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抗精神病药物可增加大鼠海马体和皮质中微管相关蛋白2的信使核糖核酸,但不增加亲环蛋白mRNA。

Antipsychotics increase microtubule-associated protein 2 mRNA but not spinophilin mRNA in rat hippocampus and cortex.

作者信息

Law Amanda J, Hutchinson Louise J, Burnet Philip W J, Harrison Paul J

机构信息

Department of Psychiatry, University of Oxford, Neurosciences Building, Warneford Hospital, Oxford, United Kingdom.

出版信息

J Neurosci Res. 2004 May 1;76(3):376-82. doi: 10.1002/jnr.20092.

Abstract

Antipsychotic (neuroleptic) drugs induce structural alterations in synaptic terminals and changes in the expression of presynaptic protein genes. Whether there are also changes in corresponding postsynaptic (dendritic) markers has not been determined. We describe the effect of 14-day treatment with typical (haloperidol, chlorpromazine) or atypical (clozapine, olanzapine, risperidone) antipsychotics on the expression of two dendritic protein genes, microtubule-associated protein 2 (MAP2) and spinophilin, using in situ hybridization, in the rat hippocampus, retrosplenial, and occipitoparietal cortices. MAP2 mRNA was increased modestly in the dentate gyrus and retrosplenial cortex by chlorpromazine, risperidone, and olanzapine and in the occipitoparietal cortex by chlorpromazine, haloperidol, and risperidone. None of the antipsychotics affected spinophilin mRNA in any area. Overall, these results show a modulation of MAP2 gene expression, likely reflecting functional or structural changes in the dendritic tree in response to some typical and atypical antipsychotics. The lack of change in spinophilin mRNA suggests that dendritic spines are not affected selectively by the drugs. The data provide further evidence that antipsychotics regulate genes involved in synaptic structure and function. Such actions may underlie their long-term effects on neural plasticity in areas of the brain implicated in the pathology of schizophrenia.

摘要

抗精神病药物(神经阻滞剂)可诱导突触终末的结构改变以及突触前蛋白基因表达的变化。相应的突触后(树突)标志物是否也发生变化尚未确定。我们使用原位杂交技术,描述了用典型抗精神病药物(氟哌啶醇、氯丙嗪)或非典型抗精神病药物(氯氮平、奥氮平、利培酮)进行14天治疗对大鼠海马体、压后皮质和枕顶叶皮质中两个树突蛋白基因——微管相关蛋白2(MAP2)和亲棘蛋白表达的影响。氯丙嗪、利培酮和奥氮平使齿状回和压后皮质中的MAP2 mRNA适度增加,氯丙嗪、氟哌啶醇和利培酮使枕顶叶皮质中的MAP2 mRNA适度增加。所有抗精神病药物均未影响任何区域的亲棘蛋白mRNA。总体而言,这些结果表明MAP2基因表达受到调节,这可能反映了树突对某些典型和非典型抗精神病药物的反应中发生的功能或结构变化。亲棘蛋白mRNA缺乏变化表明树突棘未受到药物的选择性影响。这些数据进一步证明抗精神病药物可调节参与突触结构和功能的基因。此类作用可能是它们对精神分裂症病理涉及的脑区神经可塑性产生长期影响的基础。

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