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肌肉减少性肥胖中的异常蛋白周转和运动合成代谢抵抗。

Abnormal protein turnover and anabolic resistance to exercise in sarcopenic obesity.

机构信息

1Department of Health and Kinesiology, Texas A&M University, College Station, TX 77843-4243.

出版信息

FASEB J. 2013 Oct;27(10):3905-16. doi: 10.1096/fj.12-224006. Epub 2013 Jun 26.

Abstract

Obesity may impair protein synthesis rates and cause anabolic resistance to growth factors, hormones, and exercise, ultimately affecting skeletal muscle mass and function. To better understand muscle wasting and anabolic resistance with obesity, we assessed protein 24-h fractional synthesis rates (24-h FSRs) in selected hind-limb muscles of sedentary and resistance-exercised lean and obese Zucker rats. Despite atrophied hind-limb muscles (-28% vs. lean rats), 24-h FSRs of mixed proteins were significantly higher in quadriceps (+18%) and red or white gastrocnemius (+22 or +38%, respectively) of obese animals when compared to lean littermates. Basal synthesis rates of myofibrillar (+8%) and mitochondrial proteins (-1%) in quadriceps were not different between phenotypes, while manufacture of cytosolic proteins (+12%) was moderately elevated in obese cohorts. Western blot analyses revealed a robust activation of p70S6k (+178%) and a lower expression of the endogenous mTOR inhibitor DEPTOR (-28%) in obese rats, collectively suggesting that there is an obesity-induced increase in net protein turnover favoring degradation. Lastly, the protein synthetic response to exercise of mixed (-7%), myofibrillar (+6%), and cytosolic (+7%) quadriceps subfractions was blunted compared to the lean phenotype (+34, +40, and +17%, respectively), indicating a muscle- and subfraction-specific desensitization to the anabolic stimulus of exercise in obese animals.

摘要

肥胖可能会损害蛋白质合成率,并导致生长因子、激素和运动的合成代谢抵抗,最终影响骨骼肌的质量和功能。为了更好地了解肥胖症与肌肉减少症和合成代谢抵抗的关系,我们评估了久坐和抗阻运动的瘦型和肥胖型 Zucker 大鼠选定后肢肌肉的蛋白质 24 小时分数合成率(24-h FSRs)。尽管后肢肌肉萎缩(比瘦型大鼠减少 28%),但与瘦型同窝仔相比,肥胖型动物的股四头肌(增加 18%)和红色或白色比目鱼肌(分别增加 22%或 38%)的混合蛋白 24-h FSRs 显著升高。股四头肌肌原纤维(增加 8%)和线粒体蛋白质(-1%)的基础合成率在表型之间没有差异,而胞质蛋白质(增加 12%)的合成则适度升高。Western blot 分析显示,肥胖大鼠的 p70S6k 显著激活(增加 178%),内源性 mTOR 抑制剂 DEPTOR 的表达降低(减少 28%),这表明存在肥胖诱导的净蛋白质周转率增加,有利于降解。最后,与瘦型表型相比(分别增加 34%、40%和 17%),混合(-7%)、肌原纤维(+6%)和胞质(+7%)股四头肌亚组分的蛋白质合成对运动的反应减弱,表明肥胖动物的肌肉和亚组分对运动的合成代谢刺激存在特异性脱敏。

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