• Elena Antontseva, Natalia Bondar, Vasiliy Reshetnikov, and Tatiana Merkulova.
• Department of Molecular Genetics, Institute of Cytology and Genetics, Lavrentiev Ave, 10, Novosibirsk 630090, Russia. Electronic address: antontseva@bionet.nsc.ru.
• Neuroscience. 2020 Aug 10; 441: 226-238.

AbstractThe myelination of axons, which is performed in brain tissues by specialized glial cells (oligodendrocytes) is crucial for correct formation of the complicated neural circuitry necessary for normal cognition, sensation, and motor function. Myelin-related anomalies are seen in many neurodegenerative diseases and in psychiatric disorders, including major depressive disorder and post-traumatic stress disorder. Chronic stress involving chronic stress early in life is believed to be a major etiological factor of neuropsychiatric disorders. Although molecular and cellular mechanisms underlying stress-induced psychopathologies are actively investigated, there is still little data about the role that is played in the development of these pathologies by myelin and oligodendrocyte impairments caused by chronic stress. In this article, after brief review of published data on myelin abnormalities in stress-related psychiatric disorders, we focus on recent cellular and molecular discoveries in various rodent models including models of chronic unpredictable stress, social isolation stress, chronic social defeat stress, and chronic immobilization stress. We also attempt to compile and analyze currently scarce data on myelin-related impairments resulting from early postnatal stress.Copyright © 2020 IBRO. Published by Elsevier Ltd. All rights reserved.

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