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环境刺激与抗精神病药物对前脑c-fos激活作用之间的相互作用。

Interactions between environmental stimulation and antipsychotic drug effects on forebrain c-fos activation.

作者信息

Murphy C A, Feldon J

机构信息

Behavioral Neurobiology Laboratory, Swiss Federal Institute of Technology (ETH-Zurich), Schorenstrasse 16, CH-8603, Schwerzenbach, Switzerland.

出版信息

Neuroscience. 2001;104(3):717-30. doi: 10.1016/s0306-4522(01)00110-5.

DOI:10.1016/s0306-4522(01)00110-5
PMID:11440804
Abstract

The immediate-early gene product Fos is differentially induced in the rat brain by the antipsychotic drugs haloperidol and clozapine. It is often claimed that although both drugs induce Fos in the nucleus accumbens, haloperidol but not clozapine increases Fos-like immunoreactivity in the striatum, whereas clozapine but not haloperidol increases Fos-like immunoreactivity in prefrontal cortex. Investigations of antipsychotic drug effects on Fos have typically administered high doses with pronounced sedative effects to behaviorally naive animals. In the present study, we compared the effects of low doses of haloperidol (0.1 mg/kg) and clozapine (5 mg/kg) on Fos-like immunoreactivity in rats which were either behaviorally naive, exposed to a novel environment or tested for two-way active avoidance. We determined that haloperidol increased Fos in the striatum and nucleus accumbens regardless of testing condition whereas clozapine markedly reduced the induction of Fos by behavioral testing in these regions; moreover, haloperidol dramatically increased prefrontal cortical Fos expression in animals placed in a novel environment, but not in testing-naive controls. From these results we suggest that antipsychotic drug-induced patterns of Fos expression in the rat are highly dependent on animals' concurrent behavioral status, perhaps reflecting neuroanatomically specific interactions between antipsychotic drugs and environmental stressors which also may occur in the schizophrenic condition.

摘要

抗精神病药物氟哌啶醇和氯氮平在大鼠脑中对即早基因产物Fos的诱导存在差异。人们常称,尽管两种药物都能在伏隔核中诱导Fos表达,但氟哌啶醇而非氯氮平会增加纹状体中Fos样免疫反应性,而氯氮平而非氟哌啶醇会增加前额叶皮质中的Fos样免疫反应性。以往关于抗精神病药物对Fos影响的研究通常给行为未成熟的动物施用具有明显镇静作用的高剂量药物。在本研究中,我们比较了低剂量氟哌啶醇(0.1毫克/千克)和氯氮平(5毫克/千克)对行为未成熟、暴露于新环境或接受双向主动回避测试的大鼠Fos样免疫反应性的影响。我们确定,无论测试条件如何,氟哌啶醇都会增加纹状体和伏隔核中的Fos表达,而氯氮平在这些区域通过行为测试显著降低Fos的诱导;此外,氟哌啶醇会显著增加置于新环境中的动物前额叶皮质Fos的表达,但在未进行测试的对照动物中则不会。从这些结果我们推测,抗精神病药物在大鼠中诱导的Fos表达模式高度依赖于动物同时存在的行为状态,这可能反映了抗精神病药物与环境应激源之间神经解剖学上特定的相互作用,而这种相互作用在精神分裂症状态下也可能发生。

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