SRT2104 extends survival of male mice on a standard diet and preserves bone and muscle mass

  • Evi M. Mercken
  • , Sarah J. Mitchell
  • , Alejandro Martin-Montalvo
  • , Robin K. Minor
  • , Maria Almeida
  • , Ana P. Gomes
  • , Morten Scheibye-Knudsen
  • , Hector H. Palacios
  • , Jordan J. Licata
  • , Yongqing Zhang
  • , Kevin G. Becker
  • , Husam Khraiwesh
  • , José A. González-Reyes
  • , José M. Villalba
  • , Joseph A. Baur
  • , Peter Elliott
  • , Christoph Westphal
  • , George P. Vlasuk
  • , James L. Ellis
  • , David A. Sinclair
  • Michel Bernier, Rafael de Cabo

Research output: Contribution to journalArticlepeer-review

222 Scopus citations

Abstract

Increased expression of SIRT1 extends the lifespan of lower organisms and delays the onset of age-related diseases in mammals. Here, we show that SRT2104, a synthetic small molecule activator of SIRT1, extends both mean and maximal lifespan of mice fed a standard diet. This is accompanied by improvements in health, including enhanced motor coordination, performance, bone mineral density, and insulin sensitivity associated with higher mitochondrial content and decreased inflammation. Short-term SRT2104 treatment preserves bone and muscle mass in an experimental model of atrophy. These results demonstrate it is possible to design a small molecule that can slow aging and delay multiple age-related diseases in mammals, supporting the therapeutic potential of SIRT1 activators in humans.

Original languageEnglish
Pages (from-to)787-796
Number of pages10
JournalAging Cell
Volume13
Issue number5
DOIs
StatePublished - Oct 1 2014

Keywords

  • Healthspan
  • Inflammation
  • Lifespan
  • Muscle wasting
  • Osteoporosis
  • Sirtuins

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