慢性应激通过抑制小鼠mTORC1信号通路诱导2b型骨骼肌萎缩

Shigeko Fushimi, Tsutomu Nohno, Hironobu Katsuyama
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摘要

慢性压力引起心理和生理变化,可能对健康和福祉产生负面影响。本研究以C57BL/6雄性小鼠为研究对象,对其进行重复性水浸约束应激对模型慢性应激的影响。慢性应激小鼠血清皮质酮水平显著升高,胸腺体积和骨密度下降。此外,体重、骨骼肌质量和握力明显下降。比目鱼肌组织化学分析显示2b型肌纤维横截面积明显减少。虽然2a型肌纤维也有减少的趋势,但慢性应激对1型肌纤维没有影响。慢性应激增加了REDD1、FoxO1、FoxO3、KLF15、Atrogin1和FKBP5的表达,但不影响肌生长抑制素和肌生成素的表达。相反,慢性应激导致比目鱼肌中p-S6和p-4E-BP1水平下降。综上所述,这些结果表明,慢性应激通过抑制雷帕霉素复合物1 (rapamycin complex 1)抑制剂REDD1的上调而促进肌肉萎缩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Chronic Stress Induces Type 2b Skeletal Muscle Atrophy via the Inhibition of mTORC1 Signaling in Mice.

Chronic stress induces psychological and physiological changes that may have negative sequelae for health and well-being. In this study, the skeletal muscles of male C57BL/6 mice subjected to repetitive water-immersion restraint stress to model chronic stress were examined. In chronically stressed mice, serum corticosterone levels significantly increased, whereas thymus volume and bone mineral density decreased. Further, body weight, skeletal muscle mass, and grip strength were significantly decreased. Histochemical analysis of the soleus muscles revealed a significant decrease in the cross-sectional area of type 2b muscle fibers. Although type 2a fibers also tended to decrease, chronic stress had no impact on type 1 muscle fibers. Chronic stress increased the expression of REDD1, FoxO1, FoxO3, KLF15, Atrogin1, and FKBP5, but did not affect the expression of myostatin or myogenin. In contrast, chronic stress resulted in a decrease in p-S6 and p-4E-BP1 levels in the soleus muscle. Taken together, these results indicate that chronic stress promotes muscle atrophy by inhibiting mammalian targets of rapamycin complex 1 activity due to the upregulation of its inhibitor, REDD1.

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