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精神分裂症的神经发育机制:通过神经调节蛋白-1-ErbB4和DISC1理解产后大脑成熟障碍

Neurodevelopmental mechanisms of schizophrenia: understanding disturbed postnatal brain maturation through neuregulin-1-ErbB4 and DISC1.

作者信息

Jaaro-Peled Hanna, Hayashi-Takagi Akiko, Seshadri Saurav, Kamiya Atsushi, Brandon Nicholas J, Sawa Akira

机构信息

Department of Psychiatry and Behavioral Neurosciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

出版信息

Trends Neurosci. 2009 Sep;32(9):485-95. doi: 10.1016/j.tins.2009.05.007. Epub 2009 Aug 26.

Abstract

Schizophrenia (SZ) is primarily an adult psychiatric disorder in which disturbances caused by susceptibility genes and environmental insults during early neurodevelopment initiate neurophysiological changes over a long time course, culminating in the onset of full-blown disease nearly two decades later. Aberrant postnatal brain maturation is an essential mechanism underlying the disease. Currently, symptoms of SZ are treated with anti-psychotic medications that have variable efficacy and severe side effects. There has been much interest in the prodromal phase and the possibility of preventing SZ by interfering with the aberrant postnatal brain maturation associated with this disorder. Thus, it is crucial to understand the mechanisms that underlie the long-term progression to full disease manifestation to identify the best targets and approaches towards this goal. We believe that studies of certain SZ genetic susceptibility factors with neurodevelopmental implications will be key tools in this task. Accumulating evidence suggests that neuregulin-1 (NRG1) and disrupted-in-schizophrenia-1 (DISC1) are probably functionally convergent and play key roles in brain development. We provide an update on the role of these emerging concepts in understanding the complex time course of SZ from early neurodevelopmental disturbances to later onset and suggest ways of testing these in the future.

摘要

精神分裂症(SZ)主要是一种成人精神疾病,其中早期神经发育过程中易感基因和环境损伤所引起的紊乱会在很长一段时间内引发神经生理变化,最终在近二十年后导致全面疾病的发作。异常的产后大脑成熟是该疾病的一个重要潜在机制。目前,SZ的症状通过抗精神病药物进行治疗,这些药物疗效各异且有严重的副作用。前驱期以及通过干扰与该疾病相关的异常产后大脑成熟来预防SZ的可能性一直备受关注。因此,了解导致疾病全面显现的长期进展的机制对于确定实现这一目标的最佳靶点和方法至关重要。我们认为,对具有神经发育意义的某些SZ遗传易感性因素的研究将是完成这项任务的关键工具。越来越多的证据表明,神经调节蛋白-1(NRG1)和精神分裂症相关断裂基因-1(DISC1)可能在功能上趋同,并且在大脑发育中起关键作用。我们提供了关于这些新出现的概念在理解SZ从早期神经发育紊乱到后期发病的复杂时间过程中所起作用的最新情况,并提出了未来对其进行检验的方法。

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