β-hydroxy-β-methylbutyrate supplementation mitigates muscle atrophy induced by inactivity and protein deprivation.

IF 4.4 4区 医学 Q1 GERIATRICS & GERONTOLOGY
Xu He, Yan Li, Jun Chen, Yan Huang, Ying Zhou, Yang Li, Jing Quan
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引用次数: 0

Abstract

Muscle atrophy, resulting from physical inactivity or protein deficiency, is a significant health concern. β-hydroxy-β-methylbutyrate (HMB) has potential in preserving muscle mass, but its mechanisms in various atrophy-inducing conditions are not fully understood. This study aimed to investigate HMB's effects on muscle atrophy induced by inactivity and protein deprivation, and to elucidate the underlying molecular mechanisms. Rats were subjected to inactivity or protein-deficient diets with or without HMB supplementation. Muscle morphology, strength, and biochemical parameters were assessed. In vitro studies using C2C12 myoblasts and mouse skeletal muscle satellite cells exposed to interleukin-6 (IL-6) explored molecular pathways involved in HMB's protective effects. Inactivity and protein deprivation led to muscle atrophy, reduced strength, and altered biochemical markers. HMB supplementation partially mitigated these effects, preserving muscle mass and function. HMB attenuated atrophy markers (Muscle Atrophy F-box and Muscle RING Finger 1 (MuRF1)) and maintained myogenic factor (Myogenin (MyoG)) levels. In vitro studies revealed that HMB's protective effects were mediated through the AKT/mTOR pathway, with concurrent regulation of autophagy pathways and preservation of mitochondrial function in both myoblasts and satellite cells. HMB specifically protected satellite cell viability and function through AKT-dependent mechanisms, maintaining protein synthesis and reducing apoptosis under IL-6-induced stress conditions. HMB supplementation shows protective effects against muscle atrophy induced by inactivity and protein deprivation, through multiple mechanisms including AKT/mTOR pathway activation, autophagy regulation, and maintenance of mitochondrial function in both myoblasts and satellite cells. These findings suggest HMB as a potential therapeutic strategy for preventing muscle atrophy in various clinical scenarios.

补充β-羟基-β-甲基丁酸盐可减轻不活动和蛋白质剥夺引起的肌肉萎缩。
由于缺乏运动或缺乏蛋白质而引起的肌肉萎缩是一个重大的健康问题。β-羟基-β-甲基丁酸盐(HMB)具有保持肌肉质量的潜力,但其在各种萎缩诱导条件下的机制尚不完全清楚。本研究旨在探讨HMB在缺乏运动和蛋白质剥夺引起的肌肉萎缩中的作用,并阐明其分子机制。大鼠进行不活动或缺乏蛋白质的饮食,有或没有补充HMB。评估肌肉形态、力量和生化参数。利用暴露于白细胞介素-6 (IL-6)的C2C12成肌细胞和小鼠骨骼肌卫星细胞进行体外研究,探索了参与HMB保护作用的分子途径。缺乏运动和蛋白质剥夺导致肌肉萎缩、力量降低和生化指标改变。补充HMB部分减轻了这些影响,保留了肌肉质量和功能。HMB减弱萎缩标志物(肌萎缩F-box和肌环指1 (MuRF1)),维持肌生成因子(Myogenin (MyoG))水平。体外研究表明,HMB的保护作用是通过AKT/mTOR通路介导的,同时在成肌细胞和卫星细胞中调控自噬通路并保持线粒体功能。在il -6诱导的应激条件下,HMB通过akt依赖机制特异性地保护卫星细胞的活力和功能,维持蛋白质合成并减少细胞凋亡。在成肌细胞和卫星细胞中,补充HMB通过AKT/mTOR通路激活、自噬调节和线粒体功能维持等多种机制,显示出对不活动和蛋白质剥夺引起的肌肉萎缩的保护作用。这些发现表明HMB在各种临床情况下作为预防肌肉萎缩的潜在治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biogerontology
Biogerontology 医学-老年医学
CiteScore
8.00
自引率
4.40%
发文量
54
审稿时长
>12 weeks
期刊介绍: The journal Biogerontology offers a platform for research which aims primarily at achieving healthy old age accompanied by improved longevity. The focus is on efforts to understand, prevent, cure or minimize age-related impairments. Biogerontology provides a peer-reviewed forum for publishing original research data, new ideas and discussions on modulating the aging process by physical, chemical and biological means, including transgenic and knockout organisms; cell culture systems to develop new approaches and health care products for maintaining or recovering the lost biochemical functions; immunology, autoimmunity and infection in aging; vertebrates, invertebrates, micro-organisms and plants for experimental studies on genetic determinants of aging and longevity; biodemography and theoretical models linking aging and survival kinetics.
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