Xu Yingying, Xiao Weihua
Shanghai Key Lab of Human Performance, Shanghai University of Sport, Shanghai 200438, China; The Key Lab of Exercise and Health Sciences of Ministry of Education, Shanghai University of Sport, Shanghai 200438, China.
Ageing Res Rev. 2023 Oct 28:102106. doi: 10.1016/j.arr.2023.102106.
More than a century after the discovery of nicotinamide adenine dinucleotide (NAD), our understanding of the molecule's role in the biology of ageing continues to evolve. As a coenzyme or substrate for many enzymes, NAD governs a wide range of biological processes, including energy metabolism, genomic stability, signal transduction, and cell fate. NAD deficiency has been recognised as a bona fide hallmark of tissue degeneration, and restoring NAD homeostasis helps to rejuvenate multiple mechanisms associated with tissue ageing. The progressive loss of skeletal muscle homeostasis with age is directly associated with high morbidity, disability and mortality. The aetiology of skeletal muscle ageing is complex, involving mitochondrial dysfunction, senescence and stem cell depletion, autophagy defects, chronic cellular stress, intracellular ion overload, immune cell dysfunction, circadian clock disruption, microcirculation disorders, persistent denervation, and gut microbiota dysbiosis. This review focuses on the therapeutic potential of NAD restoration to alleviate the above pathological factors and discusses the effects of in vivo administration of different NAD boosting strategies on skeletal muscle homeostasis, aiming to provide a reference for combating skeletal muscle ageing.
在烟酰胺腺嘌呤二核苷酸(NAD)被发现一个多世纪后,我们对该分子在衰老生物学中作用的理解仍在不断发展。作为许多酶的辅酶或底物,NAD 掌管着广泛的生物过程,包括能量代谢、基因组稳定性、信号转导和细胞命运。NAD 缺乏已被公认为组织退化的一个真正标志,恢复 NAD 稳态有助于使与组织衰老相关的多种机制恢复活力。随着年龄增长,骨骼肌稳态的逐渐丧失与高发病率、残疾率和死亡率直接相关。骨骼肌衰老的病因复杂,涉及线粒体功能障碍、衰老和干细胞耗竭、自噬缺陷、慢性细胞应激、细胞内离子过载、免疫细胞功能障碍、生物钟紊乱、微循环障碍、持续性去神经支配以及肠道微生物群失调。本综述重点关注恢复 NAD 以减轻上述病理因素的治疗潜力,并讨论不同 NAD 增强策略的体内给药对骨骼肌稳态的影响,旨在为对抗骨骼肌衰老提供参考。