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精神分裂症、抑郁症和双相情感障碍中NR3A NMDA受体亚基mRNA的表达

NR3A NMDA receptor subunit mRNA expression in schizophrenia, depression and bipolar disorder.

作者信息

Mueller Helena T, Meador-Woodruff James H

机构信息

Neuroscience Graduate Program, Department of Psychiatry, Mental Health Research Institute, University of Michigan Medical School, 205 Zina Pitcher Place, Ann Arbor, MI 48109-0720, USA.

出版信息

Schizophr Res. 2004 Dec 1;71(2-3):361-70. doi: 10.1016/j.schres.2004.02.016.

Abstract

Growing evidence suggests that NMDA receptor (NMDAR) dysfunction may be involved in schizophrenia. The NMDAR is a multimeric assembly derived from seven different genes (NR1, NR2A-2D and NR3A-3B). While region-specific changes in the expression of most NMDAR subunits have been reported in schizophrenia, possible abnormalities of NR3A expression have not been investigated. Both electrophysiological and anatomical data in rodents, however, suggest that NR3A subunits could play a role in this disorder. In this study, we measured NR3A transcript levels in the dorsolateral prefrontal cortex (DLPFC) and inferior temporal neocortex in the brains of people with schizophrenia, bipolar disorder, depression, and a comparison group. This transcript was elevated by 32% in schizophrenia relative to controls, but only in the DLPFC and not inferior temporal cortical regions. Interestingly, this effect was restricted to gyral aspects of the DLPFC and did not involve sulcal areas. NR3A mRNA was significantly decreased by 12% in bipolar disorder relative to the comparison group in DLPFC, although there were no gyral versus sulcal differences. As was the case in schizophrenia, no changes in NR3A expression were observed in the inferior temporal cortex in bipolar disorder. These data indicate that the NR3A subunit is abnormally expressed in both schizophrenia and bipolar disorder.

摘要

越来越多的证据表明,N-甲基-D-天冬氨酸受体(NMDAR)功能障碍可能与精神分裂症有关。NMDAR是一种由七个不同基因(NR1、NR2A - 2D和NR3A - 3B)组成的多聚体。虽然在精神分裂症中已报道了大多数NMDAR亚基表达的区域特异性变化,但尚未对NR3A表达的可能异常进行研究。然而,啮齿动物的电生理和解剖学数据均表明,NR3A亚基可能在这种疾病中起作用。在本研究中,我们测量了精神分裂症患者、双相情感障碍患者、抑郁症患者以及一个对照组大脑背外侧前额叶皮质(DLPFC)和颞下回新皮质中NR3A转录水平。相对于对照组,精神分裂症患者的该转录本在DLPFC中升高了32%,但在颞下回皮质区域未升高。有趣的是,这种效应仅限于DLPFC的脑回部分,不涉及脑沟区域。在DLPFC中,相对于对照组,双相情感障碍患者的NR3A mRNA显著降低了12%,尽管不存在脑回与脑沟的差异。与精神分裂症的情况一样,双相情感障碍患者的颞下回皮质中未观察到NR3A表达的变化。这些数据表明,NR3A亚基在精神分裂症和双相情感障碍中均异常表达。

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