食品科学 ›› 2025, Vol. 46 ›› Issue (18): 14-24.doi: 10.7506/spkx1002-6630-20250128-205

• 肌骨健康食品专栏 • 上一篇    下一篇

运动联合营养干预在肌少-骨质疏松症防治中的机制研究进展

夏君玫,姜坦程,郝宏弢,邓琪,唐嘉岭,梁计陵   

  1. (1.中南大学体育教研部,湖南?长沙 410083;2.中南大学 运动康复与运动风险防控研究中心,湖南?长沙 410083)
  • 出版日期:2025-09-25 发布日期:2025-08-19
  • 基金资助:
    湖南省自然科学基金青年C类项目(2025JJ60799);湖南省体育局科技重点项目(2024KT005); 教育部人文社会科学研究青年基金项目(22YJC890029)

Research Progress in Mechanism of Exercise Combined with Nutritional Intervention in the Prevention and Treatment of Osteosarcopenia

XIA Junmei, JIANG Tancheng, HAO Hongtao, DENG Qi, TANG Jialing, LIANG Jiling   

  1. (1. Department of Physical Education, Central South University, Changsha 410083, China;2. Center for Sports Rehabilitation and Sports Risk Mitigation Research, Central South University, Changsha 410083, China)
  • Online:2025-09-25 Published:2025-08-19

摘要: 随着人口老龄化加剧,肌少-骨质疏松症(osteosarcopenia,OS)已成为威胁老年人健康的重要退行性疾病,其特征表现为进行性骨骼肌质量减少与骨密度降低的协同恶化,会显著增加跌倒骨折风险及全因死亡率。衰老进程中的激素紊乱、慢性炎症及机械应力缺失通过影响肌肉因子与骨源性因子分泌和肌-骨交互作用,共同导致肌骨代谢失衡。运动和营养干预是防治OS的有效策略。其中,有氧运动能够激活胰岛素样生长因子-1(insulin-like growth factor-1,IGF-1)、AMP依赖的蛋白激酶(adenosine 5’-monophosphate (AMP)-activated protein kinase,AMPK)/钙/钙调素依赖性蛋白激酶II以及Wnt1/β-catenin等信号从而延缓肌肉衰老、增加骨密度;抗阻运动则可调控Fos/Fosb、丝裂原活化蛋白激酶、磷脂酰肌醇3-激酶、蛋白激酶B和哺乳动物雷帕霉素靶蛋白(mammalian target of rapamycin,mTOR)通路从而改善维持骨代谢稳态,并促进肌肉蛋白合成。而新型运动模式如全身振动训练和血流限制训练可调控AMPK/UNC-51样激酶1、叉头盒蛋白O/过氧化物酶体增殖活化受体γ辅助活化因子1α、IGF-1/生长激素等通路,起到促进肌肉生成及骨矿化的效益。营养干预策略显示,蛋白质及其衍生物(如肌酸)通过mTORC1信号通路促进肌肉合成;VD3通过类视黄醇X受体/VD受体轴调控骨代谢平衡;钙剂与益生菌则通过调节“肠-骨轴”发挥抗炎和促骨形成作用。本研究系统阐述了运动与营养干预在调控肌-骨代谢中的协同作用机制,旨在为OS的个性化防治和精准营养策略提供理论依据和方案。

关键词: 肌少-骨质疏松症;肌少症;骨质疏松症;运动;营养

Abstract: With the intensification of population aging, osteosarcopenia (OS) has emerged as a significant degenerative disease that poses a considerable threat to the health of the elderly. It is characterized by the synergistic deterioration of progressive reduction in skeletal muscle mass and decline in bone density, which significantly increases the risk of fall, fracture, and all-cause mortality. Hormonal disorders, chronic inflammation, and the lack of mechanical stress during the aging process collectively result in an imbalance in muscle and bone metabolism, primarily by affecting the secretion of muscle-derived and bone-derived factors as well as muscle-bone interactions. Exercise and nutritional interventions have proven to be effective strategies for the prevention and treatment of OS. Aerobic exercise delays muscle aging and increases bone density by activating signaling pathways such as insulin-like growth factor-1 (IGF-1), adenosine 5’-monophosphate (AMP)-activated protein kinase (AMPK)/calcium/calmodulin-dependent protein kinase II (CaMKII) and Wnt1/β-catenin. Resistance exercise improves and maintains bone metabolic homeostasis, and promotes muscle protein synthesis by regulating the Fos/Fosb, mitogen-activated protein kinase and phosphoinositide 3-kinase (PI3K)/protein kinase B (Akt)/mammalian target of rapamycin (mTOR) signaling pathways. Whole-body vibration training and blood flow restriction training have emerged as exercise modalities to promote muscle generation and bone mineralization by modulating the AMPK/UNC-51 like autophagy activating kinase 1 (ULK1), forkhead box protein O (FoxO)/ peroxisome proliferator activated receptor γ coactivator-1α (PGC-1α), and IGF-1/growth hormone (GH) signaling pathways. Nutritional intervention strategies have demonstrated that proteins and their derivatives, such as creatine, facilitate muscle synthesis through the mTORC1 signaling pathway. Additionally, vitamin D3 regulates bone metabolic balance via the retinoid X receptor (RXR)/VD receptor (VDR) signaling pathway, while calcium supplements and probiotics exert anti-inflammatory and bone-forming effects by modulating the gut-bone axis. This review systematically elucidates the synergistic mechanism of action of exercise and nutritional interventions in regulating muscle-bone metabolism, aiming to provide a theoretical basis and framework for the personalized prevention and treatment of OS and the development of precise nutritional strategies for this disease.

Key words: osteosarcopenia; sarcopenia; osteoporosis; exercise; nutrition

中图分类号: