Characterization of MK-801-induced behavior as a putative rat model of psychosis

J Pharmacol Exp Ther. 1999 Sep;290(3):1393-408.

Abstract

The objective of this study was to characterize the behavior induced by the N-methyl-D-aspartate receptor antagonist MK-801 (dizocilpine maleate) in rats as a model of psychosis. The temporal profile, dose dependence, age, and sex differences of the behavior are described. A gas chromatographic method for the analysis of MK-801 in plasma and brain was developed. Female rats showed 4 to 10 times more MK-801-induced behavior and displayed around 25 times higher serum and brain concentrations of MK-801 than male rats. Twenty-one neuroactive compounds, including a number of excitatory amino acid-active substances, were tested for the effect on MK-801-induced behavior. Neuroleptics blocked MK-801-induced behavior in a dose-dependent manner that correlated to their antipsychotic potency in humans. Adenosine receptor agonists and an N-methyl-D-aspartate receptor-associated glycine site antagonist showed putative antipsychotic effects. In conclusion, MK-801-induced behavior represents a rat excitatory amino acid hypofunction model of psychosis that appears to be of clinical relevance and may be of value in the search for new antipsychotic agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / drug effects
  • Animals
  • Brain / metabolism
  • Disease Models, Animal
  • Dizocilpine Maleate / antagonists & inhibitors
  • Dizocilpine Maleate / blood
  • Dizocilpine Maleate / pharmacology*
  • Dose-Response Relationship, Drug
  • Excitatory Amino Acid Antagonists / pharmacology*
  • Female
  • GABA Antagonists / pharmacology
  • Isoxazoles / pharmacology
  • Male
  • Motor Activity / drug effects
  • Psychoses, Substance-Induced / etiology*
  • Psychoses, Substance-Induced / physiopathology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA / physiology
  • Sex Characteristics
  • Stereotyped Behavior / drug effects*
  • Stereotypic Movement Disorder / chemically induced

Substances

  • Excitatory Amino Acid Antagonists
  • GABA Antagonists
  • Isoxazoles
  • Receptors, GABA
  • Dizocilpine Maleate
  • acivicin