Late-life protein or isoleucine restriction impacts physiological and molecular signatures of aging.

IF 17 Q1 CELL BIOLOGY
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
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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.

晚年蛋白质或异亮氨酸限制会影响衰老的生理和分子特征。
限制蛋白质或支链氨基酸异亮氨酸的摄入可促进年轻或成年小鼠的健康并延长其寿命。然而,它们对老年动物的影响尚不清楚。在此,我们研究了雄性和雌性 C57BL/6J.Nia 小鼠从 20 个月大开始摄入所有氨基酸减少 67% 的饮食(低 AA)或仅摄入异亮氨酸饮食(低 Ile)的后果。这两种饮食方案都能在不减少热量摄入的情况下有效促进整体代谢健康。低AA和低Ile饮食都能改善虚弱的各个方面,并减缓衰老速度的多种分子指标;然而,低Ile饮食会降低雌雄小鼠的握力,并对心脏产生不同性别的影响。这些结果表明,低 AA 和低 Ile 饮食可以促进老年小鼠健康老化的各个方面,并表明类似的干预措施可能会促进老年人的健康老化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
14.70
自引率
0.00%
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