共轭亚油酸/n-3和抗阻训练对高脂饮食诱导肥胖中年小鼠肌肉质量和萎缩相关泛素连接酶表达的影响

Seung-Lyul Oh, Sang-Rok Lee, Jeong-Su Kim
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引用次数: 7

摘要

目的:探讨共轭亚油酸(CLA)/n-3补充剂和抗阻运动训练(RT)对中年高脂饮食(HFD)诱导肥胖小鼠肌肉质量和蛋白质合成/降解相关基因的影响。方法:将9月龄C57BL/6雄性小鼠随机分为5组:1)正常饮食(C), 2)高脂饮食(H), 3) H+RT (HRT), 4) H+CLA/n-3 (H- cn), 5) H+RT+CLA/n-3 (H- rtcn)。高脂肪组给予含60%脂肪的饮食20周,运动组采用加权爬梯法进行渐进式RT。CLA/n-3混合饲粮添加1%的CLA和1%的n-3。评估握力,并切除肱三头肌。RT-PCR分析转录物水平。结果:H组握力明显低于C组;H- cn组、H- rt组、H- rtn组均显著高于H组。然而,与H和H- cn组相比,只有H- rt组的肌肉质量显著提高。与C和H组相比,H- cn、H- rt和H- rtcn组中Akt的表达降低,而H、H- cn、H- rt和H- rtcn组中哺乳动物雷帕霉素靶蛋白的表达较C组增加。然而,与H和H- cn组相比,H- rtcn组atrogin1表达明显下调,H- rt和H- rtcn组MuRF1表达也降低。有趣的是,与H-CN组相比,H-RTCN组atrogin1和MuRF1下调。结论:用CLA/n-3治疗20周后,hfd介导的蛋白降解相关基因表达减弱。此外,添加或不添加CLA/n-3的RT可改善中年小鼠在HFD期间的握力和肌肉质量。因此,在高强度运动期间,含CLA/n-3的RT可能通过抑制蛋白质降解来改善肌肉力量和质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effects of conjugated linoleic acid/n-3 and resistance training on muscle quality and expression of atrophy-related ubiquitin ligases in middle-aged mice with high-fat diet-induced obesity.

Effects of conjugated linoleic acid/n-3 and resistance training on muscle quality and expression of atrophy-related ubiquitin ligases in middle-aged mice with high-fat diet-induced obesity.

Effects of conjugated linoleic acid/n-3 and resistance training on muscle quality and expression of atrophy-related ubiquitin ligases in middle-aged mice with high-fat diet-induced obesity.
[Purpose] To investigate the effects of conjugated linoleic acid (CLA)/n-3 supplements and resistance exercise training (RT) for 20 weeks on muscle quality and genes related to protein synthesis/degradation in middle-aged mice with high-fat diet (HFD)-induced obesity. [Methods] Nine-month-old C57BL/6 male mice were randomly assigned to five groups: 1) normal diet (C), 2) high-fat diet (H), 3) H+RT (HRT), 4) H+CLA/n-3 (H-CN), and 5) H+RT+CLA/n-3 (H-RTCN). HFD groups were given a diet containing 60% fat for 20 weeks, and exercised groups underwent progressive RT using weighted ladder climbing. The CLA/n-3 mixed diet contained 1% CLA and 1% n-3. Grip strength was assessed, and triceps were removed. RT-PCR was used to analyze transcript levels. [Results] Grip strength of the H group was significantly lower than that of the C group; however, those in the H-CN, H-RT, and H-RTN groups were significantly greater than that in the H group. However, the muscle quality was significantly greater only in the H-RT group compared with the H and H-CN groups. Akt expression decreased in the H-CN, H-RT, and H-RTCN groups compared with those in the C and H groups, whereas mammalian target of rapamycin expression increased in the H, H-CN, H-RT, and H-RTCN groups compared with that in the C group. However, atrogin1 was significantly downregulated in the H-RTCN group compared with that in the H and H-CN groups, and MuRF1 expression was also decreased in the H-RT and H-RTCN groups. Interestingly, atrogin1 and MuRF1 were downregulated in the H-RTCN group compared with that in the H-CN group. [Conclusion] HFD-mediated gene expression involved in protein degradation was attenuated following 20-week RT with CLA/n-3. Furthermore, RT with or without CLA/n-3 improved grip strength and muscle quality in middle-aged mice during HFD. Therefore, RT with CLA/n-3 during HFD may improve muscle strength and quality by suppressing protein degradation.
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