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dc.contributor.author Mátyás, Csaba
dc.contributor.author Németh, Balázs Tamás
dc.contributor.author Oláh, Attila
dc.contributor.author Török, Marianna
dc.contributor.author Ruppert, Mihály
dc.contributor.author Kellermayer, Dalma
dc.contributor.author Barta BA
dc.contributor.author Szabó, Gábor Balázs
dc.contributor.author Kökény, Gábor
dc.contributor.author Horvath, Eszter Mária
dc.contributor.author Bódi, Beáta
dc.contributor.author Papp, Zoltán
dc.contributor.author Merkely, Béla Péter
dc.contributor.author Radovits, Tamás
dc.date.accessioned 2018-06-22T09:14:42Z
dc.date.available 2018-06-22T09:14:42Z
dc.date.issued 2017
dc.identifier 85007236091
dc.identifier.citation pagination=326-336; journalVolume=19; journalIssueNumber=3; journalTitle=EUROPEAN JOURNAL OF HEART FAILURE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5605
dc.identifier.uri doi:10.1002/ejhf.711
dc.description.abstract AIMS: Heart failure with preserved ejection fraction (HFpEF) has a great epidemiological burden. The pathophysiological role of cyclic guanosine monophosphate (cGMP) signalling has been intensively investigated in HFpEF. Elevated levels of cGMP have been shown to exert cardioprotective effects in various cardiovascular diseases, including diabetic cardiomyopathy. We investigated the effect of long-term preventive application of the phosphodiesterase-5A (PDE5A) inhibitor vardenafil in diabetic cardiomyopathy-associated HFpEF. METHODS AND RESULTS: Zucker diabetic fatty (ZDF) rats were used as a model of HFpEF and ZDF lean rats served as controls. Animals received vehicle or 10 mg/kg body weight vardenafil per os from weeks 7 to 32 of age. Cardiac function, morphology was assessed by left ventricular (LV) pressure-volume analysis and echocardiography at week 32. Cardiomyocyte force measurements were performed. The key markers of cGMP signalling, nitro-oxidative stress, apoptosis, myocardial hypertrophy and fibrosis were examined. The ZDF animals showed diastolic dysfunction (increased LV/cardiomyocyte stiffness, prolonged LV relaxation time), preserved systolic performance, decreased myocardial cGMP level coupled with impaired protein kinase G (PKG) activity, increased nitro-oxidative stress, enhanced cardiomyocyte apoptosis, and hypertrophic and fibrotic remodelling of the myocardium. Vardenafil effectively prevented the development of HFpEF by maintaining diastolic function (decreased LV/cardiomyocyte stiffness and LV relaxation time), by restoring cGMP levels and PKG activation, by lowering apoptosis and by alleviating nitro-oxidative stress, myocardial hypertrophy and fibrotic remodelling. CONCLUSIONS: We report that vardenafil successfully prevented the development of diabetes mellitus-associated HFpEF. Thus, PDE5A inhibition as a preventive approach might be a promising option in the management of HFpEF patients with diabetes mellitus.
dc.relation.ispartof urn:issn:1388-9842
dc.title Prevention of the development of heart failure with preserved ejection fraction by the phosphodiesterase-5A inhibitor vardenafil in rats with type 2 diabetes
dc.type Journal Article
dc.date.updated 2018-06-13T15:05:22Z
dc.language.rfc3066 en
dc.identifier.mtmt 3158792
dc.identifier.wos 000397857700007
dc.identifier.pubmed 27995696
dc.contributor.department SE/AOK/I/Élettani Intézet
dc.contributor.department SE/AOK/I/Kórélettani Intézet
dc.contributor.institution Semmelweis Egyetem


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