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压力与失眠的分子关系。

The Molecular Relationship between Stress and Insomnia.

机构信息

WSU Health Sciences Spokane, Elson S. Floyd College of Medicine, Department of Translational Medicine and Physiology, 412 E. Spokane Falls Blvd, Spokane, WA, 99 202, USA.

WSU Health Sciences Spokane, Elson S. Floyd College of Medicine, Department of Translational Medicine and Physiology, Pharmaceutical and Biomedical Sciences Building, Room 213/Lab 230, 412 E. Spokane Falls Blvd, (Lab) 509-368-6809, Spokane, WA, 99 202, USA.

出版信息

Adv Biol (Weinh). 2022 Nov;6(11):e2101203. doi: 10.1002/adbi.202101203. Epub 2022 Jul 13.

DOI:10.1002/adbi.202101203
PMID:35822937
Abstract

The bi-directional relationship between sleep and stress has been actively researched as sleep disturbances and stress have become increasingly common in society. Interestingly, the brain and underlying neural circuits important for sleep regulation may respond uniquely to stress that leads to post-traumatic stress disorder (PTSD) and stress that does not. In stress that does not lead to PTSD, the hypothalamic-pituitary-adrenal axis (HPA) pathway is activated normally that results in sympathetic nervous system activation that allows the brain and body to return to baseline functioning. However, exposure to stress that leads to PTSD, causes enhanced negative feedback of this same pathway and results in long-term physiological and psychological changes. In this review, how stress regulates glucocorticoid signaling pathways in brain glial cells called astrocytes, and then mediates stress-induced insomnia are examined. Astrocytes are critical sleep regulatory cells and their connections to sleep and stress due to disturbed glucocorticoid signaling provide a novel mechanism to explain how stress leads to insomnia. This review will examine the interactions of stress neurobiology, astrocytes, sleep, and glucocorticoid signaling pathways and will examine the how stress that leads to PTSD and stress that does not impacts sleep-regulatory processes.

摘要

睡眠和压力之间的双向关系已经成为研究热点,因为睡眠障碍和压力在社会中变得越来越普遍。有趣的是,大脑和调节睡眠的潜在神经回路可能对导致创伤后应激障碍(PTSD)的压力和不导致 PTSD 的压力有独特的反应。在不导致 PTSD 的压力下,下丘脑-垂体-肾上腺轴(HPA)途径正常激活,导致交感神经系统激活,使大脑和身体恢复到基线功能。然而,导致 PTSD 的压力暴露会增强同一途径的负反馈,导致长期的生理和心理变化。在这篇综述中,研究了压力如何调节大脑神经胶质细胞(星形胶质细胞)中的糖皮质激素信号通路,然后介导应激诱导的失眠。星形胶质细胞是关键的睡眠调节细胞,由于糖皮质激素信号的紊乱,它们与睡眠和压力的联系提供了一个新的机制来解释压力如何导致失眠。本综述将探讨应激神经生物学、星形胶质细胞、睡眠和糖皮质激素信号通路的相互作用,并探讨导致 PTSD 的应激和不导致 PTSD 的应激如何影响睡眠调节过程。

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