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青春期小鼠的社会挫败应激会诱导出类似抑郁的行为,并伴有少突胶质细胞生成减少。

Social Defeat Stress in Adolescent Mice Induces Depressive-like Behaviors with Reduced Oligodendrogenesis.

作者信息

Shimizu Takeshi, Ishida Akimasa, Hagiwara Mutsumi, Ueda Yoshitomo, Hattori Atsunori, Tajiri Naoki, Hida Hideki

机构信息

Department of Neurophysiology and Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.

Department of Neurophysiology and Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-8601, Japan.

出版信息

Neuroscience. 2020 Sep 1;443:218-232. doi: 10.1016/j.neuroscience.2020.07.002. Epub 2020 Jul 9.

Abstract

Strong stress related to adverse experiences during adolescence can cause mental disorders, as well as affecting brain structure and function. However, the underlying neurobiological mechanisms remain largely unknown. To investigate whether stress induced by adverse experience during adolescence affects oligodendrocyte (OL) remodeling, social defeat stress was applied to 6-week-old adolescent mice for 10 days, followed by behavioral tests and assessments of oligodendrogenesis. Socially defeated mice showed depressive-like behaviors in behavioral experiments. Stress led to a decrease in the number of newly born OLs in the anterior cortical region and the number of proteolipid protein-positive mature OLs in the corpus callosum and posterior cerebral cortex. Fewer bromodeoxyuridine-incorporated CC1-positive mature OLs were observed in these regions in socially defeated mice. To assess whether decreased oligodendrogenesis caused by social defeat stress is related to depressive-like symptoms under stress, clemastine, a drug that induces OL generation, was administered to socially defeated adolescent mice, resulting in the rescue of the behavioral abnormalities accompanied by increased oligodendrogenesis. These findings suggest that oligodendrogenesis in adverse environments during adolescence plays a role in psychiatric disorders, and clemastine may provide a potential therapeutic drug for adolescent mental disorders, targeting OLs.

摘要

与青春期不良经历相关的强烈应激会导致精神障碍,同时影响大脑结构和功能。然而,其潜在的神经生物学机制仍 largely unknown。为了研究青春期不良经历所诱导的应激是否会影响少突胶质细胞(OL)重塑,将社会挫败应激施加于6周龄的青春期小鼠,持续10天,随后进行行为测试和少突胶质细胞生成评估。在行为实验中,遭受社会挫败的小鼠表现出类似抑郁的行为。应激导致前皮质区域新生OL数量减少,以及胼胝体和大脑后皮质中蛋白脂质蛋白阳性成熟OL数量减少。在遭受社会挫败的小鼠的这些区域中,观察到掺入溴脱氧尿苷的CC1阳性成熟OL较少。为了评估社会挫败应激导致的少突胶质细胞生成减少是否与应激下的类似抑郁症状有关,将诱导OL生成的药物氯马斯汀给予遭受社会挫败的青春期小鼠,结果行为异常得到挽救,同时少突胶质细胞生成增加。这些发现表明,青春期不良环境中的少突胶质细胞生成在精神疾病中起作用,氯马斯汀可能为针对OLs的青少年精神障碍提供一种潜在的治疗药物。

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