Department of Experimental and Clinic Medicine, Section of Psychiatry, University of Pisa, Pisa, Italy.
Département de psychiatrie et d'addictologie, AP-HP, GHU Paris Nord, DMU Neurosciences, Hopital Bichat - Claude Bernard, F-75018 Paris, France.
CNS Spectr. 2022 Jun;27(3):298-308. doi: 10.1017/S1092852921000018. Epub 2021 Jan 11.
The present paper aims at reviewing and commenting on the relationships between sleep and circadian phasing alterations and neurodegenerative/neuroprogressive processes in mood disorder. We carried out a systematic review, according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, in PubMed, PsycINFO, and Embase electronic databases for literature related to mood disorders, sleep disturbances, and neurodegenerative/neuroprogressive processes in relation to (1) neuroinflammation, (2) activation of the stress system, (3) oxidative stress, (4) accumulation of neurotoxic proteins, and (5) neuroprotection deficit. Seventy articles were collectively selected and analyzed. Experimental and clinical studies revealed that insomnia, conditions of sleep loss, and altered circadian sleep may favor neurodegeneration and neuroprogression in mood disorders. These sleep disturbances may induce a state of chronic inflammation by enhancing neuroinflammation, both directly and indirectly, via microglia and astrocytes activation. They may act as neurobiological stressors that by over-activating the stress system may negatively influence neural plasticity causing neuronal damage. In addition, sleep disturbances may favor the accumulation of neurotoxic proteins, favor oxidative stress, and a deficit in neuroprotection hence contributing to neurodegeneration and neuroprogression. Targeting sleep disturbances in the clinical practice may hold a neuroprotective value for mood disorders.
本文旨在综述和评论睡眠和昼夜节律相位改变与心境障碍中神经退行性/神经进行性过程之间的关系。我们按照系统评价和荟萃分析的首选报告项目指南,在 PubMed、PsycINFO 和 Embase 电子数据库中进行了文献检索,检索内容与心境障碍、睡眠障碍以及与(1)神经炎症、(2)应激系统激活、(3)氧化应激、(4)神经毒性蛋白积累和(5)神经保护缺陷有关的神经退行性/神经进行性过程。共选择和分析了 70 篇文章。实验和临床研究表明,失眠、睡眠不足和昼夜节律睡眠改变可能有利于心境障碍中的神经退行性变和神经进行性变。这些睡眠障碍可能通过增强小胶质细胞和星形胶质细胞的激活,直接和间接地引发慢性炎症状态。它们可能作为神经生物学应激源,通过过度激活应激系统,对神经可塑性产生负面影响,导致神经元损伤。此外,睡眠障碍可能有利于神经毒性蛋白的积累、氧化应激和神经保护不足,从而导致神经退行性变和神经进行性变。在临床实践中针对睡眠障碍进行治疗可能对心境障碍具有神经保护作用。