Krill oil attenuates obesity-induced skeletal muscle atrophy in mice

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作者
Mengqing Zhou [1 ,2 ]
Yuhong Yang [3 ]
Yan Zheng [2 ]
Zijian Wu [1 ]
Chen Chen [1 ]
Qijian Liang [1 ]
Yu Yang [1 ]
Hao Wu [1 ,2 ]
Xin Guo [1 ,2 ]
Lei Du [1 ,2 ]
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[1] Department of Nutrition and Food Hygiene, School of Public Health, Cheeloo College of Medicine, Shandong University
[2] Research Center of Translational Medicine, Jinan Central Hospital, Shandong University
[3] School of Food Science and Engineering, Qilu University of Technology (Shandong Academy of
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Obesity is associated with skeletal muscle mass loss and physical dysfunction. Krill oil(KO) has been shown to be beneficial in human health. However, the effect of KO on obesity-induced skeletal muscle atrophy is still unclear. In this study, the male C57BL/6J mice were fed a high-fat diet(HFD) for 12 weeks to induce obesity, and then were intragastric administration with 400 mg/kg bw KO for an additional 6 weeks. The results showed that KO treatment reduced body weight, fat accumulation and serum pro-inflammatory cytokines in HFD-induced obese mice. Importantly, KO treatment attenuated skeletal muscle atrophy in HFD-fed mice, as evidenced by preserving skeletal muscle mass, average myofiber cross-sectional area and grip strength. KO administration also mitigated obesity-induced ectopic lipid deposition and inflammatory response in skeletal muscle. Additionally, KO treatment inhibited the transcriptional activities of nuclear factor-κB(NF-κB) p65 and forkhead box O 3a(FoxO3a), and then down-regulated muscle atrophy F-box(MAFbx) and muscle-specific RING finger protein 1(MuRF1) protein levels in skeletal muscle from HFD-fed mice. KO administration also improved obesity-induced impaired muscle protein synthesis via activating PI3K/Akt pathway. Furthermore, KO treatment enhanced muscle mitochondrial biogenesis in HFD-induced obese mice via activating PGC-1α pathway. Collectively, KO might be developed as a potential nutritional supplement for the prevention and treatment of obesity-induced skeletal muscle atrophy.
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