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维拉帕米光学异构体对离体犬心脏窦房结起搏活动及收缩性的影响。

Effects of optical isomers of verapamil on SA nodal pacemaker activity and contractility of the isolated dog heart.

作者信息

Chiba S, Kobayashi M, Furukawa Y

出版信息

Jpn Heart J. 1978 May;19(3):409-14. doi: 10.1536/ihj.19.409.

Abstract

Using 10 isolated, blood-perfused canine atrial, and ventricular preparations, the effects of d- and l-verapamil on SA nodal pacemaker activity and contractility were investigated. l-verapamil and d-verapamil produced dose-related negative chronotropic and inotropic effects in all experiments. l-verapamil was approximately 10 time more potent than d-verapamil both in inotropism and chronotropism. Negative inotropism of either d- or l-verapamil can be reversed by injection of calcium chloride. Not only d-verapamil but also l-verapamil produced a stronger suppression at higher frequencies in both atrial and ventricular muscles.

摘要

利用10个分离的、血液灌注的犬心房和心室标本,研究了d-维拉帕米和l-维拉帕米对窦房结起搏活动和收缩性的影响。在所有实验中,l-维拉帕米和d-维拉帕米均产生剂量相关的负性变时和变力作用。l-维拉帕米在变力作用和变时作用方面的效力约为d-维拉帕米的10倍。注射氯化钙可逆转d-或l-维拉帕米的负性变力作用。d-维拉帕米和l-维拉帕米在较高频率时对心房和心室肌均产生更强的抑制作用。

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