Late-life protein or isoleucine restriction impacts physiological and molecular signatures of aging.
作者信息
Yeh Chung-Yang, Chini Lucas C S, Davidson Jessica W, Garcia Gonzalo G, Gallagher Meredith S, Freichels Isaac T, Calubag Mariah F, Rodgers Allison C, Green Cara L, Babygirija Reji, Sonsalla Michelle M, Pak Heidi H, Trautman Michaela E, Hacker Timothy A, Miller Richard A, Simcox Judith A, Lamming Dudley W
机构信息
Department of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
William S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
出版信息
Nat Aging. 2024 Dec;4(12):1760-1771. doi: 10.1038/s43587-024-00744-7. Epub 2024 Nov 27.
Restricting the intake of protein or the branched-chain amino acid isoleucine promotes healthspan and extends lifespan in young or adult mice. However, their effects when initiated in aged animals are unknown. Here we investigate the consequences of consuming a diet with 67% reduction of all amino acids (low AA) or of isoleucine alone (low Ile), in male and female C57BL/6J.Nia mice starting at 20 months of age. Both dietary regimens effectively promote overall metabolic health without reducing calorie intake. Both low AA and low Ile diets improve aspects of frailty and slow multiple molecular indicators of aging rate; however, the low Ile diet reduces grip strength in both sexes and has mixed, sexually dimorphic effects on the heart. These results demonstrate that low AA and low Ile diets can promote aspects of healthy aging in aged mice and suggest that similar interventions might promote healthy aging in older adults.