Wirtshafter D
Department of Psychology, University of Illinois at Chicago 60607-7137, USA.
Eur J Pharmacol. 1998 Oct 9;358(3):R1-3. doi: 10.1016/s0014-2999(98)00652-9.
Previous studies have shown that the atypical neuroleptic clozapine is less potent at inducing Fos expression in the dorsolateral striatum than are typical neuroleptics. We report here that pretreatment with clozapine (5-20 mg/kg) actually attenuates the striatal Fos expression induced by the typical neuroleptics haloperidol and raclopride. These results suggest clozapine has pharmacological properties which actively antagonize the effects of dopamine D2 receptor blockade on striatal immediate-early gene expression.
先前的研究表明,非典型抗精神病药物氯氮平在诱导背外侧纹状体Fos表达方面的效力低于典型抗精神病药物。我们在此报告,用氯氮平(5 - 20毫克/千克)预处理实际上会减弱典型抗精神病药物氟哌啶醇和雷氯必利诱导的纹状体Fos表达。这些结果表明氯氮平具有药理学特性,可积极拮抗多巴胺D2受体阻断对纹状体即刻早期基因表达的影响。