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组胺诱导的负性肌力作用:由H1受体介导。

Histamine-induced negative inotropism: mediation by H1-receptors.

作者信息

Zavecz J H, Levi R

出版信息

J Pharmacol Exp Ther. 1978 Aug;206(2):274-80.

PMID:682111
Abstract

Histamine is known to enhance left ventricular contractility in the guinea-pig heart by interacting with H2-receptors. We have observed that when the H2-receptor antagonists metiamide and cimetidine (3 X 10(-6) and 10(-5) M) block the positive inotropic effect of histamine, a negative inotropic effect is unmasked. This negative inotropic effect is independent of changes in rate or coronary flow, is mimicked by the selective histamine H1-receptor agonists, pyridylethylamine and thiazolylethylamine (0.3--30 microgram) and is abolished by the H1-receptor antagonist chlorpheniramine (10(-7) and 10(-6) M). Thus, the negative inotropic effect of histamine appears to be mediated by H1-receptors. Our results demonstrate that the inotropic response to histamine consists of two opposing components: an increase in contraction, mediated by H2-receptors, and a decrease in contraction, mediated by H1-receptors.

摘要

已知组胺通过与H2受体相互作用增强豚鼠心脏的左心室收缩力。我们观察到,当H2受体拮抗剂甲硫米特和西咪替丁(3×10⁻⁶和10⁻⁵M)阻断组胺的正性肌力作用时,一种负性肌力作用就会显现出来。这种负性肌力作用与心率或冠脉血流的变化无关,可被选择性组胺H1受体激动剂吡啶乙胺和噻唑乙胺(0.3 - 30微克)模拟,并被H1受体拮抗剂氯苯那敏(10⁻⁷和10⁻⁶M)消除。因此,组胺的负性肌力作用似乎是由H1受体介导的。我们的结果表明,对组胺的肌力反应由两个相反的成分组成:由H2受体介导的收缩增强,以及由H1受体介导的收缩减弱。

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