氧化磷酸化
比目鱼肌
餐后
内分泌学
糖原
内科学
碳水化合物代谢
化学
新陈代谢
葡萄糖稳态
甘油三酯
脂质代谢
高胰岛素血症
生物能学
肌萎缩
生物化学
生物
胰岛素
胆固醇
骨骼肌
医学
线粒体
胰岛素抵抗
作者
Marc T. Hamilton,Deborah G. Hamilton,Theodore W. Zderic
出处
期刊:iScience
[Cell Press]
日期:2022-08-05
卷期号:25 (9): 104869-104869
被引量:27
标识
DOI:10.1016/j.isci.2022.104869
摘要
Slow oxidative muscle, most notably the soleus, is inherently well equipped with the molecular machinery for regulating blood-borne substrates. However, the entire human musculature accounts for only ∼15% of the body's oxidative metabolism of glucose at the resting energy expenditure, despite being the body's largest lean tissue mass. We found the human soleus muscle could raise local oxidative metabolism to high levels for hours without fatigue, during a type of soleus-dominant activity while sitting, even in unfit volunteers. Muscle biopsies revealed there was minimal glycogen use. Magnifying the otherwise negligible local energy expenditure with isolated contractions improved systemic VLDL-triglyceride and glucose homeostasis by a large magnitude, e.g., 52% less postprandial glucose excursion (∼50 mg/dL less between ∼1 and 2 h) with 60% less hyperinsulinemia. Targeting a small oxidative muscle mass (∼1% body mass) with local contractile activity is a potent method for improving systemic metabolic regulation while prolonging the benefits of oxidative metabolism.
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