衰老、骨肌减少症与肌肉骨骼机械转导
Aging, Osteo-Sarcopenia, and Musculoskeletal Mechano-Transduction.
作者信息
Leser Jenna M, Harriot Anicca, Buck Heather V, Ward Christopher W, Stains Joseph P
机构信息
Department of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD, United States.
出版信息
Front Rehabil Sci. 2021;2. doi: 10.3389/fresc.2021.782848. Epub 2021 Dec 6.
The decline in the mass and function of bone and muscle is an inevitable consequence of healthy aging with early onset and accelerated decline in those with chronic disease. Termed osteo-sarcopenia, this condition predisposes the decreased activity, falls, low-energy fractures, and increased risk of co-morbid disease that leads to musculoskeletal frailty. The biology of osteo-sarcopenia is most understood in the context of systemic neuro-endocrine and immune/inflammatory alterations that drive inflammation, oxidative stress, reduced autophagy, and cellular senescence in the bone and muscle. Here we integrate these concepts to our growing understanding of how bone and muscle senses, responds and adapts to mechanical load. We propose that age-related alterations in cytoskeletal mechanics alter load-sensing and mechano-transduction in bone osteocytes and muscle fibers which underscores osteo-sarcopenia. Lastly, we examine the evidence for exercise as an effective countermeasure to osteo-sarcopenia.
骨骼和肌肉质量与功能的下降是健康衰老的必然结果,在患有慢性疾病的人群中发病更早且下降加速。这种情况被称为骨少肌症,它会导致活动减少、跌倒、低能量骨折以及共病风险增加,进而引发肌肉骨骼衰弱。骨少肌症的生物学机制在系统性神经内分泌和免疫/炎症改变的背景下最为人所理解,这些改变会引发炎症、氧化应激、自噬减少以及骨骼和肌肉中的细胞衰老。在这里,我们将这些概念与我们对骨骼和肌肉如何感知、响应和适应机械负荷的不断深入的理解相结合。我们提出,细胞骨架力学的年龄相关改变会改变骨细胞和肌纤维中的负荷感知和机械转导,这突出了骨少肌症。最后,我们研究了运动作为骨少肌症有效对策的证据。