精神分裂症的核受体和神经炎症。

Molecular Neuropsychiatry Pub Date : 2018-05-01 Epub Date: 2018-01-16 DOI:10.1159/000485565
Shan-Yuan Tsai, Vibeke S Catts, Janice M Fullerton, Susan M Corley, Stuart G Fillman, Cynthia Shannon Weickert
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引用次数: 12

摘要

几个核受体家族成员与精神分裂症和炎症有关。维生素A和D具有抗炎作用,但它们的受体(主要是核受体)尚未在精神分裂症大脑中或与神经炎症相关的研究中得到广泛研究。在细胞因子表达升高的背外侧前额叶皮层(DLPFC)中,我们检测了维生素A (RARs和RXRs)、维生素D和蛋白二硫异构酶A3 (PDIA3)受体以及核孤儿受体(NR4As)的表达。方法:采用RT-qPCR方法检测DLPFC组织中核受体mRNA水平。对高炎症性精神分裂症、低炎症性精神分裂症和低炎症性对照组进行ANCOVAs比较。结果:RARG、RXRB、NR4A1和NR4A3转录本在三组间的表达差异有统计学意义(方差分析p = 0.02-0.001)。事后检测显示,与高炎症性精神分裂症患者和对照组相比,低炎症性精神分裂症患者RARG表达显著降低,低炎症性精神分裂症患者RXRB mRNA表达显著降低。与低炎症性精神分裂症相比,高炎症性精神分裂症患者NR4A1和NR4A3 mrna水平降低,且NR4A1与对照组差异显著。结论:在精神分裂症中,参与维生素A衍生物介导作用的核受体mRNA水平随大脑炎症状态的变化而变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Nuclear Receptors and Neuroinflammation in Schizophrenia.

Introduction: Several nuclear receptor family members have been associated with schizophrenia and inflammation. Vitamins A and D exert anti-inflammatory actions, but their receptors (mainly nuclear receptors) have not been extensively studied in either schizophrenia brains or in association with neuroinflammation. We examined the expression of vitamin A (RARs and RXRs) and vitamin D and protein disulphide-isomerase A3 (PDIA3) receptors, as well as nuclear orphan receptors (NR4As), in the context of elevated cytokine expression in the dorsolateral prefrontal cortex (DLPFC).

Methods: mRNA levels of nuclear receptors were measured in DLPFC tissues via RT-qPCR. ANCOVAs comparing high inflammation schizophrenia, low inflammation schizophrenia and low inflammation control groups were performed.

Results: RARG, RXRB, NR4A1 and NR4A3 transcripts showed significant differential expression across the three groups (ANCOVA p = 0.02-0.001). Post hoc testing revealed significant reductions in RARG expression in schizophrenia with low inflammation compared to schizophrenia with high inflammation and to controls, and RXRB mRNA was significantly reduced in schizophrenia with low inflammation compared to controls. NR4A1 and NR4A3 mRNAs were decreased in schizophrenia with high inflammation compared to schizophrenia with low inflammation, with NR4A1 also significantly different to controls.

Conclusion: In schizophrenia, changes in nuclear receptor mRNA levels involved with mediating actions of vitamin A derivatives vary according to the inflammatory state of brains.

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