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A rapid method for evaluating the behavioral effects of phencyclidine-like dissociative anesthetics in mice.

G E Evoniuk, R P Hertzman, P Skolnick

Psychopharmacology 1991 DOI: 10.1007/bf02316874 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Mice
Interventions Phencyclidine dizolcipine competitive NMDA antagonists sigma-receptor ligands glycine
Key findings Dissociative anesthetics binding to NMDA-coupled cation channels produced a dose-related increase in mice falling from a platform, while other compounds did not, and glycine pretreatment reduced this effect.

Abstract

A simple and rapid method for detecting the behavioral effects of phencyclidine and related dissociative anesthetics is described. Dissociative anesthetics such as phencyclidine (PCP) and dizolcipine, which bind with high affinities at N-methyl-D-aspartate (NMDA) coupled cation channels ("PCP receptors"), produced a dose-related increase in the percentage of mice that fell from a 1.5 cm deep circular arena mounted on a 60 cm platform. A similar behavior was not manifest by other classes of compounds examined including competitive NMDA antagonists, an antagonist at strychnine-insensitive glycine receptors, and sigma-receptor ligands with moderate to low affinities for PCP receptors. Pretreatment of mice with glycine reduced in a dose-dependent manner the percentage of falls elicited by a maximally effective dose of dizolcipine. This simple procedure may prove useful for both the rapid detection of dissociative anesthetics and evaluation of putative PCP antagonists.