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Glycolytic fast-twitch muscle fiber restoration counters adverse age-related changes in body composition and metabolism

机译:糖酵解快速抽搐的肌纤维修复可抵抗与年龄相关的不利身体组成和代谢变化

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摘要

Aging is associated with the development of insulin resistance, increased adiposity, and accumulation of ectopic lipid deposits in tissues and organs. Starting in mid-life there is a progressive decline in lean muscle mass associated with the preferential loss of glycolytic, fast-twitch myofibers. However, it is not known to what extent muscle loss and metabolic dysfunction are causally related or whether they are independent epiphenomena of the aging process. Here, we utilized a skeletal-muscle-specific, conditional transgenic mouse expressing a constitutively active form of Akt1 to examine the consequences of glycolytic, fast-twitch muscle growth in young vs. middle-aged animals fed standard low-fat chow diets. Activation of the Akt1 transgene led to selective skeletal muscle hypertrophy, reversing the loss of lean muscle mass observed upon aging. The Akt1-mediated increase in muscle mass led to reductions in fat mass and hepatic steatosis in older animals, and corrected age-associated impairments in glucose metabolism. These results indicate that the loss of lean muscle mass is a significant contributor to the development of age-related metabolic dysfunction and that interventions that preserve or restore fast/glycolytic muscle may delay the onset of metabolic disease.
机译:衰老与胰岛素抵抗的发展,肥胖症的增加以及组织和器官中异位脂质沉积的积累有关。从中年开始,瘦弱的肌肉质量会逐渐下降,这与糖酵解性快肌纤维的优先损失有关。然而,尚不清楚肌肉丧失和代谢功能障碍在何种程度上因果相关,或者它们是否是衰老过程的独立现象。在这里,我们利用表达Akt1组成型活性形式的骨骼肌特异性,条件性转基因小鼠,研究了饲喂标准低脂食物的年轻与中年动物的糖酵解,快速抽搐肌肉生长的后果。 Akt1转基因的激活导致选择性骨骼肌肥大,逆转了衰老时观察到的瘦肌肉的损失。 Akt1介导的肌肉量增加导致老年动物的脂肪量减少和肝脂肪变性减少,并纠正了与年龄相关的葡萄糖代谢障碍。这些结果表明,瘦肌肉的损失是与年龄有关的代谢功能障碍发展的重要原因,并且保留或恢复快速/糖酵解性肌肉的干预措施可能会延迟代谢疾病的发作。

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