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维库溴铵及相关类似物在大鼠膈肌中产生强直后衰减所涉及机制的研究。

Examination of the mechanisms involved in tetanic fade produced by vecuronium and related analogues in the rat diaphragm.

作者信息

Gibb A J, Marshall I G

出版信息

Br J Pharmacol. 1987 Mar;90(3):511-21. doi: 10.1111/j.1476-5381.1987.tb11200.x.

Abstract

The effects of vecuronium (Org NC45), Org 7678 and Org 7684 were examined on twitches and tetani recorded from rat isolated diaphragms. Org 7678 and Org 7684 exhibited approximately one tenth of the neuromuscular blocking potency of vecuronium. At concentrations producing equivalent amounts of twitch block, Org 7684 produced significantly less tetanic fade than did vecuronium or Org 7678. In cut muscles both vecuronium and Org 7684 reduced the endplate current (e.p.c.) amplitude (Ie.p.c.), reduced e.p.c. decay time constant (tau e.p.c.), and increased the e.p.c. train rundown. The effects of vecuronium were not voltage-dependent and vecuronium did not change tau noise. The effect of Org 7684 on Ie.p.c. and tau e.p.c. became greater with hyperpolarization, but the effect on e.p.c. train rundown was not voltage-dependent. It is concluded that both vecuronium and Org 7684 produce e.p.c. train rundown and tetanic fade by a prejunctional mechanism. However, whereas postjunctionally vecuronium blocks only the acetylcholine receptor, Org 7684 blocks both the receptor and its associated ion channel.

摘要

研究了维库溴铵(Org NC45)、Org 7678和Org 7684对大鼠离体膈肌记录的单收缩和强直收缩的影响。Org 7678和Org 7684的神经肌肉阻滞效能约为维库溴铵的十分之一。在产生等量单收缩阻滞的浓度下,Org 7684引起的强直收缩衰减明显小于维库溴铵或Org 7678。在切断的肌肉中,维库溴铵和Org 7684均降低终板电流(e.p.c.)幅度(Ie.p.c.)、缩短e.p.c.衰减时间常数(tau e.p.c.)并增加e.p.c.串刺激衰减。维库溴铵的作用不依赖电压,且不改变tau噪声。Org 7684对Ie.p.c.和tau e.p.c.的作用随超极化而增强,但对e.p.c.串刺激衰减作用不依赖电压。结论是,维库溴铵和Org 7684均通过接头前机制产生e.p.c.串刺激衰减和强直收缩衰减。然而,在接头后,维库溴铵仅阻断乙酰胆碱受体,而Org 7684则同时阻断受体及其相关离子通道。

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