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[奥昔非君抗心绞痛作用的机制]

[Mechanism of the antianginal action of oxyfedrine].

作者信息

Chichkanov G G, Chumburidze V B

出版信息

Farmakol Toksikol. 1977 May-Jun;40(3):302-6.

PMID:20326
Abstract

Oxyphedrine was found to depress the tonicity of coronary vessels, increase the coronary circulation volume, the oxygen uptake by the heart and also to exert a positive inoand chronotropic action in test with urethan and cloralose anesthetized cats. These effects were caused by stimulation of the beta-adrenoreceptors of the heart and vessels. In non-anesthetized cats oxyphedrine did not produce tachycardia. Furthermore, under certain conditions (when superimposed on a preliminary administration of practolol- a beta-blocking agent) oxyphedrine can exert a direct inhibitory action on the myocardium.

摘要

在对氨基甲酸乙酯和氯醛糖麻醉的猫进行的试验中,发现去氧麻黄碱可降低冠状血管的张力,增加冠脉循环血量、心脏的摄氧量,还可产生正性肌力和变时作用。这些效应是由刺激心脏和血管的β-肾上腺素能受体引起的。在未麻醉的猫中,去氧麻黄碱不会引起心动过速。此外,在某些条件下(当预先给予β受体阻滞剂心得宁时),去氧麻黄碱可对心肌产生直接抑制作用。

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