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首页> 外文期刊>European review for medical and pharmacological sciences. >Physical inactivity induces the atrophy of skeletal muscle of rats through activating AMPK/FoxO3 signal pathway
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Physical inactivity induces the atrophy of skeletal muscle of rats through activating AMPK/FoxO3 signal pathway

机译:缺乏体育活动通过激活AMPK / FoxO3信号通路诱导大鼠骨骼肌萎缩

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OBJECTIVE: Long-term physical inactivity can cause the atrophy of skeletal muscle. The aim of this study is to explore the underlying mechanisms of physical inactivity-induced atrophy of skeletal muscle. MATERIALS AND METHODS: 14 Sprague- Dawley (SD) male rats were divided into 2 groups including normal control (NC) and hindlimb suspension (HS) groups. After two weeks of HS stimulation, the ratio between skeletal muscle weight and body weight, and cross-sectional area (CSA) of skeletal muscle fibers, were measured. Western blot was applied to evaluate the expression of proteins associated with atrophy and autophagy. The transmission electron microscope was used to observe the ultra-microstructure and the mitochondrial quality of skeletal muscle. RESULTS: The rats subjected to 2-week HS treatment presented an evident atrophy of the skeletal muscle with a significantly reduced ratio between skeletal muscle weight and body weight, and smaller cross-sectional area (CSA) of skeletal muscle fibers when compared with control rats. Meanwhile, HS stimulation resulted in the damage of mitochondria, the increased expression of MuRF1 and Atrogin-1/MAFbx, and enhanced apoptosis, as well as dysfunctional autophagy in skeletal muscle. CONCLUSIONS: HS-induced skeletal muscle atrophy involves the activation of AMPK/FoxO3 signal pathway, evidenced as AMPK phosphorylation, FoxO3 activation, and Atrogin-1 and MuRF1 up-regulation. FoxO3-mediated autophagy plays an important regulatory role in HS-induced skeletal muscle atrophy.
机译:目的:长期缺乏运动会导致骨骼肌萎缩。这项研究的目的是探索身体不活动导致骨骼肌萎缩的潜在机制。材料与方法:将14只Sprague-Dawley(SD)雄性大鼠分为2组,包括正常对照组(NC)和后肢悬液(HS)组。 HS刺激两周后,测量骨骼肌重量与体重之比,以及骨骼肌纤维的横截面积(CSA)。免疫印迹被用于评估与萎缩和自噬相关的蛋白质的表达。用透射电子显微镜观察骨骼肌的超微结构和线粒体质量。结果:经过2周HS处理的大鼠与对照组相比,骨骼肌明显萎缩,骨骼肌重量与体重之比显着降低,骨骼肌纤维横截面积(CSA)较小。同时,HS刺激导致线粒体损伤,MuRF1和Atrogin-1 / MAFbx表达增加,细胞凋亡增强以及骨骼肌自噬功能异常。结论:HS引起的骨骼肌萎缩涉及AMPK / FoxO3信号通路的激活,这可通过AMPK磷酸化,FoxO3激活以及Atrogin-1和MuRF1上调来证明。 FoxO3介导的自噬在HS诱导的骨骼肌萎缩中起重要的调节作用。

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