Vitamin D status modulates mitochondrial oxidative capacities in skeletal muscle: role in sarcopenia

• Published in: Communications biology Vol. 5; no. 1; pp. 1288 - 15
• Main Authors: Salles, Jérôme, Chanet, Audrey, Guillet, Christelle, Vaes, Anouk MM, Brouwer-Brolsma, Elske M., Rocher, Christophe, Giraudet, Christophe, Patrac, Véronique, Meugnier, Emmanuelle, Montaurier, Christophe, Denis, Philippe, Le Bacquer, Olivier, Blot, Adeline, Jourdan, Marion, Luiking, Yvette, Furber, Matthew, Van Dijk, Miriam, Tardif, Nicolas, Yves Boirie, Y., Walrand, Stéphane
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 24.11.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 13/106; 45/61; 45/77; 631/443/810; 64/110; 64/60; 692/699/1702; 82/58; Aged; Animals; Biology; Biomedical and Life Sciences; Biosynthesis; Dietary supplements; Electron transport; Energy expenditure; Energy output; Food and Nutrition; Humans; Life Sciences; Mice; Mitochondria; Mitochondria - metabolism; Muscle, Skeletal - pathology; Musculoskeletal system; Myotubes; Older people; Oxidative phosphorylation; Oxidative Stress; Phosphorylation; Rats; Sarcopenia; Sarcopenia - metabolism; Skeletal muscle; Transgenic mice; Vitamin D; Vitamin D - metabolism; Vitamin D - pharmacology; Vitamin D Deficiency - metabolism; Vitamin D Deficiency - pathology; Vitamin D receptors; Vitamin deficiency
• ISSN: 2399-3642; 2399-3642
• DOI: 10.1038/s42003-022-04246-3

Skeletal muscle mitochondrial function is the biggest component of whole-body energy output. Mitochondrial energy production during exercise is impaired in vitamin D-deficient subjects. In cultured myotubes, loss of vitamin D receptor (VDR) function decreases mitochondrial respiration rate and ATP production from oxidative phosphorylation. We aimed to examine the effects of vitamin D deficiency and supplementation on whole-body energy expenditure and muscle mitochondrial function in old rats, old mice, and human subjects. To gain further insight into the mechanisms involved, we used C2C12 and human muscle cells and transgenic mice with muscle-specific VDR tamoxifen-inducible deficiency. We observed that in vivo and in vitro vitamin D fluctuations changed mitochondrial biogenesis and oxidative activity in skeletal muscle. Vitamin D supplementation initiated in older people improved muscle mass and strength. We hypothesize that vitamin D supplementation is likely to help prevent not only sarcopenia but also sarcopenic obesity in vitamin D-deficient subjects. Vitamin D has an impact on mitochondrial biogenesis and oxidative activity in skeletal muscle both in vitro and in vivo, and vitamin D supplementation in older people may improve muscle mass and strength.