Melatonin and Exercise Counteract Sarcopenic Obesity through Preservation of Satellite Cell Function

• Published in: International journal of molecular sciences 2023-03, Vol.24 (7), p.6097
• Main Authors: Mankhong, Sakulrat, Kim, Sujin, Moon, Sohee, Lee, Jae-Seon, Cho, Eun-Jeong, Kwak, Hyo-Bum, Park, Dong-Ho, Ryu, Ji-Kan, Kang, Ju-Hee
• Format: Article
• Language: English
• Subjects: Aging; Animals; Atrophy; Attenuation; Autophagy; Calcium (mitochondrial); Cells (biology); Diet, High-Fat - adverse effects; Fitness training programs; High fat diet; Hydrogen peroxide; Hydrogen Peroxide - metabolism; Impairment; Intervention; Melatonin; Melatonin - metabolism; Melatonin - pharmacology; Mice; Mitochondria; Morbidity; Morphology; Muscle, Skeletal - metabolism; Muscles; Muscular Atrophy - metabolism; Musculoskeletal system; Myoblasts; Obesity; Obesity - metabolism; Older people; Phosphorylation; Physical training; Protein synthesis; Proteins; Sarcopenia; Sarcopenia - metabolism; Satellite cells; Senescence; Skeletal muscle
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms24076097

Sarcopenic obesity (SO) is characterized by atrophic skeletal muscle impairment (sarcopenia) and obesity, which is associated with adverse outcomes of morbidity and mortality in elderly people. We investigated the effects of melatonin and exercise training on SO in 32-week-old senescence-accelerated mouse-prone-8 (SAMP8) mice fed a normal diet or a high-fat diet for 16 weeks. Melatonin, exercise, or melatonin and exercise for 8 weeks displayed reductions in the SO-induced impairment of skeletal muscle function and atrophy. Specifically, a decrease in mitochondrial calcium retention capacity in skeletal muscles observed in the HFD-con group was attenuated in melatonin and/or exercise intervention groups. More importantly, HFD-con mice displayed a lower number of Pax7+ satellite cells (SCs) and higher expression of p16 than P8ND mice, which were attenuated by melatonin and/or exercise interventions. The cellular senescence in SC-derived primary myoblasts from HFD-con mice was significantly attenuated in myoblasts from the melatonin and/or exercise groups, which was reproduced in a senescence model of H O -treated C2C12 myoblasts. Our results suggest that melatonin and exercise training attenuate SO-induced skeletal muscle dysfunction, at least in part, through preserving the SC pool by inhibiting cellular senescence and attenuating mitochondrial dysfunction.