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NPAS2对焦虑样行为和GABAA受体的调控

NPAS2 Regulation of Anxiety-Like Behavior and GABAA Receptors.

作者信息

Ozburn Angela R, Kern Joseph, Parekh Puja K, Logan Ryan W, Liu Zheng, Falcon Edgardo, Becker-Krail Darius, Purohit Kush, Edgar Nicole M, Huang Yanhua, McClung Colleen A

机构信息

Portland Veterans Affairs Medical Center, Research and Development Service, Portland, OR, United States.

Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, OR, United States.

出版信息

Front Mol Neurosci. 2017 Nov 3;10:360. doi: 10.3389/fnmol.2017.00360. eCollection 2017.

Abstract

Abnormal circadian rhythms and circadian genes are strongly associated with several psychiatric disorders. Neuronal PAS Domain Protein 2 (NPAS2) is a core component of the molecular clock that acts as a transcription factor and is highly expressed in reward- and stress-related brain regions such as the striatum. However, the mechanism by which NPAS2 is involved in mood-related behaviors is still unclear. We measured anxiety-like behaviors in mice with a global null mutation in (Npas2 null mutant mice) and found that Npas2 null mutant mice exhibit less anxiety-like behavior than their wild-type (WT) littermates (in elevated plus maze, light/dark box and open field assay). We assessed the effects of acute or chronic stress on striatal expression, and found that both stressors increased levels of . Moreover, knockdown of in the ventral striatum resulted in a similar reduction of anxiety-like behaviors as seen in the Npas2 null mutant mouse. Additionally, we identified genes as transcriptional targets of NPAS2, found that Npas2 null mutant mice exhibit reduced sensitivity to the GABAa positive allosteric modulator, diazepam and that knockdown of reduced expression and response to diazepam in the ventral striatum. These results: (1) implicate in the response to stress and the development of anxiety; and (2) provide functional evidence for the regulation of GABAergic neurotransmission by NPAS2 in the ventral striatum.

摘要

异常的昼夜节律和昼夜节律基因与多种精神疾病密切相关。神经元PAS结构域蛋白2(NPAS2)是分子时钟的核心组成部分,作为一种转录因子,在纹状体等与奖赏和应激相关的脑区中高度表达。然而,NPAS2参与情绪相关行为的机制仍不清楚。我们检测了全局无效突变小鼠(Npas2无效突变小鼠)的焦虑样行为,发现Npas2无效突变小鼠比其野生型(WT)同窝小鼠表现出更少的焦虑样行为(在高架十字迷宫、明暗箱和旷场试验中)。我们评估了急性或慢性应激对纹状体表达的影响,发现两种应激源均增加了的水平。此外,腹侧纹状体中的敲低导致焦虑样行为的减少,与Npas2无效突变小鼠中观察到的相似。此外,我们鉴定了基因作为NPAS2的转录靶点,发现Npas2无效突变小鼠对GABAa正性变构调节剂地西泮的敏感性降低,并且腹侧纹状体中的敲低降低了表达和对地西泮的反应。这些结果:(1)表明参与应激反应和焦虑的发展;(2)为腹侧纹状体中NPAS2对GABA能神经传递的调节提供了功能证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db00/5675889/bf76ddec3adc/fnmol-10-00360-g0001.jpg

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