Literature DB >> 23682161

Rapamycin extends life and health in C57BL/6 mice.

Yiqiang Zhang1, Alex Bokov, John Gelfond, Vanessa Soto, Yuji Ikeno, Gene Hubbard, Vivian Diaz, Lauren Sloane, Keith Maslin, Stephen Treaster, Samantha Réndon, Holly van Remmen, Walter Ward, Martin Javors, Arlan Richardson, Steven N Austad, Kathleen Fischer.   

Abstract

Target of rapamycin inhibition by rapamycin feeding has previously been shown to extend life in genetically heterogeneous mice. To examine whether it similarly affected mouse health, we fed encapsulated rapamycin or a control diet to C57BL/6Nia mice of both sexes starting at 19 months of age. We performed a range of health assessments 6 and 12 months later. Rapamycin feeding significantly reduced mTOR activity in most but not all tissues. It also reduced total and resting metabolic rate during the light (inactive) phase of the light:dark cycle in females only but had no effect on spontaneous activity or metabolism during the dark (active) phase of either sex. Males only had less fragmented sleep when fed rapamycin, whereas stride length and rotarod performance were improved in both sexes. Survival was also improved by this late-life rapamycin feeding, and some pathological lesions were delayed. We found no adverse health consequences associated with rapamycin treatment.

Entities:  

Keywords:  Aging; Health span; Rapamycin; Sex differences.

Mesh:

Substances:

Year:  2013        PMID: 23682161      PMCID: PMC4038246          DOI: 10.1093/gerona/glt056

Source DB:  PubMed          Journal:  J Gerontol A Biol Sci Med Sci        ISSN: 1079-5006            Impact factor:   6.053


  50 in total

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Journal:  J Gerontol A Biol Sci Med Sci       Date:  2005-12       Impact factor: 6.053

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Journal:  Autophagy       Date:  2007-11-21       Impact factor: 16.016

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  153 in total

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Review 4.  Healthspan and longevity can be extended by suppression of growth hormone signaling.

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Review 5.  Rapamycin and ageing: when, for how long, and how much?

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6.  Rapamycin and dietary restriction induce metabolically distinctive changes in mouse liver.

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8.  eRapa restores a normal life span in a FAP mouse model.

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9.  Lifespan extension and cancer prevention in HER-2/neu transgenic mice treated with low intermittent doses of rapamycin.

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10.  Comparison of rapamycin schedules in mice on high-fat diet.

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