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Cardioprotective effect of benidipine on cardiac performance and remodeling in failing rat hearts.

Cardioprotective effect of benidipine on cardiac performance and remodeling in failing rat hearts. Research Abstract Details 

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  • Cardioprotective effect of benidipine on cardiac performance and remodeling in failing rat hearts. Abstract Text:

    tomoyuki ohnoTomoyuki Ohno,naohiko kobayashiNaohiko Kobayashi,kohtaro yoshidaKohtaro Yoshida,hiromichi fukushimaHiromichi Fukushima,hiroaki matsuokaHiroaki Matsuoka,tomoyuki ohnoTomoyuki Ohno,naohiko kobayashiNaohiko Kobayashi,kohtaro yoshidaKohtaro Yoshida,hiromichi fukushimaHiromichi Fukushima,hiroaki matsuokaHiroaki Matsuoka,

    BackgroundWe have known that endothelial nitric-oxide synthase (eNOS) and oxidative stress may play a key role in cardiac performance in failing rat hearts. However, the interactions between eNOS or oxidative stress and bradykinin (BK) under treatment of calcium channel blockers (CCBs) remain unknown. To elucidate the mechanism underlying the cardioprotective effect of long-acting dihydropyridine CCBs, we evaluated the effect of benidipine on the BK-eNOS and NAD(P)H oxidase pathway in Dahl salt-sensitive (DS) rats with heart failure.Methods11-week-old DS rats were treated with one of the following drug combinations for 7 weeks until the onset of the failing stage: vehicle, BK B2 receptor antagonist (FR172357 (FR)) alone, hydralazine, benidipine, and benidipine plus FR. The left ventricular end-systolic pressure-volume relationship (ESPVR) (contractility: Ees) was evaluated using a conductance catheter.ResultsDownregulated Ees and per cent of fractional shortening (%FS) assessed by echocardiography and eNOS expression in the failing stage were both significantly increased by using benidipine; this result was not found, however, when using FR alone or hydralazine or benidipine plus FR. Upregulated expression of NAD(P)H oxidase p22phox and p47phox and lectin-like oxidized low-density lipoprotein receptor-1, and downregulated superoxide dismutase-1 (SOD-1) were significantly ameliorated by benidipine, but not by FR alone or by hydralazine or benidipine plus FR. Benidipine effectively inhibited vascular lesion formation and suppressed atrial natriuretic peptide (ANP) and transforming growth factor-beta1 (TGF-beta1), but this was not the case when using FR alone or hydralazine or benidipine plus FR.ConclusionsThese results suggest that benidipine may be useful for cardioprotective agents in preventing the cardiac dysfunction and remodeling associated with the BK-eNOS and oxidative stress pathway.American Journal of Hypertension (2008);21 2. 224-230. doi:10.1038/ajh.2007.51American Journal of Hypertension (2008);21 2. 224-230. doi:10.1038/ajh.2007.51.

    Cardioprotective effect of benidipine on cardiac performance and remodeling in failing rat hearts. Publishing Authors By Initials

    t ohnoT Ohno,n kobayashiN Kobayashi,k yoshidaK Yoshida,h fukushimaH Fukushima,h matsuokaH Matsuoka,t ohnoT Ohno,n kobayashiN Kobayashi,k yoshidaK Yoshida,h fukushimaH Fukushima,h matsuokaH Matsuoka,

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    Cardioprotective effect of benidipine on cardiac performance and remodeling in failing rat hearts. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: American journal of hypertension : journal of the

    VOLUME: 21

    Page Numbers: 224-30

    Journal Abbreviation: Am. J. Hypertens.

    ISSN: 0895-7061

    DAY: 10

    MONTH: 01

    YEAR: 2008

    Cardioprotective effect of benidipine on cardiac performance and remodeling in failing rat hearts. Information

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    LANGUAGE: eng

    NlmUniqueID: 8803676

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    Grant and Affiliation Information for Cardioprotective effect of benidipine on cardiac performance and remodeling in failing rat hearts.

    AFFILIATION: 1Department of Hypertension and Cardiorenal Medicine, Dokkyo University School of Medicine, Mibu, Tochigi, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Am J Hypertens

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