Vitamin D ameliorates adipose browning in chronic kidney disease cachexia

• Published in: Scientific reports Vol. 10; no. 1; pp. 14175 - 15
• Main Authors: Cheung, Wai W., Ding, Wei, Hoffman, Hal M., Wang, Zhen, Hao, Sheng, Zheng, Ronghao, Gonzalez, Alex, Zhan, Jian-Ying, Zhou, Ping, Li, Shiping, Esparza, Mary C., Lieber, Richard L., Mak, Robert H.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 25.08.2020; Nature Publishing Group; Nature Portfolio
• Subjects: 631/337; 692/4022; 692/4022/272; Adipocytes, Beige - drug effects; Adipocytes, Beige - metabolism; Adipocytes, Brown - metabolism; Adipocytes, White - metabolism; Adipose tissue; Animals; Appetite; Cachexia; Cachexia - drug therapy; Cachexia - etiology; Cachexia - physiopathology; Calcifediol - blood; Calcifediol - deficiency; Calcifediol - pharmacology; Calcifediol - therapeutic use; Calcitriol; Calcitriol - blood; Calcitriol - deficiency; Calcitriol - pharmacology; Calcitriol - therapeutic use; Collagen; Disease Models, Animal; Eating - drug effects; Fibrosis; Fibrosis - genetics; Gastrocnemius muscle; Gene Expression Regulation - drug effects; Hand Strength; Humanities and Social Sciences; Kidney diseases; Kidneys; Mice; Mice, Inbred C57BL; multidisciplinary; Muscle Fibers, Skeletal - drug effects; Muscle Fibers, Skeletal - pathology; Musculoskeletal system; Nephrectomy; Parathyroid Hormone - blood; Regeneration; Renal Insufficiency, Chronic - blood; Renal Insufficiency, Chronic - complications; Renal Insufficiency, Chronic - drug therapy; RNA, Messenger - biosynthesis; Rotarod Performance Test; Science; Science (multidisciplinary); Sequence Analysis, RNA; Skeletal muscle; Supplements; Thermogenesis; Thermogenesis - drug effects; Vitamin D; Weight Gain - drug effects
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-70190-z

Patients with chronic kidney disease (CKD) are often 25(OH)D 3 and 1,25(OH) 2 D 3 insufficient. We studied whether vitamin D repletion could correct aberrant adipose tissue and muscle metabolism in a mouse model of CKD-associated cachexia. Intraperitoneal administration of 25(OH)D 3 and 1,25(OH) 2 D 3 (75 μg/kg/day and 60 ng/kg/day respectively for 6 weeks) normalized serum concentrations of 25(OH)D 3 and 1,25(OH) 2 D 3 in CKD mice. Vitamin D repletion stimulated appetite, normalized weight gain, and improved fat and lean mass content in CKD mice. Vitamin D supplementation attenuated expression of key molecules involved in adipose tissue browning and ameliorated expression of thermogenic genes in adipose tissue and skeletal muscle in CKD mice. Furthermore, repletion of vitamin D improved skeletal muscle fiber size and in vivo muscle function, normalized muscle collagen content and attenuated muscle fat infiltration as well as pathogenetic molecular pathways related to muscle mass regulation in CKD mice. RNAseq analysis was performed on the gastrocnemius muscle. Ingenuity Pathway Analysis revealed that the top 12 differentially expressed genes in CKD were correlated with impaired muscle and neuron regeneration, enhanced muscle thermogenesis and fibrosis. Importantly, vitamin D repletion normalized the expression of those 12 genes in CKD mice. Vitamin D repletion may be an effective therapeutic strategy for adipose tissue browning and muscle wasting in CKD patients.