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在小鼠大脑中过度表达 munc18-1a 引起的行为、神经化学和形态变化:与精神分裂症的相关性。

Behavioral, neurochemical and morphological changes induced by the overexpression of munc18-1a in brain of mice: relevance to schizophrenia.

机构信息

Centro de Investigación Biomédica en Red de Salud Mental CIBERSAM, Spain.

出版信息

Transl Psychiatry. 2013 Jan 22;3(1):e221. doi: 10.1038/tp.2012.149.

Abstract

Overexpression of the mammalian homolog of the unc-18 gene (munc18-1) has been described in the brain of subjects with schizophrenia. Munc18-1 protein is involved in membrane fusion processes, exocytosis and neurotransmitter release. A transgenic mouse strain that overexpresses the protein isoform munc18-1a in the brain was characterized. This animal displays several schizophrenia-related behaviors, supersensitivity to hallucinogenic drugs and deficits in prepulse inhibition that reverse after antipsychotic treatment. Relevant brain areas (that is, cortex and striatum) exhibit reduced expression of dopamine D(1) receptors and dopamine transporters together with enhanced amphetamine-induced in vivo dopamine release. Magnetic resonance imaging demonstrates decreased gray matter volume in the transgenic animal. In conclusion, the mouse overexpressing brain munc18-1a represents a new valid animal model that resembles functional and structural abnormalities in patients with schizophrenia. The animal could provide valuable insights into phenotypic aspects of this psychiatric disorder.

摘要

在精神分裂症患者的大脑中已经描述了哺乳动物 unc-18 基因(munc18-1)同源物的过表达。Munc18-1 蛋白参与膜融合过程、胞吐作用和神经递质释放。描述了一种在大脑中过表达蛋白同工型 munc18-1a 的转基因小鼠品系。这种动物表现出几种与精神分裂症相关的行为、致幻药物的超敏反应以及在抗精神病药物治疗后逆转的预脉冲抑制缺陷。相关脑区(即皮层和纹状体)表现出多巴胺 D1 受体和多巴胺转运体表达减少,同时增强了安非他命诱导的体内多巴胺释放。磁共振成像显示转基因动物的灰质体积减少。总之,过表达大脑 munc18-1a 的小鼠代表了一种新的有效动物模型,类似于精神分裂症患者的功能和结构异常。该动物可以为这种精神障碍的表型方面提供有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/157b/3566728/6be67bd638e1/tp2012149f1.jpg

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