Oxiracetam and D-pyroglutamic acid antagonize a disruption of passive avoidance behaviour induced by the N-methyl-D-aspartate receptor antagonist 2-amino-5-phosphonovalerate

Psychopharmacology (Berl). 1990;100(1):130-1. doi: 10.1007/BF02245803.

Abstract

Intracerebroventricular administration (6 micrograms/2 microliters) of D-2-amino-5-phosphonovalerate (AP-5), a specific antagonist of the NMDA receptors, prior to training impaired the passive avoidance in a retention test in rat. Pretreatment with oxiracetam and D-pyroglutamic acid at doses ranging from 50 to 500 mg/kg SC dose-dependently prevented the disruptive effect of AP-5. This finding indicates that an interaction with excitatory amino acid NMDA type receptors may be important in behavioural effects of the two pyrrolidinone derivatives.

MeSH terms

  • Animals
  • Avoidance Learning / drug effects*
  • Injections, Intraventricular
  • Male
  • Motor Activity / drug effects
  • Pyrrolidines / pharmacology*
  • Pyrrolidinones / pharmacology*
  • Pyrrolidonecarboxylic Acid / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Neurotransmitter / drug effects*
  • Valine / analogs & derivatives*
  • Valine / antagonists & inhibitors
  • Valine / pharmacology

Substances

  • Pyrrolidines
  • Pyrrolidinones
  • Receptors, N-Methyl-D-Aspartate
  • Receptors, Neurotransmitter
  • 2-amino-5-phosphopentanoic acid
  • Valine
  • oxiracetam
  • Pyrrolidonecarboxylic Acid