Suppr超能文献

麻醉机制:综述

Mechanisms of anaesthesia: a review.

作者信息

Roth S H

出版信息

Can Anaesth Soc J. 1980 Sep;27(5):433-9. doi: 10.1007/BF03007039.

Abstract

Anaesthesia is a drug-induced reversible perturbation of neuronal activity. Since a wide variety of structurally unrelated substances are capable of producing this phenomenon, it has been generally accepted that anaesthetics produce their effects through non-specific hydrophobic interactions. Results of recent studies in whole animal and cellular (membrane) preparations demonstrate that a unitary theory of action does not exist. Anaesthetics can produce a spectrum of activity in the central nervous system, and different agents produce different patterns of activity. At the cellular and membrane level, differential effects have been observed, structural dependent differences occur and optical isomers display very different activities. The perturbation (fluidity change) of membrane components does not appear to be uniform for all anaesthetics. It is concluded that anaesthetics are selective agents, and produce their effects at multiple sites and through a variety of mechanisms.

摘要

麻醉是药物诱导的神经元活动的可逆性扰动。由于多种结构不相关的物质都能够产生这种现象,人们普遍认为麻醉药通过非特异性疏水相互作用产生其效应。最近在全动物和细胞(膜)制剂中的研究结果表明不存在单一的作用理论。麻醉药可在中枢神经系统产生一系列活性,不同的药物产生不同的活性模式。在细胞和膜水平上,已观察到差异效应,出现结构依赖性差异,光学异构体表现出非常不同的活性。膜成分的扰动(流动性变化)似乎并非对所有麻醉药都是一致的。结论是麻醉药是选择性药物,通过多种机制在多个部位产生其效应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验