Key result
Krill oil administration attenuated skeletal muscle atrophy, preserved muscle mass and grip strength, and reduced ectopic lipid deposition in high-fat diet-induced obese mice.
Why the study?
Obesity is associated with skeletal muscle mass loss and physical dysfunction, but the effect of krill oil on obesity-induced skeletal muscle atrophy remains unclear.
Does krill oil attenuate obesity-induced skeletal muscle atrophy in high-fat diet-induced obese mice?
Does krill oil attenuate obesity-induced skeletal muscle atrophy in high-fat diet-induced obese mice?
Krill oil supplementation may attenuate obesity-induced skeletal muscle atrophy by reducing inflammation, improving protein synthesis, and enhancing mitochondrial biogenesis in a preclinical model.
Hypothesis-generating for krill oil in obese mice; human trials required before clinical consideration.
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-kappa B (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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Zhou et al. (2024) studied Obesity-induced skeletal muscle atrophy. Krill oil vs. HFD-fed mice without krill oil was evaluated on Skeletal muscle atrophy (muscle mass, myofiber cross-sectional area, grip strength). Krill oil administration attenuated skeletal muscle atrophy, preserved muscle mass and grip strength, and reduced ectopic lipid deposition in high-fat diet-induced obese mice.
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