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应激激活不确定核并调节海马-内侧前额叶皮质通路的可塑性。

Stress activates the nucleus incertus and modulates plasticity in the hippocampo-medial prefrontal cortical pathway.

作者信息

Rajkumar Ramamoorthy, Wu You, Farooq Usman, Tan Wei Hao, Dawe Gavin S

机构信息

Department of Pharmacology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore; Neurobiology and Ageing Programme, Life Sciences Institute, National University of Singapore, Singapore; Singapore Institute for Neurotechnology (SINAPSE), Singapore.

Department of Pharmacology, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, Singapore; Neurobiology and Ageing Programme, Life Sciences Institute, National University of Singapore, Singapore; Singapore Institute for Neurotechnology (SINAPSE), Singapore.

出版信息

Brain Res Bull. 2016 Jan;120:83-9. doi: 10.1016/j.brainresbull.2015.10.010. Epub 2015 Oct 31.

DOI:10.1016/j.brainresbull.2015.10.010
PMID:26529052
Abstract

The nucleus incertus (NI) is a small cluster of brainstem neurons presumed to play a role in stress responses. We show that swim stress (normal water: 30 min and cold water: 20 min) and elevation stress robustly induced c-Fos expression in the NI and significantly suppressed long-term potentiation (LTP) in the hippocampo-medial prefrontal cortical (HP-mPFC) pathway. To examine whether activation of CRF1 receptors in the NI plays a role in the suppression of HP-mPFC LTP, antalarmin, a specific CRF1 receptor antagonist, was infused directly into the NI either before presentation of (1) elevation stress or (2) high frequency stimulation. As predicted, the intra-NI infusion of antalarmin reversed the elevation stress-induced suppression of LTP in the HP-mPFC pathway. This report suggests that the CRF1 receptor in the NI contributes to stress-related impairment in plasticity of the HP-mPFC pathway. The findings suggest that the NI-HP-mPFC is a stress responsive circuit in the rodent brain.

摘要

不确定核(NI)是脑干中一小群神经元,推测其在应激反应中发挥作用。我们发现游泳应激(常温水:30分钟和冷水:20分钟)和高架应激能强烈诱导NI中c-Fos表达,并显著抑制海马-内侧前额叶皮质(HP-mPFC)通路中的长时程增强(LTP)。为了研究NI中CRF1受体的激活是否在抑制HP-mPFC LTP中起作用,在呈现(1)高架应激或(2)高频刺激之前,将特异性CRF1受体拮抗剂安他拉美直接注入NI。正如预期的那样,向NI内注入安他拉美可逆转高架应激诱导的HP-mPFC通路中LTP的抑制。本报告表明,NI中的CRF1受体导致了HP-mPFC通路可塑性的应激相关损伤。这些发现表明,NI-HP-mPFC是啮齿动物大脑中的一个应激反应回路。

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