Effects of the NMDA antagonists CPP and MK-801 on delayed conditional discrimination

Psychopharmacology (Berl). 1989;98(4):556-60. doi: 10.1007/BF00441959.

Abstract

N-methyl-D-aspartate (NMDA) receptor/channel antagonists have previously been shown to impair spatial working memory and hippocampal long-term potentiation. The present experiment investigated the effects of a variety of doses of NMDA antagonists on a working memory task in rats involving an auditory delayed conditional discrimination. Signal detection analysis and an exponential memory decay model were used to extract independent measures of stimulus discriminability and rate of forgetting. A competitive NMDA antagonist, (CPP, 0.33, 1.0, 10.0 mg/kg, IP) produced a reduction in discriminability which was linearly related to log dose, but which was only clear at the 10 mg/kg dose. Rate of forgetting was not increased by any dose. Similar results were obtained with a non-competitive antagonist (MK-801, 0.1, 0.33 mg/kg, IP). These data suggest that doses of NMDA receptor channel antagonists sufficient to disrupt hippocampal long-term potentiation and radial arm maze performance will also disrupt delayed conditional discrimination. The effect on delayed conditional discrimination is due to a disruption of stimulus discriminability and not to an increased rate of forgetting. The extent to which these effects relate to the reported changes in hippocampal long-term potentiation and radial arm maze performance remains to be determined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticonvulsants / pharmacology*
  • Aspartic Acid / analogs & derivatives*
  • Aspartic Acid / antagonists & inhibitors
  • Dibenzocycloheptenes / pharmacology*
  • Discrimination, Psychological / drug effects*
  • Dizocilpine Maleate
  • Dose-Response Relationship, Drug
  • Male
  • N-Methylaspartate
  • Piperazines / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Stereotyped Behavior / drug effects

Substances

  • Anticonvulsants
  • Dibenzocycloheptenes
  • Piperazines
  • Aspartic Acid
  • N-Methylaspartate
  • Dizocilpine Maleate
  • 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid