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Computerized measurement of MK-801-elicited popping and hyperactivity in mice.

R B Rosse, J Mastropaolo, D M Sussman, L Koetzner, C B Morn, S I Deutsch

Clinical neuropharmacology October 1, 1995 DOI: 10.1097/00002826-199510000-00008 via PubMed

Summary

AI-generated from the abstract

MK-801, a compound that blocks NMDA glutamate receptors, causes hyperactivity, repetitive behaviors, and explosive jumping (popping) in mice. A computerized system was developed to automatically measure popping and hyperactivity by detecting vertical platform movements. This method quantifies the number, force, and duration of jumps more precisely than human observation. The antipsychotic haloperidol significantly reduced both popping and hyperactivity caused by MK-801. The authors suggest this automated approach could improve preclinical screening of potential antipsychotic drugs and help clarify the mechanisms behind MK-801-induced behaviors.

Study at a glance

Characteristics Experimental study Peer reviewed
Population Mice
Interventions MK-801 haloperidol
Key finding A computerized method can automatically measure MK-801-elicited popping and hyperactivity in mice, and haloperidol significantly reduces these behaviors.

Abstract

MK-801, a high-affinity phencyclidine (PCP) analogue, is a noncompetitive antagonist of the N-methyl-D-aspartate (NMDA) subclass of glutamate receptor that elicits hyperactivity, stereotypic behaviors, and "popping," an explosive episodic jumping behavior, in mice. The schizophreniform psychosis precipitated by PCP in humans has stimulated interest in studying MK-801-elicited mouse behaviors for their potential development as animal models of idiopathic psychosis. We describe a computerized method for measuring popping and hyperactivity elicited by MK-801 in mice, based on vertical displacements of a platform. This computerized procedure allows for the automatic measurement of discrete "pops" per individual episode of popping behavior, the force of each one of the explosive jumps, and the duration of discrete episodes of popping; these latter measures could not be easily ascertained by visual inspection alone. Moreover, the computerized measurements facilitate quantitative evaluation of the effects of pharmacological manipulations on MK-801-elicited popping. For example, the antipsychotic haloperidol was shown to reduce significantly both MK-801-induced popping and hyperactivity. Ideally, MK-801-elicited mouse popping and hyperactivity will serve as a useful preclinical screening paradigm for potential antipsychotic medications. Additionally, it is hoped that the use of this automated system will contribute to a greater understanding of the mechanisms of MK-801-induced popping and hyperactivity.

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