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终纹床核中促肾上腺皮质释放因子受体 2 的过度表达可改善恐惧孵育模型中创伤后应激障碍样症状。

Overexpression of corticotropin-releasing factor receptor type 2 in the bed nucleus of stria terminalis improves posttraumatic stress disorder-like symptoms in a model of incubation of fear.

机构信息

The Leslie and Susan Gonda (Goldschmied) Multidisciplinary Brain Research Center, Bar-Ilan University, Ramat-Gan; The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan.

出版信息

Biol Psychiatry. 2013 Dec 1;74(11):827-36. doi: 10.1016/j.biopsych.2013.05.039. Epub 2013 Jul 17.

Abstract

BACKGROUND

Posttraumatic stress disorder (PTSD) is a severe, persistent psychiatric disorder in response to a traumatic event, causing intense anxiety and fear. These responses may increase over time upon conditioning with fear-associated cues, a phenomenon termed fear incubation. Corticotropin-releasing factor receptor type 1 (CRFR1) is involved in activation of the central stress response, while corticotropin-releasing factor receptor type 2 (CRFR2) has been suggested to mediate termination of this response. Corticotropin-releasing factor (CRF) receptors are found in stress-related regions, including the bed nucleus of stria terminalis (BNST), which is implicated in sustained fear.

METHODS

Fear-related behaviors were analyzed in rats exposed to predator-associated cues, a model of psychological trauma, over 10 weeks. Rats were classified as susceptible (PTSD-like) or resilient. Expression levels of CRF receptors were measured in the amygdala nuclei and BNST of the two groups. In addition, lentiviruses overexpressing CRFR2 were injected into the medial division, posterointermediate part of the BNST (BSTMPI) of susceptible and resilient rats and response to stress cues was measured.

RESULTS

We found that exposure to stress and stress-associated cues induced a progressive increase in fear response of susceptible rats. The behavioral manifestations of these rats were correlated both with sustained elevation in CRFR1 expression and long-term downregulation in CRFR2 expression in the BSTMPI. Intra-BSTMPI injection of CRFR2 overexpressing lentiviruses attenuated behavioral impairments of susceptible rats.

CONCLUSIONS

These results implicate the BNST CRF receptors in the mechanism of coping with stress. Our findings suggest increase of CRFR2 levels as a new approach for understanding stress-related atypical psychiatric syndromes such as PTSD.

摘要

背景

创伤后应激障碍(PTSD)是一种严重的、持久的精神障碍,是对创伤事件的反应,导致强烈的焦虑和恐惧。这些反应可能会随着时间的推移而增加,与恐惧相关的线索形成条件反射,这一现象被称为恐惧潜伏期。促肾上腺皮质释放因子受体 1(CRFR1)参与中枢应激反应的激活,而促肾上腺皮质释放因子受体 2(CRFR2)被认为介导了这种反应的终止。促肾上腺皮质释放因子(CRF)受体存在于与应激相关的区域,包括终纹床核(BNST),其与持续的恐惧有关。

方法

通过 10 周的时间,使大鼠暴露于与捕食者相关的线索中,以此来分析其与恐惧相关的行为,该模型模拟了心理创伤。大鼠被分为易感(PTSD 样)或有弹性。测量了两组杏仁核核和 BNST 中的 CRF 受体表达水平。此外,将过表达 CRFR2 的慢病毒注射到易感和有弹性大鼠的 BNST 内侧分支、后中间部分(BSTMPI),并测量对应激线索的反应。

结果

我们发现,暴露于应激和应激相关线索会导致易感大鼠的恐惧反应逐渐增加。这些大鼠的行为表现与 CRFR1 表达持续升高和 CRFR2 在 BSTMPI 中的长期下调有关。BSTMPI 内注射过表达 CRFR2 的慢病毒可减轻易感大鼠的行为障碍。

结论

这些结果表明 BNST 的 CRF 受体参与了应对压力的机制。我们的研究结果表明,增加 CRFR2 水平可能是理解 PTSD 等与压力相关的非典型精神综合征的一种新方法。

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