The present study assessed the interactions between N-methyl-D-aspartate (N
MDA) agonists or antagonists and the discriminative stimulus effects of amp
hetamine. Adult male Sprague-Dawley rats were trained to discriminate 0.5 m
g/kg i.p.) of amphetamine from saline under a two-lever fixed-ratio schedul
e of food reinforcement. During test sessions, i.p. injections of the glyci
ne site agonist D-cycloserine, the ion-channel blocker dizocilpine and the
competitive antagonist CGP 43487 were coadministered with i.p. saline or wi
th a full range of doses of amphetamine. D-Cycloserine did not substitute f
or amphetamine and attenuated the cueing effects of the drug. Both dizocilp
ine and CGP 43487 engendered intermediate levels of amphetamine-appropriate
responses and potentiated the stimulus properties of amphetamine; however,
the effects of CGP 43487 were very small and not dose-dependent. In an anc
illary experiment, the training dose of amphetamine was reduced to 0.25 mg/
kg; under these conditions dizocilpine, but not CGP 43487, produced full su
bstitution for the discriminative stimulus effects of amphetamine. These re
sults show that drugs affecting NMDA receptor-based neurotransmission can m
odulate the discriminative stimulus effects of amphetamine. (C) 2001 Lippin
cott Williams & Wilkins.