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钙拮抗剂D - 600对青蛙骨骼肌纤维的麻痹作用

Paralysis of frog skeletal muscle fibres by the calcium antagonist D-600.

作者信息

Eisenberg R S, McCarthy R T, Milton R L

出版信息

J Physiol. 1983 Aug;341:495-505. doi: 10.1113/jphysiol.1983.sp014819.

Abstract

The Ca2+ channel blocker D-600 (methoxyverapamil) paralyses single muscle fibres of the frog: fibres exposed to the drug at 7 degrees C give a single K+ contracture after which they are paralysed, unable to contract in response to electrical stimulation or further applications of K+. Paralysed fibres contract in response to caffeine and have normal resting potentials and action potentials. Fibres treated with D-600 at 22 degrees C are not paralysed. Paralysed fibres warmed to 22 degrees C recover contractile properties: they twitch and give K+ contractures. Other workers have shown that D-600 blocks a Ca2+ channel at room temperature; thus, the paralytic action of D-600 is probably mediated by a different membrane protein, perhaps a different Ca2+ channel from that blocked at room temperature. These results suggest that the binding of D-600 can disrupt the mechanism coupling electrical potential changes across the T membrane to Ca2+ release from the sarcoplasmic reticulum.

摘要

钙离子通道阻滞剂D - 600(甲氧基维拉帕米)可使青蛙的单根肌纤维麻痹:在7摄氏度下暴露于该药物的肌纤维会产生一次钾离子收缩,之后便麻痹,无法对电刺激或进一步施加的钾离子作出收缩反应。麻痹的肌纤维对咖啡因有反应而收缩,且静息电位和动作电位正常。在22摄氏度下用D - 600处理的肌纤维不会麻痹。将麻痹的肌纤维升温至22摄氏度可恢复收缩特性:它们会抽搐并产生钾离子收缩。其他研究人员表明,D - 600在室温下会阻断一种钙离子通道;因此,D - 600的麻痹作用可能是由一种不同的膜蛋白介导的,也许是一种与在室温下被阻断的钙离子通道不同的钙离子通道。这些结果表明,D - 600的结合可能会破坏将T膜上的电位变化与肌浆网中钙离子释放相偶联的机制。

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