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Obese subcutaneous adipose tissue impairs human myogenesis particularly in old skeletal muscle via resistin-mediated activation of NFκB

机译:肥胖的皮下脂肪组织会通过抵抗素介导的NFκB激活而损害人的肌生成特别是在老骨骼肌中

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摘要

Adiposity and adipokines are implicated in the loss of skeletal muscle mass with age and in several chronic disease states. The aim of this study was to determine the effects of human obese and lean subcutaneous adipose tissue secretome on myogenesis and metabolism in skeletal muscle cells derived from both young (18–30 yr) and elderly (>65 yr) individuals. Obese subcutaneous adipose tissue secretome impaired the myogenesis of old myoblasts but not young myoblasts. Resistin was prolifically secreted by obese subcutaneous adipose tissue and impaired myotube thickness and nuclear fusion by activation of the classical NFκB pathway. Depletion of resistin from obese adipose tissue secretome restored myogenesis. Inhibition of the classical NFκB pathway protected myoblasts from the detrimental effect of resistin on myogenesis. Resistin also promoted intramyocellular lipid accumulation in myotubes and altered myotube metabolism by enhancing fatty acid oxidation and increasing myotube respiration and ATP production. In conclusion, resistin derived from human obese subcutaneous adipose tissue impairs myogenesis of human skeletal muscle, particularly older muscle, and alters muscle metabolism in developing myotubes. These findings may have important implications for the maintenance of muscle mass in older people with chronic inflammatory conditions, or older people who are obese or overweight.
机译:肥胖和脂肪因子与年龄和某些慢性疾病状态有关,导致骨骼肌质量下降。这项研究的目的是确定人肥胖和瘦的皮下脂肪组织分泌基因组对年轻人(18-30岁)和老年人(> 65岁)个体骨骼肌细胞的生成和代谢的影响。肥胖的皮下脂肪组织分泌蛋白组损害了旧成肌细胞的成肌能力,但不损害年轻成肌细胞的成肌能力。肥胖的皮下脂肪组织大量分泌抵抗素,并通过激活经典的NFκB途径损害肌管厚度和核融合。肥胖的脂肪组织分泌蛋白组中抵抗素的消耗恢复了肌生成。抑制经典的NFκB通路可保护成肌细胞免受抵抗素对肌生成的不利影响。抵抗素还通过增强脂肪酸氧化并增加肌管呼吸和ATP的产生来促进肌管内肌内脂质的积累并改变肌管的代谢。总之,源自人肥胖皮下脂肪组织的抵抗素会损害人骨骼肌,特别是年长肌肉的肌发生,并改变发育中的肌管中的肌肉代谢。这些发现可能对患有慢性炎性疾病的老年人或肥胖或超重的老年人的肌肉质量的维持具有重要意义。

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