THE EFFECT OF CLOZAPINE ON FOS PROTEIN IMMUNOREACTIVITY IN THE RAT FOREBRAIN IS NOT MIMICKED BY THE ADDITION OF ALPHA(1)-ADRENERGIC OR 5HT(2) RECEPTOR BLOCKADE TO HALOPERIDOL

The involvement of alpha(1)-adrenergic and 5HT(2)-receptor blockade in the induction of Fos protein produced by the 'atypical' neuroleptic clozapine was investigated in the rat forebrain. The Fos protein immunohistochemical technique has been used to identify the anatomical substrate underlying the effects of typical and atypical neuroleptics. Clozapine (20 mg/kg) induced a significantly higher Fos protein immunoreactivity response in the medial prefrontal cortex and a significantly lower response in the dorsolateral striatum compared to the effect of haloperidol (1 mg/kg). The alpha(1)-adrenergic antagonist prazosin (0.3 and 1.0 mg/kg) and the 5HT(2) antagonist ritanserin (1 and 3 mg/kg) did not increase Fos protein immunoreactivity by themselves and did not mimic the clozapine response when co-administered with haloperidol (1 mg/kg). Consequently, this study suggests that neither alpha(1)-adrenergic receptor blockade nor the 5HT(2)-receptor blockade accounts for the unique Fos protein expression pattern produced by clozapine.