表观遗传学
蛋氨酸
生物
老年学
医学
遗传学
基因
氨基酸
作者
Ulalume Hernández-Arciga,Ceda Stamenkovic,Shweta Yadav,Chiara Nicoletti,Wafaa N. Albalawy,Farazdaq Al hammood,Tiffany Fuentes Gonzalez,Maitreyi U. Naikwadi,Aidan Graham,Christian Smarz,Gabriela Little,Sean-Paul G. Williams,Brenda McMahon,Ian Sipula,Amber Vandevender,Byron Chuan,Diana Cooke,Antônio F. M. Pinto,Lisa C. Flores,Hannah L. Hartman
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-04-16
卷期号:11 (16)
标识
DOI:10.1126/sciadv.ads1532
摘要
Aging is associated with dysregulated methionine metabolism and increased levels of enzymes in the tyrosine degradation pathway (TDP). To investigate the efficacy of targeting either methionine metabolism or the TDP for healthspan improvement in advanced age, we initiated dietary MetR or TDP inhibition in 18-month-old C57BL/6J mice. MetR significantly improved neuromuscular function, metabolic health, lung function, and frailty. In addition, we confirmed improved neuromuscular function from dietary MetR in 5XFAD mice, whose weight was not affected by MetR. We did not observe benefits with TDP inhibition. Single-nucleus RNA and ATAC sequencing of muscle revealed cell type–specific responses to MetR, although MetR did not significantly affect mouse aging epigenetic clock markers. Similarly, an 8-week MetR intervention in a human trial (NCT04701346) showed no significant impact on epigenetic clocks. The observed benefits from late-life MetR provide translational rationale to develop MetR mimetics as an antiaging intervention.
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