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氯氮平而非氟哌啶醇治疗可逆转亚慢性苯环利定诱导的条件性辨别行为破坏。

Clozapine but not haloperidol treatment reverses sub-chronic phencyclidine-induced disruption of conditional discrimination performance.

作者信息

Dunn Michael J, Killcross Simon

机构信息

Department of Health and Social Sciences (Psychology), University of Wales Institute Cardiff , Llandaff Campus, Western Avenue, Cardiff CF5 2SG, United Kingdom.

出版信息

Behav Brain Res. 2006 Dec 15;175(2):271-7. doi: 10.1016/j.bbr.2006.08.028. Epub 2006 Oct 5.

Abstract

Abusers of phencyclidine (PCP) often present with a symptom profile similar to that exhibited by schizophrenic patients. Animal models utilising such psychotomimetics are currently informing research into the condition. Accumulating evidence suggests that a central cognitive deficit in schizophrenia is the inability to use task-setting cues to guide goal directed behaviour and that this ability is mediated by prefrontal dopamine (DA). The current study used the non-competitive NMDA antagonist phencyclidine (PCP) and Haloperidol (typical antipsychotic) and Clozapine (atypical antipsychotic) in order to further investigate the influence of DAergic manipulation on a task that requires the use of conditional information to inform goal-directed performance. An instrumental conditional discrimination task was employed in which rats learn to respond appropriately according to the presence of specific auditory conditional stimuli. Probe test 1 showed impaired conditional discrimination performance following sub-chronic PCP administration (seven twice-daily injection protocol) compared to control which was reversed by acute treatment with clozapine (5 mg/kg) but not haloperidol (0.1 mg/kg) both administered 60 min pre-test. Probe test 2 (8 days post-treatment) showed enduring deficits to conditional discrimination performance that were again reversed by clozapine but not haloperidol (injection procedures as above). These results show that tasks dependent upon conditional relationships are particularly sensitive to manipulation of DAergic systems as prolonged treatment with PCP has been shown to selectively reduce prefrontal cortex (PFC) DA activity and treatment with clozapine (known to ameliorate cognitive deficits) but not haloperidol has been shown to selectively restore PFC DA levels.

摘要

苯环利定(PCP)滥用者常常表现出与精神分裂症患者相似的症状特征。利用这类拟精神病药物的动物模型目前为该病症的研究提供了依据。越来越多的证据表明,精神分裂症的一个核心认知缺陷是无法利用任务设定线索来指导目标导向行为,并且这种能力由前额叶多巴胺(DA)介导。本研究使用非竞争性NMDA拮抗剂苯环利定(PCP)、氟哌啶醇(典型抗精神病药物)和氯氮平(非典型抗精神病药物),以进一步研究多巴胺能操纵对一项需要利用条件信息来指导目标导向行为的任务的影响。采用了一种工具性条件辨别任务,其中大鼠学会根据特定听觉条件刺激的出现做出适当反应。探测测试1显示,与对照组相比,亚慢性给予PCP(每日两次,共七次注射方案)后条件辨别性能受损,在测试前60分钟给予氯氮平(5毫克/千克)急性治疗可逆转这种损伤,但氟哌啶醇(0.1毫克/千克)则不能。探测测试2(治疗后8天)显示条件辨别性能存在持久缺陷,氯氮平再次可逆转这种缺陷,但氟哌啶醇则不能(注射程序如上)。这些结果表明,依赖条件关系的任务对多巴胺能系统的操纵特别敏感,因为已表明长期给予PCP可选择性降低前额叶皮质(PFC)的DA活性,而给予氯氮平(已知可改善认知缺陷)而非氟哌啶醇已表明可选择性恢复PFC的DA水平。

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