Belelli D, Pistis M, Peters J A, Lambert J J
Department of Pharmacology and Neuroscience, Ninewells Hospital and Medical School, University of Dundee, Dundee, UK DD1 9SY.
Trends Pharmacol Sci. 1999 Dec;20(12):496-502. doi: 10.1016/s0165-6147(99)01405-4.
Research within the past decade has provided compelling evidence that anaesthetics can act directly as allosteric modulators of transmitter-gated ion channels. Recent comparative studies of the effects of general anaesthetics across a structurally homologous family of inhibitory amino acid receptors that includes mammalian GABAA, glycine and Drosophila RDL GABA receptors have provided new insights into the structural basis of anaesthetic action at transmitter-gated channels. In this article, the differential effects of general anaesthetics across inhibitory amino acid receptors and the potential relevance of such actions to general anaesthesia will be discussed.
过去十年的研究提供了令人信服的证据,表明麻醉剂可直接作为递质门控离子通道的变构调节剂。最近对包括哺乳动物GABAA、甘氨酸受体以及果蝇RDL GABA受体在内的抑制性氨基酸受体这一结构同源家族进行的全身麻醉药作用的比较研究,为全身麻醉药在递质门控通道上作用的结构基础提供了新的见解。本文将讨论全身麻醉药对抑制性氨基酸受体的不同作用以及这些作用与全身麻醉的潜在相关性。