Sedentary behavior and the biological hallmarks of aging

被引:23
|
作者
Raffin, Jeremy [1 ,7 ]
Barreto, Philipe de Souto [1 ,3 ]
Le Traon, Anne Pavy [2 ]
Vellas, Bruno [1 ,3 ]
Aubertin-Leheudre, Mylene [4 ,5 ,6 ]
Rolland, Yves [1 ,3 ]
机构
[1] Ctr Hosp Univ Toulouse, Inst Vieillissement, Ge rontopole Toulouse, 37 Jules Guesdes, F-31000 Toulouse, France
[2] CHU Toulouse, Inst Space Med & Physiol MEDES, INSERM U 1297, Neurol Dept, Toulouse, France
[3] Univ Toulouse III, CERPOP UMR 1295, Inserm, UPS, Toulouse, France
[4] Univ Qubec Montreal, Fac Sci, Dept Sci Act Phys, Montreal, PQ, Canada
[5] Inst Univ Geriatrie Montreal IUGM, Ctr Rech, CIUSSS Ctr Sud de Ile de Montreal, Montreal, PQ, Canada
[6] Univ Quebec Montreal, Fac Sci, Montreal, PQ, Canada
[7] Inst Vieillissement, Gerontopole Toulouse, Batiment B, 37 Allees Jules Guesde, F-31000 Toulouse, France
关键词
Hallmarks of aging; Sedentary behavior; Bedrest; Spaceflight; Lower limb suspension; HUMAN SKELETAL-MUSCLE; AMINO-ACID SUPPLEMENTATION; SATELLITE CELL CONTENT; DOWN BED REST; GENE-EXPRESSION; DISUSE ATROPHY; PHYSICAL INACTIVITY; PROTEIN-SYNTHESIS; LIMB IMMOBILIZATION; RESISTANCE EXERCISE;
D O I
10.1016/j.arr.2022.101807
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
While the benefits of physical exercise for a healthy aging are well-recognized, a growing body of evidence shows that sedentary behavior has deleterious health effects independently, to some extent, of physical activity levels. Yet, the increasing prevalence of sedentariness constitutes a major public health issue that contributes to pre-mature aging but the potential cellular mechanisms through which prolonged immobilization may accelerate biological aging remain unestablished. This narrative review summarizes the impact of sedentary behavior using different models of extreme sedentary behaviors including bedrest, unilateral limb suspension and space travel studies, on the hallmarks of aging such as genomic instability, telomere attrition, epigenetic alterations, loss of proteostasis, deregulated nutrient sensing, mitochondrial dysfunction, cellular senescence, stem cell exhaustion, and altered intercellular communication. We further highlight the remaining knowledge gaps that need more research in order to promote healthspan extension and to provide future contributions to the field of geroscience.
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页数:17
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