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中枢神经表观遗传调控下丘脑-垂体-肾上腺轴。

Central Neuroepigenetic Regulation of the Hypothalamic-Pituitary-Adrenal Axis.

机构信息

Max Planck Institute of Psychiatry, Munich, Germany.

Simon Fraser University, Vancouver, Canada; BC Children's Hospital Research Institute, Vancouver, Canada.

出版信息

Prog Mol Biol Transl Sci. 2018;158:105-127. doi: 10.1016/bs.pmbts.2018.04.006. Epub 2018 Jun 6.

Abstract

Dynamic adaptation to stressful life events requires the co-ordinated action of the central stress response, which is mediated by the hypothalamic-pituitary-adrenal (HPA) axis, to restore and maintain homeostasis. Excessive exposure to stress or traumatic life events, such as childhood maltreatment, has been linked to HPA axis dysfunction increasing the risk of developing stress-related psychopathologies such as major depressive disorder and post-traumatic-stress-disorder. Mounting evidence supports the notion that stressors throughout pre- and postnatal development as well as adulthood can induce neuroepigenetic regulation of gene expression within key nodes of the brain, which may in part mediate such HPA axis dysfunction. Neuroepigenetic mechanisms, particularly DNA methylation and small non-coding RNAs, are therefore considered to be molecular mechanisms by which stressful life events may perpetuate aberrant behavioral phenotypes associated with psychiatric disorders throughout one's life and even across generations. In this chapter we outline the progress made toward understanding the effects of stress-induced neuroepigenetic changes upon HPA axis function and highlight the need for novel research strategies to deepen our understanding of the establishment, maintenance and reversibility of neuroepigenetic regulation following stress to enable realization of potential novel therapeutic and preventative strategies for stress-related psychiatric disorders.

摘要

动态适应有压力的生活事件需要中枢应激反应的协调行动,这是由下丘脑-垂体-肾上腺(HPA)轴介导的,以恢复和维持体内平衡。过度暴露于压力或创伤性生活事件,如儿童期虐待,与 HPA 轴功能障碍有关,增加了发展与压力相关的精神病理的风险,如重度抑郁症和创伤后应激障碍。越来越多的证据支持这样一种观点,即产前和产后以及成年期的应激源可以诱导大脑关键节点内基因表达的神经表观遗传调控,这可能部分介导了 HPA 轴功能障碍。神经表观遗传机制,特别是 DNA 甲基化和小非编码 RNA,因此被认为是应激性生活事件可能通过一生甚至跨代持续存在与精神障碍相关的异常行为表型的分子机制。在本章中,我们概述了在理解应激诱导的神经表观遗传变化对 HPA 轴功能的影响方面所取得的进展,并强调需要新的研究策略来加深我们对应激后神经表观遗传调节的建立、维持和可逆性的理解,以实现针对与压力相关的精神障碍的潜在新的治疗和预防策略。

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