Cargando…
Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice
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 tre...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996648/ https://www.ncbi.nlm.nih.gov/pubmed/27549339 http://dx.doi.org/10.7554/eLife.16351 |
_version_ | 1782449642213998592 |
---|---|
author | Bitto, Alessandro Ito, Takashi K Pineda, Victor V LeTexier, Nicolas J Huang, Heather Z Sutlief, Elissa Tung, Herman Vizzini, Nicholas Chen, Belle Smith, Kaleb Meza, Daniel Yajima, Masanao Beyer, Richard P Kerr, Kathleen F Davis, Daniel J Gillespie, Catherine H Snyder, Jessica M Treuting, Piper M Kaeberlein, Matt |
author_facet | Bitto, Alessandro Ito, Takashi K Pineda, Victor V LeTexier, Nicolas J Huang, Heather Z Sutlief, Elissa Tung, Herman Vizzini, Nicholas Chen, Belle Smith, Kaleb Meza, Daniel Yajima, Masanao Beyer, Richard P Kerr, Kathleen F Davis, Daniel J Gillespie, Catherine H Snyder, Jessica M Treuting, Piper M Kaeberlein, Matt |
author_sort | Bitto, Alessandro |
collection | PubMed |
description | 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. DOI: http://dx.doi.org/10.7554/eLife.16351.001 |
format | Online Article Text |
id | pubmed-4996648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49966482016-08-29 Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice Bitto, Alessandro Ito, Takashi K Pineda, Victor V LeTexier, Nicolas J Huang, Heather Z Sutlief, Elissa Tung, Herman Vizzini, Nicholas Chen, Belle Smith, Kaleb Meza, Daniel Yajima, Masanao Beyer, Richard P Kerr, Kathleen F Davis, Daniel J Gillespie, Catherine H Snyder, Jessica M Treuting, Piper M Kaeberlein, Matt eLife Cancer Biology 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. DOI: http://dx.doi.org/10.7554/eLife.16351.001 eLife Sciences Publications, Ltd 2016-08-23 /pmc/articles/PMC4996648/ /pubmed/27549339 http://dx.doi.org/10.7554/eLife.16351 Text en © 2016, Bitto et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cancer Biology Bitto, Alessandro Ito, Takashi K Pineda, Victor V LeTexier, Nicolas J Huang, Heather Z Sutlief, Elissa Tung, Herman Vizzini, Nicholas Chen, Belle Smith, Kaleb Meza, Daniel Yajima, Masanao Beyer, Richard P Kerr, Kathleen F Davis, Daniel J Gillespie, Catherine H Snyder, Jessica M Treuting, Piper M Kaeberlein, Matt Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice |
title | Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice |
title_full | Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice |
title_fullStr | Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice |
title_full_unstemmed | Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice |
title_short | Transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice |
title_sort | transient rapamycin treatment can increase lifespan and healthspan in middle-aged mice |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4996648/ https://www.ncbi.nlm.nih.gov/pubmed/27549339 http://dx.doi.org/10.7554/eLife.16351 |
work_keys_str_mv | AT bittoalessandro transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT itotakashik transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT pinedavictorv transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT letexiernicolasj transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT huangheatherz transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT sutliefelissa transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT tungherman transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT vizzininicholas transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT chenbelle transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT smithkaleb transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT mezadaniel transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT yajimamasanao transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT beyerrichardp transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT kerrkathleenf transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT davisdanielj transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT gillespiecatherineh transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT snyderjessicam transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT treutingpiperm transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice AT kaeberleinmatt transientrapamycintreatmentcanincreaselifespanandhealthspaninmiddleagedmice |