Chung-Yang Yeh, Lucas C S Chini, Jessica W Davidson, Gonzalo G Garcia, Meredith S Gallagher, Isaac T Freichels, Mariah F Calubag, Allison C Rodgers, Cara L Green, Reji Babygirija, Michelle M Sonsalla, Heidi H Pak, Michaela E Trautman, Timothy A Hacker, Richard A Miller, Judith A Simcox, Dudley W Lamming
{"title":"Late-life protein or isoleucine restriction impacts physiological and molecular signatures of aging.","authors":"Chung-Yang Yeh, Lucas C S Chini, Jessica W Davidson, Gonzalo G Garcia, Meredith S Gallagher, Isaac T Freichels, Mariah F Calubag, Allison C Rodgers, Cara L Green, Reji Babygirija, Michelle M Sonsalla, Heidi H Pak, Michaela E Trautman, Timothy A Hacker, Richard A Miller, Judith A Simcox, Dudley W Lamming","doi":"10.1038/s43587-024-00744-7","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":94150,"journal":{"name":"Nature aging","volume":" ","pages":""},"PeriodicalIF":17.0000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature aging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s43587-024-00744-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
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.