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醋丁洛尔(M&B 17.803)在犬原位心脏中的血浆水平及电生理效应。

Plasma levels and electrophysiological effects of acebutolol (M & B 17.803) in the dog heart in situ.

作者信息

Amlie J P, Lessum S, Collins R F, Landmark K

出版信息

Acta Pharmacol Toxicol (Copenh). 1977 Mar;40(3):378-88.

PMID:190859
Abstract

The effect of acebutolol a beta-adrenergic receptor blocking agent was tested on the dog heart in situ. The drug decreased heart rate, and caused a reduction in the conduction velocity and a significant increase in the functional refractory period of the atrioventricular node. The functional and the effective refractory period of the right atrium was increased by acebutolol. During sinus rhythm, the drug did not affect conduction velocity in the rest of the conduction pathway. During atrial pacing, however, the intra-atrial and His-Purkinje conduction times were slightly increased. The plasma concentrations of acebutolol were in the range between 0.09 and 0.5 mug/ml, which is far below those values expected to cause a membrane-stabilizing or quinidine-like effect. The clinical applications of the results are discussed.

摘要

对阿替洛尔(一种β-肾上腺素能受体阻滞剂)在犬原位心脏上的作用进行了测试。该药物降低了心率,导致房室结的传导速度降低,功能性不应期显著延长。阿替洛尔使右心房的功能性和有效不应期延长。在窦性心律期间,该药物不影响传导系统其余部分的传导速度。然而,在心房起搏期间,心房内和希氏-浦肯野纤维的传导时间略有增加。阿替洛尔的血浆浓度在0.09至0.5微克/毫升之间,远低于预期会产生膜稳定或奎尼丁样效应的浓度值。文中讨论了这些结果的临床应用。

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