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AHR 5360C的心脏电生理效应。

Cardiac electrophysiologic effects of AHR 5360C.

作者信息

Viamonte V M, Hamra M, Rosen M R

机构信息

Department of Pharmacology, Columbia University, College of Physicians and Surgeons, New York, NY 10032.

出版信息

Eur J Pharmacol. 1988 Feb 9;146(2-3):215-22. doi: 10.1016/0014-2999(88)90295-6.

Abstract

We used microelectrode and blood superfusion techniques to study the cardiac electrophysiologic effects of a new drug, AHR 5360C, which has antihypertensive and calcium channel blocking properties in several experimental models. AHR 5360C, 10(-7) M significantly depressed the amplitude of the slow response action potential in canine Purkinje fibers. The fast response action potential was also depressed in a dose-dependent fashion, but with a threshold concentration of 5 X 10(-6) M. AHR 5360C decreased normal automaticity and barium-induced abnormal automaticity at concentrations of 5 X 10(-6) and 10(-5) M respectively, as well as ouabain-induced delayed afterdepolarizations at a threshold concentration of 10(-6) M. In blood superfusion studies; i.v. administration of AHR 5360C, 0.3 mg/kg, significantly reduced blood pressure. Doses of 1.0 mg/kg induced a high degree of A-V block, further reduction of blood pressure, and no physiological changes in heart rate and in the blood superfused fibers. In conclusion, AHR 5360C has calcium blocking properties that depress A-V conduction at concentrations that do not affect the sodium-dependent fast response action potential.

摘要

我们使用微电极和血液灌流技术来研究一种新药AHR 5360C的心脏电生理效应,该药在多个实验模型中具有降压和钙通道阻滞特性。10^(-7)M的AHR 5360C可显著降低犬浦肯野纤维慢反应动作电位的幅度。快反应动作电位也呈剂量依赖性降低,但阈值浓度为5×10^(-6)M。AHR 5360C分别在5×10^(-6)M和10^(-5)M的浓度下降低正常自律性和钡诱导的异常自律性,以及在10^(-6)M的阈值浓度下降低哇巴因诱导的延迟后除极。在血液灌流研究中,静脉注射0.3mg/kg的AHR 5360C可显著降低血压。1.0mg/kg的剂量可引起高度房室传导阻滞、血压进一步降低,且对心率和血液灌流纤维无生理变化。总之,AHR 5360C具有钙阻滞特性,在不影响钠依赖性快反应动作电位的浓度下可抑制房室传导。

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