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Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts.

Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts. Research Abstract Details 

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  • Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts. Abstract Text:

    satoshi yamamotoSatoshi Yamamoto,noriko matsumotoNoriko Matsumoto,mitsuo kanazawaMitsuo Kanazawa,marie fujitaMarie Fujita,masanori takaokaMasanori Takaoka,yasuo matsumuraYasuo Matsumura,

    We investigated the role of endothelin-A (ETA) and endothelin-B (ETB) receptors in ischemia/reperfusion-induced cardiac dysfunction and norepinephrine overflow using isolated rat hearts. According to the Langendorff technique, isolated hearts were subjected to 40 minutes of global ischemia followed by 30 minutes of reperfusion. Ischemia/reperfusion led to decreases in left ventricular developed pressure and coronary flow, and an increase in left ventricular end-diastolic pressure compared with pre-ischemic basal levels. An ETB receptor antagonist A-192621 at 1 microM worsened ischemia/reperfusion-induced cardiac dysfunction. In contrast, an ETA receptor antagonist ABT-627 at 5 microM with or without A-192621 improved the aforementioned cardiac dysfunction, to the same extent. Norepinephrine was massively released in coronary effluent from the hearts exposed to ischemia/ reperfusion. Treatment with ABT-627 significantly suppressed the norepinephrine overflow induced by the ischemia/reperfusion whereas A-192621 further enhanced it, which was completely abolished by the concomitant treatment with ABT-627. These results suggest that the detrimental effect of ETB receptor blockade on post-ischemic cardiac function is mediated by the ETA receptor-related action and that norepinephrine overflow from sympathetic nerve endings is closely related to the antagonist-induced functional changes of post-ischemic hearts.

    Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts. Publishing Authors By Initials

    s yamamotoS Yamamoto,n matsumotoN Matsumoto,m kanazawaM Kanazawa,m fujitaM Fujita,m takaokaM Takaoka,y matsumuraY Matsumura,

    For similar abstracts research abstracts see: abstracts research

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    Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of cardiovascular pharmacology

    VOLUME: 44 Suppl 1

    Page Numbers: S394-7

    Journal Abbreviation: J. Cardiovasc. Pharmacol.

    ISSN: 1533-4023

    DAY: 19

    MONTH: Nov

    YEAR: 2004

    Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts. Information

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    LANGUAGE: eng

    NlmUniqueID: 7902492

    Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts. Keywords Mesh Terms:

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    Grant and Affiliation Information for Effects of ET(A) and ET(B) receptor blockade on post-ischemic cardiac dysfunction and norepinephrine overflow in isolated rat hearts.

    AFFILIATION: Department of Pharmacology, Osaka University of Pharmaceutical Sciences, Takatsuki, Osaka, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Cardiovasc Pharmacol

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