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[D-丙氨酸2、亮氨酸5、精氨酸6-脑啡肽(达洛啡肽)的心血管效应由外周μ-阿片受体激活介导]

[Cardiovascular effects of D-ALA2, LEU5, ARG6-enkephalin (dalargin) are mediated by peripheral mu-opioid receptor activation].

作者信息

Maslov L N, Lishmanov Iu B, Barzakh E I, Maksimov I V, Vorozgtsova I N, Bukhovets I L, Minin S M, Orlova E B, Lavrov A G, Ovchinnikov M V

出版信息

Eksp Klin Farmakol. 2008 Mar-Apr;71(2):21-8.

Abstract

It has been established that intravenous administration of dalargin at a dose of 0.1 mg/kg induced hypotensive, positive inotropic, and positive chronotropic response in patients with myocardial infarction, while not producing the "steal syndrome." The positive chronotropic effect of dalargin was mediated by peripheral mu-opioid receptors. Increase in the heart rate induced by dalargin had a reflex nature. Direct action of dalargin on the heart was accompanied by a decrease in the heart rate and a delay in the cardiac conductance in the atrioventricular junction region.

摘要

已经确定,以0.1mg/kg的剂量静脉注射达拉argin可使心肌梗死患者产生降压、正性肌力和正性变时反应,同时不会产生“窃血综合征”。达拉argin的正性变时作用是由外周μ-阿片受体介导的。达拉argin引起的心率增加具有反射性质。达拉argin对心脏的直接作用伴随着心率降低和房室交界区心脏传导延迟。

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