Suppr超能文献

信号蛋白和丛蛋白基因表达在伴有和不伴有幻听的精神分裂症患者的前额叶皮层中发生改变。

Semaphorin and plexin gene expression is altered in the prefrontal cortex of schizophrenia patients with and without auditory hallucinations.

机构信息

CIBERSAM, Spain; Departamento de Genética, Facultad de Biología, Universitat de València, INCLIVA, Valencia, Spain; Unidad de Neurobiología y Programa de Neurociencias Básicas y Aplicadas, Departamento de Biología Celular, Universitat de València, INCLIVA, Valencia, Spain.

Departamento de Genética, Facultad de Biología, Universitat de València, INCLIVA, Valencia, Spain.

出版信息

Psychiatry Res. 2015 Oct 30;229(3):850-7. doi: 10.1016/j.psychres.2015.07.074. Epub 2015 Jul 29.

Abstract

Auditory hallucinations (AH) are clinical hallmarks of schizophrenia, however little is known about molecular genetics of these symptoms. In this study, gene expression profiling of postmortem brain samples from prefrontal cortex of schizophrenic patients without AH (SNA), patients with AH (SA) and control subjects were compared. Genome-wide expression analysis was conducted using samples of three individuals of each group and the Affymetrix GeneChip Human-Gene 1.0 ST-Array. This analysis identified the Axon Guidance pathway as one of the most differentially expressed network among SNA, SA and CNT. To confirm the transcriptome results, mRNA level quantification of seventeen genes involved in this pathway was performed in a larger sample. PLXNB1, SEMA3A, SEMA4D and SEM6C were upregulated in SNA or SA patients compared to controls. PLXNA1 and SEMA3D showed down-regulation in their expression in the patient's samples, but differences remained statistically significant between the SNA patients and controls. Differences between SNA and SA were found in PLXNB1 expression which is decreased in SA patients. This study strengthens the contribution of brain plasticity in pathophysiology of schizophrenia and shows that non-hallucinatory patients present more alterations in frontal regions than patients with hallucinations concerning neural plasticity.

摘要

听觉幻觉(AH)是精神分裂症的临床特征,但对于这些症状的分子遗传学知之甚少。在这项研究中,我们比较了无 AH 的精神分裂症患者(SNA)、有 AH 的精神分裂症患者(SA)和对照受试者死后前额叶皮层脑组织样本的基因表达谱。使用每组三个个体的样本进行了全基因组表达分析,并使用 Affymetrix GeneChip Human-Gene 1.0 ST-Array。该分析确定轴突导向途径是 SNA、SA 和 CNT 之间差异表达网络之一。为了确认转录组结果,在更大的样本中对该途径的十七个基因的 mRNA 水平进行了定量。与对照组相比,PLXNB1、SEMA3A、SEMA4D 和 SEM6C 在 SNA 或 SA 患者中上调。PLXNA1 和 SEMA3D 在患者样本中的表达下调,但 SNA 患者与对照组之间的差异仍具有统计学意义。在 SA 患者中降低的 PLXNB1 表达中发现了 SNA 和 SA 之间的差异。这项研究加强了大脑可塑性在精神分裂症病理生理学中的作用,并表明非幻觉患者的前额叶区域比有幻觉的患者表现出更多的神经可塑性改变。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验