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Differential effect of long-term leucine supplementation on skeletal muscle and adipose tissue in old rats: an insulin signaling pathway approach

机译:长期补充亮氨酸对老年大鼠骨骼肌和脂肪组织的差异作用:胰岛素信号通路方法

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摘要

Leucine acts as a signal nutrient in promoting protein synthesis in skeletal muscle and adipose tissue via mTOR pathway activation, and may be of interest in age-related sarcopenia. However, hyper-activation of mTOR/S6K1 has been suggested to inhibit the first steps of insulin signaling and finally promote insulin resistance. The impact of long-term dietary leucine supplementation on insulin signaling and sensitivity was investigated in old rats (18 months old) fed a 15% protein diet supplemented (LEU group) or not (C group) with 4.5% leucine for 6 months. The resulting effects on muscle and fat were examined. mTOR/S6K1 signaling pathway was not significantly altered in muscle from old rats subjected to long-term dietary leucine excess, whereas it was increased in adipose tissue. Overall glucose tolerance was not changed but insulin-stimulated glucose transport was improved in muscles from leucine-supplemented rats related to improvement in Akt expression and phosphorylation in response to food intake. No change in skeletal muscle mass was observed, whereas perirenal adipose tissue mass accumulated (+45%) in leucine-supplemented rats. A prolonged leucine supplementation in old rats differently modulates mTOR/S6K pathways in muscle and adipose tissue. It does not increase muscle mass but seems to promote hypertrophy and hyperplasia of adipose tissue that did not result in insulin resistance.
机译:亮氨酸是通过mTOR途径激活促进骨骼肌和脂肪组织中蛋白质合成的信号营养素,可能与年龄相关的肌肉减少症有关。但是,已经提出mTOR / S6K1的过度激活会抑制胰岛素信号传导的第一步,并最终促进胰岛素抵抗。长期饮食中补充亮氨酸对胰岛素信号传导和敏感性的影响在年龄为18月的大龄大鼠中进行了研究,喂食了15%的蛋白质饮食(LEU组)或不补充(C组)4.5%的亮氨酸,持续了6个月。检查了对肌肉和脂肪的最终影响。长期饮食中亮氨酸过量的老年大鼠肌肉中的mTOR / S6K1信号通路没有明显改变,而在脂肪组织中则增加。总体葡萄糖耐量没有改变,但是补充亮氨酸的大鼠肌肉中胰岛素刺激的葡萄糖转运得到改善,这与进食后Akt表达和磷酸化的改善有关。在补充亮氨酸的大鼠中未观察到骨骼肌质量变化,而肾周脂肪组织质量累积(+ 45%)。在老年大鼠中长期补充亮氨酸会不同地调节肌肉和脂肪组织中的mTOR / S6K途径。它不会增加肌肉质量,但似乎会促进脂肪组织的肥大和增生,而不会导致胰岛素抵抗。

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