Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice

Alessandro Bitto(University of Washington), Takashi Ito(University of Washington), Victor V. Pineda(University of Washington), Nicolas J. LeTexier(University of Washington), Heather Z Huang(University of Washington), Elissa Sutlief(University of Washington), Herman Tung(University of Washington), Nicholas Vizzini(University of Washington), Belle Chen(University of Washington), Kaleb Smith(University of Washington), Daniel Meza(University of Washington), Masanao Yajima(Fred Hutch Cancer Center), Richard P. Beyer(University of Washington), Kathleen F. Kerr(University of Washington), Daniel J. Davis(University of Missouri), Catherine H. Gillespie(University of Missouri), Jessica M. Snyder(University of Washington), Piper M. Treuting(University of Washington), Matt Kaeberlein(University of Washington)
eLife
August 22, 2016
Cited by 476Open Access
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Abstract

The FDA approved drug rapamycin increases lifespan in rodents and delays age-related dysfunction in rodents and humans. Nevertheless, important questions remain regarding the optimal dose, duration, and mechanisms of action in the context of healthy aging. Here we show that 3 months of rapamycin treatment is sufficient to increase life expectancy by up to 60% and improve measures of healthspan in middle-aged mice. This transient treatment is also associated with a remodeling of the microbiome, including dramatically increased prevalence of segmented filamentous bacteria in the small intestine. We also define a dose in female mice that does not extend lifespan, but is associated with a striking shift in cancer prevalence toward aggressive hematopoietic cancers and away from non-hematopoietic malignancies. These data suggest that a short-term rapamycin treatment late in life has persistent effects that can robustly delay aging, influence cancer prevalence, and modulate the microbiome.


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