合成代谢
骨骼肌
肌萎缩
分解代谢
随机对照试验
内科学
内分泌学
维生素D与神经学
医学
化学
新陈代谢
作者
Tetsuya Kawahara,Tetsuya Inazu,Shoichi Mizuno,Naoki Tominaga,Mikio Toda,Nagahiro Toyama,Chie Kawahara,Gen Suzuki
标识
DOI:10.1016/j.metabol.2025.156240
摘要
BACKGROUND: The muscle-building and strengthening effects of the active form of vitamin D in humans remain unclear. METHODS: In this ancillary study of the Diabetes Prevention with active Vitamin D trial, we examined clinical and experimental aspects to investigate the effects and mechanisms of eldecalcitol, an active form of vitamin D, in preventing sarcopenia. We examined changes in molecules involved in muscle synthesis and degradation pathways in muscle samples from 32 participants before and after 1 year of eldecalcitol or placebo treatment. The protein levels of molecules involved in muscle synthesis and degradation pathways were examined using western blotting. Additionally, the skeletal muscle and body fat volumes were measured using bioelectrical impedance analysis with a body composition analyzer. RESULTS: We found that eldecalcitol treatment for 1 year resulted in higher phosphorylation levels of mTOR and FOXO1 signaling pathways, which are associated with increased muscle mass and strength than those with placebo treatment. Body composition measurements at 1 year showed that the eldecalcitol group had significantly higher skeletal muscle mass (1.9 % vs. -3.4 %, p = 3.26E-9) and muscle strength (4.1 % vs. -0.7 %, p = 2.57E-17), and lower fat mass (-3.2 % vs. 1.8 %, p = 1.73E-12) than those in the placebo group. CONCLUSION: This study suggested that the active form of vitamin D regulates the protein synthesis and degradation pathways in human skeletal muscle and may help prevent sarcopenia. This study was registered at UMIN clinical trials registry, UMIN 000005394.
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