组胺H1受体阻滞剂芬卡罗抗心律失常的实验研究。

Farmakologiia i toksikologiia Pub Date : 1991-09-01
G M Iakovlev, V I Skorobogatov, A S Svistov, M I Mironova
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引用次数: 0

摘要

芬卡罗是一种h1 -组胺受体阻滞剂,被用作抗组胺剂。采用非麻醉家兔心律失常实验模型,静脉给药5 mg/kg,检测和研究酚卡洛尔的抗心律失常作用。该药物对氯化钙、肾上腺素和斯特芬碱诱发的心律失常模型具有明显的抗心律失常和保护作用,而对乌头碱诱发的心律失常无影响。非卡洛尔被证明没有心脏抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The experimental anti-arrhythmia properties of the histamine H1 receptor blockader fencarol].

Phencarol, a blocker of H1-histamine receptors, is used as an antihistaminic agent. The antiarrhythmic effect of phencarol was detected and studied on experimental models of arrhythmias in non-anesthetized rabbits in a dose of 5 mg/kg intravenously. The drug was shown to possess the pronounced antiarrhythmic and protective properties on the models of calcium-chloride-, adrenaline- and strophanthine-induced arrhythmias and to exert no influence on aconitine-induced arrhythmia. Phencarol was demonstrated to have no cardiodepressive effect.

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