Comparative dopaminergic and muscarinic antagonist activity of clozapine and haloperidol

Life Sci. 1996;58(7):585-90. doi: 10.1016/0024-3205(95)02327-5.

Abstract

Clozapine is an atypical antipsychotic drug, and its dopamine and muscarinic antagonist activity has been compared with haloperidol in rodents. Elevation in rat striatal acetylcholine (ACh) and mice cerebellar cGMP has been used as an agonist response for oxotremorine and quinpirole. Pretreatment with clozapine significantly blocked oxotremorine-induced elevation in striatal ACh (p<0.01) and cerebellar cGMP(p<0.05). At the same doses, clozapine had no significant effect on quinpirole-induced increases in ACh and cGMP levels. Pretreatment with haloperidol significantly antagonized quinpirole-induced elevation in striatal ACh (p<0.01) and cerebellar cGMP(p<0.05), and haloperidol had no significant effect on oxotremorine-induced agonist responses. Thus, clozapine is antimuscarinic at a dose level that lacks dopamine antagonist properties, whereas haloperidol is a dopamine antagonist and lacks antimuscarinic activity. The atypical neuroleptic profile of clozapine may be due to its high antimuscarinic and low antidopaminergic activity.

Publication types

  • Comparative Study

MeSH terms

  • Acetylcholine / metabolism
  • Animals
  • Cerebellum / drug effects
  • Cerebellum / metabolism
  • Clozapine / pharmacology*
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism
  • Cyclic GMP / metabolism
  • Dopamine Antagonists / pharmacology*
  • Ergolines / pharmacology
  • Haloperidol / pharmacology*
  • Male
  • Mice
  • Muscarinic Antagonists / pharmacology*
  • Oxotremorine / pharmacology
  • Quinpirole
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Dopamine Antagonists
  • Ergolines
  • Muscarinic Antagonists
  • Quinpirole
  • Oxotremorine
  • Cyclic GMP
  • Clozapine
  • Haloperidol
  • Acetylcholine