Julia Margarita Reyes, Guy Hajj-Boutros, Dounia Rouabhia, José Morais, Felipe Salech, Gustavo Duque
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引用次数: 0
Abstract
Older adults experience a markedly increased risk of falls and fractures following hospital discharge, largely due to the rapid musculoskeletal deterioration associated with bed rest. Although age-related muscle and bone loss typically develops gradually, acute physical inactivity accelerates key biological processes underlying sarcopenia and osteoporosis, including muscle atrophy, anabolic resistance, increased bone resorption and reduced mechanical loading. Emerging evidence indicates that muscle, bone and adipose tissue communicate through interconnected biochemical pathways; however, the shared biological mechanisms underlying this crosstalk during acute unloading remain poorly understood. To review the effects of disuse on the muscle-bone-adipose axis, emphasizing disruption of inter-tissue signalling pathways and evaluating integrated countermeasures, a narrative review was conducted using PubMed, Scopus and Web of Science, focusing on human bed rest and disuse studies, musculoskeletal crosstalk and multimodal interventions involving exercise and nutrition in older adults. Disuse rapidly disrupts musculoskeletal homeostasis by uncoupling bone turnover and inducing muscle anabolic resistance. These changes are accompanied by alterations in myokine and osteokine signalling, including increased myostatin, reduced irisin, elevated RANKL, bone and muscle steatosis, and sclerostin upregulation, further compromising muscle-bone interactions. Evidence supports multimodal interventions combining resistance exercise with optimized protein intake (1.2-1.5 g/kg/day) and nutritional supplements, including β-hydroxy-β-methylbutyrate, vitamin D and creatine, to attenuate muscle and bone loss. Preventing disuse-related musculoskeletal decline requires recognizing muscle and bone as an integrated functional unit. Tailored multimodal strategies may preserve musculoskeletal health and functional independence in hospitalized older adults, although implementation must consider frailty, comorbidities, safety and feasibility.
老年人出院后跌倒和骨折的风险明显增加,主要是由于卧床休息导致肌肉骨骼迅速恶化。虽然与年龄相关的肌肉和骨质流失通常是逐渐发生的,但急性缺乏运动加速了肌肉减少症和骨质疏松症的关键生物过程,包括肌肉萎缩、合成代谢抵抗、骨吸收增加和机械负荷减少。新出现的证据表明,肌肉、骨骼和脂肪组织通过相互关联的生化途径进行交流;然而,在急性卸荷过程中,这种串扰背后的共同生物学机制仍然知之甚少。为了回顾废用对肌肉-骨-脂肪轴的影响,强调组织间信号通路的破坏并评估综合对策,使用PubMed, Scopus和Web of Science进行了一项叙述性回顾,重点关注老年人卧床休息和废用研究,肌肉-骨骼串扰和涉及运动和营养的多模式干预。废用通过解偶联骨转换和诱导肌肉合成代谢抵抗迅速破坏肌肉骨骼稳态。这些变化伴随着肌因子和骨因子信号的改变,包括肌生长抑制素增加、鸢尾素减少、RANKL升高、骨和肌肉脂肪变性以及硬化蛋白上调,进一步损害了肌-骨相互作用。有证据支持多模式干预,将阻力运动与优化蛋白质摄入量(1.2-1.5 g/kg/天)和营养补充剂(包括β-羟基-β-甲基丁酸盐、维生素D和肌酸)相结合,以减轻肌肉和骨质流失。预防废用相关的肌肉骨骼衰退需要认识到肌肉和骨骼是一个综合的功能单位。量身定制的多模式策略可以保护住院老年人的肌肉骨骼健康和功能独立性,尽管实施时必须考虑到虚弱、合并症、安全性和可行性。
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.