We have characterized excitatory effects of non-competitive NMDA receptor antagonists MK-801, PCP, and ketamine in the rat entorhinal cortex and in cultured primary entorhinal cortical neurons using expression of immediate early gene c-fos as nit indicator. NMDA receptor antagonists produced a strong and nose-dependent increase in c-fos mRNA and protein expression confined to neurons in the layer III of the caudal entorhinal cortex. Induction of c-fos mRNA is delayed and it is inhibited by antipsychotic drugs. Cultured entorhinal neurons are killed by high doses of MK-801 and PCP but c-fos expression is Mot induced in these neurons indicating that this in vitro model noes not fully replicate the in vivo effects of PCP-like drugs in the entorhinal cortex. Excitatory effects of the NMDA receptor antagonists may be connected with the psychotropic sine effects of these drugs and might become a useful model system to investigate neurobiology of psychosis. (C) 1999 American College of Neuropsychopharmacology. Published by Elsevier Science Inc.