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精神分裂症和双相情感障碍患者前额叶皮质中多巴胺相关转录因子Nurr1和NGFI-B的减少。

Reduction of dopamine-related transcription factors Nurr1 and NGFI-B in the prefrontal cortex in schizophrenia and bipolar disorders.

作者信息

Xing Guoqiang, Zhang Lei, Russell Shani, Post Robert

机构信息

Department of Psychiatry, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814-4799, USA.

出版信息

Schizophr Res. 2006 May;84(1):36-56. doi: 10.1016/j.schres.2005.11.006. Epub 2006 May 2.

Abstract

Abnormal cortical and subcortical dopaminergic activities are among the most consistent neuropathological findings in schizophrenia. The molecular mechanisms remain unspecified. NGFI-B and Nurr1 are two closely related transcription factors involved in dopaminergic cell differentiation, maturation, and apoptosis. NGFI-B knockout mice show attenuated behavioral response to dopamine receptor agonists, whereas Nurr1 knockout disrupts midbrain dopaminergic neuron development. To further understand the role of Nurr1 and NGFI-B in schizophrenia and bipolar disorders, we measured Nurr1 and NGFI-B mRNA in the prefrontal cortex Brodmann's areas 9 (BA 9) and BA 46 by in situ hybridization, and the protein levels in BA 9 by Western blotting, of patients with schizophrenia, major depression, and bipolar disorders, and non-psychiatric control subjects (n=15 per group). NGFI-B mRNA (P<0.05) and protein (P<0.01) were significantly lower in patients with schizophrenia (BA 9), and NGFI-B mRNA was lower in bipolar disorder (BA 9 and BA 46) than in the controls. In the deep cortical layers of BA 46, Nurr1 mRNA was significantly (P<0.05) lower in patients with bipolar disorder and schizophrenia than in the controls. Nurr1 protein in BA 9 was significantly lower in major depression (P<0.05) and lower at a trend level in schizophrenia (P=0.056) than in the controls. These data show a deficient prefrontal NGFI-B and Nurr1 expression in schizophrenia and bipolar disorder. Further study may elucidate if and how these deficiencies could be associated with abnormal dopaminergic functions seen in both illnesses.

摘要

皮质和皮质下多巴胺能活动异常是精神分裂症中最一致的神经病理学发现之一。其分子机制仍不明确。NGFI-B和Nurr1是两个密切相关的转录因子,参与多巴胺能细胞的分化、成熟和凋亡。NGFI-B基因敲除小鼠对多巴胺受体激动剂的行为反应减弱,而Nurr1基因敲除则破坏中脑多巴胺能神经元的发育。为了进一步了解Nurr1和NGFI-B在精神分裂症和双相情感障碍中的作用,我们通过原位杂交测量了精神分裂症、重度抑郁症、双相情感障碍患者以及非精神科对照受试者(每组n = 15)前额叶皮质布罗德曼9区(BA 9)和BA 46区的Nurr1和NGFI-B mRNA,并通过蛋白质印迹法测量了BA 9区的蛋白质水平。精神分裂症患者(BA 9)的NGFI-B mRNA(P < 0.05)和蛋白质(P < 0.01)显著降低,双相情感障碍患者(BA 9和BA 46)的NGFI-B mRNA低于对照组。在BA 46的深层皮质层,双相情感障碍和精神分裂症患者的Nurr1 mRNA显著低于对照组(P < 0.05)。BA 9区的Nurr1蛋白在重度抑郁症患者中显著低于对照组(P < 0.05),在精神分裂症患者中呈趋势性降低(P = 0.056)。这些数据表明精神分裂症和双相情感障碍患者前额叶NGFI-B和Nurr1表达不足。进一步的研究可能会阐明这些缺陷是否以及如何与这两种疾病中出现的多巴胺能功能异常相关。

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