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Ketamine and phencyclidine: the good, the bad and the unexpected.

D Lodge, M S Mercier

British Journal of Pharmacology September 2015 DOI: 10.1111/bph.13222 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Topics Esketamine Ketamine
Key findings The review argues that the 1983 discovery of ketamine's and phencyclidine's NMDA receptor antagonist properties was a key step in understanding their pharmacology, including their psychotomimetic effects in humans. It contends that these findings are relevant to modern hypotheses of schizophrenia and to drug discovery, and discusses ketamine's rapid antidepressant effects in humans in relation to other glutamatergic mechanisms.

Abstract

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.

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