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Vitamin C and E Supplementation Inhibits Acute Exercise-induced Skeletal Muscle Signaling but does not Alter Maker of Muscle Adaptations

机译:补充维生素C和E抑制急性运动诱发的骨骼肌信号传导,但不会改变肌肉适应的产生者

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Aim: The aim of this study was to investigate the effects of vitamin C and E supplementation on acute exercise-induced changes of makers of skeletal muscle adaptation and its signaling pathways in mice. Methodology: Male C57BL/6 mice were assigned to one of four groups: a control group, exercise group, vitamin C and E supplemented group, and vitamin C and E supplemented exercise group. Mice in vitamin C and E supplemented group were given vitamin C (750 mg/kg weight/day) and vitamin E (150 mg/kg weight/day) for two weeks. One hour after the last supplementation, exercise group mice ran on a treadmill at 25 m/min, 8% grade for 120 min. Results: Vitamin C and supplementation attenuated exercise-induced oxidative stress (P<0.01). However, vitamin C and E supplementation with vitamins C and E did not alter the acute exercise-induced increase in gene expression of peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α), citrate synthase (CS) and vascular endothelial growth factor (VEGF). On the other hand, vitamin C and E supplementation prevented the phosphorylation of AMP activated kinase (AMPK) and p38 mitogen-activated protein kinase (p38 MAPK) following the treadmill running (P<0.05). Conclusion: These results suggest that reactive oxygen species (ROS) inhibits exercise-induced skeletal muscle signaling but does not alter mitochondrial biogenesis and angiogenesis in skeletal muscle.
机译:目的:本研究的目的是研究补充维生素C和E对急性运动诱发的小鼠骨骼肌适应性制造商及其信号传导途径变化的影响。方法:将雄性C57BL / 6小鼠分为四组之一:对照组,运动组,补充维生素C和E的组以及补充维生素C和E的运动组。补充维生素C和E的组的小鼠接受维生素C(750 mg / kg体重/天)和维生素E(150 mg / kg体重/天)两个星期。最后一次补充后一小时,运动组小鼠以5%的坡度以25 m / min的速度在跑步机上跑步120分钟。结果:补充维生素C可以减轻运动引起的氧化应激(P <0.01)。然而,补充维生素C和E并不能改变运动引起的急性过氧化物酶体增殖物激活受体-γ共激活因子1α(PGC-1α),柠檬酸合酶(CS)和血管内皮生长的基因表达增加。因子(VEGF)。另一方面,维生素C和E的添加阻止了跑步机跑步后AMP激活激酶(AMPK)和p38丝裂原激活蛋白激酶(p38 MAPK)的磷酸化(P <0.05)。结论:这些结果表明活性氧(ROS)抑制运动诱导的骨骼肌信号传导,但不会改变骨骼肌线粒体的生物发生和血管生成。

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