular mechanism by which the expression of IER3IP1 gene is regulated by cloning the 5[prime] flanking region of the human IER3IP1 gene for various promoter studies. Deletion analysis was used to identify the basal promoter activity retained at -298/-59 region and mutation analysis proved that Sp1 is a transcriptional activator of this gene expression. As an early response gene, IER3IP1 showed an increase in transcription in response to tumor necrosis factor [alpha] (TNF-[alpha]) in a time- and dose-dependent manner. This inducible response to TNF-[alpha] is mediated by the demonstration of nuclear factor [kappa]B (NF-[kappa]B) responsive element on IER3IP1 promoter sequence. From our results, we suggest that IER3IP1 gene is involved in TNF-[alpha]-me...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2953888</comments>
            <pubDate>Mon, 02 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2953888</guid>        </item>
        <item>
            <title>Increased resistance to hydrogen peroxide-induced cardiac contracture is associated with decreased myocardial oxidative stress in hypothyroid rats</title>
            <link>http://www.medworm.com/index.php?rid=2953887&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1616</link>
            <description>The purpose of this study was to determine whether decreased oxidative stress would increase the resistance to cardiac contracture induced by H2O2 in hypothyroid rats. Male Wistar rats were divided into two groups: control and hypothyroid. Hypothyroidism was induced via thyroidectomy. Four weeks post surgery, blood samples were collected to perform thyroid hormone assessments, and excised hearts were perfused at a constant flow with or without H2O2 (1 mmol/L), being divided into two sub-groups: control, hypothyroid, control + H2O2, hypothyroid + H2O2. Lipid peroxidation (LPO) was evaluated by chemiluminescence (CL) and thiobarbituric acid reactive substances (TBARS) methods, and protein oxidation by carbonyls assay in heart homogenates. Cardiac tissue was also screened for superoxide dismu...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2953887</comments>
            <pubDate>Mon, 02 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2953887</guid>        </item>
        <item>
            <title>Development and optimization of a cell-based assay for the selection of synthetic compounds that potentiate bone morphogenetic protein-2 activity</title>
            <link>http://www.medworm.com/index.php?rid=2930379&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1615</link>
            <description>In this study, we describe the development and optimization of a cell-based assay that is sensitive, reproducible, and reliable in identifying reagents that potentiate the effects of BMP-2 in inducing transdifferentiation of C2C12 myoblasts into the osteoblastic phenotype. The assay is based on a BMP-responsive Smad1-driven luciferase reporter gene. LIM mineralization protein-1 (LMP-1) is a novel intracellular LIM domain protein that has been shown by our group to enhance cellular responsiveness to BMP-2. Our previous report elucidated that the binding of LMP-1 with the WW2 domain in Smad ubiquitin regulatory factor-1 (Smurf1) rescues the osteogenic Smads from degradation. Here, using the optimized cell-based assay, we first evaluated the activity of the recombinantly prepared proteins, LM...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2930379</comments>
            <pubDate>Tue, 27 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2930379</guid>        </item>
        <item>
            <title>Ceramide induces endothelial cell senescence</title>
            <link>http://www.medworm.com/index.php?rid=2908023&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1605</link>
            <description>Ceramide has been proposed to be a mediator of replicative senescence. Our aim was to determine whether ceramide induces senescence in vascular endothelial cells. Human umbilical vein endothelial cells were cultured to different population doubling levels and ceramide levels were quantitated. The endogenous levels of ceramide increased 2.4-fold with senescence onset. Low passage cells were chronically treated with exogenous C6-ceramide. This treatment induced a senescent phenotype as measured by an inhibition of cell proliferation and DNA replication while increasing senescence-associated [beta]-galactosidase expression. This is the second cell type in which ceramide induces senescence, thus implicating ceramide as a general mediator of cellular senescence. Copyright © 2009 John Wiley &amp; S...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2908023</comments>
            <pubDate>Mon, 19 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2908023</guid>        </item>
        <item>
            <title>Integrating the cell stress response: a new view of molecular chaperones as immunological and physiological homeostatic regulators</title>
            <link>http://www.medworm.com/index.php?rid=2893788&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1609</link>
            <description>The response of cells to stress was first documented in the 1960s and 1970s and the molecular nature of the families of proteins that subserve this vital response, the molecular chaperones, were identified and subjected to critical study in the period from the late 1980s. This resulted in the rapidly advancing new field of protein folding and its role in cellular function. Emerging at the same time, but initially largely ignored, were reports that molecular chaperones could be released by cells and exist on the outer plasma membrane or in the body fluids. These secreted molecular chaperones were found to have intercellular signalling functions. There is now a growing body of evidence to support the hypothesis that molecular chaperones have properties ascribed to the Roman god Janus, the go...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2893788</comments>
            <pubDate>Wed, 14 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2893788</guid>        </item>
        <item>
            <title>Changes in the mRNA expression of osteoblast-related genes in response to [beta]3-adrenergic agonist in UMR106 cells</title>
            <link>http://www.medworm.com/index.php?rid=2889844&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1617</link>
            <description>In conclusion, [beta]3-AR activation in rat osteoblasts induced alteration in the expression of osteoblast-related transcription factor genes as well as genes required for bone formation and resorption. The present results also suggest that, besides [beta]2-AR, [beta]3-AR is another AR subtype responsible for the sympathetic nervous system-induced bone remodeling. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2889844</comments>
            <pubDate>Tue, 13 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2889844</guid>        </item>
        <item>
            <title>Organ preservation solutions attenuate accumulation and nuclear translocation of hypoxia-inducible factor-1[alpha] in the hepatoma cell line HepG2</title>
            <link>http://www.medworm.com/index.php?rid=2875131&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1608</link>
            <description>In conclusion, preservation solutions attenuate accumulation and nuclear translocation of the transcription factor HIF-1[alpha], and this property is seemingly related to their chemical composition (L-arginine, [alpha]-ketoglutarate). Thus, it appears feasible to design preservation solution specifically to modify HIF-1[alpha] accumulation and nuclear translocation. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2875131</comments>
            <pubDate>Thu, 08 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2875131</guid>        </item>
        <item>
            <title>The effect of 5 days of aspartate and asparagine supplementation on glucose transport activity in rat muscle</title>
            <link>http://www.medworm.com/index.php?rid=2875130&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1606</link>
            <description>The consumption of protein supplements containing amino acids is increasing around the world. Aspartate (Asp) and asparagine (Asn) are amino acids metabolized by skeletal muscle. This metabolism involves biochemical pathways that are involved in increasing Krebs cycle activity via anaplerotic reactions, resulting in higher glutamine concentrations. A connection between amino acid supplementation, glycogen concentration, and glucose uptake has been previously demonstrated. The purpose of this study was to evaluate the effect of Asp and Asn supplementation on glucose uptake in rats using three different glycogen concentrations. The results indicate that Asp and Asn supplementation in rats with high glycogen concentrations (fed state) further increased the glycogen concentration in the muscle...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2875130</comments>
            <pubDate>Thu, 08 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2875130</guid>        </item>
        <item>
            <title>Rate of T alleles and TT genotype at MTHFR 677C-&gt;T locus or C alleles and CC genotype at MTHFR 1298A-&gt;C locus among healthy subjects in Turkey: impact on homocysteine and folic acid status and reference intervals</title>
            <link>http://www.medworm.com/index.php?rid=2807052&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1610</link>
            <description>This study was designed to determine the rate of MTHFR 677C-&gt;T and 1298A-&gt;C mutations, and their influence on serum folate, Hcy and vitamin B12 status and the reference intervals in 402 healthy Turkish adults. The rate of MTHFR 677C-&gt;T or 1298A-&gt;C mutations was 50.7% or 54.7%, respectively. The MTHFR 677C-&gt;T mutation-specific reference intervals for serum folate and tHcy were characterized by marked shifts in their upper limits. In homozygote subjects for MTHFR 677C-&gt;T serum folate concentration was lower and serum tHcy concentration was higher than those in the wild genotype; all subjects had lower serum folate and 54% of the subjects had higher tHcy concentrations than the cutoff values of [le]10 nmol/L and [ge]12 µmol/L, respectively. Serum vitamin B12 status was similar in all genotyp...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2807052</comments>
            <pubDate>Thu, 17 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2807052</guid>        </item>
        <item>
            <title>TNF-[alpha], a potent lipid metabolism regulator</title>
            <link>http://www.medworm.com/index.php?rid=2795917&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1596</link>
            <description>As a multifunctional cytokine, tumor necrosis factor alpha (TNF-[alpha]) exerts a series of biological actions in different cells, tissues, organs, and species and has been demonstrated to regulate and interfere with energy metabolism, especially lipid homeostasis. A large body of researches suggested that the effects of TNF-[alpha] on lipid metabolism mainly include five aspects: (1) suppresses free fatty acid (FFA) uptake and promotes lipogenesis; (2) induces lipolysis; (3) inhibits lipid-metabolism-related enzymes activity; (4) regulates cholesterol metabolism; (5) regulates other adipocyte-derived adipokines. The molecular mechanisms underlying these actions are complex and several signal transduction pathways might be involved. Regulation of metabolism-related gene expression at trans...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2795917</comments>
            <pubDate>Mon, 14 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2795917</guid>        </item>
        <item>
            <title>Effect of stress and stress hormones on the hormone (insulin) binding of Tetrahymena</title>
            <link>http://www.medworm.com/index.php?rid=2777760&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1592</link>
            <description>The unicellular Tetrahymena pyriformis GL produce, store and secrete vertebrate-like hormones. In earlier experiments the effect of different stressors on the hormone levels of Tetrahymena was studied and an elevation of these was found. In the present experiments the hormone binding was investigated, using flow cytometric method. FITC-insulin binding was elevated after concentrated (5, 10, or 20 mg ml-1) NaCl or 0.01%, 0.1%, or 0.05% formaldehyde treatment, or after thermal stress (37°C). Serotonin given together with NaCl increased and together with formaldehyde decreased the binding. Histamine always decreased the binding and insulin was indifferent. Four hours after osmotic stress, hormone binding significantly decreased and this was not influenced by hormones. However, 4 h after form...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2777760</comments>
            <pubDate>Tue, 08 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2777760</guid>        </item>
        <item>
            <title>Mechanism of cell death by 5-aminolevulinic acid-based photodynamic action and its enhancement by ferrochelatase inhibitors in human histiocytic lymphoma cell line U937</title>
            <link>http://www.medworm.com/index.php?rid=2768337&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1603</link>
            <description>Photodynamic therapy (PDT) for tumors is based on the tumor-selective accumulation of a photosensitizer, protoporphyrin IX (PpIX), followed by irradiation with visible light. However, the molecular mechanism of cell death caused by PDT has not been fully elucidated. The 5-aminolevulinic acid (ALA)-based photodynamic action (PDA) was dependent on the accumulation of PpIX, the level of which decreased rapidly by eliminating ALA from the incubation medium in human histiocytic lymphoma U937 cells. PDA induced apoptosis characterized by lipid peroxidation, increase in Bak and Bax/Bcl-xL, decrease in Bid, membrane depolarization, cytochrome c release, caspase-3 activation, phosphatidylserine (PS) externalization. PDT-induced cell death seemed to occur predominantly via apoptosis through distribu...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2768337</comments>
            <pubDate>Thu, 03 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2768337</guid>        </item>
        <item>
            <title>Effects of insulin replacement on cardiac apoptotic and survival pathways in streptozotocin-induced diabetic rats</title>
            <link>http://www.medworm.com/index.php?rid=2740796&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1601</link>
            <description>Increased myocyte apoptosis in diabetic hearts has been previously reported. Therefore, the purpose of this study was to evaluate the effects of insulin on cardiac apoptotic, hypertrophic, and survival pathways in streptozotocin (STZ)-induced diabetic rats. Forty-eight male Wistar rats at 8 weeks of age were randomly divided into control group (Control), STZ-induced (65 mg/kg STZ i.v.) Type 1-like diabetic rats (DM), and DM rats with 4 IU insulin replacement (DI) for 4 and 8 weeks, respectively. The levels of protein involved in cardiac apoptotic, hypertrophic, and survival pathways were measured by Western blotting. Cardiac mitochondrial-dependent apoptotic pathways, such as Bad, cytosolic cytochrome c, activated caspase 9 and 3, and calcineurin-nuclear factor activation transcription 3 (...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2740796</comments>
            <pubDate>Thu, 27 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2740796</guid>        </item>
        <item>
            <title>IgLON cell adhesion molecules regulate synaptogenesis in hippocampal neurons</title>
            <link>http://www.medworm.com/index.php?rid=2737169&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1600</link>
            <description>IgLON cell adhesion molecules (CAMs) belonging to the immunoglobulin superfamily comprise of LAMP, neurotrimin (Ntm), OBCAM, and Kilon. In the present study, we performed the single and double transfection of IgLON gene constructs into hippocampal neurons in vitro and evaluated synaptic number. The quantitative analysis showed that the single over-expression of LAMP or OBCAM increased synaptic number, while the over-expression of Kilon reduced synaptic number and Ntm had no effects. The double over-expression of Kilon-Ntm, Kilon-OBCAM, LAMP-Ntm, and Ntm-OBCAM decreased synaptic number and that of Kilon-LAMP and LAMP-OBCAM had no effect. These results suggest that IgLON CAMs participate in regulating synapse formation in hippocampal neurons. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2737169</comments>
            <pubDate>Wed, 26 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2737169</guid>        </item>
        <item>
            <title>Interaction of diphtheria toxin (fragment A) with actin</title>
            <link>http://www.medworm.com/index.php?rid=2737173&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1590</link>
            <description>It was shown by gel filtration and viscosity measurements that N-terminal fragment (FA) of diphtheria toxin (DT) can interact with both G- and F-actin (filamentous actin). Elution profiles on Sephadex G-100 indicated the formation of a binary complex of fragment A (FA) with globular actin monomer (G-actin), which was inhibited by gelsolin. Deoxyribonuclease I (DNase I) in turn appeared to interact with this complex. Tritiated FA was found to bind to F-actin stoichiometrically. This binding was inhibited again by gelsolin and G-actin, but not by DNase I. The binding of FA inhibited polymerization of G-actin and induced a time-dependent breakdown of F-actin under polymerization conditions. Inhibition of its ADP-ribosyltransferase activity did not have any effect on the interactions of FA wit...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2737173</comments>
            <pubDate>Tue, 25 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2737173</guid>        </item>
        <item>
            <title>A JNK inhibitor SP600125 induces defective cytokinesis and enlargement in P19 embryonal carcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=2737172&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1597</link>
            <description>While analyzing the role of c-Jun NH2-terminal kinase (JNK) in neurogenesis in P19 embryonal carcinoma cells, we noticed that treatment with SP600125, a JNK inhibitor, increased the cell size markedly. SP600125-induced enlargement of P19 cells was time- and dose-dependent. The increased cell size in response to SP600125 was also detected in B6mt-1 embryonic stem cells. SP600125 treatment inhibited cell growth and increased DNA contents, indicating the inhibition of cell proliferation resulting from endoreduplication. Concurrently, the gene expression of p21, a regulator of G2/M arrest as well as G1 arrest, was increased in cells treated with SP600125. The increased cell size in response to SP600125 was detected even in P19 cells treated with colcemide, an inhibitor of cell cycle progressio...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2737172</comments>
            <pubDate>Tue, 25 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2737172</guid>        </item>
        <item>
            <title>Polymorphisms of DNA base-excision repair genes APE/Ref-1 and XRCC1 are not associated with the risk for Graves' disease</title>
            <link>http://www.medworm.com/index.php?rid=2737171&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1595</link>
            <description>Oxidative stress has been implicated in etiopathogenesis of Graves' disease (GD). Increased lipid peroxidation and oxidative DNA damage have been found in GD patients. Oxidative DNA damage is mainly repaired by the base-excision repair (BER) pathway. Polymorphisms in DNA-repair genes have been associated with the increased risk of various diseases and could also be related to the etiology of GD. Therefore, we conducted a study including 197 patients with GD and age- and sex-matched 303 healthy subjects to examine the role of single-nucleotide polymorphisms of BER genes, APE/Ref-1 (codon 148) and XRCC1 (codons 194 and 399) as a risk factor for GD. These polymorphisms were determined by quantitative real-time PCR and melting curve analysis using LightCycler. No significant association was ob...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2737171</comments>
            <pubDate>Tue, 25 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2737171</guid>        </item>
        <item>
            <title>Changes of glycogen content in liver, skeletal muscle, and heart from fasted rats</title>
            <link>http://www.medworm.com/index.php?rid=2737170&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1602</link>
            <description>Glycogen content of white and red skeletal muscles, cardiac muscle, and liver was investigated in conditions where changes in plasma levels of non-esterified fatty acids (NEFA) occur. The experiments were performed in fed and 12 and 48 h-fasted rats. The animals were also submitted to swimming for 10 and 30 min. Glycogen content was also investigated in both pharmacologically induced low plasma NEFA levels fasted rats and pharmacologically induced high plasma NEFA levels fed rats. The participation of Akt and glycogen synthase kinase-3 (GSK-3) in the changes observed was investigated. Plasma levels of NEFA, glucose, and insulin were determined in all conditions. Fasting increased plasma NEFA levels and reduced glycogen content in the liver and skeletal muscles. However, an increase of glyc...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2737170</comments>
            <pubDate>Tue, 25 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2737170</guid>        </item>
        <item>
            <title>Characterization and comparison of adipose tissue-derived cells from human subcutaneous and omental adipose tissues</title>
            <link>http://www.medworm.com/index.php?rid=2711590&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1591</link>
            <description>Different fat depots contribute differently to disease and function. These differences may be due to the regional variation in cell types and inherent properties of fat cell progenitors. To address the differences of cell types in the adipose tissue from different depots, the phenotypes of freshly isolated adipose tissue-derived cells (ATDCs) from subcutaneous (SC) and omental (OM) adipose tissues were compared using flow cytometry. Our results showed that CD31-CD34+CD45-CD90-CD105-CD146+ population, containing vascular smooth muscle cells and pericytes, was specifically defined in the SC adipose tissue while no such population was observed in OM adipose tissue. On the other hand, CD31-CD34+CD45-CD90-CD105-CD146- population, which is an undefined cell population, were found solely in OM ad...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2711590</comments>
            <pubDate>Tue, 18 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2711590</guid>        </item>
        <item>
            <title>Chronic exercise decreases cytokine production in healthy rat skeletal muscle</title>
            <link>http://www.medworm.com/index.php?rid=2698913&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1594</link>
            <description>In conclusion, exercise training induced decreased cytokine protein expression in the skeletal muscle. These data show that in healthy rats, 8-week moderate-intensity aerobic training down regulates skeletal muscle production of cytokines involved in the onset, maintenance and regulation of inflammation, and that the response is heterogeneous according to fibre composition. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2698913</comments>
            <pubDate>Thu, 13 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2698913</guid>        </item>
        <item>
            <title>Biological markers in cerebrospinal fluid (CSF) and evaluation of in vitro effect of CSF on PC12 cell line viability in Alzheimer's disease</title>
            <link>http://www.medworm.com/index.php?rid=2644554&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1588</link>
            <description>The definite diagnosis of Alzheimer's disease (AD) is based on post mortem pathological examination. To date, there is no laboratory test that can discriminate AD patients from healthy individuals. In the perspective of recent knowledge, there are three cerebrospinal fluid (CSF) markers which have the highest sensitivity and specificity: A[beta]1-40, A[beta]1-42, and p-tau. In the present study, 15 'Probable Alzheimer's Disease' (PAD) patients and 15 control subjects were included. PAD patients were selected from the patients of Dokuz Eylül University Neurology Department Dementia outpatient clinic and control subjects were selected from the patients who were undergone epidural anesthesia because of any surgical operation. The concentrations of Ab1-40, Ab1-42, and p-tau in CSF were quanti...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2644554</comments>
            <pubDate>Mon, 27 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2644554</guid>        </item>
        <item>
            <title>Up-regulation of the tight-junction protein ZO-1 by substance P and IGF-1 in A431 cells</title>
            <link>http://www.medworm.com/index.php?rid=2644553&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1587</link>
            <description>The formation of a barrier by tight junctions is important in epithelia of various tissues. Substance P (SP) and insulin-like growth factor (IGF)-1 synergistically promote barrier function in the corneal epithelium. We have now examined the effects of SP and IGF-1 on expression of the tight-junction protein zonula occludens (ZO)-1 in A431 human epidermoid carcinoma cells. Reverse transcription-polymerase chain reaction (RT-PCR) and immunoblot analyses revealed that SP and IGF-1 increased the amounts of ZO-1 mRNA and protein in these cells in a concentration-dependent manner, with neither SP nor IGF-1 alone having such an effect. The SP- and IGF-1-induced up-regulation of ZO-1 was accompanied by phosphorylation of extracellular signal-regulated kinase (ERK), and both of these effects were b...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2644553</comments>
            <pubDate>Mon, 27 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2644553</guid>        </item>
        <item>
            <title>Vitamin C and E combination modulates oxidative stress induced by X-ray in blood of smoker and nonsmoker radiology technicians</title>
            <link>http://www.medworm.com/index.php?rid=2641172&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1589</link>
            <description>X-ray radiation is detrimental to human cells and may lead to development of life-threatening diseases. Cigarette smoke contains about 500 chemicals that include organic and oxidant compounds whereas vitamin C and E (VCE) have scavenger effects on the compounds. We investigated effects of VCE administration on X-ray-induced oxidative toxicity in blood of smoker and nonsmoker X-ray technicians.Twenty technicians and 30 healthy age-matched subjects control were used in the study. Ten of the X-ray technicians and 15 of the control were smokers. Blood samples were taken from the control. Oral vitamin C (500 mg) and vitamin E (150 mg) were daily supplemented to the smoker and nonsmoker X-ray technicians for 5 weeks. Blood samples were taken from the X-ray technicians after and before 5 weeks. P...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2641172</comments>
            <pubDate>Sun, 26 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2641172</guid>        </item>
        <item>
            <title>Effects of [beta]-carotene on antioxidant status in rats with chronic alcohol consumption</title>
            <link>http://www.medworm.com/index.php?rid=2641171&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1579</link>
            <description>This study examined the effects of [beta]-carotene on antioxidant status in rats with chronic alcohol consumption. At the beginning of experiment (week 0), according to both the plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities, rats (n = 24) were divided into 3 groups and fed with a standard diet (group C), a diet containing ethanol (group E), or a diet containing ethanol and [beta]-carotene (group E+B). After 10 weeks, plasma AST and ALT, fat accumulation in the liver, antioxidant enzyme activities in erythrocytes and the liver, malondialdehyde (MDA), and [alpha]-tocopherol and retinol in plasma and hepatic samples were analyzed. The chronic alcohol diet significantly increased AST and ALT levels in plasma, and these changes were prevented by supplemen...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2641171</comments>
            <pubDate>Sun, 26 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2641171</guid>        </item>
        <item>
            <title>Ketogenesis evaluation in perfused liver of diabetic rats submitted to short-term insulin-induced hypoglycemia</title>
            <link>http://www.medworm.com/index.php?rid=2625258&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1586</link>
            <description>Ketogenesis, inferred by the production of acetoacetate plus ß-hydroxybutyrate, in isolated perfused livers from 24-h fasted diabetic rats submitted to short-term insulin-induced hypoglycemia (IIH) was investigated. For this purpose, alloxan-diabetic rats that received intraperitoneal regular insulin (IIH group) or saline (COG group) injection were compared. An additional group of diabetic rats which received oral glucose (gavage) (100 mg kg-1) 15 min after insulin administration (IIH + glucose group) was included. The studies were performed 30 min after insulin (1.0 U kg-1) or saline injection. The ketogenesis before octanoate infusion was diminished (p &lt; 0.05) in livers from rats which received insulin (COG vs. IIH group) or insulin plus glucose (COG vs. IIH + glucose group). However, t...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2625258</comments>
            <pubDate>Tue, 21 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2625258</guid>        </item>
        <item>
            <title>HERC1 polymorphisms: population-specific variations in haplotype composition</title>
            <link>http://www.medworm.com/index.php?rid=2615248&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1582</link>
            <description>Human HERC1 is one of six HERC proteins and may play an important role in intracellular membrane trafficking. The human HERC1 gene is suggested to have been affected by local positive selection. To assess the global frequency distributions of coding and non-coding single nucleotide polymorphisms (SNPs) in the HERC1 gene, we developed a new simultaneous genotyping method for four SNPs, and applied this method to investigate 1213 individuals from 12 global populations. The results confirmed remarked differences in the allele and haplotype frequencies between East Asian and non-East Asian populations. One of the three common haplotypes observed was found to be characteristic of East Asians, who showed a relatively uniform distribution of haplotypes. Information on haplotypes would be useful f...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2615248</comments>
            <pubDate>Sat, 18 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2615248</guid>        </item>
        <item>
            <title>Human insulin A-chain peptide analog(s) with in vitro biological activity</title>
            <link>http://www.medworm.com/index.php?rid=2615249&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1584</link>
            <description>In a previous study, we showed that a synthetic human insulin 1-chain analog, named analog (3) was capable of mimicking in vitro effects of native insulin, including stimulation of cell proliferation, glucose uptake and glycogen synthesis. Here, we have synthesized three new analogs (6, 9, 12) of the human A-chain, bearing or not their N- or C-terminal residue, to determine the structural features which are responsible for their biological properties. In vitro experiments clearly demonstrated that the N-terminal part of the peptides is required for the biological activity of the molecules, suggesting its crucial role in the mechanism underlying the cellular effect. Our findings may help to better understand the mechanism of interaction between insulin and its receptor. In addition, the pre...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2615249</comments>
            <pubDate>Thu, 16 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2615249</guid>        </item>
        <item>
            <title>Pulmonary antioxidant defences and protein damage during the ageing process of both sexes</title>
            <link>http://www.medworm.com/index.php?rid=2587657&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1585</link>
            <description>The free radical theory holds that the senescence is caused by oxidative damage that results from an imbalance between reactive oxygen and nitrogen species (RONS) and antioxidant defences. Hence, it plays an important role in the field of gerontology. We evaluated, in male and female rats, the activities of the antioxidant enzymes catalase (CAT), glutathione peroxidase (GPx), and total superoxide dismutase (tSOD), as well as oxidative protein damage in pulmonary tissue at 3, 6, 12, and 20 months of age. The results show an increase in the activities of all antioxidant enzymes at 12 months of age in female rats, suggesting an association with the reproductive life cycle. Protein damage in female pulmonary tissues did not change significantly throughout the ageing process. In male rats, the ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2587657</comments>
            <pubDate>Wed, 08 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2587657</guid>        </item>
        <item>
            <title>Determination of the lactate threshold and maximal blood lactate steady state intensity in aged rats</title>
            <link>http://www.medworm.com/index.php?rid=2579699&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1580</link>
            <description>The reliability of the lactate threshold (LT) determined in aged rats and its validity to identify an exercise intensity corresponding to the maximal blood lactate steady state (MLSS) were analyzed. Eighteen male aged Wistar rats ([sim]365 days) were submitted to two incremental swimming tests until exhaustion, consisting of an initial load corresponding to 1% of body mass (BM) and increments of 1% BM at each 3-min with blood lactate ([lac]) measurements. The LT was determined by visual inspection (LTV) as well by applying a polynomial function on the [lac]/workload ratio (LTP) by considering the vertices of the curve. For the MLSS, twelve animals were submitted, on different days, to 3-4 exercise sessions of 30-min with workload corresponding to 4, 5 or 6% BM. The MLSS was considered the ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2579699</comments>
            <pubDate>Tue, 07 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2579699</guid>        </item>
        <item>
            <title>TpMRK regulates cell division of Tetrahymena in response to oxidative stress</title>
            <link>http://www.medworm.com/index.php?rid=2579700&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1583</link>
            <description>TpMRK was identified as a stress-responsive mitogen activated protein kinase (MAPK)-related kinase and has been shown to play a critical role in the stress signalling in Tetrahymena cells. Here, we found that the mRNA expression of TpMRK was correlated with cell division of Tetrahymena with decreased expression occurring in cells prior to entering synchronous cell division induced by heat treatment. Notably, cell division was delayed with a lower division index of 40% after exposure to hydrogen peroxide while 85% of cells underwent cell division synchronously at 75 min after heat treatment without the oxidative exposure. Furthermore, inactivation of TpMRK signalling by p38 MAPK inhibitor SB203580 or MEK inhibitor PD 98059 partially derepressed cell division induced by hydrogen peroxide. Ou...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2579700</comments>
            <pubDate>Mon, 06 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2579700</guid>        </item>
        <item>
            <title>The relationship between cell membrane damage and lipid peroxidation under the condition of hypoxia-reoxygenation: analysis of the mechanism using antioxidants and electron transport inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=2555482&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1578</link>
            <description>We consecutively observed lipid peroxidation and cell membrane damage under the condition of hypoxia-reoxygenation (H/R) in cells and analyzed their mechanisms by using electron transport inhibitors and an antioxidant. In H/R experiments, lipid peroxidation and cell membrane damage were observed during the hypoxia phase. In the reoxygenation phase, lipid peroxidation stopped, while cell membrane damage did not. An antioxidant, n-acetylcystein (NAC), and potassium cyanide (KCN) inhibited lipid peroxidation and cell membrane damage, while rotenone did not inhibit either of them. Although antimycin A did not inhibit lipid peroxidation, it inhibited cell membrane damage during the hypoxia phase but not during the reoxygenation phase. These results suggested that lipid peroxidation can affect c...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2555482</comments>
            <pubDate>Mon, 29 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2555482</guid>        </item>
        <item>
            <title>ICAT as a potential enhancer of monocytic differentiation: implications from the comparative proteome analysis of the HL60 cell line stimulated by all-trans retinoic acid and NSC67657</title>
            <link>http://www.medworm.com/index.php?rid=2555481&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1576</link>
            <description>A novel sterol mesylate compound (NSC67657) was recently identified and reported by National Cancer Institute that could efficiently induce the differentiation of HL60 cells into monocytes in vitro and in vivo. The expression of many proteins would have been changed during the differentiation process, and some proteins may have played key roles in the differentiation of HL60 cell line induced by this drug. Therefore, we treated HL60 cells with NSC67657 and all-trans retinoic acid (ATRA) to identify the differentially expressed proteins and determine their functions in cellular differentiation. Of the 45 differentially expressed protein spots investigated, 24 were either elevated or decreased in both the monocytic and granulocytic differentiating HL60 cells, 8 showed significant changes onl...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2555481</comments>
            <pubDate>Mon, 29 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2555481</guid>        </item>
        <item>
            <title>Effect of Terminalia chebula aqueous extract on oxidative stress and antioxidant status in the liver and kidney of young and aged rats</title>
            <link>http://www.medworm.com/index.php?rid=2503520&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1581</link>
            <description>We evaluated the preventive effects of Terminalia chebula (T. chebula) aqueous extract on oxidative and antioxidative status in liver and kidney of aged rats compared to young albino rats. The concentrations of malondialdehyde (MDA), lipofuscin (LF), protein carbonyls (PCO), activities of xantione oxidase (XO), manganese-superoxide dismutase (MnSOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione-S-transferase (GST), and glucose-6-phosphate dehydrogenase (G6PDH), levels of glutathione (GSH), vitamin C and vitamin E were used as biomarkers. In the liver and kidney of aged animals, enhanced oxidative stress was accompanied by compromised antioxidant defences. Administration of aqueous extract of T. cheubla effectively modulated oxidative stress and enha...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503520</comments>
            <pubDate>Wed, 24 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2503520</guid>        </item>
        <item>
            <title>Pulsatilla decoction and its active ingredients inhibit secretion of NO, ET-1, TNF-[alpha], and IL-1[alpha] in LPS-induced rat intestinal microvascular endothelial cells</title>
            <link>http://www.medworm.com/index.php?rid=2439768&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1570</link>
            <description>To investigate the pharmacological mechanism of the traditional Chinese medicine, Pulsatilla decoction (PD), the levels of nitric oxide (NO), endothelin-1 (ET-1), tumor necrosis factor-[alpha] (TNF-[alpha]), and interleukin-1[alpha] (IL-1[alpha]) secreted by cultured rat intestinal microvascular endothelial cells (RIMECs) were determined after treatment with PD and its seven active ingredients, namely anemoside B4, anemonin, berberine, jatrorrhizine, palmatine, aesculin, and esculetin. RIMECs were challenged with lipopolysaccharide (LPS) at 1 µg ml-1 for 3 h and then treated with PD at 1, 5, and 10 mg ml-1 and its seven ingredients at 1, 5, and 10 µg ml-1 for 21 h, respectively. The results revealed that PD, anemonin, berberine, and esculetin inhibited the production of NO; PD, anemonin,...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2439768</comments>
            <pubDate>Thu, 28 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2439768</guid>        </item>
        <item>
            <title>Antioxidant enzymes and melatonin levels in patients with bronchial asthma and chronic obstructive pulmonary disease during stable and exacerbation periods</title>
            <link>http://www.medworm.com/index.php?rid=2439771&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1569</link>
            <description>In conclusion, we observed that oxidative stress in the exacerbation period of patients with BA and COPD increased whereas the antioxidant enzymes and melatonin values reduced. The episodes of BA or COPD might be associated with elevated levels of oxidative stress. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2439771</comments>
            <pubDate>Wed, 27 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2439771</guid>        </item>
        <item>
            <title>Genotyping of five single nucleotide polymorphisms in the OCA2 and HERC2 genes associated with blue-brown eye color in the Japanese population</title>
            <link>http://www.medworm.com/index.php?rid=2439770&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1572</link>
            <description>Human eye color is a polymorphic phenotype influenced by multiple genes. It has recently been reported that three single nucleotide polymorphisms (SNPs) within intron 1 of the OCA2 gene (rs7495174, rs4778241, rs4778138) and two SNPs in intron 86 (rs12913832) and the 3[prime] UTR region (rs1129038) of the HERC2 gene - located in the upstream of the OCA2 locus - have a high statistical association with human eye color. The present study is the first to examine in detail the genotype and haplotype frequencies for these five SNPs in an Asian (Japanese) population (n = 523) comprising solely brown-eyed individuals. Comparison of the genotype and haplotype distributions in Japanese with those in African and European subjects revealed significant differences between Japanese and other populations...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2439770</comments>
            <pubDate>Tue, 26 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2439770</guid>        </item>
        <item>
            <title>Age associated high level of major vault protein is p53 dependent</title>
            <link>http://www.medworm.com/index.php?rid=2439769&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1571</link>
            <description>In this study, designed to elucidate the regulation of MVP in young and senescent HDFs, we examined the levels of transcriptional factors for the MVP gene, which revealed that among the putative transcriptional factors, p53 decreased only in young HDFs, but not in senescent HDFs in response to H2O2 treatment in the same mode as the expression of MVP. Moreover, the phosphorylation status of p53 increased only in senescent HDFs but not in young HDFs in response to H2O2 treatment. Therefore, we tested the possibility of MVP regulation by p53 status. MVP is upregulated in p53 over-expressing young HDFs, while MVP is downregulated in p53-specific small interfering RNA (siRNA)-transfected senescent HDFs, which suggests that the expression of MVP would be p53 dependent. Furthermore, using chromat...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2439769</comments>
            <pubDate>Tue, 26 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2439769</guid>        </item>
        <item>
            <title>TSH induces co-localization of TSH receptor and Na/K-ATPase in human erythrocytes</title>
            <link>http://www.medworm.com/index.php?rid=2432101&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1567</link>
            <description>In conclusion our results are compatible with the existence, in erythrocytes, of a functional TSHR that interacts with Na/K-ATPase after TSH treatment, thus suggesting a novel cell signalling pathway, potentially active in local circulatory control. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2432101</comments>
            <pubDate>Fri, 22 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2432101</guid>        </item>
        <item>
            <title>Are nociceptin(1-13)NH2 and its structural analogue [ORN9]nociceptin(1-13)NH2 able to affect brain antioxidant status in control and kainic acid-treated rats?</title>
            <link>http://www.medworm.com/index.php?rid=2396709&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1566</link>
            <description>In-vivo effects of nociceptin (N/OFQ(1-13)NH2) on the levels of lipid peroxidation and cell enzyme (superoxide dismutase, glutathione peroxidase and glutathione reductase) and non-enzyme (glutathione) antioxidants in brain of control and kainic acid-treated rats were studied. N/OFQ(1-13)NH2 effects were compared with those of its structural analogue [Orn9]N/OFQ(1-13)NH2. Kainic acid (25 µg, i.c.v) increased the lipid peroxidation (4 and 24 h after kainic acid treatment) and decreased the glutathione level (1 h after kainic acid injection). We failed to find, any changes in antioxidant enzyme activities, independently of the time of kainic acid treatment. At the background of kainic acid-effects, N/OFQ(1-13)NH2 and [Orn9] N/OFQ(1-13)NH2, injected 30 min before kainic acid, had no effects o...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2396709</comments>
            <pubDate>Fri, 08 May 2009 02:02:28 +0100</pubDate>
            <guid isPermaLink="false">2396709</guid>        </item>
        <item>
            <title>Association of a new intronic polymorphism of the SOD2 gene (G1677T) with cancer</title>
            <link>http://www.medworm.com/index.php?rid=2380004&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1560</link>
            <description>There is growing evidence of the correlation between cancer and reactive oxygen species (ROS), especially superoxide. Low expression levels of the Mn-superoxide dismutase (SOD2) enzyme have been reported in cancer patients. Genetic variation in the regulatory regions of the SOD2 gene may increase the risk of cancer. We identified a genetic variation (G1677T, rs2Y758Y339) in the vicinity of the enhancer region located in intron 2 of the SOD2 gene that creates a potential glucocorticoid responsive element, and developed an assay to screen DNA samples of 220 individuals (73 control, 59 prostate cancer survival individuals and 88 lung cancer biopsies). There were no significant differences in the genotype frequency distribution among prostate, lung cancer and control (p = 0.074 and 0.057, resp...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2380004</comments>
            <pubDate>Thu, 30 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2380004</guid>        </item>
        <item>
            <title>Characterization of pharmacogenetically relevant CYP2D6 and ABCB1 gene polymorphisms in a Portuguese population sample</title>
            <link>http://www.medworm.com/index.php?rid=2380005&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1561</link>
            <description>In this study the frequency of the pharmacologically relevant CYP2D6*3, *4, *5, *6 allelic variants and gene duplication, and ABCB1 C1236T and C3435T gene polymorphisms and their haplotypes was determined in a population sample of 100 Portuguese healthy subjects. CYP2D6 allele frequencies were 1.4% (*3), 13.3% (*4), 2.8% (*5), 1.8% (*6) and 6.1% (gene duplication), with 5% of the individuals classified as PM and 8.4% as UM. The frequencies obtained for the non-functional alleles and for the CYP2D6 gene duplication are in agreement with other South European populations, and reinforce the previously suggested south/north gradient of CYP2D6 duplications. Allelic frequencies for the ABCB1 polymorphisms were 52% (3435C) and 54% (1236C) and the most common haplotype (1236C-3435C) occurred with a...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2380005</comments>
            <pubDate>Wed, 29 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2380005</guid>        </item>
        <item>
            <title>Retraction</title>
            <link>http://www.medworm.com/index.php?rid=2363623&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1565</link>
            <description>No Abstract. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2363623</comments>
            <pubDate>Fri, 24 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2363623</guid>        </item>
        <item>
            <title>Note from the Editor</title>
            <link>http://www.medworm.com/index.php?rid=2363622&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1564</link>
            <description>No Abstract. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2363622</comments>
            <pubDate>Fri, 24 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2363622</guid>        </item>
        <item>
            <title>Over-expression of SUMO-1 induces the up-regulation of heterogeneous nuclear ribonucleoprotein A2/B1 isoform B1 (hnRNP A2/B1 isoform B1) and uracil DNA glycosylase (UDG) in hepG2 cells</title>
            <link>http://www.medworm.com/index.php?rid=2352976&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1562</link>
            <description>In this report, we have found that PIASx[alpha], PIASx[beta], and PIASy are highly expressed in liver as well as testis by tissue distribution studies. We thus aimed to identify any SUMO-1 related proteins in liver cancer cells by two-dimensional gel electrophoresis and mass spectrometry. Two up-regulated proteins, heterogeneous nuclear ribonucleoprotein A2/B1 isoform B1 (hnRNP A2/B1 isoform B1) and uracil DNA glycosylase (UDG), have been identified in the EGFP-SUMO-1 over-expressing HepG2 cells. The up-regulation is suggested to be mediated via changes at the translational level or protection from degradation by western blotting and RT-PCR. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2352976</comments>
            <pubDate>Tue, 21 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2352976</guid>        </item>
        <item>
            <title>Parathyroid hormone inhibits phosphorylation of mitogen-activated protein kinase (MAPK) ERK1/2 through inhibition of c-Raf and activation of MKP-1 in osteoblastic cells</title>
            <link>http://www.medworm.com/index.php?rid=2352975&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1568</link>
            <description>Parathyroid hormone (PTH) regulation of mitogen-activated protein kinases (MAPK) ERK1/2 contributes to PTH regulation of osteoblast growth and apoptosis. We investigated the mechanisms by which PTH inhibits ERK1/2 activity in osteoblastic UMR 106-01 cells. Treatment with PTH significantly inhibited phosphorylated ERK1/2 between 5 and 60 min. Transient transfection of cells with a cDNA encoding MAPK phosphatase-1 (MKP-1) resulted in 30-40% inhibition of pERK1/2; however MKP-1 protein levels were only significantly stimulated by PTH after 30 mins, suggesting another mechanism for the early phase of pERK1/2 inhibition. The active upstream kinase c-Raf phosphorylation at serine 338 (ser338) was significantly inhibited by PTH treatment within 5 min and transfection of the cells with constitutiv...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2352975</comments>
            <pubDate>Tue, 21 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2352975</guid>        </item>
        <item>
            <title>Low concentration of lipopolysaccharide acts on MC3T3-E1 osteoblasts and induces proliferation via the COX-2-independent NF[kappa]B pathway</title>
            <link>http://www.medworm.com/index.php?rid=2352974&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1563</link>
            <description>The translocations of lipopolysaccharide (LPS) from the gut and its effects on bone healing are usually of clinical interest during bone fracture. As already widely stuided, Cyclooxygenase-2 (COX-2) is a key enzyme for prostaglandin E2 (PGE2) production, which induces the nuclear factor kappa B (NF[kappa]B) activation and is beneficial to fracture healing. In order to know their roles in skeletal regeneration, mouse MC3T3-E1 osteoblasts were treated with NF[kappa]B inhibitor BAY 11-7082 and sc791 (a selective COX-2 inhibitor), in the presence of LPS. Interestingly, LPS could induce osteoblasts proliferation through increasing NF[kappa]B activation and translocation. This induction was not related to COX-2 expression, suggesting that LPS-induced NF[kappa]B activiation is independent of COX-...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2352974</comments>
            <pubDate>Tue, 21 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2352974</guid>        </item>
        <item>
            <title>Growth factors and glucose homeostasis in diabetic rats: effects of exercise training</title>
            <link>http://www.medworm.com/index.php?rid=2346646&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1556</link>
            <description>To investigate the alterations of glucose homeostasis and variables of the insulin-like growth factor-1 (IGF-1) growth system in sedentary and trained diabetic (TD) rats, Wistar rats were divided into sedentary control (SC), trained control (TC), sedentary diabetic (SD), and TD groups. Diabetes was induced by Alloxan (35 mg kg-1 b.w.). Training program consisted of swimming 5 days week-1, 1 h day-1, during 8 weeks. Rats were sacrificed and blood was collected for determinations of serum glucose, insulin, growth hormone (GH), IGF-1, and IGF binding protein-3 (IGFBP-3). Muscle and liver were removed to evaluate glycogen content. Cerebellum was extracted to determinate IGF-1 content. Diabetes decreased serum GH, IGF-1, IGFBP-3, liver glycogen, and cerebellum IGF-1 peptide content in baseline ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2346646</comments>
            <pubDate>Mon, 20 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2346646</guid>        </item>
        <item>
            <title>Antioxidant effect of diphenyl diselenide on oxidative stress caused by acute physical exercise in skeletal muscle and lungs of mice</title>
            <link>http://www.medworm.com/index.php?rid=2346645&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1559</link>
            <description>This study was designed to examine if diphenyl diselenide (PhSe)2, an organoselenium compound, attenuates oxidative stress caused by acute physical exercise in skeletal muscle and lungs of mice. Swiss mice were pre-treated with (PhSe)2 (5 mg kg-1 day-1) for 7 days. At the 7th day, the animals were submitted to acute physical exercise which consisted of continuous swimming for 20 min. The animals were euthanized 1 and 24 h after the exercise test. The levels of thiobarbituric acid reactive species (TBARS), non-protein thiols (NPSH) and ascorbic acid and the activity of catalase (CAT) were measured in the lungs and skeletal muscle of mice. Glycogen content was determined in the skeletal muscle of mice. Parameters in plasma (urea and creatinine) were determined. The results demonstrated an in...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2346645</comments>
            <pubDate>Mon, 20 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2346645</guid>        </item>
        <item>
            <title>Increased glycated calmodulin in the submandibular salivary glands of streptozotocin-induced diabetic rats</title>
            <link>http://www.medworm.com/index.php?rid=2339904&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1555</link>
            <description>Non-enzymatic glycosylation, a post translational protein modification may be implicated in the diabetes complications. Calmodulin is an important calcium binding protein that complexed with Ca2+ may be implicated in salivary gland secretory process. Glycated calmodulin has shown to be less effective in binding calcium. The aim of this study was to determine whether the concentration of glycated-calmodulin may be elevated in the submandibular salivary glands of streptozotocin-induced diabetic rats. Diabetes was induced by an intraperitoneal injection of spreptozotocin, and hyperglycemia was confirmed 72 h after injection using a glucosimeter. Thirty days after the induction of diabetes, submandibular salivary glands were used for the analysis of glycated and non-glycated calmodulin, using ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2339904</comments>
            <pubDate>Sat, 18 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2339904</guid>        </item>
        <item>
            <title>An investigation of the relationship between SULT1A1 Arg213His polymorphism and lung cancer susceptibility in a Turkish population</title>
            <link>http://www.medworm.com/index.php?rid=2325818&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1558</link>
            <description>Human sulfotransferase 1A1 (SULT1A1), the most expressed isoform of the phenol SULT1 subfamily, is an important member of sulfotransferase superfamily. A transition, G to A at position 638, in SULT1A1 gene, results in Arg213His change. This single nucleotide polymorphism reduces the activity and thermostability of SULT1A1 enzyme. Thus, in the present study the relationship between SULT1A1 Arg213His polymorphism and lung cancer was investigated. One hundred and six case and 271 control samples were studied using PCR-RFLP. There was no significant difference in genotype and allele distribution between lung cancer and control populations (p = 0.07; p = 0.06, respectively). Compared with the SULT1A1*1/SULT1A1*1 genotype the variant SULT1A1 genotype (SULT1A1*1/SULT1A1*2 or SULT1A1*2/SULT1A1*2) ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2325818</comments>
            <pubDate>Sat, 11 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2325818</guid>        </item>
        <item>
            <title>In vitro effects of 2-methoxyestradiol on cell numbers, morphology, cell cycle progression, and apoptosis induction in oesophageal carcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=2325822&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1557</link>
            <description>The influence of 2-methoxyestradiol (2-ME) was investigated on cell numbers, morphology, cell cycle progression, and apoptosis induction in an oesophageal carcinoma cell line (WHCO3). Dose-dependent studies (1 × 10-9M-1 × 10-6M) revealed that 2-ME significantly reduced cell numbers to 60% in WHCO3 after 72 h of exposure at a concentration of 1 × 10-6M compared to vehicle-treated cells. Morphological studies entailing light-, fluorescent-, as well as transmission electron microscopy (TEM) confirmed 2-ME's antimitotic effects. These results indicated hallmarks of apoptosis including cell shrinkage, hypercondensation of chromatin, cell membrane blebbing, and apoptotic bodies in treated cells. Flow cytometric analyses demonstrated an increase in the G2/M-phase after 2-ME exposure; thus prev...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2325822</comments>
            <pubDate>Thu, 02 Apr 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2325822</guid>        </item>
        <item>
            <title>Proliferation- and migration-enhancing effects of ginseng and ginsenoside Rg1 through IGF-I- and FGF-2-signaling pathways on RSC96 Schwann cells</title>
            <link>http://www.medworm.com/index.php?rid=2296467&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1554</link>
            <description>The aim of the present study is to evaluate the proliferation- and migration-enhancing effects of ginseng and its component, ginsenoside (Rg1) on RSC96 Schwann cells. We investigated the molecular signaling pathways, which include: (1) survival signaling, IGFs-IGFIR-Akt-Bcl2 and proliferative signaling, cell cycle factors and mitogen-activated protein kinase (MAPK) pathways, (2) migrating and anti-scar signaling, FGF-2-uPA-MMPs.We treated RSC96 cells with different concentrations (100, 200, 300, 400, 500 µg ml-1) of ginseng and its constituent, Rg1 (5, 10, 15, 20, 25 µg ml-1). We observed a proliferative effect in a dose-dependent manner by PCNA western blotting assay, MTT assay, and wound healing test. Furthermore, we also found in the results of western blotting assay, ginseng and Rg1 ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2296467</comments>
            <pubDate>Sun, 29 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2296467</guid>        </item>
        <item>
            <title>Levels of lipid peroxidation, nitric oxide, and antioxidant vitamins in plasma of patients with fibromyalgia</title>
            <link>http://www.medworm.com/index.php?rid=2296470&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1548</link>
            <description>The etiology of fibromyalgia is not clearly understood. In recent years, a few studies have investigated the possible role of reactive oxygen species (ROS) in the etiology and pathogenesis of fibromyalgia. The aim of this study was to investigate plasma antioxidant vitamins, lipid peroxidation (LP), and nitric oxide (NO) levels in patients with fibromyalgia and controls. The study was performed on the blood plasma of 30 female patients and 30 age-matched controls. After a fast of 12 h, blood samples were taken, and plasma samples were obtained for measurement of vitamins A, C, E, and [beta]-carotene concentrations and levels of LP and NO. Concentrations of vitamins A (p &lt; 0.01) and E (p &lt; 0.001) were significantly lower in patients with fibromyalgia than in controls, and LP levels were sig...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2296470</comments>
            <pubDate>Tue, 24 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2296470</guid>        </item>
        <item>
            <title>Effect of zinc supplementation on the antioxidant, copper, and iron status of physically active adolescents</title>
            <link>http://www.medworm.com/index.php?rid=2257769&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1550</link>
            <description>In conclusion, our study indicates that the use of 22 mg d-1 of supplemental zinc during 12 week in adolescent athletes did not affect growth, improved markers of antioxidant status but reduced plasma iron and copper. Therefore, it appears that the use of zinc supplementation by healthy adolescent athletes benefits their antioxidant capacity but impairs copper and iron nutritional status. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2257769</comments>
            <pubDate>Thu, 12 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2257769</guid>        </item>
        <item>
            <title>Erdosteine modulates radiocontrast-induced hepatotoxicity in rat</title>
            <link>http://www.medworm.com/index.php?rid=2257773&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1546</link>
            <description>It has been suggested that reactive oxygen species (ROS) plays an important role in radio contrast media (RCM)-induced ischemia reperfusion tissue injury although antioxidants may have protective effects on the injury. We investigated the effects of erdosteine as an antioxidant agent on RCM-induced liver toxicity in rats by evaluation of lipid peroxidation (as TBARS), catalase (CAT), superoxide dismutase (SOD), reduced glutathione (GSH) and glutathione peroxidase (GSH-Px) values and histological evaluation. Twenty-one rats were equally divided into three groups as follows: control, RCM, and RCM plus erdosteine. RCM was intraperitoneally administered for 1 day. Erdosteine was administered orally for 2 days after RCM administration. Liver samples were taken from the rats and they homogenized...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2257773</comments>
            <pubDate>Tue, 10 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2257773</guid>        </item>
        <item>
            <title>Effects of cholesterol and docosahexaenoic acid on cell viability and (Ca2+)i levels in acutely isolated mouse thymocytes</title>
            <link>http://www.medworm.com/index.php?rid=2257772&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1549</link>
            <description>We investigated the effects of lipids on thymocyte function. The effects of application of cholesterol or docosahexaenoic acid (DHA), a C22, omega-3 (n-3) polyunsaturated fatty acid (PUFA), on viability and intracellular calcium concentrations of acutely isolated mouse thymocytes were investigated using flow cytometry. Cholesterol (100 µM) caused significant cell death after 30-60 min whether or not calcium was present in the medium. Cell death was associated with an elevation of intracellular calcium whether or not calcium was present in the extracellular medium. However, the elevation of calcium concentration was not responsible for the cell death since calcium levels in the presence of ionomycin rose higher without significant cell death. DHA had similar actions but was more potent, ca...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2257772</comments>
            <pubDate>Tue, 10 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2257772</guid>        </item>
        <item>
            <title>Pre-steady state kinetics of ATP hydrolysis by Na,K-ATPase</title>
            <link>http://www.medworm.com/index.php?rid=2257771&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1545</link>
            <description>Fast reaction kinetics of ATP hydrolysis by Na,K-ATPase has been investigated by following absorption pattern of pH sensitive dye in stopped flow spectrophotometer. Distinct pre-steady state phase signal could be recorded with an initial decrease in acidity followed by increase in acidity. Average half time for H+ absorption and peak alkalinity was, respectively, 30 ms and 60 ms. Under optimal Na+ (120 mM) and K+ (30 mM) concentrations, magnitude of both H+ absorption and H+ release are found to be about 1.0 H+/ATPase molecule. H+ absorption and release decreased with decrease in Na+ concentration, H+ release was more affected. Both H+ absorption and H+ release are found to be independent of K+ concentration in the pre-steady state phase. No H+ absorption or release was observed following ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2257771</comments>
            <pubDate>Tue, 10 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2257771</guid>        </item>
        <item>
            <title>Alteration of Ca2+-ATPase activity in the homogenate, plasma membrane and microsomes of the salivary glands of streptozotocin-induced diabetic rats</title>
            <link>http://www.medworm.com/index.php?rid=2257770&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1544</link>
            <description>Diabetes has been implicated in the dryness of the mouth, loss of taste sensation, sialosis, and other disorders of the oral cavity, by impairment of the salivary glands. The aim of the present study was to examine the plasma membrane, microsomal, and homogenate Ca2+-ATPase activity in the rat submandibular and parotid salivary glands of streptozotocin-induced diabetes. We have also examined the influence of the acidosis state on this parameter. Diabetes was induced by an intraperitoneal injection of streptozotocin and acidosis was induced by daily injection of NH4Cl. At 15 and 30 days after diabetes induction, the animals were euthanized and the submandibular and parotid salivary glands were removed and analyzed. Ca2+-ATPase (total, independent, and dependent) was determined in the homoge...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2257770</comments>
            <pubDate>Mon, 09 Mar 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2257770</guid>        </item>
        <item>
            <title>Calmodulin effects on steroids-regulated plasma membrane calcium pump activity</title>
            <link>http://www.medworm.com/index.php?rid=2197257&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1543</link>
            <description>We examined the role of PMCA isoforms composition and CaM effect in regulation of Ca2+ uptake by estradiol, dehydroepiandrosterone (DHEA), pregnenolone (PREG), and their sulfates in a concentration range from 10-9 to 10-6 M, using the membranes from rat cortical synaptosomes, differentiated PC12 cells, and human erythrocytes. In excitable membranes with full set of PMCAs steroids apparently increased Ca2+ uptake, although to a variable extent. In most of the cases, CaM decreased transport by 30-40% below controls. Erythrocyte PMCA was regulated by the steroids somewhat differently than excitable cells. CaM strongly increased the potency for Ca2+ extrusion in membranes incubated with 17-[beta]-estradiol and PREG. Our results indicated that steroids may sufficiently control cytoplasmic calci...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2197257</comments>
            <pubDate>Wed, 18 Feb 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2197257</guid>        </item>
        <item>
            <title>Impact of estradiol on insulin signaling in the rat heart</title>
            <link>http://www.medworm.com/index.php?rid=2197256&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1542</link>
            <description>In this study we examine the impact of estradiol (E2) on insulin signaling in the rat heart. Ovariectomized female rats were treated with E2 6 h prior to analysis of basal protein and mRNA content of insulin signaling molecules, and additionally with insulin 30 min before the experiment to delineate E2 effects on phosphorylations and molecular associations relevant for insulin signaling. The results show that E2 decreased insulin receptor (IR) tyrosine phosphorylation, while it did not alter IR protein and mRNA content. E2 administration did not change IR substrate 1 (IRS-1) protein content and tyrosine phosphorylation, while decreased mRNA content and increased its association with the p85 subunit of phosphatidylinositol 3-kinase (PI3K). E2 decreased protein and mRNA content of IR substra...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2197256</comments>
            <pubDate>Wed, 18 Feb 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2197256</guid>        </item>
        <item>
            <title>A preliminary study of human paraoxonase and PON 1 L/M55-PON 1 Q/R 192 polymorphisms in Turkish patients with coronary artery disease</title>
            <link>http://www.medworm.com/index.php?rid=2197255&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1539</link>
            <description>Paraoxonase 1 (PON 1) is a high-density lipoprotein (HDL)-associated enzyme with antioxidant function protecting low-density lipoprotein (LDL) from oxidation. PON 1 has two amino acid polymorphisms in coding region; L/M 55 and Q/R 192. These polymorphisms modulate paraoxonase activity of the enzyme. PON 1 activity decreases in coronary artery disease (CAD). In the present study, distribution of PON 1 L/M 55 and Q/R 192 polymorphisms and the effect of these polymorphisms on the activities of PON 1, and on the severity of CAD in 277 CAD (+) patient and 92 CAD (-) subjects were examined. PON 1 L/M 55 and Q/R 192 genotypes were determined by PCR, RFLP and agarose gel electrophoresis techniques. Genotype distributions and allele frequencies for PON 1 Q/R 192 polymorphism were not significantly ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2197255</comments>
            <pubDate>Wed, 18 Feb 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2197255</guid>        </item>
        <item>
            <title>Regulation of inflammation in the adipose tissue in cancer cachexia: effect of exercise</title>
            <link>http://www.medworm.com/index.php?rid=2197254&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1540</link>
            <description>The paraneoplastic syndrome of cachexia is considered a degenerative chronic inflammatory disease, being deeply related to the increase of pro-inflammatory factors, especially tumour necrosis factor alpha (TNF-[alpha]). It is known that the adipose tissue is affected by cachexia and contributing with the secretion of pro-inflammatory factors which reach the adjacent tissues and the circulation. The effect of pro-inflammatory factors is balanced by the effect of anti-inflammatory factors, such as interleukin 10 (IL-10). The IL-10/TNF-[alpha] ratio has been recently postulated as a marker for the assessment of the degree of inflammation, which correlates with disease-associated morbidity and mortality. In order to counteract inflammation in chronic disease, our group has currently adopted ch...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2197254</comments>
            <pubDate>Wed, 18 Feb 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2197254</guid>        </item>
        <item>
            <title>Leptin transport in the central nervous system</title>
            <link>http://www.medworm.com/index.php?rid=2171037&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1538</link>
            <description>Synthesized and released by the adipose tissue, leptin is the widely studied 167-amino acid hormonal protein product of the obesity gene. Originally leptin was defined in association with satiety and energy balance and claimed to be an anti-obesity factor that functioned via a feedback effect from adipocytes to hypothalamus. There is a growing body of evidence that emphasizes the importance of leptin in the regulation of food intake and body weight in animals and humans, alike. Other research findings point out that it plays a role in the regulation of the metabolism, sexual development, reproduction, hematopoiesis, immunity, gastrointestinal functions, sympathetic activation, and angiogenesis. The aim of this review is to evaluate the relation between leptin and the central nervous system...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2171037</comments>
            <pubDate>Tue, 10 Feb 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2171037</guid>        </item>
        <item>
            <title>Glucose deprivation increases nuclear DNA repair protein Ku and resistance to radiation induced oxidative stress in human cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=2171038&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1541</link>
            <description>Recent studies have indicated that nutrient deprivation particularly glucose may play a major role in tumor cell tolerance to a generally oxidative stress environment in solid tumors. Here, we studied the impact of glucose deprivation on the response of human colon (HT29) and prostate (DU145) cancer cells to [gamma] radiation. A significant decrease in intracellular glucose level was observed in glucose deprived cells as measured by bioreductive assay. The survival of HT29 and DU145 were increased by 30 and 100% respectively when these cells were exposed to [gamma] radiation in the absence of glucose compared to that in the presence of glucose. In glucose depleted medium, glutathione (GSH), a free radical scavenger, content remained the same, and showed no correlation with the radiation re...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2171038</comments>
            <pubDate>Mon, 09 Feb 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2171038</guid>        </item>
        <item>
            <title>I405V and TaqIB polymorphisms of the cholesteryl ester transfer protein and their relation to serum lipid and lipoprotein levels in a Turkish population</title>
            <link>http://www.medworm.com/index.php?rid=2127142&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1536</link>
            <description>In conclusion, our results indicate that I405V polymorphism may affect the HDL-C levels in Turkish population. The association of this polymorphism and HDL-C levels could be modified by other factors, such as gender and TG levels. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2127142</comments>
            <pubDate>Fri, 23 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2127142</guid>        </item>
        <item>
            <title>Matrix metalloproteinase-2 and -9 activities in human keloids, hypertrophic and atrophic scars: a pilot study</title>
            <link>http://www.medworm.com/index.php?rid=2127143&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1537</link>
            <description>This study is the first to relate scar formation relationship in regard to gelatinase activation ratio in a keloid, hypertrophic and atrophic scar patient group which is chosen appropriate in age and sex. Copyright © 2009 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2127143</comments>
            <pubDate>Thu, 22 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2127143</guid>        </item>
        <item>
            <title>Cell biochemistry and function and the integration of biomedical research (location, location, location)</title>
            <link>http://www.medworm.com/index.php?rid=2114310&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1535</link>
            <description>No Abstract. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114310</comments>
            <pubDate>Thu, 01 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114310</guid>        </item>
        <item>
            <title>Protective effect of aminoguanidine against oxidative stress and bladder injury in cyclophosphamide-induced hemorrhagic cystitis in rat</title>
            <link>http://www.medworm.com/index.php?rid=2114319&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1534</link>
            <description>Cyclophosphamide (CP) is an antineoplastic agent that is used for the treatment of many neoplastic diseases. Hemorrhagic cystitis (HC) is a major dose limiting side effect of CP. Recent studies show that aminogaunidine, an inhibitor of inducible nitric oxide synthase is a potent antioxidant and prevents changes caused by oxidative stress such as depletion of antioxidant activity and tissue injury. The purpose of the study is to investigate the effect of aminoguanidine on parameters of oxidative stress, antioxidant enzymes and bladder injury caused by CP. Adult male rats were randomly divided into four groups. Control rats were administered saline; the AG control group received 200 mg/kg body wt of aminoguanidine; The CP group received a single injection of CP at the dose of 150 mg/kg body ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114319</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114319</guid>        </item>
        <item>
            <title>Effects of short chain fatty acids on effector mechanisms of neutrophils</title>
            <link>http://www.medworm.com/index.php?rid=2114318&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1533</link>
            <description>Short chain fatty acids (SCFAs) are metabolic by products of anerobic bacteria fermentation. These fatty acids, despite being an important fuel for colonocytes, are also modulators of leukocyte function. The aim of this study was to evaluate the effects of SCFAs (acetate, propionate, and butyrate) on function of neutrophils, and the possible mechanisms involved. Neutrophils obtained from rats by intraperitoneal lavage 4 h after injection of oyster glycogen solution (1%) were treated with non toxic concentrations of the fatty acids. After that, the following measurements were performed: phagocytosis and destruction of Candida albicans, production of ROS (O2[bull]-, H2O2, and HOCl) and degranulation. Gene expression (p47phox and p22phox) and protein phosphorylation (p47phox) were analyzed by...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114318</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114318</guid>        </item>
        <item>
            <title>KAI1/CD82 decreases Rac1 expression and cell proliferation through PI3K/Akt/mTOR pathway in H1299 lung carcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=2114317&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1532</link>
            <description>We report here, that a KAI1/CD82-induced phenotypic change was involved in the decrease of Rac1 expression and GTPase activity. However, we found that KAI1/CD82 did not regulate Rac1 mRNA levels. This suggests the existence of another regulatory mechanism of Rac1 protein maturation or activation. To identify the signaling pathway of Rac1 regulation, we investigated the PI3K/Akt/mTOR pathway, since the PI3K/Akt pathway regulates Rac1 activation and mTOR is known to play a regulatory role in protein translation. H1299/CD82-transfectants showed lower mTOR expression and cell growth than the control group. The data obtained from this study suggested that KAI1/CD82 decreased the metastatic phenotype of H1299 lung carcinoma cells by down-regulating Rac1 expression through the PI3K/Akt/mTOR pathw...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114317</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114317</guid>        </item>
        <item>
            <title>Oxidative stress resistance through blocking Hsp60 translocation followed by SAPK/JNK inhibition in aged human diploid fibroblasts</title>
            <link>http://www.medworm.com/index.php?rid=2114316&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1531</link>
            <description>The stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK) pathway is a well-known senescence-related stress activated protein kinase. Multiple environmental stresses induce programmed cell death, such as apoptosis. Normal human diploid fibroblast (HDF) cells have a limited life span in vitro, halting proliferation after a fixed number of cell divisions. Aged passage HDF showed resistance to oxidative stress involving heat shock proteins (Hsp60) through a mechanism involving the translocation of Hsp60 from the mitochondria to the cytosol. The present study showed that the translocation of Hsp60 from the mitochondria to the cytosol followed by high levels of p-SAPK/JNK activation as a result of oxidative stress was observed in the young cells only. The inhibition of SAPK/JNK act...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114316</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114316</guid>        </item>
        <item>
            <title>Evidence that L-glutamine is better than L-alanine as gluconeogenic substrate in perfused liver of weaned fasted rats submitted to short-term insulin-induced hypoglycaemia</title>
            <link>http://www.medworm.com/index.php?rid=2114315&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1530</link>
            <description>Gluconeogenesis in livers from overnight fasted weaned rats submitted to short-term insulin-induced hypoglycaemia (IIH) was investigated. For this purpose, a condition of hyperinsulinemia/hypoglycaemia was obtained with an intraperitoneal (ip) injection of regular insulin (1.0 U kg-1). Control group (COG group) received ip saline. The studies were performed 30 min after insulin (IIH group) or saline (COG group) injection. The livers from IIH and COG rats were perfused with L-alanine (5 mM), L-lactate (2 mM), L-glutamine (10 mM) or glycerol (2 mM). Hepatic glucose, L-lactate and pyruvate production from L-alanine was not affected by IIH. In agreement with this result, the hepatic ability in producing glucose from L-lactate or glycerol remained unchanged (IIH group vs. COG group). However, l...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114315</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114315</guid>        </item>
        <item>
            <title>TGF[beta]3 and loading increases osteocyte survival in human cancellous bone cultured ex vivo</title>
            <link>http://www.medworm.com/index.php?rid=2114314&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1529</link>
            <description>The goal of this study was to assess the effect of the addition of TGF[beta]3, alone or in combination with loading, on the survival of osteocytes in 3D human explant cancellous bone during long-term culture in an ex vivo loading bioreactor. Human cancellous bone explants were cultured for up to 14 days with or without TGF[beta]3 (15 ng ml-1) and with or without loading (300 cycles, at 1 Hz, producing 4000 microstrain). Bone core response was visualized using undecalcified histology with morphological methods after embedding with Technovit 9100 New® resin. Histological examination revealed normal gross level bone structure with or without the application of load or the addition of TGF[beta]3. The viability of the osteocytes within the bone was assessed by lactate dehydrogenase (LDH) activ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114314</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114314</guid>        </item>
        <item>
            <title>Protective action of indole-3-acetic acid on induced hepatocarcinoma in mice</title>
            <link>http://www.medworm.com/index.php?rid=2114313&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1528</link>
            <description>In this study, we report the protective effects of IAA on diethylnitrosamine (DEN)-induced hepatocarcinogenesis. BALB/c mice received daily IAA at 50 (T50), 250 (T250), and 500 (T500) mg Kg-1 per body mass by gavage for 15 days. At day 15, animals were administered DEN and sacrificed 4 h later. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed in sera. In addition, hepatomorphologic alterations, activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR), gene expression of antioxidant enzymes and DNA integrity were evaluated in the liver. IAA administration did not show any alterations in any of the parameters available, except for a reduction of the gene expression for antioxidant enzymes by 55, 56, ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114313</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114313</guid>        </item>
        <item>
            <title>How applicable is the general adaptation syndrome to the unicellular Tetrahymena?</title>
            <link>http://www.medworm.com/index.php?rid=2114312&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1527</link>
            <description>Hormone receptors, hormones and signal transduction pathways characteristic of higher vertebrates can be observed also in the unicellular Tetrahymena. Previous work showed that stress conditions (starvation, high temperature, high salt concentration, formaldehyde or alcohol treatment) elevated the intracellular level of four hormones (ACTH, endorphin, serotonin and T3). Here, the effect of other stressors (CuSO4 poisoning, tryptophan hydroxylase inhibitor parachlorphenylalanine (PCPA) treatment) on the same and other hormones (epinephrine, insulin, histamine) was studied, using immunocytochemistry and flow cytometric analysis. It was found, that each effect increased the intracellular hormone contents, but some hormones (histamine, T3) were less reactive. Insulin - which is a life-saving f...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114312</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114312</guid>        </item>
        <item>
            <title>Effects of arachidonic acid and docosahexaenoic acid on differentiation and mineralization of MC3T3-E1 osteoblast-like cells</title>
            <link>http://www.medworm.com/index.php?rid=2114311&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1526</link>
            <description>Osteoblasts in culture can differentiate into mature mineralizing osteoblasts when stimulated with osteogenic agents. Clinical trials and in vivo animal studies suggest that specific polyunsaturated fatty acids (PUFAs) may benefit bone health. The aim of this study was to investigate whether arachidonic acid (AA) and docosahexaenoic acid (DHA) affect osteogenesis in osteoblasts and the transdifferentiation into adipocytes. Results from this study show that long-term exposure to AA inhibited alkaline phosphatase (ALP) activity in these cells, which might be prostaglandin E2 (PGE2)-mediated. DHA exposure also inhibited ALP activity which was evident after both short- and long-term exposures. The mechanism whereby DHA inhibits ALP activity is not clear and needs to be investigated. Although l...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2114311</comments>
            <pubDate>Tue, 23 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2114311</guid>        </item>
        <item>
            <title>The relationship of oral disturbances of diabetes mellitus patients with paraoxonase gene polymorphisms</title>
            <link>http://www.medworm.com/index.php?rid=1949489&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1519</link>
            <description>Diabetes Mellitus (DM) is a multisystemic disorder with serious complications and these patients may also have serious problems with their oral cavity probably because of the microangiopathic and neuropathic complications. In diabetic patients, there may be several problems of the oral cavity such as gingivitis, periodontitis, candidiasis, glossitis, oral ulcerations, loss of taste sensations, opportunistic infections and several other conditions dependent on these. One of the recent theories about complications in DM is the contribution of reactive oxygen radicals. Paraoxonase (PON1) is an enzyme that is synthesized in liver and having the capability of hydrolasing the active metabolite of an insectisid, parathion. Previously it was shown that there are two polymorphic areas on the PON1 g...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1949489</comments>
            <pubDate>Wed, 12 Nov 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">1949489</guid>        </item>
        <item>
            <title>Modulation of insulin release by adenosine A1 receptor agonists and antagonists in INS-1 cells: The possible contribution of 86Rb+ efflux and 45Ca2+ uptake</title>
            <link>http://www.medworm.com/index.php?rid=1922708&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1514</link>
            <description>In conclusion, stimulation of A1 receptors by receptor selective and nonselective compounds reduced insulin release which is not coupled to opening of potassium channels (86Rb+ efflux experiments) or inhibition of calcium channels (45Ca2+ uptake experiments). It may be expected that of all pleiotropic 2nd messengers, the cAMP system (not tested here) is predominant for A1 receptor effects and the channel systems (K+ and Ca2+) are of minor importance and do not contribute to insulin release though being coupled to the receptor in other tissues. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1922708</comments>
            <pubDate>Fri, 31 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1922708</guid>        </item>
        <item>
            <title>Pax9 mediated cell survival in oral squamous carcinoma cell enhanced by c-myb</title>
            <link>http://www.medworm.com/index.php?rid=1922707&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1522</link>
            <description>This study examined the anti-apoptotic roles of Pax9 and c-myb, and clarified interaction between the two genes in KB cells. Inhibition of Pax9 caused the induction of apoptosis with enhanced cleavage of caspase-3 and PARP, accelerated Bax, and reduced Bcl-2 expression. Transducing c-myb cells with adenovirus c-myb (Ad/c-myb) were induced cell growth and inhibited apoptosis, but dominant-negative myb cells (Ad/DN-myb) were not affected. Pax9 was upregulated in the Ad/c-myb cells with simultaneous decrease in the Ad/DN-myb infection. However, c-myb remained unaffected in the Pax9 small interfering RNA (siRNA) transfected cells. Moreover, the Pax9 siRNA transfected cells and Ad/DN-myb infected cells were able to arrest the cell cycle at the G0 phase. This suggests that Pax9 and c-myb express...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1922707</comments>
            <pubDate>Fri, 31 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1922707</guid>        </item>
        <item>
            <title>Stretch-induced activation of ERK in myocytes is p38 and calcineurin-dependent</title>
            <link>http://www.medworm.com/index.php?rid=1913215&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1518</link>
            <description>Activation of specific mitogen-activated protein kinases (MAPKs) has been suggested to be involved in phenotype modulation of cells subjected to mechanical strain, which may be common to different mechano-sensitive cell types. We have submitted C2C12 myocytes to a static stretch and examined its effect upon the activation of ERK. Stretch induced a rapid but transient activation of ERK. This activation was however prevented when cells were pre-treated with inhibitors of p38 and calcineurin. The dependence of strain-induced ERK activation upon p38 suggests a cross-talk between these two pathways when mediating a response to a mechanical stimulus in this cell type. This suggests that cross relationships between these MAP kinases may be of crucial importance for myocyte phenotype modulation an...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1913215</comments>
            <pubDate>Wed, 29 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1913215</guid>        </item>
        <item>
            <title>Inhibitory effect of mesenchymal stem cells on lymphocyte proliferation</title>
            <link>http://www.medworm.com/index.php?rid=1913216&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1523</link>
            <description>We investigated the mechanism underlying the inhibitory effect of rat mesenchymal stem cells (MSCs) on non-specific mitogen-stimulated lymphocytes (LCs) and lymphoblasts (LBs). We used MSCs of passages 2-8 prepared from Sprague-Dawley (SD) rats. LCs were isolated from the spleens of SD rats. Mixed LCs reactions of mitomycin C-treated MSCs with concanavalin A (ConA)-stimulated LCs or LBs were performed, and the proliferation inhibition effect was tested by MTS assay. The cytotoxicity of MSCs against naïve and ConA-stimulated LBs was detected, after co-culturing for 24 h, by lactate dehydrogenase release assay. The rate of apoptosis of ConA-stimulated LBs was measured by flow cytometry after incubation with MSCs for 9 h in the ratio 10:1. The MSCs were treated with Fas ligand (FasL), transf...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1913216</comments>
            <pubDate>Mon, 27 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1913216</guid>        </item>
        <item>
            <title>Antimicrobial activity of endemic Crataegus tanacetifolia (Lam.) Pers and observation of the inhibition effect on bacterial cells</title>
            <link>http://www.medworm.com/index.php?rid=1898293&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1515</link>
            <description>The objective of the present study was to determine antimicrobial activity and the activity mechanism of C. tanacetifolia plant extract. The leaves of C. tanacetifolia, which is an endemic plant, were extracted using methanol and tested against 10 bacterial and 4 yeast strains by using a drop method. It was observed that the plant extract had antibacterial effects on Bacillus subtilis, Shigella, Staphylococcus aureus, and Listeria monocytogenes among the microorganisms that were tested. Minimum inhibitory concentration (MIC) results obtained at the end of an incubation of 24 h were found to be [ge]6.16 mg ml-1 for B. subtilis, (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1898293</comments>
            <pubDate>Wed, 22 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1898293</guid>        </item>
        <item>
            <title>Glucose metabolism by lymphocytes, macrophages, and tumor cells from Walker 256 tumor-bearing rats supplemented with fish oil for one generation</title>
            <link>http://www.medworm.com/index.php?rid=1898292&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1520</link>
            <description>Here we investigated the effect of lifelong supplementation of the diet with coconut fat (CO, rich in saturated fatty acids) or fish oil (FO, rich in n-3 polyunsaturated fatty acids) on tumor growth and lactate production from glucose in Walker 256 tumor cells, peritoneal macrophages, spleen, and gut-associated lymphocytes. Female Wistar rats were supplemented with CO or FO prior to mating and then throughout pregnancy and gestation and then the male offspring were supplemented from weaning until 90 days of age. Then they were inoculated subcutaneously with Walker 256 tumor cells. Tumor weight at 14 days in control rats (those fed standard chow) and CO supplemented was approximately 30 g. Supplementation of the diet with FO significantly reduced tumor growth by 76%. Lactate production (nmo...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1898292</comments>
            <pubDate>Wed, 22 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1898292</guid>        </item>
        <item>
            <title>Mechanism of 3-nitropropionic acid-induced membrane permeability transition of isolated mitochondria and its suppression by L-carnitine</title>
            <link>http://www.medworm.com/index.php?rid=1893197&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1521</link>
            <description>3-Nitropropionic acid (3NP) functions as an irreversible inhibitor of succinic acid dehydrogenase (complex II) and induces neuronal disorders in rats similar to those in patients with Huntington's disease. It is well known that L-carnitine (LC), a carrier of long chain fatty acid into the mitochondrial matrix, attenuates the neuronal degeneration in 3NP-treated rats. From these findings it has been suggested that 3NP induces certain neuronal cell death through mitochondrial dysfunction and that LC preserves the neurons against the dysfunction of mitochondria caused by 3NP. However, the detailed mechanism of cell death by 3NP and the protective actions of LC against the mitochondrial dysfunction have not been fully elucidated yet. Thus, we studied the molecular mechanism of the effects of 3...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1893197</comments>
            <pubDate>Wed, 22 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1893197</guid>        </item>
        <item>
            <title>Dynorphin inhibits NEP activity in R1.1 mouse thymoma cells</title>
            <link>http://www.medworm.com/index.php?rid=1893198&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1524</link>
            <description>In this study, on R1.1 cells, NEP activity was inhibited by [kappa]-opioid polypeptide dynorphin (10-8-10-6 M) and by thiorphan (2 × 10-4 M), a known inhibitor of NEP (30 min treatment). NEP inhibition by dynorphin was stronger than by thiorphan. A non-opioid opioid mechanism of action was mostly involved in this inhibition. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1893198</comments>
            <pubDate>Tue, 21 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1893198</guid>        </item>
        <item>
            <title>Soy lecithin supplementation alters macrophage phagocytosis and lymphocyte response to concanavalin A: a study in alloxan-induced diabetic rats</title>
            <link>http://www.medworm.com/index.php?rid=1864339&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1517</link>
            <description>In conclusion, lymphocyte and macrophage function were altered by lecithin supplementation, indicating an immunomodulatory effect of phosphatidylcholine. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1864339</comments>
            <pubDate>Fri, 10 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1864339</guid>        </item>
        <item>
            <title>Apolipoprotein E genotype is related to nitric oxide production in platelets</title>
            <link>http://www.medworm.com/index.php?rid=1864340&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1516</link>
            <description>In this study, the relationship between APOE genotype and oxidative stress markers, both in AD patients and controls, was evaluated. The AD group showed an increase in the content of thiobarbituric acid-reactive substances (TBARS) and in the activities of nitric oxide synthase (NOS) and Na, K-ATPase, when compared to controls. Both groups had a similar cGMP content and superoxide dismutase activity. APOE [epsiv]4 allele carriers showed higher NOS activity than non-carriers. These results suggest a possible influence of APOE genotype on nitric oxide (NO) production that might enhance the effects of age-related specific factor(s) associated with neurodegenerative disorders. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1864340</comments>
            <pubDate>Wed, 08 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1864340</guid>        </item>
        <item>
            <title>Liver glycogen metabolism during short-term insulin-induced hypoglycemia in fed rats</title>
            <link>http://www.medworm.com/index.php?rid=1801397&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1501</link>
            <description>The activities of glycogen phosphorylase and synthase during infusions of glucagon, isoproterenol, or cyanide in isolated liver of fed rats submitted to short-term insulin-induced hypoglycemia (IIH) was investigated. A condition of hyperinsulinemia/hypoglycemia was obtained with an intraperitoneal injection of regular insulin (1.0 U kg-1). The control group received ip saline. The experiments were carried out 60 min after insulin (IIH group) or saline (COG group) injection. The rats were anesthetized and after laparotomy, blood was collected from the vena cava for glucose and insulin measurements. The liver was then infused with glucagon (1 nM), isoproterenol (2 µM), or cyanide (0.5 mM) during 20 min and a sample of the organ was collected for determination of the activities of glycogen p...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1801397</comments>
            <pubDate>Thu, 18 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1801397</guid>        </item>
        <item>
            <title>Potency and property of DNA conformational damage determine ATM activation: two new DNA topological probes</title>
            <link>http://www.medworm.com/index.php?rid=1787390&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1510</link>
            <description>In this report we chose a couple of intercalating analogues and a Chinese traditional medicine Tanshinone IIA as probes to investigate the response of DNA damage sensor ataxia-telangiectasia mutated (ATM) protein toward the DNA topological change in vivo. The two analogues 1a (3-(4-Methyl-piperazin)-8-oxo-8H-acenaphtho [1,2-b]pyrrole -9-carbonitrile) and 3a (3-(3-Dimethylamino-propylamino)-8-oxo-8H-acenaphtho[1,2-b]pyrrole-9- carbonitrile) could unwind double helix to different extents, whereas Tanshinone IIA could wind the double helix. Using a combination of circular dichroism (CD) studies and immunoflurescence assays, we found for the first time that the ATM protein kinase can respond to the unwinding chromatin conformational damage caused by 1a and 3a, while it could not be activated b...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1787390</comments>
            <pubDate>Thu, 11 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1787390</guid>        </item>
        <item>
            <title>Interleukin-18 and gestosis: correlation with Helicobacter pylori seropositivity</title>
            <link>http://www.medworm.com/index.php?rid=1767256&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1503</link>
            <description>We report similar values of IL-18 in our pre-eclamptic patients and in healthy parturient women (respectively 350 ± 150 vs. 399 ± 132 pg ml-1; p = 0.23). However the seropositivity for H. pylori was 84 and 32% (p &lt; 0.001), and anti-Cag-A antibodies were present respectively in 80 and 28% of the two populations. On the basis of our data we hypothesize that H. pylori infection from Cag-A strains can be involved in some cases of PE and that the microorganism could modulate IL-18 release. In fact, differences on IL-18 production have been described by different authors between pre-eclamptic and healthy pregnant women, independently from infective pathology. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1767256</comments>
            <pubDate>Sat, 06 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1767256</guid>        </item>
        <item>
            <title>A general response to stressors by the unicellular Tetrahymena: effect of stress on the hormone levels</title>
            <link>http://www.medworm.com/index.php?rid=1767257&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1508</link>
            <description>Hormone (ACTH, endorphin, serotonin and T3) content of the unicellular Tetrahymena was studied by using immunocytochemical and flow cytometry methods. The cells were previously treated with different concentrations of salts (NaCl or KCl for 1 h), were kept in low (+4°C) or high (+37°C) temperature for 1 h and were treated with formaldehyde or ethanol. High concentrations of salts (20 mg ml-1 medium), all levels (0.1, 0.05, 0.01%) of formaldehyde and high temperature almost doubled the hormone contents and 0.1% alcohol also significantly elevated them. The experiments call attention to the presence of a general adaptation syndrome (GAS)-like phenomenon at a unicellular level and points to the possibility of deduction of GAS to a low level of phylogeny. Copyright © 2008 John Wiley &amp; Sons,...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1767257</comments>
            <pubDate>Fri, 05 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1767257</guid>        </item>
        <item>
            <title>Cytochrome P450 2J2*7 polymorphisms in Japanese, Mongolians and Ovambos</title>
            <link>http://www.medworm.com/index.php?rid=1731878&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1512</link>
            <description>This study is the first to investigate the distribution of the CYP2J2*7 gene polymorphisms in Japanese, Mongolians, and Ovambos. These data will be informative and facilitate genetic association studies, in Asian and African populations for CYP2J2-related diseases such as cardiovascular disorders. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1731878</comments>
            <pubDate>Wed, 27 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1731878</guid>        </item>
        <item>
            <title>Reye's and Reye's-like syndromes</title>
            <link>http://www.medworm.com/index.php?rid=1712489&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1465</link>
            <description>The review reports various questions about Reye's syndrome and Reye's-like syndromes. Although there is a significant decrease in the classic Reye's syndrome cases, because of the reduced employment of salicylates in children (salicylate seems to be the most important inducing factor of the syndrome in paediatric subjects affected by viral infection), the problem is still of interest considering the presence of different Reye's-like forms. All these pathological situations are associated with various aetiologic or predisposing causes that are examined in the text. Particular attention is placed on metabolic disorders, especially of fatty acid metabolism, and also of one amino acid. In fact, a latent form can also be the basis of possible biochemical disturbances induced by various exogenou...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1712489</comments>
            <pubDate>Tue, 19 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1712489</guid>        </item>
        <item>
            <title>Membrane protein analysis of human breast cancer cell line MCF-7 by different membrane washing methods</title>
            <link>http://www.medworm.com/index.php?rid=1703321&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1507</link>
            <description>Membrane and membrane-associated proteins are rich in known or potential pharmaceutical drug targets for carcinogenesis. In order to systemically analyze membrane proteins of human breast cancer, we isolated membrane from MCF-7 cells by sequential extraction by washing with three different buffers, namely, phosphate buffer (5 mM, pH 8.0), Tris (40 mM, pH 9.5), and sodium carbonate (100 mM pH 11). The extracted proteins were separated by two-dimensional gel electrophoresis (2-DE) using cup-loading and were then analyzed by peptide mass fingerprinting (PMF). A total of 137 spots from the gels of the three procedures were successfully identified. They corresponded to 79 distinct proteins. Among them, 22 exclusive proteins belonging to each washing procedure were also found, including P-glycop...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1703321</comments>
            <pubDate>Thu, 14 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1703321</guid>        </item>
        <item>
            <title>Hypercapnia protects erythrocytes against free radical damage induced by hypoxia in exposed rats</title>
            <link>http://www.medworm.com/index.php?rid=1687738&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1509</link>
            <description>Several studies report that hypoxic exposure induces free radical oxidative damage in various tissues. The mechanism of this damage includes membrane lipid peroxidation which can be easily detected by measuring fluorescent end-products of the process, i.e. lipofuscin-like pigments. Four day exposure of rats to hypoxia (10% O2) increased the level of lipofuscin-like pigments in erythrocytes up to 9 fold. This increase was completely prevented when the animals were exposed to hypercapnia (4.3% CO2) in addition to hypoxia. We studied the possible mechanism of the hypercapnic protection on isolated erythrocyte membranes in vitro. Lipid peroxidation was initiated by incubation of the membranes with iron ions and ascorbate. Production of malonaldehyde, the precursor of lipofuscin-like pigments, ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1687738</comments>
            <pubDate>Fri, 08 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1687738</guid>        </item>
        <item>
            <title>L-Carnitine suppresses oleic acid-induced membrane permeability transition of mitochondria</title>
            <link>http://www.medworm.com/index.php?rid=1687739&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1506</link>
            <description>In this study, we investigated whether L-carnitine suppresses oleic acid-induced MPT using isolated mitochondria from rat liver. Oleic acid-induced MPT in isolated mitochondria, inhibited endogenous respiration, caused membrane depolarization, and increased large amplitude swelling, and cytochrome c (Cyt. c) release from mitochondria. L-Carnitine was indispensable to [beta]-oxidation of oleic acid in the mitochondria, and this reaction required ATP and coenzyme A (CoA). In the presence of ATP and CoA, L-carnitine stimulated oleic acid oxidation and suppressed the oleic acid-induced depolarization, swelling, and Cyt. c release. L-Carnitine also contributed to maintaining mitochondrial function, which was decreased by the generation of free fatty acids with the passage of time after isolatio...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1687739</comments>
            <pubDate>Thu, 07 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1687739</guid>        </item>
        <item>
            <title>Production of cachexia mediators by Walker 256 cells from ascitic tumors</title>
            <link>http://www.medworm.com/index.php?rid=1644282&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1497</link>
            <description>In neoplasic cachexia, chemical mediators seem to act as initiators or perpetuators of this process. Walker 256 cells, whose metabolic properties have so far been little studied with respect to cancer cachexia, are used as a model for the study of this syndrome. The main objective of this research was to pinpoint the substances secreted by these cells that may contribute to the progression of the cachectic state. Since inflammatory mediators seem to be involved in the manifestation of this syndrome, the in vitro production of nitric oxide (NO), cytokines (tumor necrosis factor alpha (TNF-[alpha]) and interleukin-6 (IL-6)), and prostaglandin E2 (PGE2) was evaluated in Walker 256 cells isolated from ascitic tumors. After 4 or 5 h, a significant increase in NO production was observed (2.55 ±...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1644282</comments>
            <pubDate>Wed, 23 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1644282</guid>        </item>
        <item>
            <title>Subcellular localization of human heparanase and its alternative splice variant in COS-7 cells</title>
            <link>http://www.medworm.com/index.php?rid=1644285&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1492</link>
            <description>Heparanase, the enzyme that degrades heparan sulfate, has been implicated to play important and characteristic roles in organogenesis, tissue organization, cell migration, and tumor metastasis. Clarification of its expression, its intracellular sorting, and its secretion is, therefore, of much importance to understand its role in cell biology. In addition to the 1.7 Kb transcript previously reported, we detected a 1.5 Kb transcript of human heparanase by RT-PCR. The smaller transcript was shown to be an alternatively spliced variant lacking exon 5, which contains the essential glutamic acid residue required for enzyme activity. When expressed in COS-7 cells this variant did not show any heparanase activity. Full-length heparanase and the exon 5-deleted splice variant were expressed in COS-...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1644285</comments>
            <pubDate>Mon, 21 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1644285</guid>        </item>
        <item>
            <title>Comparative study of the residues 63 and 67 on the HLA-B molecule in patients with Takayasu's arteritis and tuberculosis</title>
            <link>http://www.medworm.com/index.php?rid=1644284&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1505</link>
            <description>Takayasu's arteritis (TA) and tuberculosis (TB) have been associated with major histocompatibility complex genes, especially HLA-B alleles. However, different HLA-B alleles have been detected in these diseases. The aim of the study was to compare the distribution of the residues 63 and 67 on the HLA-B molecule in patients with TA and TB in order to establish a genetic relationship between these two diseases. HLA-B sequences obtained in 30 patients with TB were compared to those previously reported in TA and healthy controls. 8 out of 30 TB patients studied (26.6%) presented at least one allele with glutamic acid at position 63 and serine at position 67. This was observed in 73% of the TA patients (p = 0.0005). Ten TB (10/30 = 33.3%) and two TA patients (2/26 = 7.7%) did not show similarity...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1644284</comments>
            <pubDate>Mon, 21 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1644284</guid>        </item>
        <item>
            <title>Manganese superoxide dismutase (MnSOD) genetic polymorphism is associated with risk of early-onset prostate cancer</title>
            <link>http://www.medworm.com/index.php?rid=1644283&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1504</link>
            <description>Prostate cancer continues to be the most frequently diagnosed neoplasm, and the second leading cause of cancer-related mortality in men. Oxidative stress may enhance prostatic carcinogenesis. Manganese superoxide dismutase (MnSOD) is the only known superoxide scavenger in mitochondria. It plays a key role in antioxidant defense as mitochondria are important for oxidative metabolism coupled to the electron transport chain and oxidative phosphorylation and hence, ROS production. A T[rarr]C single nucleotide substitution, resulting in a Val[rarr]Ala change at position 9 (Ala-9Val), which alters the secondary structure of the protein, has been noted to affect transport of MnSOD into the mitochondria. We have determined the MnSOD genotype in 85 prostate cancer cases and 151 control subjects. Al...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1644283</comments>
            <pubDate>Mon, 21 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1644283</guid>        </item>
        <item>
            <title>Advanced glycation end products serve as ligands for lectin-like oxidized low-density lipoprotein receptor-1(LOX-1): biochemical and binding characterizations assay</title>
            <link>http://www.medworm.com/index.php?rid=1636472&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1502</link>
            <description>Advanced glycation end products (AGEs) are a class of complex heterogeneous compounds which accumulate with age and is known to be involved in the pathogenesis of several diseases from diabetes to atherosclerosis. AGEs serve as ligands for multiple receptors including scavenger receptor (SR-A), CD36, and SR-B[Igr]. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) plays an important role in both atherosclerosis and is found to be an endothelial cell receptor for AGEs. To explore the binding characterization of AGEs to LOX-1, AGEs were prepared by three different reducing sugars (d-glucose, d-fructose, and d-ribose) and the biochemical characterization including, free amino groups, free amine content, fructosamine residues, carbonyl content, fluorescence, and absorbance were d...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636472</comments>
            <pubDate>Sat, 19 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636472</guid>        </item>
        <item>
            <title>Adipose-derived stem cell: a better stem cell than BMSC</title>
            <link>http://www.medworm.com/index.php?rid=1636480&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1488</link>
            <description>To further study the proliferation and multi-differentiation potentials of adipose-derived stem cells (ADSCs), the cells were isolated with improved methods and their growth curves were achieved with cck-8. Surface protein expression was analyzed by flow cytometry to characterize the cell phenotype. The multi-lineage potential of ADSCs was testified by differentiating cells with adipogenic, chondrogenic, osteogenic, and myogenic inducers. The results showed that about 5 × 105 stem cells could be obtained from 400 to 600 mg adipose tissue. The ADSCs can be continuously cultured in vitro for up to 1 month without passage and they have several logarithmic growth phases during the culture period. Also, the flow cytometry analysis showed that ADSCs expressed high levels of stem cell-related an...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636480</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636480</guid>        </item>
        <item>
            <title>Neurite outgrowth of NG108-15 cells induced by heat shock protein 90 inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=1636479&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1458</link>
            <description>We previously reported that radicicol (Rad) and geldanamycin (Geld), heat shock protein 90 (Hsp90) inhibitors, potentiate neurite growth of cultured sensory neurons from chick embryo. We now show that the antibiotics induce neurite growth in NG108-15 cells. Treatment of the cells with these drugs caused transient decrease in protein levels of Raf1, ERK1/2, phosphorylated ERK1/2, Akt1, and CDK4. The neurite growth of NG108-15 induced by the inhibitors was blocked by actynomycin D, but the neurite growth stimulated by dbcAMP in the cells was not affected. The neurite growth could be due to a change in the synthesis of some specific protein(s) and is speculated to be due to the transient downregulation of particular-signaling molecules stabilized by Hsp90. Copyright © 2008 John Wiley &amp; Sons,...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636479</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636479</guid>        </item>
        <item>
            <title>MTHFR C677T polymorphism in chronic pancreatitis and pancreatic adenocarcinoma</title>
            <link>http://www.medworm.com/index.php?rid=1636478&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1487</link>
            <description>In this study, we tested whether MTHFR C677T polymorphism is associated with chronic pancreatitis and pancreatic adenocarcinoma in the Serbian population. DNA was extracted from blood samples of 51 chronic pancreatitis patients, 21 pancreatic adenocarcinoma patients, and a control group consisting of 50 healthy smokers. The MTHFR C677T polymorphism was analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. Although, no statistically significant differences were observed in the distribution of MTHFR genotype or allele frequencies between patients and control groups, the results showed an increased frequency of homozygotes for MTHFR C677T polymorphism in chronic pancreatitis patients (14%) and a decreased frequency in pancreatic adenocarcinoma pa...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636478</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636478</guid>        </item>
        <item>
            <title>Three single nucleotide polymorphisms leading to non-synonymous amino acid substitution in the human ribonuclease 2 and angiogenin genes exhibit markedly less genetic heterogeneity in six populations</title>
            <link>http://www.medworm.com/index.php?rid=1636477&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1498</link>
            <description>Angiogenin and ribonuclease 2 (RNase 2) are members of the human RNase superfamily. Although three potential single nucleotide polymorphisms (SNPs) in these genes, which could give rise to an amino acid substitution in the protein, have been identified, relevant population data are not available, and accordingly they have not been applied to clinical-genetic analysis. For this purpose, a novel genotyping method for each SNP using the mismatched PCR-restriction fragment length polymorphism technique has been developed. Using this method, the genotype distribution of each SNP was investigated in six populations: Japanese (n = 167), Korean (n = 90), Mongolian (n = 92), Ovambos (n = 86), Turkish (n = 87), and German (n = 70). In all the populations, only one genotype was found in each SNP. Irr...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636477</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636477</guid>        </item>
        <item>
            <title>Antioxidant status and lipid peroxidation in the blood of breast cancer patients of different ages</title>
            <link>http://www.medworm.com/index.php?rid=1636476&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1499</link>
            <description>In this study we investigated the level of oxidative stress and antioxidant (AO) status in the blood of breast cancer patients of different ages. The level of lipid hydroperoxides (LP) was measured in blood plasma and the activities of copper, zinc superoxide dismutase (CuZnSOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione reductase (GR) enzymes, as well as the level of total glutathione (GSH) and CuZnSOD protein were measured in blood cells of breast cancer patients and age-matched healthy subjects. Our results showed that breast carcinoma is related to increase of lipid peroxidation in plasma with concomitant decrease of AO defense capacity in blood cells, which becomes more pronounced during aging of the patients. Suppression of CuZnSOD activity related to breast cance...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636476</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636476</guid>        </item>
        <item>
            <title>Effects of a selective Rho-kinase inhibitor Y-27632 on oxidative stress parameters in acute dichlorvos poisoning in rats</title>
            <link>http://www.medworm.com/index.php?rid=1636475&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1500</link>
            <description>In conclusion, our results suggest that Rho-kinase pathway is involved in organophosphate intoxication, and a decrease in cardiac paraoxonase activities may play a role in the pathogenesis of acute organophosphate poisoning in rats. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636475</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636475</guid>        </item>
        <item>
            <title>Effect of endurance training upon lipid metabolism in the liver of cachectic tumour-bearing rats</title>
            <link>http://www.medworm.com/index.php?rid=1636474&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1495</link>
            <description>The syndrome of cancer cachexia is accompanied by several alterations in lipid metabolism, and the liver is markedly affected. Previous studies showed that moderate exercise training may prevent liver fat accumulation through diminished delivery of lipids to the liver, increased hepatic oxidation and increased incorporation of triacylglycerol (TAG) into very low density lipoprotein (VLDL). Our aim was to examine the influence of moderate intensity training (8 weeks) upon TAG content, VLDL assembly and secretion, apolipoprotein B (apoB) and microsomal transfer protein (MTP) gene expression in the liver of cachectic tumour-bearing rats. Animals were randomly assigned to a sedentary control (SC), sedentary tumour-bearing (ST) or exercise-trained control (EC) or to an exercise trained tumour-b...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636474</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636474</guid>        </item>
        <item>
            <title>TGF-[alpha] induces upregulation and nuclear translocation of Hes1 in glioma cell</title>
            <link>http://www.medworm.com/index.php?rid=1636473&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1494</link>
            <description>Both the Notch-signaling pathway and extracellular signal regulated kinase (ERK) cascade are involved in a wide variety of biological processes, such as proliferation, differentiation, survival, and tumorigenesis. Their dysregulation in recent studies have been shown to be associated with glioma formation. Here, we show that transforming growth factor-[alpha] (TGF-[alpha]) stimulated glioma cell line U251 growth and can partly compensate for the inhibitory effect of Notch-signaling inhibitor DAPT. The effect of TGF-[alpha] on ERK1/2 phosphorylation was prompt and transient and could be inhibited by mitogen-activated/extracellular signal-regulated kinase kinase 1/2 (MEK1/2) specific inhibitor PD98059. Moreover, TGF-[alpha] was capable of up-regulating Hairy-enhancer of split1 (Hes1) express...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1636473</comments>
            <pubDate>Thu, 17 Jul 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1636473</guid>        </item>
        <item>
            <title>Comparison of plasma leptin and zinc levels in elite athletes and sedentary people</title>
            <link>http://www.medworm.com/index.php?rid=1533015&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1480</link>
            <description>In consideration of leptin effects such as reducing food intake and increasing energy consumption, many researchers have sought to examine the relation between leptin and exercise. The presence of reports arguing that zinc, can be a mediator in leptin production indicates a possible relation between zinc and leptin. The present study aims to determine plasma leptin levels in elite weightlifters and examine their relation with zinc. The study enrolled 30 healthy volunteers in the 18-27 age range. The subjects were allocated to groups in equal numbers: Group 1, Control Group: the group included subjects who did not exercise regularly. Group 2, Elite Weightlifter Group: the group included elite weight lifters who were selected to the national team in their weight classes, who exercised regula...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1533015</comments>
            <pubDate>Sat, 21 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1533015</guid>        </item>
        <item>
            <title>Antagonistic effect of EGF on FAK phosphorylation/dephosphorylation in a cell</title>
            <link>http://www.medworm.com/index.php?rid=1504659&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1457</link>
            <description>In this study, we found that the quantitative change of phosphorylated FAK was bell-shaped time-dependently by EGF stimulation in immortalized human keratinocyte (HaCaT). EGF enhanced FAK phosphorylation and cell spreading in adhering HaCaT cells with low-phosphorylated FAK. On the other hand, spread HaCaT cells having high-phosphorylated FAK changed to round shapes with FAK dephosphorylation 15 min after EGF stimulation. Pharmacological agents, U0126 and PD98059 (mitogen-activated protein kinases (MAPK) kinases (MEK) inhibitors), and AG1478 (an EGF receptor kinase inhibitor) blocked the cell rounding and FAK dephosphorylation. In addition, the EGFR-MAPK signaling pathway had an influence on cell migration by regulating FAK dephosphorylation of keratinocytes in response of EGF, since the M...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1504659</comments>
            <pubDate>Wed, 11 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1504659</guid>        </item>
        <item>
            <title>Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent</title>
            <link>http://www.medworm.com/index.php?rid=1504661&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1493</link>
            <description>To elucidate molecular and cellular mechanisms of peroxisome biogenesis, we have isolated Chinese hamster ovary (CHO) cell mutants defective in peroxisome biogenesis by making use of enhanced green fluorescent protein (EGFP) and a frameshift-inducing mutagen ICR191. CHO-TKa cells stably expressing Pex2p were transformed with a cDNA encoding EGFP fused with peroxisomal targeting signal type 2 (PTS2-EGFP), termed Tka/EG2. TKa/EG2 cells were mutagenized with ICR191 and cultured in the presence of P9OH (9-(1[prime]-pyrene) nonanol) followed by an exposure to UV. P9OH/UV-resistant and morphologically peroxisome-deficient mutant cells were isolated by directly observing cytosolic localization of EGFP, without cell staining. By a combination of cell-fusion and PEX transfection, we determined comp...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1504661</comments>
            <pubDate>Tue, 10 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1504661</guid>        </item>
        <item>
            <title>Hepatic denervation impairs the assembly and secretion of VLDL-TAG</title>
            <link>http://www.medworm.com/index.php?rid=1504660&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1476</link>
            <description>VLDL secretion is a regulated process that depends on the availability of lipids, apoB and MTP. Our aim was to investigate the effect of liver denervation upon the secretion of VLDL and the expression of proteins involved in this process. Denervation was achieved by applying a 85% phenol solution onto the portal tract, while control animals were treated with 9% NaCl. VLDL secretion was evaluated by the Tyloxapol method. The hepatic concentration of TAG and cholesterol, and the plasma concentration of TAG, cholesterol, VLDL-TAG, VLDL-cholesterol and HDL-cholesterol were measured, as well as mRNA expression of proteins involved in the process of VLDL assembly. Hepatic acinar distribution of MTP and apoB was evaluated by immunohistochemistry. Denervation increased plasma concentration of chol...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1504660</comments>
            <pubDate>Tue, 10 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1504660</guid>        </item>
        <item>
            <title>Relation of glutathione S-transferase T1, M1 and P1 genotypes and breast cancer risk</title>
            <link>http://www.medworm.com/index.php?rid=1485560&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1490</link>
            <description>The aim of this study was to investigate associations between genetic variability in specific Glutathione S-transferases (GST) genes (GSTM1, GSTT1 and GSTP1) and susceptibility to breast cancer. Genotypes of blood specimen DNA were determined for 65 women with incident cases of breast cancer and 108 control subjects. Associations between specific genotypes and the development of breast cancer were examined by the use of logistic regression to calculate odds ratios (ORs) and 95% confidence intervals (CIs). Neither GSTT1 nor GSTM1 homozygous null genotype was associated with a significant increased risk of developing breast cancer. The presence of valine alleles compared to isoleucine alleles in codon 105 in GSTP1 did not increase the risk of breast cancer development. The risk of breast can...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1485560</comments>
            <pubDate>Tue, 03 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1485560</guid>        </item>
        <item>
            <title>Effects of oral L-arginine supplementation on blood pressure and asymmetric dimethylarginine in stress-induced preeclamptic rats</title>
            <link>http://www.medworm.com/index.php?rid=1485561&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1491</link>
            <description>This study was carried out to elucidate the role of asymmetric dimethylarginine (ADMA) and nitric oxide (NO) in preeclampsia development, and to investigate the effect of L-arginine supplementation in rats. Preeclampsia was induced in pregnant rats using a stress model. L-arginine was administered orally and ADMA, urinary nitrate, and protein levels were measured on the 20th day of pregnancy. Compared with the group of rats that are normally pregnant, the levels of blood pressure (BP), protein excretion, and ADMA were significantly increased in preeclampsia which returned to normal levels following the supplementation of L-arginine. Both group of rats had similar urine nitrate levels. Arginine-ADMA-NO pathway is affected in preeclampsia. L-arginine supplementation decreased hypertension (H...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1485561</comments>
            <pubDate>Mon, 02 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1485561</guid>        </item>
        <item>
            <title>Antioxidant protection during ageing and senescence in chloroplasts of tobacco with modulated life span</title>
            <link>http://www.medworm.com/index.php?rid=1478923&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1481</link>
            <description>We studied changes in antioxidant protection during ageing and senescence in chloroplasts of tobacco (Nicotiana tabacum L., cv. Wisconsin) with introduced SAG12 promoter fused with ipt gene for cytokinin synthesis (transgenic plants with increased levels of cytokinins, SAG) or without it (control). Old leaves of SAG plants as well as their chloroplasts maintained higher physiological parameters compared to controls; accordingly, we concluded that their ageing was diverted due to increased cytokinin content. The chloroplast antioxidant protection did not decrease as well. Although antioxidant protection usually decreased in whole leaves of senescing control plants, ascorbate peroxidase (APX) and dehydroascorbate reductase (DHAR) activity, which maintained the high redox state of ascorbate, ...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1478923</comments>
            <pubDate>Sat, 31 May 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1478923</guid>        </item>
        <item>
            <title>Mitochondria as the target for mildronate's protective effects in azidothymidine (AZT)-induced toxicity of isolated rat liver mitochondria</title>
            <link>http://www.medworm.com/index.php?rid=1473388&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1486</link>
            <description>Previously mildronate, an aza-butyrobetaine derivative, was shown to be a cytoprotective drug, through its mechanism of action of inhibition of carnitine palmitoyltransferase-1, thus protecting mitochondria from long-chain fatty acid accumulation and subsequent damage. Recently in an azidothymidine (AZT)-induced cardiotoxicity model in vivo (in mice), we have found mildronate's ability of protecting heart tissue from nuclear factor [kappa]B abnormal expression. Preliminary data also demonstrate cerebro- and hepatoprotecting properties of mildronate in AZT-toxicity models. We suggest that mildronate may target its action predominantly to mitochondria. The present study in isolated rat liver mitochondria was designed to clarify mitochondrial targets for mildronate by using AZT as a model com...</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1473388</comments>
            <pubDate>Thu, 29 May 2008 04:00:00 +0100</pubDate>
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        <item>
            <title>4-Amino-3-acetylquinoline-induced apoptosis of murine L1210 leukemia cells involves ROS-mitochondrial-mediated death signaling and activation of p38 MAPK</title>
            <link>http://www.medworm.com/index.php?rid=1473387&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1485</link>
            <description>In this study, we investigated whether AAQ has cytotoxicity in murine L1210 leukemia cells. Results from cell proliferation assays showed that AAQ caused significant decrease in cell number in a dose-dependent manner. The cell death induced by AAQ appeared to involve apoptosis, based on evidence from apoptotic DNA fragmentation, flow cytometry, fluorescence microscopy, and Western blot analyses. We found that AAQ-treated cells had activated p38 MAPK and that apoptosis was processed through a reactive oxygen species (ROS)-dependent mitochondrial pathway. In summary, our results suggest that AAQ can induce apoptosis, at least in part, through the activation of the p38 MAPK pathway in L1210 leukemia cells. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1473387</comments>
            <pubDate>Thu, 29 May 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1473387</guid>        </item>
        <item>
            <title>Nitric oxide-mediated activation of NADPH oxidase by salbutamol during acute asthma in children</title>
            <link>http://www.medworm.com/index.php?rid=1473386&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1484</link>
            <description>This study concludes that salbutamol treatment enhances superoxide anion production in asthma patients through NO-mediated mechanisms, however it exerts beneficial antioxidant effects through activation of catalase and attenuation of lipid peroxidation. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1473386</comments>
            <pubDate>Thu, 29 May 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1473386</guid>        </item>
        <item>
            <title>Mitochondrial AIF protein involved in skeletal muscle regeneration</title>
            <link>http://www.medworm.com/index.php?rid=1473385&amp;cid=s_33761_60_f&amp;fid=33761&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1002%252Fcbf.1483</link>
            <description>We report here that 100 µM hydrogen peroxide (H2O2) induced the proliferation of C2C12 myoblasts and over-expression of AIF simultaneously in vitro. Immunofluorescence showed that the over-expression of AIF was located in the cytoplasm. The immunopositive AIF was detected in nuclei 27 days after denervation of skeletal muscle, but in the cytoplasm it was detected 27 days after fiber-damaged skeletal muscle. AIF may be a factor involved in skeletal muscle regeneration. Copyright © 2008 John Wiley &amp; Sons, Ltd. (Source: Cell Biochemistry and Function)</description>
            <author>Cell Biochemistry and Function</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1473385</comments>
            <pubDate>Thu, 29 May 2008 04:00:00 +0100</pubDate>
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