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对箭毒在运动终板作用的重新审视。

A re-examination of curare action at the motor endplate.

作者信息

Katz B, Miledi R

出版信息

Proc R Soc Lond B Biol Sci. 1978 Dec 4;203(1151):119-33. doi: 10.1098/rspb.1978.0096.

Abstract

Recent evidence indicates that curare, in addition to its competitive' interference with endplate receptors, can block open ionic channels by a 'non-competitive' action on the activated acetylcholine-receptor complex. These findings called for further study of the kinetic behaviour of endplate channels and their modification by curare. Examining impulse-evoked endplate currents and acetylcholine-induced current fluctuations, it is found that the lifetime of the open channel is shortened by relatively high concentrations of curare (greater than 5 micrometer), an effect which shows up most strikingly at hyperpolarized levels of membrane potential (-130 mV and above). No shortening of this kind is observed when a neuromuscular block of equal or greater intensity is produced by a dose of alpha-bungarotoxin. Two other neuromuscular blocking agents, gallamine and pancuronium are shown to have an action on channel kinetics which cannot be explained by competitive receptor binding, but conforms to the hypothesis of rapidly repeated blocking and unblocking of individual ion channels, which had been proposed originally to account for the endplate action of local anaesthetics.

摘要

最近有证据表明,箭毒除了对终板受体有竞争性干扰外,还可通过对激活的乙酰胆碱受体复合物的“非竞争性”作用来阻断开放的离子通道。这些发现促使人们进一步研究终板通道的动力学行为及其被箭毒修饰的情况。通过检测冲动诱发的终板电流和乙酰胆碱诱导的电流波动发现,相对高浓度的箭毒(大于5微摩尔)会缩短开放通道的寿命,这种效应在超极化膜电位水平(-130毫伏及以上)最为明显。当用一定剂量的α-银环蛇毒素产生同等强度或更强强度的神经肌肉阻滞时,未观察到这种缩短现象。另外两种神经肌肉阻滞剂加拉明和泮库溴铵对通道动力学有作用,这种作用不能用竞争性受体结合来解释,但符合最初为解释局部麻醉药的终板作用而提出的关于单个离子通道快速反复阻断和解除阻断的假说。

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