早期生活压力和炎症:对啮齿动物关键实验方法的系统回顾。

Brain and neuroscience advances Pub Date : 2020-12-28 eCollection Date: 2020-01-01 DOI:10.1177/2398212820978049
Ethan G Dutcher, E A Claudia Pama, Mary-Ellen Lynall, Shahid Khan, Menna R Clatworthy, Trevor W Robbins, Edward T Bullmore, Jeffrey W Dalley
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摘要

反复产妇分离是研究早期慢性压力与其神经精神和身体后果之间关系的最广泛使用的临床前方法。在这项系统综述中,我们确定了46项进行重复母体分离或单次母体分离的研究,并报告了白细胞介素1b、白细胞介素-6、白细胞白细胞介质-10、肿瘤坏死因子α或小胶质细胞活化和密度的测量。我们报告说,在短期内和后期生活压力的背景下,反复的母亲分离会在不同组织中产生促炎免疫后果。重复母体分离的动物在与人类精神疾病有关的关键大脑区域表现出更大的小胶质细胞激活和升高的促炎细胞因子信号传导。值得注意的是,在没有后期生活压力的情况下,重复的母体分离通常对任何组织中的细胞因子表达没有长期影响。这些观察结果表明,在有早期生活压力史的人类中报告的炎症信号升高可能是持续暴露于压力源以及对压力源增强的神经和/或免疫反应的共同结果。最后,我们的发现为未来的研究提供了详细的指导,这些研究质疑早期生活压力和炎症在严重抑郁症等疾病中的因果作用。
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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Early-life stress and inflammation: A systematic review of a key experimental approach in rodents.

Repeated maternal separation is the most widely used pre-clinical approach to investigate the relationship between early-life chronic stress and its neuropsychiatric and physical consequences. In this systematic review, we identified 46 studies that conducted repeated maternal separation or single-episode maternal separation and reported measurements of interleukin-1b, interleukin-6, interleukin-10, tumour necrosis factor-alpha, or microglia activation and density. We report that in the short-term and in the context of later-life stress, repeated maternal separation has pro-inflammatory immune consequences in diverse tissues. Repeated maternal separation animals exhibit greater microglial activation and elevated pro-inflammatory cytokine signalling in key brain regions implicated in human psychiatric disorders. Notably, repeated maternal separation generally has no long-term effect on cytokine expression in any tissue in the absence of later-life stress. These observations suggest that the elevated inflammatory signalling that has been reported in humans with a history of early-life stress may be the joint consequence of ongoing stressor exposure together with potentiated neural and/or immune responsiveness to stressors. Finally, our findings provide detailed guidance for future studies interrogating the causal roles of early-life stress and inflammation in disorders such as major depression.

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