Aging Cell

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

Experiments in animalsInterventions
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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.

From the paper

Animals

In the SRT2104 group, 14 mice were censored due to vets orders (n = 2; 74 weeks age, 97 weeks age), prolapsed anus (n = 1; 79 weeks age), or experimental procedures (n = 11; 40 weeks age, 115 weeks age), leaving 86 mice for the survival analysis.

Methods, Survival study

Quoted word for word from the full text on PubMed Central.