Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramadori, Giorgio, Coppari, Roberto
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091526/
https://www.ncbi.nlm.nih.gov/pubmed/21464518
_version_ 1782203270414991360
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