Rollema H, Lu Y, Schmidt A W, Zorn S H
Pfizer Inc., Department of Neuroscience, Groton, CT 06340, USA.
Eur J Pharmacol. 1997 Nov 5;338(2):R3-5. doi: 10.1016/s0014-2999(97)81951-6.
Clozapine (1-10 mg/kg s.c.) produces a selective increase in dopamine release in rat prefrontal cortex which is, in large part (approximately 50%), mediated via activation of 5-HT1A receptors. Clozapine is a moderately potent, partial 5-HT1A receptor agonist and activation of 5-HT1A receptors may contribute to its efficacy against negative symptoms and reduced extrapyramidal side effect liability. Agonist affinity for 5-HT1A receptors could thus be a desirable feature in the design of new antipsychotics.
氯氮平(1-10毫克/千克,皮下注射)可使大鼠前额叶皮质中的多巴胺释放选择性增加,这在很大程度上(约50%)是通过5-羟色胺1A受体的激活介导的。氯氮平是一种中等效力的5-羟色胺1A受体部分激动剂,5-羟色胺1A受体的激活可能有助于其抗阴性症状的疗效,并降低锥体外系副作用的可能性。因此,对5-羟色胺1A受体的激动剂亲和力可能是新型抗精神病药物设计中一个理想的特性。