Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ehninger, Dan, Neff, Frauke, Xie, Kan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Basel 2014
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
_version_ 1782341058562097152
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