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Longevity, aging and rapamycin
The federal drug administration (FDA)-approved compound rapamycin was the first pharmacological agent shown to extend maximal lifespan in both genders in a mammalian species. A major question then is whether the drug slows mammalian aging or if it has isolated effects on longevity by suppressing can...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Basel
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207939/ https://www.ncbi.nlm.nih.gov/pubmed/25015322 http://dx.doi.org/10.1007/s00018-014-1677-1 |
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author | Ehninger, Dan Neff, Frauke Xie, Kan |
author_facet | Ehninger, Dan Neff, Frauke Xie, Kan |
author_sort | Ehninger, Dan |
collection | PubMed |
description | The federal drug administration (FDA)-approved compound rapamycin was the first pharmacological agent shown to extend maximal lifespan in both genders in a mammalian species. A major question then is whether the drug slows mammalian aging or if it has isolated effects on longevity by suppressing cancers, the main cause of death in many mouse strains. Here, we review what is currently known about the effects that pharmacological or genetic mammalian target of rapamycin (mTOR) inhibition have on mammalian aging and longevity. Currently available evidence seems to best fit a model, wherein rapamycin extends lifespan by suppressing cancers. In addition the drug has symptomatic effects on some aging traits, such as age-related cognitive impairments. |
format | Online Article Text |
id | pubmed-4207939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Basel |
record_format | MEDLINE/PubMed |
spelling | pubmed-42079392014-10-28 Longevity, aging and rapamycin Ehninger, Dan Neff, Frauke Xie, Kan Cell Mol Life Sci Review The federal drug administration (FDA)-approved compound rapamycin was the first pharmacological agent shown to extend maximal lifespan in both genders in a mammalian species. A major question then is whether the drug slows mammalian aging or if it has isolated effects on longevity by suppressing cancers, the main cause of death in many mouse strains. Here, we review what is currently known about the effects that pharmacological or genetic mammalian target of rapamycin (mTOR) inhibition have on mammalian aging and longevity. Currently available evidence seems to best fit a model, wherein rapamycin extends lifespan by suppressing cancers. In addition the drug has symptomatic effects on some aging traits, such as age-related cognitive impairments. Springer Basel 2014-07-12 2014 /pmc/articles/PMC4207939/ /pubmed/25015322 http://dx.doi.org/10.1007/s00018-014-1677-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Review Ehninger, Dan Neff, Frauke Xie, Kan Longevity, aging and rapamycin |
title | Longevity, aging and rapamycin |
title_full | Longevity, aging and rapamycin |
title_fullStr | Longevity, aging and rapamycin |
title_full_unstemmed | Longevity, aging and rapamycin |
title_short | Longevity, aging and rapamycin |
title_sort | longevity, aging and rapamycin |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207939/ https://www.ncbi.nlm.nih.gov/pubmed/25015322 http://dx.doi.org/10.1007/s00018-014-1677-1 |
work_keys_str_mv | AT ehningerdan longevityagingandrapamycin AT nefffrauke longevityagingandrapamycin AT xiekan longevityagingandrapamycin |