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        <title>Cardiovascular Drugs and Therapy 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 'Cardiovascular Drugs and Therapy' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Cardiovascular+Drugs+and+Therapy&t=Cardiovascular+Drugs+and+Therapy&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 09:32:32 +0100</lastBuildDate>
        <item>
            <title>Effects of Candesartan on Left Ventricular Function, Aldosterone and BNP in Chronic Heart Failure</title>
            <link>http://www.medworm.com/index.php?rid=5666990&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F138u6303g6q51x17%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In CandHeart, the addition of candesartan to standard medical treatment did not reduce circulating BNP more than standard
 therapy (primary endpoint), but it significantly improved LV function and produced a marked decrease in aldosterone levels
 at study end.
 
 
 
 
	Content Type Journal ArticlePages 1-13DOI 10.1007/s10557-012-6370-8Authors
		Aneta Aleksova, Cardiovascular Department, “Ospedali Riuniti” and University of Trieste, Trieste, ItalySerge Masson, Department of Cardiovascular Research, Istituto di Ricerche Farmacologiche “Mario Negri”, via Giuseppe La Masa 19, 20156 Milan, ItalyAldo P. Maggioni, ANMCO Research Center, Florence, ItalyDonata Lucci, ANMCO Research Center, Florence, ItalyRenato Urso, ANMCO Research Center, Florence, ItalyLidia Staszew...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666990</comments>
            <pubDate>Thu, 02 Feb 2012 18:16:26 +0100</pubDate>
            <guid isPermaLink="false">5666990</guid>        </item>
        <item>
            <title>Modulatory Effect of Fenofibrate on Endothelial Production of Neutrophil Chemokines IL-8 and ENA-78</title>
            <link>http://www.medworm.com/index.php?rid=5638316&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk7u854383g536811%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Fenofibrate blunts IL-1β-mediated ENA-78 production with no effect on IL-8. This represents a novel mechanism by which fenofibrate
 exerts anti-inflammatory effects and should be further explored.
 
 
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s10557-011-6368-7Authors
		Elvin Tyrone Price, University of Arkansas for Medical Sciences, Little Rock, AR, USAGregory James Welder, Department of Pharmacotherapy and Translational Research, University of Florida College of Pharmacy, Gainesville, FL, USAIssam Zineh, Department of Pharmacotherapy and Translational Research, University of Florida College of Pharmacy, Gainesville, FL, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638316</comments>
            <pubDate>Tue, 24 Jan 2012 12:27:21 +0100</pubDate>
            <guid isPermaLink="false">5638316</guid>        </item>
        <item>
            <title>Hypertension in the US Black Population: Risk Factors, Complications, and Potential Impact of Central Aortic Pressure on Effective Treatment</title>
            <link>http://www.medworm.com/index.php?rid=5597173&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6036344lp45n6013%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;There is an urgent need to successfully control hypertension in the black population. Although data are limited in blacks,
 evidence suggests that central blood pressure warrants more continued assessment in future clinical studies.
 
 
 
 
	Content Type Journal ArticleCategory Review ArticlePages 1-9DOI 10.1007/s10557-011-6367-8Authors
		Keith C. Ferdinand, Division of Cardiology, Tulane University School of Medicine and Association of Black Cardiologists, Inc., 1430 Tulane Ave, SL-48, New Orleans, LA 70112, USARaymond R. Townsend, University of Pennsylvania, Philadelphia, PA, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5597173</comments>
            <pubDate>Fri, 13 Jan 2012 16:48:36 +0100</pubDate>
            <guid isPermaLink="false">5597173</guid>        </item>
        <item>
            <title>Cardiovascular Pharmacotherapy can Reduce Mortality</title>
            <link>http://www.medworm.com/index.php?rid=5597174&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw8041021991q7l56%2F</link>
            <description>Content Type Journal ArticleCategory ISCP President's LetterPages 1-2DOI 10.1007/s10557-011-6369-6Authors
		Juan-Carlos Kaski, St. George’s, University of London, London, United Kingdom
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5597174</comments>
            <pubDate>Fri, 13 Jan 2012 16:48:35 +0100</pubDate>
            <guid isPermaLink="false">5597174</guid>        </item>
        <item>
            <title>Investigating the Signal Transduction Pathways Underlying Remote Ischemic Conditioning in the Porcine Heart</title>
            <link>http://www.medworm.com/index.php?rid=5559754&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3n0441368u7t3q65%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In the porcine heart, both RIPC and RIPerC both reduce myocardial infarct size and with RIPC but not RIPerC this cardioprotective
 effect is associated with the activation of the PI3K-Akt pathway at reperfusion.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10557-011-6364-yAuthors
		D. J. Hausenloy, The Hatter Cardiovascular Institute, University College London Hospital &amp; Medical School, London, UKE. K. Iliodromitis, 2nd University Department of Cardiology, Attikon General Hospital, Medical School, University of Athens, Athens, GreeceI. Andreadou, Department of Pharmaceutical Chemistry, School of Pharmacy, University of Athens, Athens, GreeceA. Papalois, 2nd University Department of Cardiology, Attikon General Hospital, Medical School, University of Athe...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559754</comments>
            <pubDate>Fri, 30 Dec 2011 07:08:58 +0100</pubDate>
            <guid isPermaLink="false">5559754</guid>        </item>
        <item>
            <title>In Vivo and In Vitro Protective Effects of Pentamethylquercetin on Cardiac Hypertrophy</title>
            <link>http://www.medworm.com/index.php?rid=5537564&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk454014323713m24%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;PMQ has significant protective effects on cardiac hypertrophy through up-regulating the mRNA and protein levels of PPAR α
 and PPAR β involved in the process of inflammation response and cardiac fibrosis.
 
 
 
 
	Content Type Journal ArticlePages 1-12DOI 10.1007/s10557-011-6363-zAuthors
		Ting He, Department of Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaLei Chen, Department of Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaYong Chen, Department of Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaYi Han, Department of Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, ChinaWei...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5537564</comments>
            <pubDate>Tue, 20 Dec 2011 06:43:32 +0100</pubDate>
            <guid isPermaLink="false">5537564</guid>        </item>
        <item>
            <title>Stem Cell Therapy for Arterial Restenosis: Potential Parameters Contributing to the Success of Bone Marrow-Derived Mesenchymal Stromal Cells</title>
            <link>http://www.medworm.com/index.php?rid=5515264&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F07j35g73uk240k23%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;MSCs play an immunomodulatory paracrine role when injected in rats submitted to carotid arteriotomy, accompanied by the release
 of VEGF, possibly contributing to the accelerated repair of the injured vascular wall.
 
 
 
 
	Content Type Journal ArticlePages 1-13DOI 10.1007/s10557-011-6359-8Authors
		Amalia Forte, Department of Experimental Medicine, Second University of Naples, Via L. De Crecchio, 7-80138 Naples, ItalyBarbara Rinaldi, Department of Experimental Medicine, Second University of Naples, Via L. De Crecchio, 7-80138 Naples, ItalyLoredana Sodano, Department of Experimental Medicine, Second University of Naples, Via L. De Crecchio, 7-80138 Naples, ItalyLiberato Berrino, Department of Experimental Medicine, Second University of Naples, Via L. De Crecchio, 7-...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515264</comments>
            <pubDate>Wed, 14 Dec 2011 06:57:38 +0100</pubDate>
            <guid isPermaLink="false">5515264</guid>        </item>
        <item>
            <title>Mechanistic Insights into Arterial Repair with Mesenchymal Stromal Cells</title>
            <link>http://www.medworm.com/index.php?rid=5504587&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F736182j101l48661%2F</link>
            <description>Content Type Journal ArticleCategory EDITORIALPages 1-3DOI 10.1007/s10557-011-6362-0Authors
		Peter J. Psaltis, Division of Cardiovascular Diseases, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5504587</comments>
            <pubDate>Mon, 12 Dec 2011 17:12:00 +0100</pubDate>
            <guid isPermaLink="false">5504587</guid>        </item>
        <item>
            <title>It is Time to Reconsider the Cardiovascular Protection Afforded by RAAS Blockade - Overview of RAAS Systems</title>
            <link>http://www.medworm.com/index.php?rid=5486645&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm885507200201765%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;More than a century has passed since the renin-angiotensin-aldosterone system (RAAS) was discovered in 1897. Both circulatory
 and tissue RAAS have been found to be essential for regulation of the functions of the whole body, organs, tissues and cells.
 There is no doubt that the RAAS plays fundamental physiological roles in maintaining homeostasis, but it can also contribute
 to organ pathophysiology and tissue damages in some situations. Today, the usefulness of RAAS blockade is well-established
 in the management of a variety of cardiovascular disorders worldwide. However, the latest findings in this field are still
 providing us with new and unexpected insights into the pathophysiology of cardiovascular diseases. Such developments include
 dual blockade therapy with...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486645</comments>
            <pubDate>Tue, 06 Dec 2011 17:03:42 +0100</pubDate>
            <guid isPermaLink="false">5486645</guid>        </item>
        <item>
            <title>Nitrates and Other Nitric Oxide Donors in Cardiology - Current Positioning and Perspectives</title>
            <link>http://www.medworm.com/index.php?rid=5476320&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx32w1550m72825x5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Nitric oxide donors have been commonly used in the therapy of cardiovascular disease for more than 150&amp;nbsp;years. In spite of
 this longevity and the popularity of their use, it appears somewhat paradoxical that there is no current consistent use among
 cardiologists, as to both their indications and their optimal mode of administration. In part this results from their contradictory
 pharmacodynamics: when given acutely, their effectiveness is undisputable; however, their long-term efficacy is potentially
 limited by the development of tolerance and the induction of endothelial dysfunction, which may have negative prognostic implications.
 This review reports recent biochemical and pathophysiological acquisitions, re-examines the role of nitrates and other nitric
 oxid...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476320</comments>
            <pubDate>Thu, 01 Dec 2011 19:29:53 +0100</pubDate>
            <guid isPermaLink="false">5476320</guid>        </item>
        <item>
            <title>Nonclinical Pharmacokinetics of a New Nonpeptide V2 Receptor Antagonist, Tolvaptan</title>
            <link>http://www.medworm.com/index.php?rid=5449668&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1122987023g62n49%2F</link>
            <description>Abstract
 Purpose&amp;nbsp;&amp;nbsp;To evaluate the pharmacokinetic profile of tolvaptan.
 
 
 
 Method&amp;nbsp;&amp;nbsp;The nonclinical pharmacokinetic profile of [14C]tolvaptan was evaluated in an absorption, distribution, and excretion study in rats after single oral administration. An
 in vitro protein binding study was also performed.
 
 
 
 
 Results&amp;nbsp;&amp;nbsp;The tolvaptan-derived radioactivity was rapidly absorbed and extensively distributed to all tissues in rats. The radioactivity
 levels were greatest in the gastrointestinal tract and liver, though the levels in the cerebrum, cerebellum and medulla oblongata
 were low. The serum and tissue concentrations of radioactivity, and serum concentration of tolvaptan in male and female rats
 showed a marked sex difference. The radioactivity was cros...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449668</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:31 +0100</pubDate>
            <guid isPermaLink="false">5449668</guid>        </item>
        <item>
            <title>Effects of Tolvaptan on Volume Overload in Japanese Patients with Heart Failure: Results of a Phase II, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study</title>
            <link>http://www.medworm.com/index.php?rid=5449669&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg01413146061k243%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Once-daily tolvaptan (15, 30 or 45&amp;nbsp;mg) was effective and tolerable as an add-on treatment to furosemide therapy in Japanese
 HF patients with volume overload.
 
 
 
 
	Content Type Journal ArticlePages 1-13DOI 10.1007/s10557-011-6303-yAuthors
		Masunori Matsuzaki, Division of Cardiology, Department of Medicine and Clinical Science, Yamaguchi University Graduate School of Medicine, Yamaguchi, JapanMasatsugu Hori, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, JapanTohru Izumi, Department of Cardio-Angiology, Kitasato University School of Medicine, 1-15-1 Kitasato, Minamiku, Sagamihara, Kanagawa 252-0373, JapanHidetsugu Asanoi, Imizu City Hospital, Toyama, JapanTakayoshi Tsutamoto, Department of Cardiovascular and Respiratory Medicine, Shiga U...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449669</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:30 +0100</pubDate>
            <guid isPermaLink="false">5449669</guid>        </item>
        <item>
            <title>Phase III Clinical Pharmacology Study of Tolvaptan</title>
            <link>http://www.medworm.com/index.php?rid=5449672&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7j8430476600677p%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Tolvaptan exerts diuretic effects and causes body weight loss at the low dose of 7.5&amp;nbsp;mg; however, these effects were less
 than those elicited by 15&amp;nbsp;mg tolvaptan.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s10557-011-6349-xAuthors
		Takayuki Inomata, Department of Cardio-Angiology, Kitasato University School of Medicine, 1-15-1 Kitasato, Minamiku, Sagamihara, Kanagawa, 252–0373, JapanTohru Izumi, Department of Cardio-Angiology, Kitasato University School of Medicine, 1-15-1 Kitasato, Minamiku, Sagamihara, Kanagawa, 252–0373, JapanMasunori Matsuzaki, Department of Medicine and Clinical Science, Yamaguchi University Graduate School of Medicine, Ube, JapanMasatsugu Hori, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japa...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449672</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:29 +0100</pubDate>
            <guid isPermaLink="false">5449672</guid>        </item>
        <item>
            <title>Efficacy and Safety of Tolvaptan in Heart Failure Patients with Sustained Volume Overload despite the Use of Conventional Diuretics: A Phase III Open-Label Study</title>
            <link>http://www.medworm.com/index.php?rid=5449671&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp2586l642086466m%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This study confirms the efficacy and safety of 15&amp;nbsp;mg/day tolvaptan for 7–14&amp;nbsp;days in Japanese HF patients with volume overload
 despite conventional diuretics.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6348-yAuthors
		Masatake Fukunami, Cardiovascular Center, Osaka General Medical Center, 3-1-56 Bandai-Higashi, Sumiyoshi-ku, Osaka, 558-8558 JapanMasunori Matsuzaki, Department of Medicine and Clinical Science, Yamaguchi University Graduate School of Medicine, Ube, JapanMasatsugu Hori, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, JapanTohru Izumi, Department of Cardio-Angiology, Kitasato University School of Medicine, Sagamihara, Japanfor the Tolvaptan Investigators
	

	
		Journal Cardiovascular Drugs and Th...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449671</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:29 +0100</pubDate>
            <guid isPermaLink="false">5449671</guid>        </item>
        <item>
            <title>Anti-edematous Effects of Tolvaptan in Experimental Rodent Models</title>
            <link>http://www.medworm.com/index.php?rid=5449670&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fft8298674uw20q1r%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Tolvaptan had anti-edematous effects in two different rat models. By increasing free water excretion, tolvaptan may be more
 advantageous for certain patients than loop diuretics because it does not cause electrolyte loss, and may prevent electrolyte
 abnormities, such as hyponatremia. These results suggest that tolvaptan has potential clinical benefits for the treatment
 of edema.
 
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10557-011-6355-zAuthors
		Toshiki Miyazaki, First Institute of New Drug Discovery, Otsuka Pharmaceutical Co., Ltd, 463-10 Kagasuno, Kawauchi-cho, Tokushima, 771-0192 JapanYuki Sakamoto, First Institute of New Drug Discovery, Otsuka Pharmaceutical Co., Ltd, 463-10 Kagasuno, Kawauchi-cho, Tokushima, 771-0192 JapanTatsuya Yamashita, Fi...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449670</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:29 +0100</pubDate>
            <guid isPermaLink="false">5449670</guid>        </item>
        <item>
            <title>Effects of Tolvaptan on Systemic and Renal Hemodynamic Function in Dogs with Congestive Heart Failure</title>
            <link>http://www.medworm.com/index.php?rid=5449673&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn62q36309v7x1210%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Tolvaptan elicited a potent aquaretic response and reduced the cardiac preload without unfavorable effects on systemic or
 renal hemodynamics, the renin–angiotensin–aldosterone system, or the sympathetic nervous system in CHF dogs. Thus, tolvaptan
 may offer a novel approach to remove excess water congestion from patients with CHF.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6350-4Authors
		Toshiyuki Onogawa, First institute of New Drug Discovery, Otsuka Pharmaceutical Co., Ltd, Tokushima, JapanYuki Sakamoto, First institute of New Drug Discovery, Otsuka Pharmaceutical Co., Ltd, Tokushima, JapanShigeki Nakamura, First institute of New Drug Discovery, Otsuka Pharmaceutical Co., Ltd, Tokushima, JapanSunao Nakayama, First institute of New Dr...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449673</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:28 +0100</pubDate>
            <guid isPermaLink="false">5449673</guid>        </item>
        <item>
            <title>Erratum to: Tolvaptan for Heart Failure Patients with Volume Overload</title>
            <link>http://www.medworm.com/index.php?rid=5449674&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6t253772u1634wr2%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s10557-011-6360-2Authors
		Masatsugu Hori, Osaka Medical Center for Cancer and Cardiovascular Diseases, 1-3-3 Nakamichi, Higashinari-ku, Osaka, 537-8511 Japan
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449674</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:27 +0100</pubDate>
            <guid isPermaLink="false">5449674</guid>        </item>
        <item>
            <title>Pharmacokinetics, Pharmacodynamics and Safety of Tolvaptan, A Novel, Oral, Selective Nonpeptide AVP V2-receptor Antagonist: Results of Single- and Multiple-Dose Studies in Healthy Japanese Male Volunteers</title>
            <link>http://www.medworm.com/index.php?rid=5449676&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv523l1415318q17k%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Single and multiple oral doses of tolvaptan exhibited dose-dependent aquaretic effects. Tolvaptan was well tolerated at all
 doses tested.
 
 
 
 
	Content Type Journal ArticlePages 1-13DOI 10.1007/s10557-011-6299-3Authors
		Seong Ryul Kim, Department of Clinical Research and Development, Otsuka Pharmaceutical Co., Ltd, 3-2-27 Otedori, Chuo-ku, Osaka, 540–0021 JapanTomoko Hasunuma, Kitasato University Research Center for Clinical Pharmacology, 5-9-1 Shirokane, Minato-ku, Tokyo, 108–8642 JapanOsamu Sato, Department of Clinical Research and Development, Otsuka Pharmaceutical Co., Ltd, 3-2-27 Otedori, Chuo-ku, Osaka, 540–0021 JapanTadashi Okada, Department of Clinical Research and Development, Otsuka Pharmaceutical Co., Ltd, 3-2-27 Otedori, Chuo-ku, Osaka, 540–0...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449676</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:26 +0100</pubDate>
            <guid isPermaLink="false">5449676</guid>        </item>
        <item>
            <title>Efficacy and Safety of Tolvaptan in Heart Failure Patients with Volume Overload Despite the Standard Treatment with Conventional Diuretics: A Phase III, Randomized, Double-blind, Placebo-controlled Study (QUEST Study)</title>
            <link>http://www.medworm.com/index.php?rid=5449675&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm32h2131g612762u%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Tolvaptan reduced volume overload and improved congestive symptoms associated with HF by a potent water diuresis (aquaresis).
 
 
 
	Content Type Journal ArticlePages 1-13DOI 10.1007/s10557-011-6304-xAuthors
		Masunori Matsuzaki, Department of Medicine and Clinical Science, Yamaguchi University Graduate School of Medicine, Ube, JapanMasatsugu Hori, Osaka Medical Center for Cancer and Cardiovascular Disease, 1-3-3 Nakamichi, Higashinari-ku, Osaka, 537–8511 JapanTohru Izumi, Department of Cardio-Angiology, Kitasato University School of Medicine, Sagamihara, JapanMasatake Fukunami, Cardiovascular Center, Osaka General Medical Center, Osaka, Japanfor the Tolvaptan Investigators
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Sou...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449675</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:26 +0100</pubDate>
            <guid isPermaLink="false">5449675</guid>        </item>
        <item>
            <title>Nonclinical Safety Profile of Tolvaptan</title>
            <link>http://www.medworm.com/index.php?rid=5449677&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flk7j128169t1p667%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Nonclinical toxicity that precludes the safe administration of tolvaptan to humans was not observed. However, appropriate
 cautions should be taken in women of childbearing potential.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s10557-011-6356-yAuthors
		Akihide Oi, Drug Safety Research Center, Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd, 463-10 Kagasuno, Kawauchi-cho, Tokushima, 771-0192 JapanKatsumi Morishita, Drug Safety Research Center, Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd, 463-10 Kagasuno, Kawauchi-cho, Tokushima, 771-0192 JapanTakumi Awogi, Drug Safety Research Center, Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd, 463-10 Kagasuno, Kawauchi-cho, Tokushima, 771-0192 JapanAtsushi Ozaki, Departme...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449677</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:25 +0100</pubDate>
            <guid isPermaLink="false">5449677</guid>        </item>
        <item>
            <title>Inhibition of Secretory Phospholipase A2 in Patients with Acute Coronary Syndromes: Rationale and Design of the Vascular Inflammation Suppression to Treat Acute Coronary Syndrome for 16 Weeks (VISTA-16) Trial</title>
            <link>http://www.medworm.com/index.php?rid=5449678&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6t28g85342183u76%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;sPLA2 inhibition has the potential to exert a favorable effect on the artery wall. The VISTA-16 study will determine whether varespladib
 methyl has a beneficial impact on cardiovascular events in patients with an acute coronary syndrome.
 
 
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s10557-011-6358-9Authors
		Stephen J. Nicholls, Cleveland Clinic Coordinating Center for Clinical Research, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USAMatthew A. Cavender, Department of Cardiovascular Medicine, Cleveland Clinic, Mail Code JJ-65, 9500, Euclid Avenue, Cleveland, OH 44195, USAJohn J. P. Kastelein, Academic Medical Center, University of Amsterdam, Amsterdam, The NetherlandsGregory Schwartz, VA Medical Center and University of Colorado Denver, De...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449678</comments>
            <pubDate>Wed, 23 Nov 2011 16:33:41 +0100</pubDate>
            <guid isPermaLink="false">5449678</guid>        </item>
        <item>
            <title>Simvastatin Ameliorates Angiotensin II-Induced Endothelial Dysfunction Through Restoration of Rho-BH4-eNOS-NO Pathway</title>
            <link>http://www.medworm.com/index.php?rid=5421834&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy565k4620152g1j0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Endothelial dysfunction contributes to the initiation and development of hypertension. We previously found that simvastatin
 moderately decreases blood pressure in 2-kidney-2-clip (2k2c) renal hypertension, but the precise mechanisms are still unclear.
 The present study was designed to examine the protective actions of simvastatin in 2k2c-evoked endothelial dysfunction and
 also delineate the underlying mechanisms. Here we show that 2k2c-induced elevation in plasma angiotensin II impaired acetylcholine-induced
 endothelium-dependent vascular relaxation, suppressed endothelial NO synthase (eNOS) activity and reduced nitric oxide (NO)
 production. Additionally, the levels of tetrahydrobiopterin (BH4), an essential cofactor of eNOS, as well as the activity
 of GTP cyclohy...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421834</comments>
            <pubDate>Mon, 14 Nov 2011 16:52:44 +0100</pubDate>
            <guid isPermaLink="false">5421834</guid>        </item>
        <item>
            <title>The Chemical Compound PTC124 Does Not Affect Cellular Electrophysiology of Cardiac Ventricular Myocytes</title>
            <link>http://www.medworm.com/index.php?rid=5407571&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F686574667u252741%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;PTC124 has no acute or long-term effects on rabbit ventricular action potentials. These experiments form the basis for future
 studies evaluating the use of this therapy in preventing potentially lethal arrhythmias in patients with BrS and/or conduction
 disease.
 
 
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s10557-011-6352-2Authors
		Tamara T. Koopmann, Heart Failure Research Center, Department of Clinical and Experimental Cardiology, Academic Medical Center, Amsterdam, The NetherlandsArie O. Verkerk, Heart Failure Research Center, Department of Anatomy, Embryology &amp; Physiology, Academic Medical Center, Amsterdam, The NetherlandsConnie R. Bezzina, Heart Failure Research Center, Department of Clinical and Experimental Cardiology, Academic Medical Center, A...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407571</comments>
            <pubDate>Tue, 08 Nov 2011 06:50:42 +0100</pubDate>
            <guid isPermaLink="false">5407571</guid>        </item>
        <item>
            <title>The Pleiotropic Effects of Statins in the Prevention of Atherosclerosis</title>
            <link>http://www.medworm.com/index.php?rid=5386028&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp861608g4863g167%2F</link>
            <description>Content Type Journal ArticleCategory EDITORIALPages 1-3DOI 10.1007/s10557-011-6353-1Authors
		Wei Kong, Department of Physiology and Pathophysiology, Peking University Health Sciences Center, Beijing, 100191 ChinaYi Zhu, Department of Physiology and Pathophysiology, Peking University Health Sciences Center, Beijing, 100191 China
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5386028</comments>
            <pubDate>Fri, 04 Nov 2011 05:44:35 +0100</pubDate>
            <guid isPermaLink="false">5386028</guid>        </item>
        <item>
            <title>Simvastatin Suppresses Apoptosis in Vulnerable Atherosclerotic Plaques Through Regulating the Expression of p53, Bcl-2 and Bcl-xL</title>
            <link>http://www.medworm.com/index.php?rid=5360205&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe285m0671p885255%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;In the present study, we show novel data to suggest that simvastatin could suppress apoptosis in vulnerable atherosclerotic
 plaques of apoE−/− mice by regulating the expression of apoptosis-related proteins, such as p53, Bcl-2 and Bcl-xL.
 
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s10557-011-6347-zAuthors
		Weiwei Qin, The Key Laboratory of Geriatrics, Beijing Hospital &amp; Beijing Institute of Geriatrics, Ministry of Health, Beijing, 100730 ChinaYonggang Lu, The Key Laboratory of Geriatrics, Beijing Hospital &amp; Beijing Institute of Geriatrics, Ministry of Health, Beijing, 100730 ChinaChengyan Zhan, Shanghai PuNan Hospital, Shanghai, 200125 ChinaTao Shen, The Key Laboratory of Geriatrics, Beijing Hospital &amp; Beijing Institute of Geriatrics, Ministry of ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5360205</comments>
            <pubDate>Fri, 28 Oct 2011 17:25:00 +0100</pubDate>
            <guid isPermaLink="false">5360205</guid>        </item>
        <item>
            <title>Systematic Review and Meta-Analysis: Renin-Angiotensin System Inhibitors in the Prevention of Atrial Fibrillation Recurrences. An Unfulfilled Hope</title>
            <link>http://www.medworm.com/index.php?rid=5335446&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv9280806g1765126%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Currently there is no role for ARBs in secondary prevention of AF. With regard to ACEIs, the data are not strong enough for
 a conclusion, although the efficacy is expected to be the same as that of ARBs.
 
 
 
 
	Content Type Journal ArticleCategory Review ArticlePages 1-8DOI 10.1007/s10557-011-6346-0Authors
		Marcello Disertori, Department of Cardiology, Santa Chiara Hospital, Largo Medaglie d’Oro, 38122 Trento, ItalySimona Barlera, Department of Cardiovascular Research, Istituto Mario Negri, Milan, ItalyLidia Staszewsky, Department of Cardiovascular Research, Istituto Mario Negri, Milan, ItalyRoberto Latini, Department of Cardiovascular Research, Istituto Mario Negri, Milan, ItalySilvia Quintarelli, Department of Cardiology, Santa Chiara Hospital, Largo Medaglie...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5335446</comments>
            <pubDate>Tue, 18 Oct 2011 15:57:29 +0100</pubDate>
            <guid isPermaLink="false">5335446</guid>        </item>
        <item>
            <title>The MAGIC Study and the Gastrointestinal Effects of Low-Dose Aspirin</title>
            <link>http://www.medworm.com/index.php?rid=5335447&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu0k2661587114436%2F</link>
            <description>Content Type Journal ArticleCategory EditorialPages 1-2DOI 10.1007/s10557-011-6345-1Authors
		John McNeil, Department of Epidemiology &amp; Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Alfred Centre, 99 Commercial Road, Melbourne, Victoria 3004, AustraliaAndrew Tonkin, Department of Epidemiology &amp; Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Alfred Centre, 99 Commercial Road, Melbourne, Victoria 3004, Australia
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5335447</comments>
            <pubDate>Mon, 17 Oct 2011 16:04:28 +0100</pubDate>
            <guid isPermaLink="false">5335447</guid>        </item>
        <item>
            <title>LOX-1, Oxidative Stress and Inflammation: A Novel Mechanism for Diabetic Cardiovascular Complications</title>
            <link>http://www.medworm.com/index.php?rid=5314226&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx2582142l7884w90%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diabetes mellitus is a common metabolic disease characterized by a state of oxidative stress, inflammation and endothelial
 dysfunction. This malady can lead to a number of complications such as ischemic heart disease, nephropathy, neuropathy, retinopathy
 and impaired wound healing. The etiology of diabetic complications is multifactorial, and is closely associated with oxidative
 stress and inflammation. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), a receptor for oxidized low density
 lipoprotein (ox-LDL), plays critical roles in multiple signal transduction pathways and is involved in the process of oxidative
 stress and inflammation. Recent studies provide important insights into the roles of LOX-1 in the development and progression
 of diabetic ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314226</comments>
            <pubDate>Wed, 12 Oct 2011 16:04:59 +0100</pubDate>
            <guid isPermaLink="false">5314226</guid>        </item>
        <item>
            <title>Anti-Inflammatory Effects of Varespladib Methyl in Diabetic Patients with Acute Coronary Syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5314227&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe26702672327wn20%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Varespladib significantly reduces the post-ACS inflammatory response in those with and without diabetes. These responses were
 greater in diabetic subjects compared to non-diabetic subjects.
 
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10557-011-6344-2Authors
		Robert S. Rosenson, Mount Sinai School of Medicine, 1425 Madison Ave., New York, NY 10029, USAHeather Fraser, Anthera Pharmaceuticals, Inc., 25801 Industrial Blvd., Suite B, Hayward, CA 94545, USAMichael A. Goulder, Worldwide Clinical Trials, Isaac Newton Centre, Nottingham Science Park, Nottingham, UK NG7 2RHColin Hislop, Anthera Pharmaceuticals, Inc., 25801 Industrial Blvd., Suite B, Hayward, CA 94545, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314227</comments>
            <pubDate>Tue, 11 Oct 2011 15:49:42 +0100</pubDate>
            <guid isPermaLink="false">5314227</guid>        </item>
        <item>
            <title>Aliskiren and Valsartan Reduce Myocardial AT1 Receptor Expression and Limit Myocardial Infarct Size in Diabetic Mice</title>
            <link>http://www.medworm.com/index.php?rid=5314228&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn2463um0047h56h1%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;AL, dose dependently limited myocardial IS in mice with type-2 diabetes mellitus. At doses shown to limit IS in non-diabetic
 animals, VA failed to reduce IS in Db/Db mice. However, at higher dose (16&amp;nbsp;mg/kg/d), VA reduced IS. Both drugs reduced the
 expression of AT1R and increased myocardial levels of the longevity genes Sirt1 and PGC-1α along with increased Akt and eNOS
 phosphorylation.
 
 
 
 
	Content Type Journal ArticlePages 1-11DOI 10.1007/s10557-011-6339-zAuthors
		Yumei Ye, The Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, MRB 5:108, 301 University Blvd., Galveston, TX 77555, USAJinqiao Qian, The Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, MRB 5:108, 301 University Blvd....</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314228</comments>
            <pubDate>Mon, 10 Oct 2011 15:01:15 +0100</pubDate>
            <guid isPermaLink="false">5314228</guid>        </item>
        <item>
            <title>Angiogenesis is a Link Between Atherosclerosis and Tumorigenesis: Role of LOX-1</title>
            <link>http://www.medworm.com/index.php?rid=5296820&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe610326k85u34663%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Angiogenesis is defined as the formation of new blood vessels sprouting from pre-existing vessels. It plays an important role
 not only in physiological situations such as embryonic vascular development and wound healing, but also in pathological conditions
 including atherogenesis and evolution and spread of certain tumors. Lectin-like oxidized low-density lipoprotein receptor-1
 (LOX-1), a receptor for oxidized low density lipoprotein (ox-LDL), is mainly expressed in endothelial cells. It has diverse
 physiological functions and it could be a link between atherogenesis and tumorigenesis. The risk factors for atherosclerosis
 like hypertension, diabetes mellitus and hyperlipidemia are associated with LOX-1. Dyslipidemia and obesity are also being
 recognized as risk fa...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296820</comments>
            <pubDate>Tue, 04 Oct 2011 05:49:09 +0100</pubDate>
            <guid isPermaLink="false">5296820</guid>        </item>
        <item>
            <title>Oxidized LDL, LOX-1 and Atherosclerosis</title>
            <link>http://www.medworm.com/index.php?rid=5273500&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Faw613h0748x55712%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An elevated level of low density lipoprotein (LDL) cholesterol constitutes a major risk factor for genesis of atherosclerosis.
 Ox-LDL plays a more important role in the genesis and progression of atherosclerosis than the native LDL. Ox-LDL leads to
 endothelial dysfunction leading to expression of adhesion molecules and recruitment of monocyte in subendothelial space. Ox-LDL
 is taken up by macrophages via scavenger receptors, such as SR-A1, SR-A2 and LOX-1. Lately, LOX-1, a type II membrane protein
 receptor of ox-LDL, has gained much importance in relation to effects of ox-LDL on endothelial biology. Endothelial cells
 primarily express LOX-1 as receptor for ox-LDL and ox-LDL has been shown to upregulate expression of LOX-1. In addition, ox-LDL
 promotes the growth a...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273500</comments>
            <pubDate>Tue, 27 Sep 2011 05:50:36 +0100</pubDate>
            <guid isPermaLink="false">5273500</guid>        </item>
        <item>
            <title>Beta-Blocker Dose Up-Titration or Addition of Ivabradine in Stable Angina: More is Not Necessarily Better</title>
            <link>http://www.medworm.com/index.php?rid=5260423&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa70m473155154458%2F</link>
            <description>Content Type Journal ArticleCategory EditorialPages 1-2DOI 10.1007/s10557-011-6340-6Authors
		Raymond W. Sy, Concord Clinical School, University of Sydney, Sydney, AustraliaSaul B. Freedman, Concord Clinical School, University of Sydney, Sydney, Australia
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260423</comments>
            <pubDate>Tue, 20 Sep 2011 05:47:40 +0100</pubDate>
            <guid isPermaLink="false">5260423</guid>        </item>
        <item>
            <title>Stroke Prevention in Atrial Fibrillation</title>
            <link>http://www.medworm.com/index.php?rid=5237003&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdlp0506155243536%2F</link>
            <description>Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6334-4Authors
		Jonathan P. Piccini, Division of Cardiology, Duke Clinical Research Institute, Duke University School of Medicine, Durham, USAThomas W. Wallace, Heart Clinic Arkansas, Little Rock, AR, USAManesh R. Patel, Division of Cardiology, Duke Clinical Research Institute, Duke University School of Medicine, Durham, USARichard C. Becker, Division of Cardiology, Duke Clinical Research Institute, Duke University School of Medicine, Durham, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237003</comments>
            <pubDate>Fri, 16 Sep 2011 16:43:25 +0100</pubDate>
            <guid isPermaLink="false">5237003</guid>        </item>
        <item>
            <title>High Dose Statin Treatment and New Onset Diabetes</title>
            <link>http://www.medworm.com/index.php?rid=5237004&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk7q61k08m8306661%2F</link>
            <description>Content Type Journal ArticleCategory ISCP President’s PagePages 1-2DOI 10.1007/s10557-011-6338-0Authors
		Juan Carlos Kaski, Cardiovascular Sciences Research Centre, St. George’s, University of London, Cranmer Terrace, London, SW17 0RE UK
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237004</comments>
            <pubDate>Tue, 13 Sep 2011 15:52:39 +0100</pubDate>
            <guid isPermaLink="false">5237004</guid>        </item>
        <item>
            <title>Novel Concepts in the Genesis of Hypertension: Role of LOX-1</title>
            <link>http://www.medworm.com/index.php?rid=5237005&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj7wml31r72x65j19%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hypertension is a common disease and a potent risk factor for cardiovascular disease. Tremendous strides have been made in
 understanding its genesis in the last 2 decades. Hypertension is often clustered with other cardiovascular risk factors, such
 as dyslipidemia and diabetes. The state of hypertension is often associated with increased vascular oxidative stress. Oxidative
 stress promotes proliferation and hypertrophy of vascular smooth muscle cell and collagen deposition, leading to thickening
 of the vascular media and narrowing of the vascular lumen. Oxidative stress also injures endothelium, impairs endothelium-dependent
 vascular relaxation and increases vascular contractile activity. Further, oxidative stress also oxidizes LDL-cholesterol.
 It has been shown t...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237005</comments>
            <pubDate>Mon, 12 Sep 2011 15:51:36 +0100</pubDate>
            <guid isPermaLink="false">5237005</guid>        </item>
        <item>
            <title>LOX-1/LOXIN: The Yin/Yang of Atheroscleorosis</title>
            <link>http://www.medworm.com/index.php?rid=5208331&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh863330381n0r92p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Atherosclerosis is the first cause of death in industrialized countries. Together with traditional risk factors (male gender,
 hypercholesterolemia, hypertension, diabetes, smoking and age), non-traditional risk factors have also been described as predisposing
 to this disease. Among these, oxidized low density lipoproteins (OxLDL) have been described in correlation to many proatherogenic
 processes. Many of the effects of OxLDL are mediated by the lectin like oxidized low density lipoprotein receptor 1 (LOX-1),
 expressed on endothelial cells, macrophages, SMCs and platelets. LOX-1 is encoded by the lectin like oxidized low density
 lipoprotein receptor 1 (OLR1) gene, located in the p12.3–p13.2 region of human chromosome 12. Variations on this gene have been studied ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208331</comments>
            <pubDate>Fri, 09 Sep 2011 05:48:43 +0100</pubDate>
            <guid isPermaLink="false">5208331</guid>        </item>
        <item>
            <title>Do Atherosclerosis and Obesity-Associated Susceptibility to Cancer Share Causative Link to oxLDL and LOX-1?</title>
            <link>http://www.medworm.com/index.php?rid=5183642&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff8u616341605235u%2F</link>
            <description>Content Type Journal ArticlePages 1-11DOI 10.1007/s10557-011-6330-8Authors
		Magomed Khaidakov, Central Arkansas Veterans Healthcare Center and the University of Arkansas for Medical Sciences, 4301 W Markham, Slot 532, Little Rock, AR 72205, USAJawahar L. Mehta, Central Arkansas Veterans Healthcare Center and the University of Arkansas for Medical Sciences, 4301 W Markham, Slot 532, Little Rock, AR 72205, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5183642</comments>
            <pubDate>Wed, 31 Aug 2011 15:52:57 +0100</pubDate>
            <guid isPermaLink="false">5183642</guid>        </item>
        <item>
            <title>LOX-1 and Obesity</title>
            <link>http://www.medworm.com/index.php?rid=5183641&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp8827110815w77kl%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Obesity is one of the most common lifestyle-related diseases. Being closely associated with insulin resistance, hypertension
 and dyslipidemia, it is also a component of metabolic syndrome and is involved in the development of atherosclerosis and cardiovascular
 and renal ailments. Obesity is also accompanied with a state of chronic inflammation. Lectin-like oxidized low-density lipoprotein
 receptor-1 (LOX-1), a receptor for oxidized low density lipoprotein (ox-LDL), is expressed not only in endothelial cells,
 but also in macrophages, vascular smooth muscle cells, platelets and adipocytes. LOX-1 binds multiple ligands, has diverse
 physiological functions and plays a critical role in the signal transduction. It may well turn out to be a key, or very important,
 factor...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5183641</comments>
            <pubDate>Wed, 31 Aug 2011 15:52:57 +0100</pubDate>
            <guid isPermaLink="false">5183641</guid>        </item>
        <item>
            <title>Reduction of Cerebral Infarct Size by Dronedarone</title>
            <link>http://www.medworm.com/index.php?rid=5183643&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx81v956544tu35n0%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Dronedarone administered before and after MCAO reduces IS and improves FA and neurological outcome in transient cerebral ischemia.
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10557-011-6336-2Authors
		Tobias Engelhorn, Department of Neuroradiology, University of Erlangen-Nuremberg, Schwabachanlage 6, 91054 Erlangen, GermanyMarc A. Schwarz, Department of Neuroradiology, University of Erlangen-Nuremberg, Schwabachanlage 6, 91054 Erlangen, GermanyGerd Heusch, Institute for Pathophysiology, University School of Medicine, Essen, GermanyArnd Doerfler, Department of Neuroradiology, University of Erlangen-Nuremberg, Schwabachanlage 6, 91054 Erlangen, GermanyRainer Schulz, Institute for Physiology, Justus-Liebig University, Giessen, Germany
	

	
		Journal Cardiov...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5183643</comments>
            <pubDate>Wed, 31 Aug 2011 15:52:55 +0100</pubDate>
            <guid isPermaLink="false">5183643</guid>        </item>
        <item>
            <title>LOX-1 and Angiotensin Receptors, and Their Interplay</title>
            <link>http://www.medworm.com/index.php?rid=5161403&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp404650115m320q4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The renin-angiotensin system (RAS) plays an important role in regulating blood pressure, water-salt balance and the pathogenesis
 of cardiovascular diseases. Angiotensin II (Ang II) is the physiologically active mediator and mediates the main pathophysiological
 actions in RAS. Ang II exerts the effects by activating its receptors, primarily type 1 (AT1R) and type 2 (AT2R). Most of
 the known pathophysiological effects of Ang II are mediated by AT1R activation. The precise physiological function of AT2R
 is still not clear. Generally, AT2R is considered to oppose the effects of AT1R. Lectin-like oxidized low-density lipoprotein
 scavenger receptor-1 (LOX-1) is one of the major receptors responsible for binding, internalizing and degrading ox-LDL. The
 activation of LOX-...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161403</comments>
            <pubDate>Mon, 22 Aug 2011 15:58:43 +0100</pubDate>
            <guid isPermaLink="false">5161403</guid>        </item>
        <item>
            <title>LOX-1: A Critical Player in the Genesis and Progression of Myocardial Ischemia</title>
            <link>http://www.medworm.com/index.php?rid=5161404&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa7471nrw87774770%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Myocardial ischemia is the most common cause of mortality and morbidity in the developed countries and rapidly becoming a
 common malady in the developing countries. Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), encoded by the
 OLR1 gene, is a scavenger receptor that plays a fundamental role in the genesis and progression of atherosclerosis and its
 complications. LOX-1 has been identified as a major receptor for oxidized low-density lipoprotein (ox-LDL) in endothelial
 cells, cardiomyocytes and fibroblast. In vitro and in vivo studies show that LOX-1 is upregulated during acute myocardial
 ischemia, and continues to be upregulated during chronic ischemia. Further, LOX-1 inhibition reduces ischemic myocardial injury
 and limits cardiac remodeling. LOX...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161404</comments>
            <pubDate>Wed, 17 Aug 2011 05:54:59 +0100</pubDate>
            <guid isPermaLink="false">5161404</guid>        </item>
        <item>
            <title>Oxidized Low Density Lipoproteins-Do We Know Enough About Them?</title>
            <link>http://www.medworm.com/index.php?rid=5161405&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F31811047176m1732%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since the discovery of oxidized low density lipoprotein (Ox-LDL), over 5,000 articles have appeared on the topic with over
 400 articles appearing every year during the past decade. LDL contains esterified polyunsaturated fatty acid containing lipids,
 such as, phosphatidylcholine (PtdCho) and cholesterol esters (CE). Peroxidation of polyunsaturated fatty acid (PUFA) containing
 lipids has been known for a long time. Numerous studies have documented that peroxidized lipids as well as products derived
 from their decomposition, particularly aldehydes, have deleterious biological properties. This concept has been exemplified
 in the study of atherosclerosis. A plethora of in vitro and animal studies, as well as human epidemiological and correlatory
 studies, have supporte...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161405</comments>
            <pubDate>Tue, 16 Aug 2011 06:14:26 +0100</pubDate>
            <guid isPermaLink="false">5161405</guid>        </item>
        <item>
            <title>Prospective Cohort Study of Gastrointestinal Complications and Vascular Diseases in Patients Taking Aspirin: Rationale and Design of the MAGIC Study</title>
            <link>http://www.medworm.com/index.php?rid=5131913&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjj3n79706n563014%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The MAGIC study will yield important findings with regard to the prevalence and incidence of gastrointestinal complications
 and related risk factors for low-dose aspirin users. It may also report that use of anti-secretory agents such as proton pump
 inhibitors reduces the risk of such complications.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6328-2Authors
		Hideki Origasa, Division of Biostatistics and Clinical Epidemiology, University of Toyama, 2630 Sugitani, Toyama, 930-0194 JapanShinya Goto, Department of Internal Medicine, Tokai University, Isehara, Tokyo, JapanKazuyuki Shimada, Department of Cardiology, Jichi Medical University, Shimotsuke, Tochigi, JapanShinichiro Uchiyama, Department of Neurology, Tokyo Women’s Medical Universit...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131913</comments>
            <pubDate>Sat, 13 Aug 2011 06:13:44 +0100</pubDate>
            <guid isPermaLink="false">5131913</guid>        </item>
        <item>
            <title>Efficacy of Ivabradine in Combination with Beta-Blocker Versus Uptitration of Beta-Blocker in Patients with Stable Angina</title>
            <link>http://www.medworm.com/index.php?rid=5126180&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F02g235gk48858776%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These results suggest that combining ivabradine with low dose bisoprolol in stable angina patients produces additional antianginal
 and anti-ischemic benefits and improves chronotropic reserve.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10557-011-6327-3Authors
		E. Amosova, National Medical University, Kiev, UkraineE. Andrejev, National Medical University, Kiev, UkraineI. Zaderey, National Medical University, Kiev, UkraineU. Rudenko, National Medical University, Kiev, UkraineC. Ceconi, Department of Cardiology, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, ItalyR. Ferrari, Department of Cardiology and LTTA Centre, University Hospital of Ferrara and Salvatore Maugeri Foundation, IRCCS, Lumezzane, Italy
	

	
		Journal Cardiovascular Drugs an...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126180</comments>
            <pubDate>Wed, 10 Aug 2011 15:40:02 +0100</pubDate>
            <guid isPermaLink="false">5126180</guid>        </item>
        <item>
            <title>LOX-1: A New Target for Therapy for Cardiovascular Diseases</title>
            <link>http://www.medworm.com/index.php?rid=5126181&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F25144n72r47g4851%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is much interest in the role of oxidant stress in an ever-increasing list of disease states. However, the precise mediator
 of oxidant stress and the stressor molecule/s have not been identified. Accordingly, trials of inhibitors of oxidant stress
 in animal models of disease states have met only limited success. The trials of traditional anti-oxidant vitamins have been
 largely unsuccessful in the treatment of a wide array of disease states in humans. Recent identification of LOX-1 in vascular
 endothelial cells and its activation by oxidant species have led to a marked improvement in our understanding of the pathology
 of several cardiovascular disease states. Here, we review the disease states where therapy targeted at LOX-1 inhibition might
 be helpful.
 
 
	C...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126181</comments>
            <pubDate>Mon, 08 Aug 2011 19:51:32 +0100</pubDate>
            <guid isPermaLink="false">5126181</guid>        </item>
        <item>
            <title>The Discovery of LOX-1, its Ligands and Clinical Significance</title>
            <link>http://www.medworm.com/index.php?rid=5096755&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh24473654771857v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;LOX-1 is an endothelial receptor for oxidized low-density lipoprotein (oxLDL), a key molecule in the pathogenesis of atherosclerosis.The
 basal expression of LOX-1 is low but highly induced under the influence of proinflammatory and prooxidative stimuli in vascular
 endothelial cells, smooth muscle cells, macrophages, platelets and cardiomyocytes. Multiple lines of in vitro and in vivo
 studies have provided compelling evidence that LOX-1 promotes endothelial dysfunction and atherogenesis induced by oxLDL.
 The roles of LOX-1 in the development of atherosclerosis, however, are not simple as it had been considered. Evidence has
 been accumulating that LOX-1 recognizes not only oxLDL but other atherogenic lipoproteins, platelets, leukocytes and CRP.
 As results, LOX-1 not...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5096755</comments>
            <pubDate>Mon, 01 Aug 2011 05:32:29 +0100</pubDate>
            <guid isPermaLink="false">5096755</guid>        </item>
        <item>
            <title>LOX-1 Transcription</title>
            <link>http://www.medworm.com/index.php?rid=5088083&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy4h112575712vll1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The importance of the lectin-like oxidized LDL receptor (LOX-1) gene in cardiovascular and other diseases is slowly being
 revealed. LOX-1 gene expression appears to be a “canary in a coal mine” for atherogenesis, being strongly up-regulated early
 on in a number of cell types when they are activated, and predicting the sites of future disease. From this early time point
 the LOX-1 protein often participates in the disease process itself. While gene/protein expression can be regulated on a multiplicity
 of levels, the most basic and important mode of regulation is usually transcriptional. There are very few studies on the transcriptional
 regulation of the human LOX-1 promoter; fewer still on definitive mapping of the transcription factors involved. It is known
 tha...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088083</comments>
            <pubDate>Wed, 27 Jul 2011 15:51:26 +0100</pubDate>
            <guid isPermaLink="false">5088083</guid>        </item>
        <item>
            <title>C-Reactive Protein, Statins and the Risk of Vascular Events: A Better Understanding</title>
            <link>http://www.medworm.com/index.php?rid=5088084&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F62u4856772077123%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The association between C-reactive protein (CRP) and cardiovascular disease has been under investigation for more than sixty
 years. Lately, findings from the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin
 (JUPITER) trial opened a new frontier: that of prescribing statins for vascular events risk reduction based upon the baseline
 CRP levels in otherwise healthy adults. Although the results from the JUPITER were impressive, ambiguities and arguments about
 this association have remained. Moreover, the results of a report by Heart Protection Study investigators have added to the
 complexities of the correlation between CRP levels and the risk of vascular events. In this review, a summary of the structural
 and functiona...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088084</comments>
            <pubDate>Tue, 26 Jul 2011 15:48:34 +0100</pubDate>
            <guid isPermaLink="false">5088084</guid>        </item>
        <item>
            <title>Cardioprotective Effect of 3-Iodothyronamine in Perfused Rat Heart Subjected to Ischemia and Reperfusion</title>
            <link>http://www.medworm.com/index.php?rid=5070127&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk80g1051j4173674%2F</link>
            <description>In conclusion, in isolated rat heart T1AM produces a cardioprotective effect which is mediated by a protein kinase C and KATP+-dependent pathway and is probably linked to modulation of mitochondrial permeability transition and/or ischemic arrest time.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10557-011-6320-xAuthors
		Sabina Frascarelli, Dipartimento di Scienze dell’Uomo e dell’Ambiente, University of Pisa, Via Roma 55, 56126 Pisa, ItalySandra Ghelardoni, Dipartimento di Scienze dell’Uomo e dell’Ambiente, University of Pisa, Via Roma 55, 56126 Pisa, ItalyGrazia Chiellini, Dipartimento di Scienze dell’Uomo e dell’Ambiente, University of Pisa, Via Roma 55, 56126 Pisa, ItalyElena Galli, Scuola Superiore S. Anna, Pisa, ItalyFrancesca Ronca, Dipartimento di Scienze dell...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5070127</comments>
            <pubDate>Mon, 25 Jul 2011 05:33:54 +0100</pubDate>
            <guid isPermaLink="false">5070127</guid>        </item>
        <item>
            <title>Abdominal Surgical Incision Induces Remote Preconditioning of Trauma (RPCT) via Activation of Bradykinin Receptors (BK2R) and the Cytochrome P450 Epoxygenase Pathway in Canine Hearts</title>
            <link>http://www.medworm.com/index.php?rid=5070128&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3w7773v216112326%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These results suggest that BK and the EETs share cardioprotective properties in a large animal model of RPCT.
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10557-011-6321-9Authors
		Garrett J. Gross, Department of Pharmacology and Toxicology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USAJohn E. Baker, Department of Pharmacology and Toxicology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USAJeannine Moore, Department of Pharmacology and Toxicology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USAJohn R. Falck, Departments of Biochemistry and Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USAKasem Nithipatikom, Department o...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5070128</comments>
            <pubDate>Mon, 25 Jul 2011 05:33:53 +0100</pubDate>
            <guid isPermaLink="false">5070128</guid>        </item>
        <item>
            <title>Effect of Aliskiren in Patients with Heart Failure According to Background Dose of ACE Inhibitor: A Retrospective Analysis of the Aliskiren Observation of Heart Failure Treatment (ALOFT) Trial</title>
            <link>http://www.medworm.com/index.php?rid=5063517&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpr6w132505w08405%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Aliskiren causes neurohumoral suppression in heart failure, even in patients treated with ≥recommended-dose of ACE inhibitor.
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10557-011-6319-3Authors
		Novalia P. Sidik, British Heart Foundation Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow, G12 8TA UKScott D. Solomon, Cardiovascular Division, Brigham &amp; Women’s Hospital, Boston, MA, USARoberto Latini, Department of Cardiovascular Research, Istituto di Ricerche Farmacologiche Mario Negri, Milan, ItalyAldo P. Maggioni, ANMCO Research Center, Florence, ItalyMelanie Wright, Novartis Pharma AG, Basel, SwitzerlandClaudio R. Gimpelewicz, Novartis Pharma AG, Basel, SwitzerlandBertram Pitt, University of Michigan, Ann Arbor, MI...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063517</comments>
            <pubDate>Thu, 21 Jul 2011 18:04:43 +0100</pubDate>
            <guid isPermaLink="false">5063517</guid>        </item>
        <item>
            <title>Inhibition of the Cerebral Renin-Angiotensin System to Limit Cognitive Decline in Elderly Hypertensive Persons</title>
            <link>http://www.medworm.com/index.php?rid=5063518&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0274k41614730318%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s10557-011-6316-6Authors
		Lionel H. Opie, Hatter Cardiovascular Research Institute, Department of Medicine, University of Cape Town Faculty of Health Sciences and Groote Schuur Hospital, Observatory, Cape Town, 7925 South Africa
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063518</comments>
            <pubDate>Tue, 19 Jul 2011 23:37:41 +0100</pubDate>
            <guid isPermaLink="false">5063518</guid>        </item>
        <item>
            <title>The Difficult Task of Teaching Cardiovascular Pharmacotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5063519&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh314j08t4m243711%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s10557-011-6317-5Authors
		Juan-Carlos Kaski, St. George’s, University of London, London, UK
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063519</comments>
            <pubDate>Tue, 19 Jul 2011 05:44:37 +0100</pubDate>
            <guid isPermaLink="false">5063519</guid>        </item>
        <item>
            <title>Cardiac Resynchronization in Mild Heart Failure: All Issues Resolved?</title>
            <link>http://www.medworm.com/index.php?rid=5063520&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1005837kp8535443%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s10557-011-6318-4Authors
		Alexander H. Maass, Department of Cardiology, Thoraxcenter, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063520</comments>
            <pubDate>Tue, 19 Jul 2011 05:44:35 +0100</pubDate>
            <guid isPermaLink="false">5063520</guid>        </item>
        <item>
            <title>Cardiac Resynchronization Therapy in Patients with Mild Heart Failure: A Systematic Review and Meta-Analysis of Randomized Controlled Trials</title>
            <link>http://www.medworm.com/index.php?rid=5030270&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu2qg3l51v5523671%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This meta-analysis suggests that CRT could improve the prognosis in patients with mild heart failure and ventricular dyssynchrony,
 but these improvements are accompanied by more adverse events. Since most patients in the included trials had received ICD
 therapy, our analysis suggests that CRT could offer an additional benefit.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6313-9Authors
		Ronghui Tu, Department of Geriatric Cardiology, First Afiliated Hospital, Guangxi Medical University, 22 Shuangyong Road, 530000 Nanning, Guangxi, People’s Republic of ChinaGuoqiang Zhong, Department of Geriatric Cardiology, First Afiliated Hospital, Guangxi Medical University, 22 Shuangyong Road, 530000 Nanning, Guangxi, People’s Republic of ChinaZhiyu ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030270</comments>
            <pubDate>Wed, 13 Jul 2011 06:03:16 +0100</pubDate>
            <guid isPermaLink="false">5030270</guid>        </item>
        <item>
            <title>The Impact of Age on Effects of Pre-hospital Initiation of High Bolus Dose of Tirofiban Before Primary Angioplasty for ST-Elevation Myocardial Infarction</title>
            <link>http://www.medworm.com/index.php?rid=5030271&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0v48l328p76v617x%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The effect of pre-hospital initiation of high bolus dose tirofiban on myocardial reperfusion, as determined by ST-segment
 resolution is highest in the elderly patients. However, this was associated with a trend towards more bleeding complications,
 resulting in a balanced clinical effect after 30-day follow-up. Future studies should evaluate whether the elderly STEMI patient
 may benefit from highly effective and safer antiplatelet therapy.
 
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s10557-011-6314-8Authors
		Renicus S. Hermanides, Department of Cardiology, Isala Klinieken. locatie Weezenlanden, Groot Wezenland 20, 8011 JW Zwolle, The NetherlandsGert van Houwelingen, Department of Cardiology, Medisch Spectrum Twente, Enschede, The NetherlandsJan Paul O...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030271</comments>
            <pubDate>Mon, 11 Jul 2011 05:35:15 +0100</pubDate>
            <guid isPermaLink="false">5030271</guid>        </item>
        <item>
            <title>Erratum to: Design and Rationale of Japanese Evaluation Between Formula of Azelnidipine and Amlodipine Add on Olmesartan to Get Antialbuminuric Effect Study (J-FLAG)</title>
            <link>http://www.medworm.com/index.php?rid=5009801&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg1654158868258j5%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s10557-011-6315-7Authors
		Katsuyuki Ando, Department of Nephrology and Endocrinology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113–8655 JapanMasakazu Haneda, Division of Metabolism and Biosystemic Science, Department of Medicine, Asahikawa Medical University, 1-1, 2–1 Midorigaokahigashi, Asahikawa, Hokkaido 078–8510, JapanSadayoshi Ito, Division of Nephrology, Endocrinology, and Vascular Medicine, Department of Internal Medicine, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980–8574 JapanNaoki Kashihara, Division of Nephrology, Department of Internal Medicine, Kawasaki Medical School, 557 Matsushima, Kurashiki, Okayama 701–0192, JapanKoichi Node, Department of ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5009801</comments>
            <pubDate>Wed, 06 Jul 2011 05:53:54 +0100</pubDate>
            <guid isPermaLink="false">5009801</guid>        </item>
        <item>
            <title>Atorvastatin Protects against Ischemia-Reperfusion Injury in Fructose-Induced Insulin Resistant Rats</title>
            <link>http://www.medworm.com/index.php?rid=4946486&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe37n45u83p301136%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Atorvastatin conferred significant protection against MI-RP injury and alleviated HFr induced IRS possibly by increasing NOS
 expression through Akt dependent pathway.
 
 
 
 
	Content Type Journal ArticlePages 1-13DOI 10.1007/s10557-011-6312-xAuthors
		Prem Prakash, Pharmacology Division, CSIR-Central Drug Research Institute, 1. M.G. Marg, Lucknow, UP 226001, IndiaVivek Khanna, Pharmacology Division, CSIR-Central Drug Research Institute, 1. M.G. Marg, Lucknow, UP 226001, IndiaVishal Singh, Pharmacology Division, CSIR-Central Drug Research Institute, 1. M.G. Marg, Lucknow, UP 226001, IndiaAnupam Jyoti, Pharmacology Division, CSIR-Central Drug Research Institute, 1. M.G. Marg, Lucknow, UP 226001, IndiaManish Jain, Pharmacology Division, CSIR-Central Drug Research Insti...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946486</comments>
            <pubDate>Tue, 14 Jun 2011 05:50:37 +0100</pubDate>
            <guid isPermaLink="false">4946486</guid>        </item>
        <item>
            <title>Inhibition of Phosphodiesterases Leads to Prevention of the Mitochondrial Permeability Transition Pore Opening and Reperfusion Injury in Cardiac H9c2 Cells</title>
            <link>http://www.medworm.com/index.php?rid=4913452&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft75014n265n306k6%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Inhibition of PDEs prevents the mPTP opening by inactivating GSK-3β through PKA and PKG. GSK-3β is a common downstream target
 of PKA and PKG. Inhibition of PDEs may be a useful approach to prevent reperfusion injury.
 
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s10557-011-6310-zAuthors
		Guillaume Chanoit, Department of Anesthesiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USAJuan Zhou, Department of Anesthesiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USASungRyul Lee, Department of Anesthesiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USARachel McIntosh, Department of Anesthesiology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913452</comments>
            <pubDate>Sat, 04 Jun 2011 06:01:55 +0100</pubDate>
            <guid isPermaLink="false">4913452</guid>        </item>
        <item>
            <title>Mesenchymal Stem Cells for Cardiovascular Regeneration</title>
            <link>http://www.medworm.com/index.php?rid=4903986&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg312p007w6874204%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite recent studies suggesting that the heart has instrinsic mechanisms of self-regeneration following myocardial infarction,
 it cannot regenerate itself to an optimal level. Mesenchymal stem cells (MSCs) are currently being investigated for regeneration
 of mesenchyme-derived tissues, such as bone, cartilage and tendon. In vitro evidence suggests that MSCs can also differentiate
 into cardiomyogenic and vasculogenic lineages, offering another cell source for cardiovascular regeneration. In vivo, MSCs
 may contribute to the re-growth and protection of vasculature and cardiomyocytes, mediated by paracrine actions, and/or persist
 within the myocardium in a differentiated state; although proof of cardiomyocytic phenotype and functional integration remains
 elusive. He...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903986</comments>
            <pubDate>Fri, 03 Jun 2011 05:57:22 +0100</pubDate>
            <guid isPermaLink="false">4903986</guid>        </item>
        <item>
            <title>Design and Rationale of Japanese Evaluation Between Formula of Azelnidipine and Amlodipine Add on Olmesartan to Get Antialbuminuric Effect Study (J-FLAG)</title>
            <link>http://www.medworm.com/index.php?rid=4903987&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp52x477271828n21%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The present trial is expected to clarify whether the sympatholytic CCB azelnidipine is a beneficial second-line choice for
 RAS inhibitor-treated hypertensive patients with CKD, such as diabetic nephropathy.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10557-011-6309-5Authors
		Katsuyuki Ando, Department of Nephrology and Endocrinology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 JapanMasakazu Haneda, Division of Metabolism and Biosystemic Science, Department of Medicine, Asahikawa Medical University, 1-1, 2-1 Midorigaokahigashi, Asahikawa, Hokkaido 078-8510, JapanSadayoshi Ito, Division of Nephrology, Endocrinology, and Vascular Medicine, Department of Internal Medicine, Tohoku University Graduate School of Medicin...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903987</comments>
            <pubDate>Fri, 03 Jun 2011 05:57:21 +0100</pubDate>
            <guid isPermaLink="false">4903987</guid>        </item>
        <item>
            <title>Granulocyte Colony Stimulating Factor in the Treatment of Cardiac Ischemic Disease. A Decade has Passed: Is it Time to Give Up?</title>
            <link>http://www.medworm.com/index.php?rid=4903988&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff24qv173016l6g45%2F</link>
            <description>Content Type Journal ArticlePages 1-5DOI 10.1007/s10557-011-6308-6Authors
		Ruy Andrade N. Louzada, Departamento de Biociências e Atividade Física, CCS, Escola de Educação Física e Desportos, Ilha do Fundão, Universidade Federal do Rio de Janeiro (UFRJ), Carlos Chagas Filho av, 540, 21941–599 Rio de Janeiro, RJ, BrazilJoão Pedro Saar Werneck-de-Castro, Departamento de Biociências e Atividade Física, CCS, Escola de Educação Física e Desportos, Ilha do Fundão, Universidade Federal do Rio de Janeiro (UFRJ), Carlos Chagas Filho av, 540, 21941–599 Rio de Janeiro, RJ, Brazil
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903988</comments>
            <pubDate>Wed, 01 Jun 2011 05:58:37 +0100</pubDate>
            <guid isPermaLink="false">4903988</guid>        </item>
        <item>
            <title>Polymorphisms of the Beta Adrenergic Receptor Predict Left Ventricular Remodeling Following Acute Myocardial Infarction</title>
            <link>http://www.medworm.com/index.php?rid=4903990&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl436726117177412%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;We found that polymorphisms of the β1-AR and β2-AR genes are associated with differential LV remodeling in patients treated
 with a β1 receptor antagonist following STEMI.
 
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s10557-011-6307-7Authors
		Rhondalyn C. McLean, Division of Cardiology, Department of Medicine, The Johns Hopkins Medical Institutions, Baltimore, MD, USAGlenn A. Hirsch, Division of Cardiology, Department of Medicine, The Johns Hopkins Medical Institutions, Baltimore, MD, USALewis C. Becker, Division of Cardiology, Department of Medicine, The Johns Hopkins Medical Institutions, Baltimore, MD, USALaura Kasch-Semenza, The Johns Hopkins School of Medicine, The McKusick-Nathans Institute of Genetic Medicine, Baltimore, MD, USAGary Gerstenblit...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903990</comments>
            <pubDate>Mon, 30 May 2011 16:49:44 +0100</pubDate>
            <guid isPermaLink="false">4903990</guid>        </item>
        <item>
            <title>Effects of Omega-3 Fatty Acid for Sudden Cardiac Death Prevention in Patients with Cardiovascular Disease: A Contemporary Meta-Analysis of Randomized, Controlled Trials</title>
            <link>http://www.medworm.com/index.php?rid=4903989&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl71j3l87218qg763%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In the era of guidelines-adjusted treatment for CVD secondary prevention, omega-3 fatty acids do not appear to reduce SCD.
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s10557-011-6306-8Authors
		Qi Chen, Institute of Geriatric Cardiology, The General Hospital of the People’s Liberation Army, 28 Fuxing Road, Beijing, CountryLiu-Quan Cheng, Department of Radiology, The General Hospital of the People’s Liberation Army, 28 Fuxing Road, Beijing, CountryTie-Hui Xiao, Institute of Geriatric Cardiology, The General Hospital of the People’s Liberation Army, 28 Fuxing Road, Beijing, CountryYu-Xiao Zhang, Institute of Geriatric Cardiology, The General Hospital of the People’s Liberation Army, 28 Fuxing Road, Beijing, CountryMei Zhu, Institute of Geriatric Car...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903989</comments>
            <pubDate>Mon, 30 May 2011 16:49:44 +0100</pubDate>
            <guid isPermaLink="false">4903989</guid>        </item>
        <item>
            <title>Protection of Endothelial Cells, Inhibition of Neointimal Hyperplasia by β-elemene in an Injured Artery</title>
            <link>http://www.medworm.com/index.php?rid=4903991&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc77501u4j3h64223%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Our results indicate that β-elemene is effective in protecting the endothelial cells from injury induced by hydrogen peroxide
 in vitro, inhibiting smooth muscle cell proliferation/migration and inhibiting neointima formation in vivo after vascular
 injury.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6305-9Authors
		Lingyan Wu, Key Laboratory of Biorheological Science and Technology (Chongqing University), Ministry of Education, Chongqing Engineering Lab. in Vascular Implants, Bioengineering College of Chongqing University, Chongqing, 400044 ChinaGuixue Wang, Key Laboratory of Biorheological Science and Technology (Chongqing University), Ministry of Education, Chongqing Engineering Lab. in Vascular Implants, Bioengineering College of Chongq...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903991</comments>
            <pubDate>Mon, 23 May 2011 17:04:02 +0100</pubDate>
            <guid isPermaLink="false">4903991</guid>        </item>
        <item>
            <title>Reduced Thrombin Generation and Soluble P-selectin After Intravenous Enoxaparin During PCI</title>
            <link>http://www.medworm.com/index.php?rid=4842755&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F043v352m672840j4%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Intravenous enoxaparin induced target F Xa inhibition (&amp;gt;0.6&amp;nbsp;IU/ml) for 60&amp;nbsp;min in 82% of study patients. During the 6&amp;nbsp;h of
 monitoring, a decrease of thrombin generation (F1 + 2) and sP-selectin levels were observed.
 
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s10557-011-6301-0Authors
		J. Kvasnička, Center for Thrombosis Research, General Teaching Hospital, Charles University, Karlovo n. 32, Prague, 121 11 Czech RepublicJ. Horák, 2nd Department of Internal Medicine, General Teaching Hospital, Charles University, U nemocnice 2, Prague, Czech RepublicZ. Zenáhlíková, Center for Thrombosis Research, General Teaching Hospital, Charles University, Karlovo n. 32, Prague, 121 11 Czech RepublicTomáš Kvasnička, Center for Thrombosis R...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4842755</comments>
            <pubDate>Mon, 16 May 2011 08:42:09 +0100</pubDate>
            <guid isPermaLink="false">4842755</guid>        </item>
        <item>
            <title>Heart Protection by Combination Therapy with Esmolol and Milrinone at Late-Ischemia and Early Reperfusion</title>
            <link>http://www.medworm.com/index.php?rid=4821802&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc7338g2673556wq0%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Late-ischemia/early reperfusion therapy with esmolol + milrinone additively reduces LV-IS associated with robust activation
 of myocardial PKA and subsequent Akt-antiapoptotic pathway.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6302-zAuthors
		Ming-He Huang, Department of Internal Medicine, Cardiology Division (M-HH, YW, VN, SR, BFU, KF), University of Texas Medical Branch, Galveston, TX, USAYewen Wu, Department of Internal Medicine, Cardiology Division (M-HH, YW, VN, SR, BFU, KF), University of Texas Medical Branch, Galveston, TX, USAVincent Nguyen, Department of Internal Medicine, Cardiology Division (M-HH, YW, VN, SR, BFU, KF), University of Texas Medical Branch, Galveston, TX, USASaurabh Rastogi, Department of Internal Medicine, Car...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4821802</comments>
            <pubDate>Wed, 11 May 2011 15:46:40 +0100</pubDate>
            <guid isPermaLink="false">4821802</guid>        </item>
        <item>
            <title>Reduction of Myocardial Infarct Size by Dronedarone in Pigs—A Pleiotropic Action?</title>
            <link>http://www.medworm.com/index.php?rid=4805752&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx781gx8v25631832%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The beneficial effect of dronedarone is attributed to cardioprotective properties, possibly through attenuation of calcium
 overload during myocardial ischemia/reperfusion.
 
 
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s10557-011-6300-1Authors
		Andreas Skyschally, Institut für Pathophysiologie, Universitätsklinikum Essen, Hufelandstr. 55, 45122 Essen, GermanyGerd Heusch, Institut für Pathophysiologie, Universitätsklinikum Essen, Hufelandstr. 55, 45122 Essen, Germany
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4805752</comments>
            <pubDate>Wed, 04 May 2011 14:51:29 +0100</pubDate>
            <guid isPermaLink="false">4805752</guid>        </item>
        <item>
            <title>Tolvaptan for Heart Failure Patients with Volume Overload</title>
            <link>http://www.medworm.com/index.php?rid=4782299&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy75167754706x42n%2F</link>
            <description>Content Type Journal ArticlePages 1-4DOI 10.1007/s10557-011-6298-4Authors
		Masatsugu Hori, Osaka Medical Center for Cancer and Cardiovascular Diseases, 1-3-3 Nakamichi, Higashinari-ku, Osaka, 537-8511 Japan
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4782299</comments>
            <pubDate>Mon, 02 May 2011 14:59:29 +0100</pubDate>
            <guid isPermaLink="false">4782299</guid>        </item>
        <item>
            <title>MicroRNA Involvement in Immune Activation During Heart Failure</title>
            <link>http://www.medworm.com/index.php?rid=4745113&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6vu885m8t59r1135%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Heart failure is one of the common end stages of cardiovascular diseases, the leading cause of death in developed countries.
 Molecular mechanisms underlying the development of heart failure remain elusive but there is a consistent observation of chronic
 immune activation and aberrant microRNA (miRNA) expression that is present in failing hearts. This review will focus on the
 interplay between the immune system and miRNAs as factors that play a role during the development of heart failure. Several
 studies have shown that heart failure patients can be characterized by a sustained innate immune activation. The role of inflammatory
 signaling is discussed and TLR4 signaling, IL-1β, TNFα and IL-6 expression appears to coincide with the development of heart
 failure. Fu...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4745113</comments>
            <pubDate>Tue, 19 Apr 2011 07:13:14 +0100</pubDate>
            <guid isPermaLink="false">4745113</guid>        </item>
        <item>
            <title>Disassociation Between Left Ventricular Mechanical and Electrical Properties in Ischemic Rat Heart After G-CSF Treatment</title>
            <link>http://www.medworm.com/index.php?rid=4745115&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd488177586221v8v%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Both early and delayed administrations of G-CSF can improve electrophysiological properties after myocardial ischemia, but
 have no beneficial effects on LV mechanical remodeling.
 
 
 
 
	Content Type Journal ArticlePages 1-12DOI 10.1007/s10557-011-6294-8Authors
		Hong-Mei Liu, Institute of Cardiovascular Diseases, Pingjin Hospital, Medical College of Chinese People’s Armed Police Forces, 220 Cheng-Lin Road, Tianjin, 300162 ChinaTao Luo, Institute of Cardiovascular Diseases, Pingjin Hospital, Medical College of Chinese People’s Armed Police Forces, 220 Cheng-Lin Road, Tianjin, 300162 ChinaXin Zhou, Institute of Cardiovascular Diseases, Pingjin Hospital, Medical College of Chinese People’s Armed Police Forces, 220 Cheng-Lin Road, Tianjin, 300162 ChinaLin Cai, I...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4745115</comments>
            <pubDate>Tue, 19 Apr 2011 07:13:12 +0100</pubDate>
            <guid isPermaLink="false">4745115</guid>        </item>
        <item>
            <title>Pharmacotherapy Crisis in the Spotlight—Is Open Collaboration Between Academia and Industry the Answer?</title>
            <link>http://www.medworm.com/index.php?rid=4745114&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm15606158852tr09%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s10557-011-6297-5Authors
		Juan-Carlos Kaski, Cardiovascular Sciences Research Centre, St. George’s, University of London, London, UK
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4745114</comments>
            <pubDate>Tue, 19 Apr 2011 07:13:12 +0100</pubDate>
            <guid isPermaLink="false">4745114</guid>        </item>
        <item>
            <title>Cardiovascular Drugs and Therapy Celebrates its 25th Year of Publication with a New Section: Education in Cardiovascular Therapy</title>
            <link>http://www.medworm.com/index.php?rid=4725493&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmh863114v771204j%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s10557-011-6296-6Authors
		Willem J. Remme, Sticares Cardiovascular Research Institute, Oever 1-5, 3161GR, Rhoon, The Netherlands
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4725493</comments>
            <pubDate>Thu, 14 Apr 2011 16:59:40 +0100</pubDate>
            <guid isPermaLink="false">4725493</guid>        </item>
        <item>
            <title>Istaroxime: Is the Remedy Better than the Disease?</title>
            <link>http://www.medworm.com/index.php?rid=4710141&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj716250rt4328433%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s10557-011-6295-7Authors
		Dimitrios Farmakis, Athens University Medical School, Second Department of Cardiology, Attikon University Hospital, 28 Doukissis Plakentias St, 11523 Athens, GreeceGerasimos Filippatos, Athens University Medical School, Second Department of Cardiology, Attikon University Hospital, 28 Doukissis Plakentias St, 11523 Athens, Greece
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4710141</comments>
            <pubDate>Mon, 11 Apr 2011 15:50:17 +0100</pubDate>
            <guid isPermaLink="false">4710141</guid>        </item>
        <item>
            <title>Use of Prolonged Bivalirudin Infusions Following Percutaneous Coronary Intervention</title>
            <link>http://www.medworm.com/index.php?rid=4710142&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe618h745u24t7p75%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The strategy of prolonging the bivalirudin infusion at a reduced infusion rate for 4&amp;nbsp;h after completion of the PCI procedure
 was explored and offers promising results.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6293-9Authors
		Lynette R. Moser, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Suite 2190, Detroit, MI 48201, USACarrie W. Nemerovski, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Suite 2190, Detroit, MI 48201, USAKelley L. Good, Baxter Healthcare, McGraw Park, IL, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4710142</comments>
            <pubDate>Fri, 08 Apr 2011 17:00:24 +0100</pubDate>
            <guid isPermaLink="false">4710142</guid>        </item>
        <item>
            <title>An Introduction to Small Non-coding RNAs: miRNA and snoRNA</title>
            <link>http://www.medworm.com/index.php?rid=4686150&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk5806851905m6347%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Research into small non-coding RNAs (ncRNA) has fundamentally transformed our understanding of gene regulatory networks, especially
 at the post-transcriptional level. Although much is now known about the basic biology of small ncRNAs, our ability to recognize
 the impact of small ncRNA in disease states is preliminary, and the ability to effectively target them in vivo is very limited. However, given the larger and growing focus on targeting RNAs for disease therapeutics, what we do know
 about the intrinsic biology of these small RNAs makes them potentially attractive targets for pharmacologic manipulation.
 With that in mind, this review provides an introduction to the biology of small ncRNA, using microRNA (miRNA) and small nucleolar
 RNA (snoRNA) as examples.
 
 
	...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4686150</comments>
            <pubDate>Tue, 05 Apr 2011 16:56:43 +0100</pubDate>
            <guid isPermaLink="false">4686150</guid>        </item>
        <item>
            <title>The Emerging Role of Small Non-coding RNAs in the Failing Heart: Big Hopes for Small Molecules</title>
            <link>http://www.medworm.com/index.php?rid=4686151&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj2m3p62j6765h802%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;&amp;nbsp;
 
	Content Type Journal ArticlePages 1-1DOI 10.1007/s10557-011-6292-xAuthors
		Douglas L. Mann, Washington University School of Medicine, St. Louis, MO, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4686151</comments>
            <pubDate>Tue, 05 Apr 2011 16:56:41 +0100</pubDate>
            <guid isPermaLink="false">4686151</guid>        </item>
        <item>
            <title>List of Reviewers 2010</title>
            <link>http://www.medworm.com/index.php?rid=4664865&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F77u10513p50235q0%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s10557-011-6286-8

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4664865</comments>
            <pubDate>Tue, 29 Mar 2011 06:04:58 +0100</pubDate>
            <guid isPermaLink="false">4664865</guid>        </item>
        <item>
            <title>Age Related Issues in Reperfusion of Myocardial Infarction</title>
            <link>http://www.medworm.com/index.php?rid=4644105&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7624307982895085%2F</link>
            <description>This article reviews current
 evidence regarding management of AMI in the elderly.
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s10557-011-6288-6Authors
		Amelia Carro, Cardiovascular Sciences Research Centre, Division of Clinical Sciences, St George’s University of London, Cranmer Terrace, London, SW17 0RE UKRachel Bastiaenen, Cardiovascular Sciences Research Centre, Division of Clinical Sciences, St George’s University of London, Cranmer Terrace, London, SW17 0RE UKJuan Carlos Kaski, Cardiovascular Sciences Research Centre, Division of Clinical Sciences, St George’s University of London, Cranmer Terrace, London, SW17 0RE UK
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4644105</comments>
            <pubDate>Fri, 25 Mar 2011 05:48:33 +0100</pubDate>
            <guid isPermaLink="false">4644105</guid>        </item>
        <item>
            <title>Role of MicroRNAs in Cardiac Remodeling and Heart Failure</title>
            <link>http://www.medworm.com/index.php?rid=4637006&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F089435t3m3250845%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;MicroRNAs (miRNAs) are endogenous, short (~22 nucleotide), evolutionarily conserved, non-coding RNAs that regulate gene expression
 at the post-transcriptional level. Recent evidence suggests that miRNAs are differentially expressed in the failing myocardium
 and play an important role in progression of heart failure by targeting genes that govern diverse functions in cardiac remodeling
 process including myocyte hypertrophy, excitation-contraction coupling, increased myocyte loss, and myocardial fibrosis. In
 addition to their role in adverse cardiac remodeling, miRNAs hold promise as biomarkers of disease progression in heart failure
 given their presence in circulation and enhanced stability. Further development of miR-based therapeutics may allow for modulation
 of ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4637006</comments>
            <pubDate>Tue, 22 Mar 2011 18:09:24 +0100</pubDate>
            <guid isPermaLink="false">4637006</guid>        </item>
        <item>
            <title>Differential Effects of Vitamin D Receptor Agonists on Gene Expression in Neonatal Rat Cardiomyocytes</title>
            <link>http://www.medworm.com/index.php?rid=4632272&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl3175k147t17753n%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;VDR hormone calcitriol and its analog paricalcitol exhibit more potent effects than the prehormone calcidiol in cardiomyocytes.
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s10557-011-6287-7Authors
		J. Ruth Wu-Wong, University of Illinois at Chicago, 2201 W. Campbell Park Dr., Suite 13, Chicago, IL 60612, USAYung-Wu Chen, VidaGene, Chicago, IL USAMasaki Nakane, VidaGene, Chicago, IL USAMyles Wolf, University of Miami Miller School of Medicine, Miami, FL USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4632272</comments>
            <pubDate>Mon, 21 Mar 2011 19:11:10 +0100</pubDate>
            <guid isPermaLink="false">4632272</guid>        </item>
        <item>
            <title>Long-Term Efficacy of Adding Fenofibric Acid to Moderate-Dose Statin Therapy in Patients with Persistent Elevated Triglycerides</title>
            <link>http://www.medworm.com/index.php?rid=4616501&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6132241928581617%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The addition of fenofibric acid to moderate-dose statin in patients whose LDL-C was optimal but whose triglycerides remained
 &amp;gt;200&amp;nbsp;mg/dL led to additional improvements in non–HDL-C, ApoB, HDL-C, and triglycerides that resulted in greater proportions
 of patients attaining optimal levels of the individual parameters as well as simultaneously achieving optimal levels of these
 parameters and LDL-C.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s10557-011-6280-1Authors
		Christie M. Ballantyne, Baylor College of Medicine and Methodist DeBakey Heart and Vascular Center, 6565 Fannin St., Room A601, Houston, TX 77030, USAPeter H. Jones, Baylor College of Medicine and Methodist DeBakey Heart and Vascular Center, 6565 Fannin St., Room A601, Houston, TX ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4616501</comments>
            <pubDate>Thu, 17 Mar 2011 18:32:43 +0100</pubDate>
            <guid isPermaLink="false">4616501</guid>        </item>
        <item>
            <title>In Memoriam Elliot Rapaport</title>
            <link>http://www.medworm.com/index.php?rid=4541356&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6620w4251r871316%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s10557-011-6282-zAuthors
		Lionel H. Opie, University of Cape Town Medical School, Cape Town, South Africa
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4541356</comments>
            <pubDate>Wed, 23 Feb 2011 23:14:39 +0100</pubDate>
            <guid isPermaLink="false">4541356</guid>        </item>
        <item>
            <title>Clinical Trials Update AHA Congress 2010</title>
            <link>http://www.medworm.com/index.php?rid=4513357&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F88838m62013l3070%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The clinical trials described in this article were presented at the Late Breaking Trials and the Clinical Science: Clinical
 Reports sessions of the American Heart Association Congress held in November 2010 in Chicago. The sessions and topics chosen
 for this article reflect the scope of interest of Cardiovascular Drugs and Therapy. The presentations should be considered
 preliminary, as further analyses may be done, which could alter the final publication of the results of these studies. PROTECT
 (ProBNP Outpatient Tailored Chronic Heart Failure Therapy) was designed to test the hypothesis that adjustment of intensity
 of chronic heart failure (HF) therapy on the basis of NT-proBNP plasma level monitoring would improve outcomes. The results
 provided some support of th...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4513357</comments>
            <pubDate>Mon, 21 Feb 2011 17:08:19 +0100</pubDate>
            <guid isPermaLink="false">4513357</guid>        </item>
        <item>
            <title>Exploiting a Physiological Regulator to Improve the Efficacy and Safety of Statins</title>
            <link>http://www.medworm.com/index.php?rid=4495955&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl645l6431462m908%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s10557-011-6281-0Authors
		Saloni Gill, BABS, School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Biological Sciences Building, D26, Sydney, NSW 2052, AustraliaAndrew J. Brown, BABS, School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Biological Sciences Building, D26, Sydney, NSW 2052, Australia
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4495955</comments>
            <pubDate>Wed, 16 Feb 2011 07:02:30 +0100</pubDate>
            <guid isPermaLink="false">4495955</guid>        </item>
        <item>
            <title>Chronic Istaroxime Improves Cardiac Function and Heart Rate Variability in Cardiomyopathic Hamsters</title>
            <link>http://www.medworm.com/index.php?rid=4442703&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn52181k28n431317%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Chronic istaroxime improves cardiac function and heart rate variability in Bio TO.2 Syrian hamster model of progressive heart
 failure.
 
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s10557-011-6283-yAuthors
		Pietro Lo Giudice, Research and Development, Pharmacology Department, Sigma-Tau Industrie Farmaceutiche Riunite S.p.A., Via Pontina km 30.400, 00040 Pomezia, Rome ItalyGiovan Giuseppe Mattera, Research and Development, Pharmacology Department, Sigma-Tau Industrie Farmaceutiche Riunite S.p.A., Via Pontina km 30.400, 00040 Pomezia, Rome ItalyJean-Pierre Gagnol, University of Montpellier 1 and CNRS UMR5232, Montpellier, FranceFranco Borsini, Research and Development, Pharmacology Department, Sigma-Tau Industrie Farmaceutiche Riunite S.p.A., Via Pontina ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4442703</comments>
            <pubDate>Thu, 03 Feb 2011 21:03:57 +0100</pubDate>
            <guid isPermaLink="false">4442703</guid>        </item>
        <item>
            <title>Evaluation of the Functional Status Questionnaire in Heart Failure: A Sub-study of the Second Cardiac Insufficiency Bisoprolol Survival Study (CIBIS-II)</title>
            <link>http://www.medworm.com/index.php?rid=4442704&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd730172819132557%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The FSQ performed well in this study, provided additional information to the MLwHF questionnaire and allowed interesting comparisons
 with other chronic medical conditions. The FSQ may be a useful general QoL instrument for studies in CHF.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s10557-011-6284-xAuthors
		Siobhan Gallanagh, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, Scotland UKDavide Castagno, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, Scotland UKBen Wilson, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, Scotland UKErland Erdmann, Department III of Internal Medicine, University of Cologne, Cologne, GermanyFaiez Zannad, University of Nancy, Nancy, FranceWil...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4442704</comments>
            <pubDate>Thu, 03 Feb 2011 21:03:53 +0100</pubDate>
            <guid isPermaLink="false">4442704</guid>        </item>
        <item>
            <title>AMP-Activated Protein Kinase Inhibits Homocysteine-Induced Dysfunction and Apoptosis in Endothelial Progenitor Cells</title>
            <link>http://www.medworm.com/index.php?rid=4400800&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2512nu7t2721512q%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;AMPK activation inhibits eNOS down-regulation and Nox4-derived ROS accumulation induced by Hcy in EPCs, and may contribute
 to the protective effects of atorvastatin on endothelial function.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s10557-010-6277-1Authors
		Fang Jia, Department of Cardiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, 197 Ruijin Road II, Shanghai, 200025 People’s Republic of ChinaChunfang Wu, Department of Cardiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, 197 Ruijin Road II, Shanghai, 200025 People’s Republic of ChinaZhenyue Chen, Department of Cardiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, 197 Ruijin Road II, Shanghai, 200025 People’s Republic of...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4400800</comments>
            <pubDate>Fri, 21 Jan 2011 20:24:23 +0100</pubDate>
            <guid isPermaLink="false">4400800</guid>        </item>
        <item>
            <title>The Role of β-adrenergic Receptors in the Cardioprotective Effects of Beta-Preconditioning (βPC)</title>
            <link>http://www.medworm.com/index.php?rid=4344154&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj685538x54480w34%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Protection afforded by β-ARs stimulation, depends on activation of both β1-AR and β2-ARs but not β3-AR. With functional recovery
 as endpoint, results suggest involvement of NO in β1/β2-AR preconditioning and the Gi protein in β2-AR preconditioning. Both
 PKA and PI3-K activation were essential for β1/β2-AR cardioprotection.
 
 
 
 
	Content Type Journal ArticlePages 1-16DOI 10.1007/s10557-010-6275-3Authors
		Ruduwaan Salie, Division Medical Physiology, Department of Biomedical Sciences, Faculty of Health Sciences, University of Stellenbosch, Tygerberg, 7505 Republic of South AfricaJohannes A. Moolman, Division Medical Physiology, Department of Biomedical Sciences, Faculty of Health Sciences, University of Stellenbosch, Tygerberg, 7505 Republic of South Afric...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4344154</comments>
            <pubDate>Tue, 11 Jan 2011 18:03:06 +0100</pubDate>
            <guid isPermaLink="false">4344154</guid>        </item>
        <item>
            <title>Rationale for Combining a Direct Renin Inhibitor with other Renin- Angiotensin System Blockers. Focus on Aliskiren and Combinations</title>
            <link>http://www.medworm.com/index.php?rid=4325082&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv132685u8g848190%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Inhibition of the renin-angiotensin system has been a highly successful therapeutic approach for the prevention of hypertension-related
 end organ damage. Angiotensin converting enzyme inhibitors and angiotensin II receptor blockers lower blood pressure and reduce
 morbidity and mortality in patients with cardiovascular and kidney disease. However, progression to end-stage disease remains
 common in these patient populations. A compensatory increase in plasma renin activity occurs with the use of either angiotensin
 converting enzyme inhibitors or angiotensin II receptor blockers, thus causing increased levels of angiotensin II, which may
 limit the therapeutic effectiveness of these agents. The direct renin inhibitor, aliskiren, suppresses the renin-angiotensin
 system...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4325082</comments>
            <pubDate>Thu, 06 Jan 2011 17:55:05 +0100</pubDate>
            <guid isPermaLink="false">4325082</guid>        </item>
        <item>
            <title>Phosphatidylcholine-Rich Nanoliposomes: Potential Tools for Serum C-Reactive Protein Reduction?</title>
            <link>http://www.medworm.com/index.php?rid=4322938&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F578w042l874g1332%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s10557-010-6279-zAuthors
		Amirhossein Sahebkar, Cardiovascular Research Center, Avicenna Research Institute, Mashhad University of Medical Sciences (MUMS), P. O. Box: 91775-1365, Mashhad, Iran
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4322938</comments>
            <pubDate>Wed, 05 Jan 2011 16:50:42 +0100</pubDate>
            <guid isPermaLink="false">4322938</guid>        </item>
        <item>
            <title>President’s Page</title>
            <link>http://www.medworm.com/index.php?rid=4319236&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk0u45005k2010722%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6276-2Authors
		Juan-Carlos Kaski, St. George’s, University of London, London, UK
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4319236</comments>
            <pubDate>Tue, 04 Jan 2011 17:53:22 +0100</pubDate>
            <guid isPermaLink="false">4319236</guid>        </item>
        <item>
            <title>Achievement of Lipid Targets with the Combination of Rosuvastatin and Fenofibric Acid in Patients with Type 2 Diabetes Mellitus</title>
            <link>http://www.medworm.com/index.php?rid=4285718&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F83qq351873703j30%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;A significantly greater proportion of T2DM patients achieved individual and combined lipid targets when treated with the combination
 of R + FA than corresponding-dose R monotherapies.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6273-5Authors
		Robert S. Rosenson, Mount Sinai Heart, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, NY 10029-6574, USADawn M. Carlson, Abbott, Abbott Park, IL USAMaureen T. Kelly, Abbott, Abbott Park, IL USACarolyn M. Setze, Abbott, Abbott Park, IL USABoaz Hirshberg, AstraZeneca LP, Wilmington, DE USAJames C. Stolzenbach, Abbott, Abbott Park, IL USALaura A. Williams, Abbott, Abbott Park, IL USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascul...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4285718</comments>
            <pubDate>Mon, 20 Dec 2010 22:17:23 +0100</pubDate>
            <guid isPermaLink="false">4285718</guid>        </item>
        <item>
            <title>Blockade of the Renin-Angiotensin System Ameliorates Apelin Production in 3T3-L1 Adipocytes</title>
            <link>http://www.medworm.com/index.php?rid=4267299&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb3321t416267587p%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Our study suggests that RAS blockers achieve their beneficial effects by their enhancement of adipocyte secretion of apelin.
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6274-4Authors
		Wei-Wen Hung, Division of Endocrinology and Metabolism, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, TaiwanTusty-Jiuan Hsieh, Department of Medical Genetics, College of Medicine, Kaohsiung Medical University, Kaohsiung, TaiwanTzu Lin, Department of Medical Genetics, College of Medicine, Kaohsiung Medical University, Kaohsiung, TaiwanPong-Chun Chou, Division of Endocrinology and Metabolism, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, TaiwanPi-Jung Hsiao, Division of Endocrinology and Metabolism, D...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4267299</comments>
            <pubDate>Wed, 15 Dec 2010 15:55:36 +0100</pubDate>
            <guid isPermaLink="false">4267299</guid>        </item>
        <item>
            <title>Statins in Heart Failure—Where Do We Stand?</title>
            <link>http://www.medworm.com/index.php?rid=4242516&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl03723886p401575%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;HMG Co-A reductase inhibitors (statins) are a group of drugs which lower cholesterol by inhibiting the conversion of HMG Co-A
 to mevalonate early in the cholesterol synthetic pathway. They are used in the primary and secondary prevention of cardiovascular
 events in patients deemed to be at increased risk and their benefit in patients with ischaemic heart disease is well supported.
 Their use in patients with heart failure (HF) however, is controversial. Evidence from observational and mechanistic studies
 suggests that statins should benefit patients with HF. However, larger randomised controlled trials have failed to demonstrate
 these expected benefits. The aim of this review article is to summarise the data from trials of statin use in patients with
 HF and attempt...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4242516</comments>
            <pubDate>Mon, 06 Dec 2010 18:46:51 +0100</pubDate>
            <guid isPermaLink="false">4242516</guid>        </item>
        <item>
            <title>President’s Page</title>
            <link>http://www.medworm.com/index.php?rid=4191544&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa59167mt68375uw3%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6272-6Authors
		Jay N. Cohn, University of Minnesota, Minneapolis, MN USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4191544</comments>
            <pubDate>Fri, 19 Nov 2010 17:03:03 +0100</pubDate>
            <guid isPermaLink="false">4191544</guid>        </item>
        <item>
            <title>Pre-treatment with a DPP-4 Inhibitor is Infarct Sparing in Hearts from Obese, Pre-diabetic Rats</title>
            <link>http://www.medworm.com/index.php?rid=4187368&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnwv252r05257118w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cardiovascular risk is closely associated with insulin resistance and type 2 diabetes. Therapy based on the actions of GLP-1
 is currently seen as a novel approach to treat this disease. The aims of this study was therefore to use an animal model to
 determine whether (i) pre-treatment of obese, insulin resistant but pre-diabetic rats with a DPP4 inhibitor, PFK275-055, could
 protect the heart from ischaemia/reperfusion injury and (ii) the possible mechanisms involved in such protection. Obese, pre-diabetic
 rats (DIO) were treated for 4&amp;nbsp;weeks with 10&amp;nbsp;mg/kg/day of the DPP4 inhibitor PFK275-055. Ex vivo perfusion was used to subject
 hearts to ischaemia/reperfusion to determine infarct size, functional recovery and post-ischaemic activation of proteins associat...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4187368</comments>
            <pubDate>Thu, 18 Nov 2010 17:54:43 +0100</pubDate>
            <guid isPermaLink="false">4187368</guid>        </item>
        <item>
            <title>Erythropoietin (EPO) Affords More Potent Cardioprotection by Activation of Distinct Signaling to Mitochondrial Kinases Compared with Carbamylated EPO</title>
            <link>http://www.medworm.com/index.php?rid=4089512&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd223v020742682u0%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;EPO affords more potent protection against infarction than does CEPO by distinct activation of signaling leading to phosphorylation
 of pro-survival protein kinases in mitochondria upon reperfusion.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6265-5Authors
		Takahiro Sato, Division of Cardiology, Second Department of Internal Medicine, Sapporo Medical University School of Medicine, South-1 West-16, Chuo-ku, Sapporo, 060-8543 JapanMasaya Tanno, Division of Cardiology, Second Department of Internal Medicine, Sapporo Medical University School of Medicine, South-1 West-16, Chuo-ku, Sapporo, 060-8543 JapanTakayuki Miki, Division of Cardiology, Second Department of Internal Medicine, Sapporo Medical University School of Medicine, South-1 West-16, Chuo-ku, Sa...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4089512</comments>
            <pubDate>Sat, 16 Oct 2010 09:03:25 +0100</pubDate>
            <guid isPermaLink="false">4089512</guid>        </item>
        <item>
            <title>Efficacy and Safety of Rosuvastatin 5 mg in Combination with Fenofibric Acid 135 mg in Patients with Mixed Dyslipidemia – A Phase 3 Study</title>
            <link>http://www.medworm.com/index.php?rid=4089513&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv76197513880687l%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;In conclusion, rosuvastatin 5&amp;nbsp;mg + fenofibric acid 135&amp;nbsp;mg resulted in comprehensive improvements in the lipid profile of patients
 with mixed dyslipidemia without unanticipated adverse events.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6266-4Authors
		Eli M. Roth, Sterling Research Group, 2230 Auburn Avenue, Cincinnati, OH 45219, USARobert S. Rosenson, Mount Sinai School of Medicine, New York, NY USADawn M. Carlson, Abbott, Abbott Park, IL USASandra M. Fukumoto, Abbott, Abbott Park, IL USACarolyn M. Setze, Abbott, Abbott Park, IL USAJames W. Blasetto, AstraZeneca LP, Wilmington, DE USANardev S. Khurmi, AstraZeneca LP, Wilmington, DE USAJames C. Stolzenbach, Abbott, Abbott Park, IL USALaura A. Williams, Abbott, Abbott Park, IL USA
	

	
		Jour...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4089513</comments>
            <pubDate>Sat, 16 Oct 2010 09:03:24 +0100</pubDate>
            <guid isPermaLink="false">4089513</guid>        </item>
        <item>
            <title>Resveratrol Confers Endothelial Protection in Insulin-Dependent Diabetes Mellitus</title>
            <link>http://www.medworm.com/index.php?rid=4068269&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frn54643329177rn7%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6267-3Authors
		Zoltan Ungvari, Reynolds Oklahoma Center on Aging, Donald W. Reynolds Department of Geriatric Medicine, University of Oklahoma Health Sciences Center, 975 N. E. 10th Street - BRC 1303, Oklahoma City, OK 73104, USAAnna Csiszar, Reynolds Oklahoma Center on Aging, Donald W. Reynolds Department of Geriatric Medicine, University of Oklahoma Health Sciences Center, 975 N. E. 10th Street - BRC 1303, Oklahoma City, OK 73104, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4068269</comments>
            <pubDate>Mon, 11 Oct 2010 16:48:44 +0100</pubDate>
            <guid isPermaLink="false">4068269</guid>        </item>
        <item>
            <title>Heterogeneous Postprandial Lipoprotein Responses in the Metabolic Syndrome, and Response to Fenofibrate Therapy</title>
            <link>http://www.medworm.com/index.php?rid=4037524&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F33532112jqm4p334%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Late postprandial triglyceride responders have attenuated clearance of large VLDL particles, but they were more responsive
 to fenofibrate.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6264-6Authors
		Robert S. Rosenson, Mount Sinai Heart, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1070, New York, NY 10017, USAIrene B. Helenowski, Department of Preventive Medicine, Northwestern University, Chicago, IL USAChristine C. Tangney, Department of Clinical Nutrition, Rush University Medical Center, Chicago, IL USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4037524</comments>
            <pubDate>Mon, 04 Oct 2010 14:48:03 +0100</pubDate>
            <guid isPermaLink="false">4037524</guid>        </item>
        <item>
            <title>G-CSF and Erythropoietin Combination Therapy for Infarct Repair: Two Plus Two Equals Two?</title>
            <link>http://www.medworm.com/index.php?rid=4026156&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc82wq1719v51g703%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6268-2Authors
		Carrie M. Quinn, Division of Cardiovascular Diseases and Cardiovascular Research Institute, University of Kansas Medical Center and Hospital, 3901 Rainbow Blvd, Rm. 1001, Eaton Hall, MS 3006, Kansas City, KS 66160, USABuddhadeb Dawn, Division of Cardiovascular Diseases and Cardiovascular Research Institute, University of Kansas Medical Center and Hospital, 3901 Rainbow Blvd, Rm. 1001, Eaton Hall, MS 3006, Kansas City, KS 66160, USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4026156</comments>
            <pubDate>Fri, 01 Oct 2010 06:58:39 +0100</pubDate>
            <guid isPermaLink="false">4026156</guid>        </item>
        <item>
            <title>Effects of Sphingosine-1-Phosphate on Acute Contractile Heart Failure (ACHF)</title>
            <link>http://www.medworm.com/index.php?rid=3978038&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F428013874623vv27%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6258-4Authors
		Gaurang Prabhakar Deshpande, University of Cape Town, Cape Town, South AfricaJoy McCarthy, University of Cape Town, Cape Town, South AfricaHarshawardhan Mardikar, Spandan Heart Institute and Research Center, Nagpur, IndiaSandrine Lecour, University of Cape Town, Cape Town, South AfricaLionel Opie, University of Cape Town, Cape Town, South Africa
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3978038</comments>
            <pubDate>Tue, 14 Sep 2010 06:00:09 +0100</pubDate>
            <guid isPermaLink="false">3978038</guid>        </item>
        <item>
            <title>Cytochrome P450 Pathway Contributes to Methanandamide-induced Vasorelaxation in Rat Aorta</title>
            <link>http://www.medworm.com/index.php?rid=3934062&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7017r237x2u40103%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Methanandamide endothelium-dependent vasorelaxation is mediated by CB1 and CB2 cannabinoid receptors. The NO- and CYP-mediated pathways contribute in a concurrent manner in this vascular effect. Stimulation
 of both cannabinoid receptor subtypes is indistinctly linked to NO or CYP routes to cause vasorelaxation.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6261-9Authors
		Visitación López-Miranda, Dpto. Farmacología y Nutrición, Facultad Ciencias de la Salud, Universidad Rey Juan Carlos, Avda. Atenas s/n, 28922 Alcorcón, Madrid SpainM. Teresa Dannert, Dpto. Farmacología, Facultad de Medicina, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040 Madrid, SpainEsperanza Herradón, Dpto. Farmacología y Nutrición, Facultad Ciencias de la ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3934062</comments>
            <pubDate>Fri, 03 Sep 2010 17:27:23 +0100</pubDate>
            <guid isPermaLink="false">3934062</guid>        </item>
        <item>
            <title>Cytokine Combination Therapy with Erythropoietin and Granulocyte Colony Stimulating Factor in a Porcine Model of Acute Myocardial Infarction</title>
            <link>http://www.medworm.com/index.php?rid=3930075&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn852q4p332186476%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Our findings indicate that EPO+GCSF combination therapy promotes stabilization of cardiac function after acute MI. However,
 combination therapy does not seem to be superior to monotherapy with either EPO or GCSF.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6263-7Authors
		Franca S. Angeli, Division of Cardiology, Department of Medicine, University of California, 505 Parnassus Avenue, L-523, Box 0103, San Francisco, CA 94143-0103, USANicolas Amabile, Division of Cardiology, Department of Medicine, University of California, 505 Parnassus Avenue, L-523, Box 0103, San Francisco, CA 94143-0103, USAMia Shapiro, Division of Cardiology, Department of Medicine, University of California, 505 Parnassus Avenue, L-523, Box 0103, San Francisco, CA 94143-0103, US...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3930075</comments>
            <pubDate>Thu, 02 Sep 2010 06:49:14 +0100</pubDate>
            <guid isPermaLink="false">3930075</guid>        </item>
        <item>
            <title>Efficacy of Simvastatin in Reducing Aortic Dilatation in Mouse Models of Abdominal Aortic Aneurysm</title>
            <link>http://www.medworm.com/index.php?rid=3930077&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm7g3j787j1723705%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In this study involving two mouse models of AAA, simvastatin had limited efficacy in restricting aortic dilatation but substantial
 ability to reduce atheroma progression.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6262-8Authors
		Jonathan Golledge, The Vascular Biology Unit, Department of Surgery, School of Medicine, James Cook University, Townsville, QLD Australia 4811Bradford Cullen, The Vascular Biology Unit, Department of Surgery, School of Medicine, James Cook University, Townsville, QLD Australia 4811Corey Moran, The Vascular Biology Unit, Department of Surgery, School of Medicine, James Cook University, Townsville, QLD Australia 4811Catherine Rush, The Vascular Biology Unit, Department of Surgery, School of Medicine, James Cook University, To...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3930077</comments>
            <pubDate>Thu, 02 Sep 2010 06:49:12 +0100</pubDate>
            <guid isPermaLink="false">3930077</guid>        </item>
        <item>
            <title>Cardiovascular Pharmacotherapy 2010</title>
            <link>http://www.medworm.com/index.php?rid=3930076&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwx5m031354537g08%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6260-xAuthors
		Jay N. Cohn, University of Minnesota, Minneapolis, MN USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3930076</comments>
            <pubDate>Thu, 02 Sep 2010 06:49:12 +0100</pubDate>
            <guid isPermaLink="false">3930076</guid>        </item>
        <item>
            <title>Pharmacologic Therapy for Non ST-segment Elevation Acute Coronary Syndromes: Focus on Antithrombotic Therapy</title>
            <link>http://www.medworm.com/index.php?rid=3878090&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F613532567p564721%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Antithrombotic therapy constitutes the basis of the management of acute coronary syndromes. It combines antiplatelet and anticoagulant
 therapy. Antiplatelet agents should combine aspirin and agents acting through the ADP pathway such as clopidogrel; newer antiplatelet
 agents such as prasugrel or ticagrelor have superior anti-ischemic efficacy, compared with clopidogrel. Intravenous glycoprotein
 IIb/IIIa inhibitors may be used in selected patients at high risk undergoing percutaneous coronary interventions. Unfractionated
 heparin constitutes the reference anticoagulant treatment. Enoxaparin provides slightly better anti-ischemic efficacy. Newer
 agents, such as bivalirudin or fondaparinux, reduce bleeding complications, with no improvement in anti-ischemic efficacy.
...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3878090</comments>
            <pubDate>Tue, 17 Aug 2010 05:55:39 +0100</pubDate>
            <guid isPermaLink="false">3878090</guid>        </item>
        <item>
            <title>Cardioprotection in the Clinical Setting-Lessons from J-WIND Studies</title>
            <link>http://www.medworm.com/index.php?rid=3832479&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F703276313703lr56%2F</link>
            <description>Discussion&amp;nbsp;&amp;nbsp;For prevention of acute myocardial infarction, it is widely accepted to treat high risk patients with aspirin and/or statins.
 On the other hand, several medications such as angiotensin converting enzyme inhibitors, aldosterone receptor antagonists
 and beta blockers have been used for the prevention of post-infarction heart failure in patients who have suffered from an
 acute myocardial infarction. However, at present we do not have an adjunctive drug therapy to reduce infarct size in the acute
 phase in patients with myocardial infarction. Recently, the J-WIND trials suggested that an infusion of human atrial natriuretic
 peptide in the acute phase and oral administration of nicorandil in the chronic phase of infarction result in a better outcome
 in patients with a...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3832479</comments>
            <pubDate>Fri, 06 Aug 2010 07:47:40 +0100</pubDate>
            <guid isPermaLink="false">3832479</guid>        </item>
        <item>
            <title>Regeneration of the Endothelium in Vascular Injury</title>
            <link>http://www.medworm.com/index.php?rid=3832480&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn531362m754v34j6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The endothelium mediates relaxations (dilatations) of the underlying vascular smooth muscle cells. The endothelium-dependent
 relaxations are due to the release of non-prostanoid vasodilator substances. The best characterized endothelium-derived relaxing
 factor (EDRF) is nitric oxide (NO). The endothelial cells also release substances (endothelium-derived hyperpolarizing factor,
 EDHF) that cause hyperpolarization of the cell membrane of the underlying vascular smooth muscle. The release of EDRF from
 the endothelium can be mediated by both pertussis toxin-sensitive Gi (alpha2-adrenergic activation, serotonin, thrombin) and insensitive Gq (adenosine diphosphate, bradykinin) coupling proteins. The ability of the endothelial cell to release relaxing factors can
 be upreg...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3832480</comments>
            <pubDate>Fri, 06 Aug 2010 07:47:39 +0100</pubDate>
            <guid isPermaLink="false">3832480</guid>        </item>
        <item>
            <title>Aldosterone Inhibition and Cardiovascular Protection: More Important Than it Once Appeared</title>
            <link>http://www.medworm.com/index.php?rid=3809882&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv71p7x5h035x5424%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Aldosterone is present and active all along the cardiovascular continuum. Excessive tissue production occurs in cardiovascular
 diseases including myocardial infarction (MI) and heart failure, resulting in a multitude of adverse effects in the cardiovascular
 system necessitating pharmacologic blockade of this neurohormone. Both human and animal studies have consistently proven the
 beneficial effects of antialdosteronics in the improvement of: 1) endothelial function, 2) modulation of inflammatory mechanisms
 between blood and the vascular wall and 3) reduction of tissue proliferation and cardiovascular remodeling leading to different
 severities of cardiovascular damage. These basic mechanisms of anti-aldosterone therapy strongly support the promising data
 observed i...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3809882</comments>
            <pubDate>Fri, 30 Jul 2010 17:02:56 +0100</pubDate>
            <guid isPermaLink="false">3809882</guid>        </item>
        <item>
            <title>Resveratrol Shows Vasoprotective Effect Reducing Oxidative Stress Without Affecting Metabolic Disturbances in Insulin-dependent Diabetes of Rabbits</title>
            <link>http://www.medworm.com/index.php?rid=3809881&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F53286hlk813704l7%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Overall, there was no noticeable difference between resveratrol treatment groups on the recovery from diabetes. Our results
 indicate that resveratrol alleviates type 1 diabetes-induced vasculopathy by decreasing vascular oxidative stress and thereby
 increasing the bioavailability of nitric oxide without changing metabolic abnormalities.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6255-7Authors
		Fatma Akar, Gazi University Department of Pharmacology, Faculty of Pharmacy Etiler Ankara TurkeyM. Bilgehan Pektas, Gazi University Department of Pharmacology, Faculty of Pharmacy Etiler Ankara TurkeyCan Tufan, Gazi University Department of Pharmacology, Faculty of Pharmacy Etiler Ankara TurkeySelen Soylemez, Gazi University Department of Pharmacology, Facult...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3809881</comments>
            <pubDate>Fri, 30 Jul 2010 17:02:56 +0100</pubDate>
            <guid isPermaLink="false">3809881</guid>        </item>
        <item>
            <title>Conventional and Novel Drug Therapeutics to Relief Myocardial Ischemia</title>
            <link>http://www.medworm.com/index.php?rid=3791854&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv651k1603086m15n%2F</link>
            <description>This article reviews drugs that alleviate the
 symptoms of chronic angina with emphasis on several novel pharmacological agents.
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6254-8Authors
		Danny Dvir, Tel Aviv University Cardiology Department, Rabin Medical Center, Petach Tikva, Sackler Faculty of Medicine 49100 Tel Aviv IsraelAlexander Battler, Tel Aviv University Cardiology Department, Rabin Medical Center, Petach Tikva, Sackler Faculty of Medicine 49100 Tel Aviv Israel
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3791854</comments>
            <pubDate>Sat, 24 Jul 2010 13:47:51 +0100</pubDate>
            <guid isPermaLink="false">3791854</guid>        </item>
        <item>
            <title>Effect of Dronedarone on Exercise Capacity and Cardiac Function in Patients With Severe Left Ventricular Dysfunction and Compensated Stable Heart Failure</title>
            <link>http://www.medworm.com/index.php?rid=3785062&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5148454r5652r453%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Short-term treatment with dronedarone did not affect exercise capacity and did not decrease LVEF in patients with severe LV
 dysfunction and compensated HF.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6251-yAuthors
		T. Barry Levine, Michigan Institute for Heart Failure and Transplant Care Farmington Hills MI USAThomas Giles, Louisiana State University School of Medicine New Orleans LA USADavid Radzik, sanofi-aventis Paris FranceJalal K. Ghali, Louisiana State University School of Medicine Shreveport LA USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3785062</comments>
            <pubDate>Fri, 23 Jul 2010 12:17:58 +0100</pubDate>
            <guid isPermaLink="false">3785062</guid>        </item>
        <item>
            <title>How to Mediate Cardioprotection in Ischemic Hearts—Accumulated Evidence of Basic Research Should Translate to Clinical Medicine</title>
            <link>http://www.medworm.com/index.php?rid=3777900&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy04646x303113511%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ischemic heart failure is one of the leading causes of death in the western countries and it is a critical issue to overcome
 ischemic heart diseases for the human health care worldwide. There are several aspects of ischemic heart failure that we need
 to seriously consider for the conquest of cardiovascular death. First of all, we need to know either causes or pathophysiology
 of the onset of coronary artery disease, the ischemia/reperfusion injury and post-infarction cardiac remodeling. Secondly,
 we need to find the potential seeds for the molecular, pharmacological, biomedical or engineering treatment to prevent or
 attenuate ischemic heart diseases. Thirdly, we need to accelerate translational research and to create the network of clinical
 trials to grow the novel...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3777900</comments>
            <pubDate>Mon, 19 Jul 2010 17:50:29 +0100</pubDate>
            <guid isPermaLink="false">3777900</guid>        </item>
        <item>
            <title>Dipyridamole with Low-Dose Aspirin Augments the Infarct Size-Limiting Effects of Simvastatin</title>
            <link>http://www.medworm.com/index.php?rid=3773707&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F342w6g48537n6513%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;During acute myocardial ischemia, DIP alone or with low-dose ASA limits IS and does not attenuate the IS-limiting effect of
 SIM as high-dose ASA.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6252-xAuthors
		Yumei Ye, The University of Texas Medical Branch Department of Biochemistry and Molecular Biology Galveston TX USABo Long, The University of Texas Medical Branch Department of Biochemistry and Molecular Biology Galveston TX USAJinqiao Qian, The University of Texas Medical Branch Department of Biochemistry and Molecular Biology Galveston TX USAJose R. Perez-Polo, The University of Texas Medical Branch Department of Biochemistry and Molecular Biology Galveston TX USAYochai Birnbaum, The University of Texas Medical Branch Department of Biochemistry an...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3773707</comments>
            <pubDate>Fri, 16 Jul 2010 18:41:09 +0100</pubDate>
            <guid isPermaLink="false">3773707</guid>        </item>
        <item>
            <title>Is Vascular Stiffness a Target for Therapy?</title>
            <link>http://www.medworm.com/index.php?rid=3773708&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa47304x59x251555%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Measurement of arterial stiffness will not only be helpful in the detection of early vascular disease but also as a tool in
 the selection and follow-up monitoring of therapeutic strategies aimed at preventing or delaying progression of vascular disease.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6250-zAuthors
		Daniel A. Duprez, University of Minnesota Cardiovascular Division, Medical School VCRC Room 270, 420 Delaware St SE, MMC 508 Minneapolis MN 55455 USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3773708</comments>
            <pubDate>Wed, 14 Jul 2010 22:48:42 +0100</pubDate>
            <guid isPermaLink="false">3773708</guid>        </item>
        <item>
            <title>The Metabolic Effects of Omega-3 Plant Sterol Esters in Mixed Hyperlipidemic Subjects</title>
            <link>http://www.medworm.com/index.php?rid=3741607&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe3511h74v5387u7u%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In patients with mixed hyperlipidemia, n-3-PSE treatment may offer a safe and effective therapy for triglyceride level reduction
 while avoiding the typical increase in LDL-C levels associated with n-3 fatty acid treatment. The observed reduction in blood
 pressure and inflammation markers warrants further evaluation. The positive effect of n-3-PSE treatment was preserved at the
 end of the follow up phase.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6249-5Authors
		Rafael Bitzur, Sheba Medical Center The Bert W. Strassburger Lipid Center Tel Hashomer IsraelHofit Cohen, Sheba Medical Center The Bert W. Strassburger Lipid Center Tel Hashomer IsraelTzafra Cohen, Enzymotec Ltd R&amp;D Department Migdal HaEmeq IsraelTali W. Dror, Enzymotec Ltd R&amp;D Department ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3741607</comments>
            <pubDate>Thu, 08 Jul 2010 16:19:02 +0100</pubDate>
            <guid isPermaLink="false">3741607</guid>        </item>
        <item>
            <title>Smoking Cessation–Recent Advances</title>
            <link>http://www.medworm.com/index.php?rid=3727692&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F764uk726466g6883%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Further studies are required to address the uncertainty that exists on the most appropriate duration of therapy as well as
 the effectiveness and safety of combination pharmacotherapy. Post-marketing surveillance continues to play an important role
 in monitoring the adverse effects events associated with these therapies.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6246-8Authors
		John J. McNeil, Monash University Department of Epidemiology &amp; Preventive Medicine, School of Public Health &amp; Preventive Medicine, Alfred Hospital Melbourne Victoria 3004 AustraliaLoretta Piccenna, Monash University Department of Epidemiology &amp; Preventive Medicine, School of Public Health &amp; Preventive Medicine, Alfred Hospital Melbourne Victoria 3004 AustraliaLisa L. Ioannide...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3727692</comments>
            <pubDate>Sun, 04 Jul 2010 22:46:38 +0100</pubDate>
            <guid isPermaLink="false">3727692</guid>        </item>
        <item>
            <title>Which Beta-Blocker is Most Effective in Heart Failure?</title>
            <link>http://www.medworm.com/index.php?rid=3727693&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkmr2347185q12244%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6247-7Authors
		Willem J. Remme, Sticares Cardiovascular Research Institute P.O. Box 882 3160 AB Rhoon The Netherlands
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3727693</comments>
            <pubDate>Fri, 02 Jul 2010 19:45:24 +0100</pubDate>
            <guid isPermaLink="false">3727693</guid>        </item>
        <item>
            <title>Role of Dual Antiplatelet Therapy in Symptomatic Patients with Established Vascular Disease: Putting the CHARISMA Trial into Therapeutic Perspective</title>
            <link>http://www.medworm.com/index.php?rid=3715533&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh05883195011p710%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Hypothesizing that dual antiplatelet therapy would provide benefit across the broad spectrum of atherothrombotic disease was
 plausible. In retrospect, it is apparent that by combining such a heterogeneous population, CHARISMA failed to show a clear
 treatment effect for DAPT and potentially masked important benefits in specific populations. Given the inherent clinical and
 biological variability among patients and disease states, difficult-to-interpret clinical data should not be dismissed. The
 current challenge is identifying clinically useful data from CHARISMA to determine the role of DAPT in contemporary clinical
 practice.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6245-9Authors
		William E. Boden, University at Buffalo School of Medicine and ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3715533</comments>
            <pubDate>Wed, 30 Jun 2010 15:21:59 +0100</pubDate>
            <guid isPermaLink="false">3715533</guid>        </item>
        <item>
            <title>Cardioprotection in the Clinical Setting</title>
            <link>http://www.medworm.com/index.php?rid=3715534&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkq720v07u378j567%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Reperfusion therapy is the primary treatment of acute myocardial infarction and must be applied as soon as possible to limit
 the ischemic insult. Unfortunately, reperfusion is responsible for additional myocardial damage likely involving opening of
 the mitochondrial permeability transition pore. Ischemic postconditioning is a powerful intervention that dramatically reduces
 lethal reperfusion injury. Several clinical studies using angioplasty postconditioning now support its protective effects
 in patients with an acute myocardial infarction. Alternatively, pharmacological postconditioning could afford comparable protection
 and be applied to a much larger number of patients. Indeed, the mitochondrial permeability transition pore inhibitor cyclosporine
 A has been sho...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3715534</comments>
            <pubDate>Tue, 29 Jun 2010 16:33:25 +0100</pubDate>
            <guid isPermaLink="false">3715534</guid>        </item>
        <item>
            <title>Neonatal Exendin-4 Leads to Protection from Reperfusion Injury and Reduced Rates of Oxidative Phosphorylation in the Adult Rat Heart</title>
            <link>http://www.medworm.com/index.php?rid=3708016&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F604x575540228951%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;A short course of Exendin-4 in the neonatal period leads to protection from ischemic injury and a preconditioned mitochondrial
 phenotype in the adult rat.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6242-zAuthors
		Suzanne B. Brown, Hospital of the University of Pennsylvania Philadelphia PA USAJoseph R. Libonati, University of Pennsylvania School of Nursing Philadelphia PA USAMary A. Selak, Children’s Hospital of Philadelphia Philadelphia PA USARichard P. Shannon, Hospital of the University of Pennsylvania Philadelphia PA USARebecca A. Simmons, Hospital of the University of Pennsylvania Philadelphia PA USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3708016</comments>
            <pubDate>Sat, 26 Jun 2010 16:21:49 +0100</pubDate>
            <guid isPermaLink="false">3708016</guid>        </item>
        <item>
            <title>Secondary Prevention of CAD with ACE Inhibitors: A Struggle Between Life and Death of the Endothelium</title>
            <link>http://www.medworm.com/index.php?rid=3700429&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F33742j8225v16n43%2F</link>
            <description>We report our experience
 in this context with perindopril.
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6244-xAuthors
		Roberto Ferrari, Arcispedale S. Anna Hospital Chair of Cardiology, University of Ferrara, Cardiovascular Institute C.rso Giovecca 203 Ferrara 44100 ItalyGabriele Guardigli, University Hospital of Ferrara Ferrara ItalyClaudio Ceconi, Arcispedale S. Anna Hospital Chair of Cardiology, University of Ferrara, Cardiovascular Institute C.rso Giovecca 203 Ferrara 44100 Italy
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3700429</comments>
            <pubDate>Fri, 25 Jun 2010 16:54:15 +0100</pubDate>
            <guid isPermaLink="false">3700429</guid>        </item>
        <item>
            <title>Atherosclerotic Plaque Regression: Fact or Fiction?</title>
            <link>http://www.medworm.com/index.php?rid=3667744&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftj3p5v8347087157%2F</link>
            <description>This article reviews
 the existing evidence underpinning current therapeutic strategies aimed at achieving atherosclerotic plaque regression. In
 this review we also discuss imaging modalities for the assessment of plaque regression, predictors of regression and whether
 plaque regression is associated with a survival benefit.
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6241-0Authors
		Nesan Shanmugam, St George’s University of London Division of Cardiac and Vascular Sciences Cranmer Terrace London SW17 0RE UKAna Román-Rego, St George’s University of London Division of Cardiac and Vascular Sciences Cranmer Terrace London SW17 0RE UKPeter Ong, St George’s University of London Division of Cardiac and Vascular Sciences Cranmer Terrace London SW17 0RE UKJuan Carlos Kaski, St...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3667744</comments>
            <pubDate>Mon, 14 Jun 2010 14:06:54 +0100</pubDate>
            <guid isPermaLink="false">3667744</guid>        </item>
        <item>
            <title>Rapamycin can Inhibit the Development of Chlamydia pneumoniae, which Might Partly Contribute to the Prevention of In-stent Restenosis</title>
            <link>http://www.medworm.com/index.php?rid=3653542&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh640200p24034034%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Sufficient rapamycin can inhibit the growth of C. pneumoniae effectively, but it should be applied at the early stage of the chlamydial infections. Rapamycin eluting-stents can induce
 a high enough local concentration of rapamycin. This provides a possibility for us to suppose that the beneficial effect of
 rapamycin in preventing in-stent restenosis might partly be explained by its inhibitory effects on the growth of C. pneumoniae.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6238-8Authors
		Ying Yan, University of Oulu Department of Medical Microbiology PO BOX 5000 90014 Oulu FinlandSylvi Silvennoinen-Kassinen, University of Oulu Department of Medical Microbiology PO BOX 5000 90014 Oulu FinlandMaija Leinonen, National Institute for Health and Welfar...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3653542</comments>
            <pubDate>Wed, 09 Jun 2010 09:13:45 +0100</pubDate>
            <guid isPermaLink="false">3653542</guid>        </item>
        <item>
            <title>Postconditioning in Reperfusion Injury: A Status Report</title>
            <link>http://www.medworm.com/index.php?rid=3653543&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fggn56q8145160643%2F</link>
            <description>This article will primarily discuss the existing literature regarding protection of Postcon on the heart, but there is a potential
 for future research into other organ systems to identify beneficial effects of Postcon on tissue reperfusion injury, particularly
 in patients undergoing surgical revascularization.
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6240-1Authors
		Zhi-Qing Zhao, Mercer University School of Medicine Cardiovascular Research Laboratory Savannah GA USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3653543</comments>
            <pubDate>Wed, 09 Jun 2010 09:13:43 +0100</pubDate>
            <guid isPermaLink="false">3653543</guid>        </item>
        <item>
            <title>Cardiovascular Risks of Anemia Correction with Erythrocyte Stimulating Agents: Should Blood Viscosity Be Monitored for Risk Assessment?</title>
            <link>http://www.medworm.com/index.php?rid=3626902&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx0487402418165q8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To date, all major clinical trials for anemia correction using erythrocyte stimulating agents (ESAs) failed to show improved
 outcomes for cardiovascular disease (CVD), stroke, and vascular thrombosis. Even moderate elevations in hemoglobin (e.g.,
 to 13&amp;nbsp;g/dL) using erythropoietin have been associated with significantly increased risk of thrombotic cardiovascular events
 and heart failure. This review presents a biophysical rationale for increased risk of CVD among certain patients treated with
 ESAs and suggests a risk management approach based on blood viscosity. Whole blood viscosity is a key determinant of the work
 of the heart, and elevated blood viscosity appears to be both a strong predictor of cardiovascular disease and an important
 pathophysiological fac...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3626902</comments>
            <pubDate>Tue, 01 Jun 2010 06:05:19 +0100</pubDate>
            <guid isPermaLink="false">3626902</guid>        </item>
        <item>
            <title>Mechanism of Cardioprotection by Early Ischemic Preconditioning</title>
            <link>http://www.medworm.com/index.php?rid=3611037&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq152125q24743538%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A series of brief ischemia/reperfusion cycles (termed ischemic preconditioning, IPC) limits myocardial injury produced by
 a subsequent prolonged period of coronary artery occlusion and reperfusion. Over the last 2 decades our understanding of IPC’s
 mechanism has increased exponentially. Hearts exposed to IPC have a better metabolic and ionic status during prolonged ischemia
 compared to naïve hearts. However, this difference is not thought to be the main mechanism by which IPC protects against infarction.
 Signaling pathways that are activated by IPC distinguish IPC hearts from naïve hearts. During the trigger phase of IPC, adenosine,
 bradykinin and opioid receptors are occupied. Although these three receptors trigger signaling through divergent pathways,
 the si...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3611037</comments>
            <pubDate>Thu, 27 May 2010 11:01:04 +0100</pubDate>
            <guid isPermaLink="false">3611037</guid>        </item>
        <item>
            <title>The Second Window of Preconditioning (SWOP) Where Are We Now?</title>
            <link>http://www.medworm.com/index.php?rid=3600749&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw0116g41052677j2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A standard ischemic preconditioning (IPC) stimulus of one or more brief episodes of non-lethal myocardial ischemia and reperfusion
 elicits a bi-phasic pattern of cardioprotection. The first phase manifests almost immediately following the IPC stimulus and
 lasts for 1–2&amp;nbsp;h, after which its effect disappears (termed classical or early IPC). The second phase of cardioprotection appears
 12–24&amp;nbsp;h later and lasts for 48–72&amp;nbsp;h (termed the Second Window of Protection [SWOP] or delayed or late IPC). The cardioprotection
 conferred by delayed IPC is robust and ubiquitous but is not as powerful as early IPC. Although there are some similarities
 in the mechanisms underlying early and delayed IPC, one of the major distinctions between the two is the latter’s ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3600749</comments>
            <pubDate>Sat, 22 May 2010 16:49:37 +0100</pubDate>
            <guid isPermaLink="false">3600749</guid>        </item>
        <item>
            <title>Application of Direct Renin Inhibition to Chronic Kidney Disease</title>
            <link>http://www.medworm.com/index.php?rid=3582764&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl8t6132p7hmg206u%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;High dose ARB therapy or combination therapies with ACE inhibitors and ARBs have shown beneficial effects on surrogate markers
 of chronic kidney disease. Early data based on urinary protein excretion rates as a surrogate marker for renal function suggest
 a possibly novel role for aliskiren alone or in combination with ARBs in chronic kidney disease.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6232-1Authors
		Christian W. Mende, University of California at San Diego Department of Medicine 6950 Fairway Road La Jolla CA 92037 USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3582764</comments>
            <pubDate>Wed, 19 May 2010 17:59:51 +0100</pubDate>
            <guid isPermaLink="false">3582764</guid>        </item>
        <item>
            <title>Mitochondria and GSK-3β in Cardioprotection Against Ischemia/Reperfusion Injury</title>
            <link>http://www.medworm.com/index.php?rid=3582763&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv610246v5k64255t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The mitochondrion is a powerhouse of the cell, a platform of cell signaling and decision-maker of cell death, including death
 by ischemia/reperfusion. Ischemia shuts off ATP production by mitochondria, and cell viability is compromised by energy deficiency
 and build-up of cytotoxic metabolites during ischemia. Furthermore, the mitochondrial permeability transition pore (mPTP)
 is primed by ischemia to open upon reperfusion, leading to reperfusion-induced cell necrosis. mPTP opening can be suppressed
 by ischemic preconditioning (IPC) and other interventions that induce phosphorylation of GSK-3β. Activation of the mitochondrial
 ATP-sensitive K+ channel (mKATP channel) is an important signaling step in a trigger phase of IPC, which ultimately enhances GSK-3β phosphor...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3582763</comments>
            <pubDate>Wed, 19 May 2010 17:59:51 +0100</pubDate>
            <guid isPermaLink="false">3582763</guid>        </item>
        <item>
            <title>Rationale, design and population baseline characteristics of the PERFORM Vascular Project: an ancillary study of the Prevention of cerebrovascular and cardiovascular Events of ischemic origin with teRutroban in patients with a history oF ischemic strOke or tRansient ischeMic attack (PERFORM) trial</title>
            <link>http://www.medworm.com/index.php?rid=3582765&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4161h6054180p532%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The PERFORM Vascular Project will investigate terutroban’s effect on vascular structure and function in patients with a history
 of ischemic stroke or TIAs.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6231-2Authors
		Michael G. Hennerici, University of Heidelberg Department of Neurology Mannheim GermanyMichiel L. Bots, University Medical Center Utrecht Julius Center for Health Sciences and Primary Care Utrecht The NetherlandsIan Ford, Robertson Centre for Biostatistics Glasgow UKStéphane Laurent, Hôpital Européen Georges Pompidou Department of Pharmacology and INSERM U970 Paris FrancePierre Jean Touboul, Hôpital Bichat Department of Neurology and Stroke Center Paris France
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3582765</comments>
            <pubDate>Wed, 19 May 2010 17:59:50 +0100</pubDate>
            <guid isPermaLink="false">3582765</guid>        </item>
        <item>
            <title>Hydralazine does not Ameliorate Nitric Oxide Resistance in Chronic Heart Failure</title>
            <link>http://www.medworm.com/index.php?rid=3582766&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbn622q6368155436%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The results of the present study do not support the assumption that hydralazine could be viewed as a “NO enhancer”; there
 is no evidence of attenuation of NO resistance by hydralazine treatment.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6233-0Authors
		Yuliy Y. Chirkov, Cardiology Unit, Vascular Disease and Therapeutics Research Group, Basil Hetzel Institute, The Queen Elizabeth Hospital, School of Medicine, The University of Adelaide Adelaide AustraliaMichele De Sciscio, Cardiology Unit, Vascular Disease and Therapeutics Research Group, Basil Hetzel Institute, The Queen Elizabeth Hospital, School of Medicine, The University of Adelaide Adelaide AustraliaAaron L. Sverdlov, Cardiology Unit, Vascular Disease and Therapeutics Research Group, Basil ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3582766</comments>
            <pubDate>Wed, 19 May 2010 17:59:48 +0100</pubDate>
            <guid isPermaLink="false">3582766</guid>        </item>
        <item>
            <title>Role of the Renin-Angiotensin System in Cardiovascular Disease</title>
            <link>http://www.medworm.com/index.php?rid=3553605&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv701j52177718856%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6230-3Authors
		Jay N. Cohn, University of Minnesota Medical School Department of Medicine, Cardiovascular Division Mayo Mail Code 508, 420 Delaware Street Southeast Minneapolis MN 55455 USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3553605</comments>
            <pubDate>Sat, 08 May 2010 10:14:03 +0100</pubDate>
            <guid isPermaLink="false">3553605</guid>        </item>
        <item>
            <title>Hypoxia Inducible Factor-1 Protects Against Nitrate Tolerance and Stunning in Rabbit Cardiac Myocytes</title>
            <link>http://www.medworm.com/index.php?rid=3491663&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0628r4342583nj25%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;We found that upregulation of HIF-1 could protect isolated cardiac myocytes against nitrate tolerance through a cyclic GMP
 protein kinase-independent mechanism and through a kinase-dependent mechanism in stunning.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6229-9Authors
		Tao Tan, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School Heart and Brain Circulation Laboratory, Department of Physiology and Biophysics 675 Hoes Lane West Piscataway NJ 08854 USAHarvey R. Weiss, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School Heart and Brain Circulation Laboratory, Department of Physiology and Biophysics 675 Hoes Lane West Piscataway NJ 08854 USA
	

	
		Journal Cardiovascular Drugs and Th...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3491663</comments>
            <pubDate>Tue, 20 Apr 2010 11:03:32 +0100</pubDate>
            <guid isPermaLink="false">3491663</guid>        </item>
        <item>
            <title>Practical Strategies for the Management of Anticoagulation Therapy: Unsolved Issues in the Cardiac Catheterization Laboratory</title>
            <link>http://www.medworm.com/index.php?rid=3477033&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk54n46624555681r%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The published evidence supports the updates to the guidelines. Updated guidelines still have knowledge gaps which require
 the application of clinical discretion by the cardiologist.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6226-zAuthors
		José G. Díez, Texas Heart Institute, Baylor College of Medicine St. Luke’s Episcopal Hospital 1709 Dryden Rd., BCM 620, Suite 9.40 Houston TX 77030 USAJames M. Wilson, Texas Heart Institute, Baylor College of Medicine St. Luke’s Episcopal Hospital 1709 Dryden Rd., BCM 620, Suite 9.40 Houston TX 77030 USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3477033</comments>
            <pubDate>Tue, 13 Apr 2010 18:18:11 +0100</pubDate>
            <guid isPermaLink="false">3477033</guid>        </item>
        <item>
            <title>A Multicenter, Eight-Week Treatment, Single-Step Titration, Open-Label Study Assessing the Percentage of Korean Dyslipidemic Patients Achieving LDL Cholesterol Target with Atorvastatin Starting Doses of 10 mg, 20 mg and 40 mg</title>
            <link>http://www.medworm.com/index.php?rid=3469164&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa42m624507240j60%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Patient-tailored statin therapy according to an individual’s risk category and LDL-C levels was safe and effective with a
 quick achievement of LDL-C target in Korean dyslipidemic patients.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6225-0Authors
		Cheol Whan Lee, Asan Medical Center Seoul South KoreaSang-Hong Baek, The Catholic University of Korea Division of Cardiology, Seoul St. Mary’s Hospital 505 Banpo-dong, Seocho-gu Seoul 137-701 South KoreaTaek-Jong Hong, Pusan National University Hospital Busan South KoreaYoung-Jin Choi, Hallym University Sacred Heart Hospital Anyang Gyeonggi South KoreaYoung-Jo Kim, Yeungnam University Hospital Daegu South KoreaTae-Hoon Ahn, Gachon University Gil Medical Center Incheon South KoreaSang-Hyun Ihm, The Cath...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3469164</comments>
            <pubDate>Sat, 10 Apr 2010 07:49:00 +0100</pubDate>
            <guid isPermaLink="false">3469164</guid>        </item>
        <item>
            <title>Additive Effect of TAK-491, a New Angiotensin Receptor Blocker, and Pioglitazone, in Reducing Myocardial Infarct Size</title>
            <link>http://www.medworm.com/index.php?rid=3469165&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk743322103823715%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;TAK-491 and PIO independently limited myocardial IS in a dose-dependent fashion; and the effects were additive. The mechanism
 of protection and the role of TAK-491 in this clinical setting should be further investigated.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6227-yAuthors
		Yumei Ye, The University of Texas Medical Branch The Department of Biochemistry and Molecular Biology Galveston TX USAKyle T. Keyes, The University of Texas Medical Branch The Department of Biochemistry and Molecular Biology Galveston TX USAChong F. Zhang, The University of Texas Medical Branch The Department of Biochemistry and Molecular Biology Galveston TX USAJose R. Perez-Polo, The University of Texas Medical Branch The Department of Biochemistry and Molecular Biology Ga...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3469165</comments>
            <pubDate>Thu, 08 Apr 2010 18:02:01 +0100</pubDate>
            <guid isPermaLink="false">3469165</guid>        </item>
        <item>
            <title>Role of Beta-Adrenergic Receptor Gene Polymorphisms in the Long-Term Effects of Beta-Blockade with Carvedilol in Patients with Chronic Heart Failure</title>
            <link>http://www.medworm.com/index.php?rid=3426320&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F46g68g3123k51275%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Beta1-AR Arg389Gly and beta2-AR Arg16Gly SNPs are not related to the response to carvedilol therapy. In contrast, the Gln27Glu
 SNP is a determinant of the LVEF response to this agent in patients with chronic HF.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6220-5Authors
		Marco Metra, University of Brescia Institute of Cardiology, Department of Experimental and Applied Medicine Brescia ItalyLoredana Covolo, University of Brescia Institute of Hygiene, Epidemiology and Public Health, Department of Experimental and Applied Medicine Brescia ItalyNatalia Pezzali, University of Brescia Institute of Cardiology, Department of Experimental and Applied Medicine Brescia ItalyValerio Zacà, University of Brescia Institute of Cardiology, Department of Experimental ...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3426320</comments>
            <pubDate>Tue, 30 Mar 2010 05:46:30 +0100</pubDate>
            <guid isPermaLink="false">3426320</guid>        </item>
        <item>
            <title>The PACIFIC (Prevention of AtherothrombotiC Incidents Following Ischemic Coronary attack) Registry: Rationale and Design of a 2-Year Study in Patients Initially Hospitalised with Acute Coronary Syndrome in Japan</title>
            <link>http://www.medworm.com/index.php?rid=3426319&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F47h3841x2758j70v%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The PACIFIC Registry will give insights as to the Japanese epidemiology of ACS: recurrence of atherothrombotic events in the
 same or other vascular territories.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6223-2Authors
		Katsumi Miyauchi, Juntendo University Department of Cardiovascular Medicine, School of Medicine 2-1-1 Hongo Bunkyo-ku Tokyo 113-8421 JapanYoshihiro Morino, Tokai University Department of Cardiology, School of Medicine Isehara JapanKengo Tsukahara, Yokohama City University Medical Center Division of cardiology Yokohama JapanHideki Origasa, University of Toyama Division of Biostatistics and Clinical Epidemiology Toyama JapanHiroyuki Daida, Juntendo University Department of Cardiovascular Medicine, School of Medicine 2-1-1 Hongo Bunkyo-...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3426319</comments>
            <pubDate>Tue, 30 Mar 2010 05:46:30 +0100</pubDate>
            <guid isPermaLink="false">3426319</guid>        </item>
        <item>
            <title>Transitory Activation of AMPK at Reperfusion Protects the Ischaemic-Reperfused Rat Myocardium Against Infarction</title>
            <link>http://www.medworm.com/index.php?rid=3367109&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv16886p8t1382613%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Our data demonstrated that, in our ex vivo model of myocardial ischaemia-reperfusion injury, AMPK activation in early reperfusion
 is associated with a reduction in infarct size.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6222-3Authors
		Marta A. Paiva, University College London Hospitals and Medical School The Hatter Cardiovascular Institute 67 Chenies Mews London WC1E 6HX UKLino M. Gonçalves, Coimbra University Hospital and Coimbra Medical School Basic Research in Cardiology Unit, IBILI Coimbra PortugalLuis A. Providência, Coimbra University Hospital and Coimbra Medical School Basic Research in Cardiology Unit, IBILI Coimbra PortugalSean M. Davidson, University College London Hospitals and Medical School The Hatter Cardiovascular Institute 67 Che...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3367109</comments>
            <pubDate>Sun, 14 Mar 2010 11:27:56 +0100</pubDate>
            <guid isPermaLink="false">3367109</guid>        </item>
        <item>
            <title>Effects of Eprosartan on Diastolic Function and Neurohormones in Patients with Hypertension and Diastolic Dysfunction</title>
            <link>http://www.medworm.com/index.php?rid=3367110&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu21t4tt30182j7g6%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Lowering blood pressure, either with eprosartan or other anti-hypertensives in hypertensive patients with diastolic dysfunction
 did not change diastolic function after 6&amp;nbsp;months of treatment, but was associated with a decrease of NT-proBNP.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6221-4Authors
		Adriaan A. Voors, University Medical Centre Groningen Department of Cardiology PO Box 30.001 9700 RB Groningen The NetherlandsRuud M. van de Wal, St. Antonius Hospital Nieuwegein Nieuwegein The NetherlandsJasper W. L Hartog, University Medical Centre Groningen Department of Cardiology PO Box 30.001 9700 RB Groningen The NetherlandsRichard G. Vijn, Refaja Hospital Stadskanaal Stadskanaal The NetherlandsYoran M. Hummel, University Medical Centre Groninge...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3367110</comments>
            <pubDate>Sun, 14 Mar 2010 11:27:55 +0100</pubDate>
            <guid isPermaLink="false">3367110</guid>        </item>
        <item>
            <title>Prevention of Peri-procedural Myocardial Injury Using a Single High Loading Dose of Rosuvastatin</title>
            <link>http://www.medworm.com/index.php?rid=3360420&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgnr7304p37515785%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;A single high loading dose of rosuvastatin reduces the incidence of peri-procedural myocardial necrosis and infarction effectively.
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6224-1Authors
		Serkan Cay, Yuksek Ihtisas Heart-Education and Research Hospital Department of Cardiology Ankara TurkeyGoksel Cagirci, Ministry of Health Dışkapı Yıldırım Beyazıt Research and Educational Hospital Department of Cardiology Ankara TurkeyNihat Sen, Mustafa Kemal University, Faculty of Medicine Department of Cardiology Hatay TurkeyYucel Balbay, Yuksek Ihtisas Heart-Education and Research Hospital Department of Cardiology Ankara TurkeyTahir Durmaz, Ataturk Education and Research Hospital Department of Cardiology Ankara TurkeySinan Aydogdu, Yuksek Ihtisas Heart-Edu...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3360420</comments>
            <pubDate>Thu, 11 Mar 2010 02:45:03 +0100</pubDate>
            <guid isPermaLink="false">3360420</guid>        </item>
        <item>
            <title>Cyclosporine A at Reperfusion Reduces Infarct Size in Pigs</title>
            <link>http://www.medworm.com/index.php?rid=3312807&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fru51066276210108%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s10557-010-6219-yAuthors
		Andreas Skyschally, Institut für Pathophysiologie, Universitätsklinikum Essen Hufelandstraße 55 45122 Essen GermanyRainer Schulz, Institut für Pathophysiologie, Universitätsklinikum Essen Hufelandstraße 55 45122 Essen GermanyGerd Heusch, Institut für Pathophysiologie, Universitätsklinikum Essen Hufelandstraße 55 45122 Essen Germany
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3312807</comments>
            <pubDate>Thu, 25 Feb 2010 06:56:10 +0100</pubDate>
            <guid isPermaLink="false">3312807</guid>        </item>
        <item>
            <title>Erratum to: Resveratrol: A Multifunctional Compound Improving Endothelial Function</title>
            <link>http://www.medworm.com/index.php?rid=3285200&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr15j21368332n0r3%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s10557-010-6218-zAuthors
		Huige Li, Johannes Gutenberg University Department of Pharmacology Obere Zahlbacher Strasse 67 55131 Mainz GermanyUlrich Förstermann, Johannes Gutenberg University Department of Pharmacology Obere Zahlbacher Strasse 67 55131 Mainz Germany
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3285200</comments>
            <pubDate>Wed, 17 Feb 2010 18:31:19 +0100</pubDate>
            <guid isPermaLink="false">3285200</guid>        </item>
        <item>
            <title>Modulation of Programmed Forms of Cell Death by Intracoronary Levosimendan During Regional Myocardial Ischemia in Anesthetized Pigs</title>
            <link>http://www.medworm.com/index.php?rid=3281050&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0794m3542l123520%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Such effects of intracoronary levosimendan bolus administration during regional myocardial ischemia indicate the occurrence
 of cardio-protection by modulation of programmed form of cell death.
 
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6217-0Authors
		Elena Grossini, University of East Piedmont “A. Avogadro” Department of Clinical and Experimental Medicine, Physiology Section Via Solaroli 17 28100 Novara ItalyPhilippe Primo Caimmi, Ospedale Maggiore della Carità Department of Cardiac Surgery C.so Mazzini 18 28100 Novara ItalyFrancesca Platini, University of East Piedmont “A. Avogadro” Department of Food, Chemical, Pharmaceutical and Pharmacological Sciences (DISCAFF) Novara ItalyClaudio Molinari, University of East Piedmont “A. Avogadro...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3281050</comments>
            <pubDate>Tue, 16 Feb 2010 18:08:22 +0100</pubDate>
            <guid isPermaLink="false">3281050</guid>        </item>
        <item>
            <title>Granulocyte-colony Stimulating Factor Treatment of Chronic Myocardial Infarction</title>
            <link>http://www.medworm.com/index.php?rid=3232817&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl80741k02q0867vu%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These data clearly show that G-CSF treatment was unable to restore cardiac function impaired by myocardial infarction either
 with classical approach or long term low dose administration.
 
 
 
	Content Type Journal ArticleDOI 10.1007/s10557-010-6215-2Authors
		Ruy A. N. Louzada, UFRJ Laboratório de Cardiologia Celular e Molecular do Instituto de Biofísica Carlos Chagas Filho Rio de Janeiro CEP 21941-902 BrasilPatricia F. Oliveira, UFRJ Laboratório de Cardiologia Celular e Molecular do Instituto de Biofísica Carlos Chagas Filho Rio de Janeiro CEP 21941-902 BrasilJoao Paulo A. Cavalcanti-de-Albuquerque, EEFD—UFRJ Laboratório de Biologia do Exercício do Departamento de Biociências e Atividade Física Rio de Janeiro CEP 21941-599 BrasilLeandro Cunha-Carvalho, E...</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3232817</comments>
            <pubDate>Mon, 01 Feb 2010 18:05:47 +0100</pubDate>
            <guid isPermaLink="false">3232817</guid>        </item>
        <item>
            <title>President’s Page: ISCP’s Educational Goals</title>
            <link>http://www.medworm.com/index.php?rid=3228661&amp;cid=s_33443_7_f&amp;fid=33443&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx8646un371377l8t%2F</link>
            <description>Content Type Journal ArticleDOI 10.1007/s10557-010-6216-1Authors
		Jay N. Cohn, University of Minnesota Medical School Cardiovascular Division, Mayo Mail Code 508 420 Delaware Street Southeast Minneapolis MN 55455 USA
	

	
		Journal Cardiovascular Drugs and TherapyOnline ISSN 1573-7241Print ISSN 0920-3206 (Source: Cardiovascular Drugs and Therapy)</description>
            <author>Cardiovascular Drugs and Therapy</author>
            <type>journals</type>
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            <pubDate>Fri, 29 Jan 2010 12:18:32 +0100</pubDate>
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