Lodge D, Mercier M S
Centre for Synaptic Plasticity, School of Physiology and Pharmacology, University of Bristol, Bristol, UK.
Br J Pharmacol. 2015 Sep;172(17):4254-76. doi: 10.1111/bph.13222. Epub 2015 Jul 28.
The history of ketamine and phencyclidine from their development as potential clinical anaesthetics through drugs of abuse and animal models of schizophrenia to potential rapidly acting antidepressants is reviewed. The discovery in 1983 of the NMDA receptor antagonist property of ketamine and phencyclidine was a key step to understanding their pharmacology, including their psychotomimetic effects in man. This review describes the historical context and the course of that discovery and its expansion into other hallucinatory drugs. The relevance of these findings to modern hypotheses of schizophrenia and the implications for drug discovery are reviewed. The findings of the rapidly acting antidepressant effects of ketamine in man are discussed in relation to other glutamatergic mechanisms.
本文回顾了氯胺酮和苯环己哌啶的历史,从它们作为潜在临床麻醉剂的开发,到滥用药物、精神分裂症动物模型,再到潜在的速效抗抑郁药。1983年发现氯胺酮和苯环己哌啶的N-甲基-D-天冬氨酸(NMDA)受体拮抗特性,是理解它们药理学的关键一步,包括它们在人体中的拟精神病效应。这篇综述描述了这一发现的历史背景和过程,以及它向其他致幻药物的扩展。本文还回顾了这些发现与现代精神分裂症假说的相关性以及对药物发现的意义。文中讨论了氯胺酮在人体中的速效抗抑郁作用的发现与其他谷氨酸能机制的关系。