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精神分裂症的转化研究:精神分裂症和啮齿动物动机的剖析。

Schizophrenia in translation: dissecting motivation in schizophrenia and rodents.

机构信息

Department of Psychiatry, Columbia University, New York, NY, USA.

出版信息

Schizophr Bull. 2012 Nov;38(6):1111-7. doi: 10.1093/schbul/sbs114. Epub 2012 Sep 26.

DOI:10.1093/schbul/sbs114
PMID:23015686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3494038/
Abstract

The negative symptoms of schizophrenia include deficits in motivation, for which there is currently no treatment available. Animal models provide a powerful tool for identifying the potential pathophysiological mechanisms underlying the motivation deficits of schizophrenia with the aim of discovering novel treatment targets. The success of such an approach critically depends on meticulously detailed analysis of motivational phenotypes in patients and in animal models. Here, we review the results of recent human behavioral and imaging studies of motivation, and we relate those findings to the results from animal studies, including a mouse model of striatal dopamine D2 receptor hyperfunction. The motivational deficit in patients with schizophrenia is not due to an inability to experience pleasure in the moment as hedonic reaction appears intact in patients. Instead, the motivation deficit represents a reduced capacity for anticipating future pleasure resulting from goal-directed action. The diminished anticipation appears to be a consequence of an inability to accurately represent the expected reward values of actions. A strikingly similar phenotype in incentive motivation has also been described in mice with striatal dopamine D2 receptor hyperfunction. These convergent findings identify potential pathophysiological mechanisms that underlie the deficit in anticipatory motivation, and importantly, the mouse model provides a tool for investigating novel treatment strategies, which we discuss here.

摘要

精神分裂症的阴性症状包括动机缺陷,目前尚无可用的治疗方法。动物模型为确定精神分裂症动机缺陷的潜在病理生理机制提供了强有力的工具,旨在发现新的治疗靶点。这种方法的成功与否关键取决于对患者和动物模型中动机表型的细致详细分析。在这里,我们回顾了最近关于动机的人类行为和成像研究的结果,并将这些发现与动物研究的结果进行了关联,包括纹状体多巴胺 D2 受体功能亢进的小鼠模型。精神分裂症患者的动机缺陷不是由于无法即时体验到愉悦,因为愉悦反应在患者中似乎是完整的。相反,动机缺陷代表了由于目标导向的行动而导致对未来愉悦的预期能力降低。这种预期的减少似乎是由于无法准确表示动作的预期奖励值的结果。纹状体多巴胺 D2 受体功能亢进的小鼠中也描述了一种激励动机的惊人相似表型。这些趋同的发现确定了潜在的病理生理机制,这些机制是预测性动机缺陷的基础,重要的是,该小鼠模型为研究新的治疗策略提供了工具,我们在这里对此进行了讨论。

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本文引用的文献

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