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

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Evi M. Mercken
  • Sarah J. Mitchell
  • Alejandro Martin-Montalvo
  • Robin K. Minor
  • Maria Almeida
  • Ana P. Gomes
  • 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

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.

OriginalsprogEngelsk
TidsskriftAging Cell
Vol/bind13
Udgave nummer5
Sider (fra-til)787-796
Antal sider10
ISSN1474-9718
DOI
StatusUdgivet - 1 okt. 2014
Eksternt udgivetJa

ID: 172128335