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The recovery trajectory of adolescent social defeat stress-induced behavioral 1H-MRS metabolites and myelin changes in Balb/c mice

机译:Balb / c小鼠青春期社交挫折应激行为1H-MRS代谢产物和髓磷脂变化的恢复轨迹

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摘要

Adolescent exposure to social stress precipitates emotion-related disorders and affects the development and function of medial prefrontal cortex (mPFC). However, this adversity-induced behavioral and neurological changes remain not fully explored. Adolescent Balb/c mice were subjected to intermittent social defeat stress during postnatal days 28 to 42. Proton magnetic resonance spectroscopy (1H-MRS) measurements, behavioral tests and immunohistochemistry were performed one day or 3 weeks after the last stress episode. Defeated mice exhibited hypoactivity and social avoidance with the latter lasting into the early adulthood, while the anxiety level was unchanged. Social defeat experience lead to temporary decreases in the levels of total creatines (Cr + pCr) and Glx (Glu + Gln), but a delayed increase of N- acetylaspartate (NAA) levels. These alternations were accompanied with a persistent reduction of myelin basic protein expression although the number of mature oligodendrocyte did not change. These findings provide evidence that adolescent adverse social experience permanently impairs the emotion-related behavioral performance and induces biochemical and molecular changes in the brain which at least lasts into early adulthood, thus enhancing our understanding of the neurobiology of social defeat stress. Our finding also implicates that NAA signals on MRS may reflect myelin status.
机译:青少年遭受社会压力会加剧情绪相关的疾病,并影响内侧前额叶皮层(mPFC)的发育和功能。但是,这种逆境引起的行为和神经学变化仍未得到充分探讨。青春期Balb / c小鼠在出生后28到42天间遭受间歇性社交挫败压力。质子磁共振波谱( 1 H-MRS)测量,行为测试和免疫组化在术后1天或3周进行最后的压力发作。击败的小鼠表现出机能减退和社交回避,后者持续到成年初期,而焦虑水平未变。社交失败的经历会导致总肌酸(Cr + pCr)和Glx(Glu + Gln)的水平暂时降低,但N-乙酰天门冬氨酸(NAA)水平的升高会延迟。尽管成熟的少突胶质细胞的数量没有改变,但这些交替伴随着髓磷脂碱性蛋白表达的持续降低。这些发现提供了证据,表明青春期不良的社交经历会永久损害与情感相关的行为表现,并诱发大脑中至少持续到成年的生化和分子变化,从而增强我们对社交失败压力的神经生物学的理解。我们的发现还暗示MRS上的NAA信号可能反映了髓磷脂状态。

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