Nucleus accumbens NMDA antagonist decreases locomotor activity produced by cocaine, heroin or accumbens dopamine, but not caffeine

Pharmacol Biochem Behav. 1991 Dec;40(4):841-5. doi: 10.1016/0091-3057(91)90095-j.

Abstract

Glutamatergic afferents to the nucleus accumbens (NAC) have been suggested to modulate psychostimulant-induced locomotor activation. The purpose of this study was 1) to determine the importance of nucleus accumbens N-methyl-D-aspartate (NMDA) glutamate receptors in the control of psychostimulant-induced locomotion, 2) to determine whether NMDA receptor modulation of psychostimulant-induced locomotion occurs presynaptic to or postsynaptic to NAC dopamine terminals, and 3) to determine whether NMDA receptors also modulate opiate- and caffeine-induced locomotor activation. For this purpose, rats treated with cocaine (10 mg/kg IP), dopamine (20 micrograms directly into the NAC), heroin (0.5 mg/kg SC), or caffeine (10 mg/kg SC) were challenged with intra-NAC microinfusion of 2-amino-5-phosphonovaleric acid (APV), a selective NMDA receptor antagonist. APV reduced locomotor activation induced by cocaine, heroin and intra-NAC dopamine, but not caffeine. These results suggest that NAC glutamate modulates psychomotor stimulation at the level of the NAC through an interaction with the integrated output of this region.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 2-Amino-5-phosphonovalerate / pharmacology*
  • Animals
  • Caffeine / pharmacology
  • Cocaine / pharmacology
  • Dopamine / metabolism
  • Glutamates / metabolism
  • Glutamic Acid
  • Heroin / pharmacology
  • Male
  • Motor Activity / drug effects*
  • Motor Activity / physiology
  • Nucleus Accumbens / drug effects
  • Nucleus Accumbens / physiology
  • Rats
  • Rats, Inbred Strains
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*

Substances

  • Glutamates
  • Receptors, N-Methyl-D-Aspartate
  • Caffeine
  • Glutamic Acid
  • Heroin
  • 2-Amino-5-phosphonovalerate
  • Cocaine
  • Dopamine