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Chronic social defeat reduces myelination in the mouse medial prefrontal cortex

机译:慢性社交衰竭减少了小鼠内侧前额叶皮层的髓鞘形成

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摘要

The medial prefrontal cortex (mPFC) plays a key role in top-down control of the brain’s stress axis, and its structure and function are particularly vulnerable to stress effects, which can lead to depression in humans and depressive-like states in animals. We tested whether chronic social defeat produces structural alterations in the mPFC in mice. We first performed a microarray analysis of mPFC gene expression changes induced by defeat, and biological pathway analysis revealed a dominant pattern of down-regulation of myelin-associated genes. Indeed, 69% of the most significantly down-regulated genes were myelin-related. The down regulation was confirmed by in situ hybridization histochemistry for two strongly down-regulated genes, myelin oligodendrocyte glycoprotein (Mog) and ermin (Ermn), and by immunohistochemistry for myelin basic protein. To test for stress-induced changes in myelin integrity, aurophosphate (Black Gold) myelin staining was performed on mPFC sections. Quantitative stereologic analysis showed reduced myelinated fiber length and density. Behavioral analysis confirmed that the 14-day social defeat sessions resulted in induction of depressive-like states measured in social interaction and light/dark tests. The combined data suggest that chronic social defeat induces molecular changes that reduce myelination of the prefrontal cortex, which may be an underlying basis for stress-induced depressive states.
机译:内侧前额叶皮层(mPFC)在自上而下控制大脑的压力轴中起着关键作用,其结构和功能特别容易受到压力的影响,这可能导致人的抑郁和动物的抑郁样状态。我们测试了慢性社交失败是否会在小鼠的mPFC中产生结构性改变。我们首先进行了由失败诱导的mPFC基因表达变化的微阵列分析,而生物学途径分析揭示了髓磷脂相关基因下调的主要模式。实际上,最显着下调的基因中有69%与髓磷脂有关。下调通过两个强烈下调的基因,髓鞘少突胶质细胞糖蛋白(Mog)和ermin(Ermn)的原位杂交组织化学,以及髓鞘碱性蛋白的免疫组织化学证实。为了测试压力诱导的髓磷脂完整性变化,在mPFC切片上进行了磷酸铝(黑金)髓磷脂染色。定量立体分析显示,髓鞘纤维长度和密度降低。行为分析证实,为期14天的社交挫败活动导致了在社交互动和明暗测试中测得的抑郁状态。综合数据表明,长期的社会失败导致分子变化,从而减少前额叶皮层的髓鞘形成,这可能是压力诱发的抑郁状态的基础。

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