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体力活动不足通过激活 AMPK/FoxO3 信号通路诱导大鼠骨骼肌萎缩。

Physical inactivity induces the atrophy of skeletal muscle of rats through activating AMPK/FoxO3 signal pathway.

机构信息

Graduate School, Wuhan Sports University, Wuhan, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Jan;22(1):199-209. doi: 10.26355/eurrev_201801_14118.

Abstract

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.

摘要

目的

长期不运动可导致骨骼肌萎缩。本研究旨在探讨不运动导致骨骼肌萎缩的潜在机制。

材料与方法

14 只 Sprague-Dawley(SD)雄性大鼠分为正常对照组(NC)和后肢悬吊(HS)组。经过两周的 HS 刺激后,测量骨骼肌重量与体重的比值以及骨骼肌纤维的横截面积(CSA)。采用 Western blot 评估与萎缩和自噬相关的蛋白表达。利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

接受 2 周 HS 治疗的大鼠出现明显的骨骼肌萎缩,骨骼肌重量与体重的比值显著降低,骨骼肌纤维 CSA 减小。同时,HS 刺激导致线粒体损伤、MuRF1 和 Atrogin-1/MAFbx 表达增加、凋亡增强以及骨骼肌自噬功能障碍。

结论

HS 诱导的骨骼肌萎缩涉及 AMPK/FoxO3 信号通路的激活,表现为 AMPK 磷酸化、FoxO3 激活以及 Atrogin-1 和 MuRF1 的上调。FoxO3 介导的自噬在 HS 诱导的骨骼肌萎缩中发挥重要的调节作用。

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