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Does hypothalamic SIRT1 regulate aging?
In virtually all organisms, life expectancy is profoundly affected by caloric intake. For example, dietary restriction (DR; a feeding regimen of fewer calories compared to the ad libitum level without causing malnutrition) has been shown to lengthen, whereas hypercaloric (HC) diet feeding to shorten...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Impact Journals LLC
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091526/ https://www.ncbi.nlm.nih.gov/pubmed/21464518 |
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author | Ramadori, Giorgio Coppari, Roberto |
author_facet | Ramadori, Giorgio Coppari, Roberto |
author_sort | Ramadori, Giorgio |
collection | PubMed |
description | In virtually all organisms, life expectancy is profoundly affected by caloric intake. For example, dietary restriction (DR; a feeding regimen of fewer calories compared to the ad libitum level without causing malnutrition) has been shown to lengthen, whereas hypercaloric (HC) diet feeding to shorten, lifespan. Recent findings in invertebrates indicate that specialized groups of cells (e.g.: metabolic-sensing neurons) detect changes in caloric intake and convey energy-status-variation signals to other cells in the body to regulate lifespan. In mammals, whether metabolic-sensing neurons govern aging in a cell-non-autonomous fashion is unknown. Yet, this is a captivating and testable hypothesis. |
format | Text |
id | pubmed-3091526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-30915262011-05-12 Does hypothalamic SIRT1 regulate aging? Ramadori, Giorgio Coppari, Roberto Aging (Albany NY) Research Perspective In virtually all organisms, life expectancy is profoundly affected by caloric intake. For example, dietary restriction (DR; a feeding regimen of fewer calories compared to the ad libitum level without causing malnutrition) has been shown to lengthen, whereas hypercaloric (HC) diet feeding to shorten, lifespan. Recent findings in invertebrates indicate that specialized groups of cells (e.g.: metabolic-sensing neurons) detect changes in caloric intake and convey energy-status-variation signals to other cells in the body to regulate lifespan. In mammals, whether metabolic-sensing neurons govern aging in a cell-non-autonomous fashion is unknown. Yet, this is a captivating and testable hypothesis. Impact Journals LLC 2011-03-18 /pmc/articles/PMC3091526/ /pubmed/21464518 Text en Copyright: © 2011 Ramadori and Coppari http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited |
spellingShingle | Research Perspective Ramadori, Giorgio Coppari, Roberto Does hypothalamic SIRT1 regulate aging? |
title | Does hypothalamic SIRT1 regulate aging? |
title_full | Does hypothalamic SIRT1 regulate aging? |
title_fullStr | Does hypothalamic SIRT1 regulate aging? |
title_full_unstemmed | Does hypothalamic SIRT1 regulate aging? |
title_short | Does hypothalamic SIRT1 regulate aging? |
title_sort | does hypothalamic sirt1 regulate aging? |
topic | Research Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091526/ https://www.ncbi.nlm.nih.gov/pubmed/21464518 |
work_keys_str_mv | AT ramadorigiorgio doeshypothalamicsirt1regulateaging AT coppariroberto doeshypothalamicsirt1regulateaging |