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Research Article | Open Access

Krill oil attenuates obesity-induced skeletal muscle atrophy in mice

Mengqing Zhoua,b,1Yuhong Yangc,1Yan ZhengbZijian WuaChen ChenaQijian LiangaYu YangaHao Wua,b( )Xin Guoa,b( )Lei Dua,b ( )
Department of Nutrition and Food Hygiene, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan 250012, China
Research Center of Translational Medicine, Jinan Central Hospital, Shandong University, Jinan 250013, China
School of Food Science and Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, China

1 These authors contributed equally to this work.

Peer review under responsibility of Beijing Academy of Food Sciences.

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Highlights

• Krill oil attenuated obesity-induced skeletal muscle atrophy in mice.

• Krill oil diminished obesity-induced lipid deposition and inflammation in skeletal muscle.

• Krill oil balanced muscle protein degradation and synthesis in obese mice.

• Krill oil promoted muscle mitochondrial biogenesis in obese mice.

Abstract

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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Food Science and Human Wellness
Article number: 9250018

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Cite this article:
Zhou M, Yang Y, Zheng Y, et al. Krill oil attenuates obesity-induced skeletal muscle atrophy in mice. Food Science and Human Wellness, 2025, 14(1): 9250018. https://doi.org/10.26599/FSHW.2024.9250018

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Received: 01 April 2023
Revised: 12 June 2023
Accepted: 21 June 2023
Published: 14 February 2025
© 2025 Beijing Academy of Food Sciences. Publishing services by Tsinghua University Press.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).