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Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction

BACKGROUND: Chronic dietary restriction (DR) has been shown to have beneficial effects on glucose homeostasis and insulin sensitivity. These factors show rapid and robust improvements when rodents were crossed over from an ad libitum (AL) diet to DR in mid life. We aimed to determine whether the ben...

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Autores principales: Cameron, Kerry M, Miwa, Satomi, Walker, Cornelia, von Zglinicki, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886267/
https://www.ncbi.nlm.nih.gov/pubmed/24764509
http://dx.doi.org/10.1186/2046-2395-1-3
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author Cameron, Kerry M
Miwa, Satomi
Walker, Cornelia
von Zglinicki, Thomas
author_facet Cameron, Kerry M
Miwa, Satomi
Walker, Cornelia
von Zglinicki, Thomas
author_sort Cameron, Kerry M
collection PubMed
description BACKGROUND: Chronic dietary restriction (DR) has been shown to have beneficial effects on glucose homeostasis and insulin sensitivity. These factors show rapid and robust improvements when rodents were crossed over from an ad libitum (AL) diet to DR in mid life. We aimed to determine whether the beneficial effects induced by short-term exposure to DR can be retained as a ‘metabolic memory’ when AL feeding is resumed (AL-DR-AL) and vice versa: whether the effects of long-term DR can be reversed by a period of AL feeding (DR-AL-DR). C57BL/6 male and female mice were used to examine sex differences (N = 10/sex/group). Mice were fed AL or DR from 3 until 15 months (baseline) and each dietary crossover lasted approximately 5 months. RESULTS: In females, body and fat mass were proportional to the changes in feeding regime and plasma insulin and glucose tolerance were unaffected by the crossovers. However, in male mice, glucose tolerance and plasma insulin levels were reversed within 6 to 12 weeks. When males returned to AL intake following 5 months DR (AL-DR-AL), body mass was maintained below baseline, proportional to changes in fat mass. Glucose tolerance was also significantly better compared to baseline. CONCLUSIONS: Male mice retained a metabolic memory of 5 months of DR feeding in terms of reduced body mass and improved glucose tolerance. This implies that some of the beneficial effects induced by a period of DR in adult life may be beneficial, even when free feeding is resumed at least in males. However, under continuous DR, lifespan extension was more prominent in females than in males.
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spelling pubmed-38862672014-01-13 Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction Cameron, Kerry M Miwa, Satomi Walker, Cornelia von Zglinicki, Thomas Longev Healthspan Research BACKGROUND: Chronic dietary restriction (DR) has been shown to have beneficial effects on glucose homeostasis and insulin sensitivity. These factors show rapid and robust improvements when rodents were crossed over from an ad libitum (AL) diet to DR in mid life. We aimed to determine whether the beneficial effects induced by short-term exposure to DR can be retained as a ‘metabolic memory’ when AL feeding is resumed (AL-DR-AL) and vice versa: whether the effects of long-term DR can be reversed by a period of AL feeding (DR-AL-DR). C57BL/6 male and female mice were used to examine sex differences (N = 10/sex/group). Mice were fed AL or DR from 3 until 15 months (baseline) and each dietary crossover lasted approximately 5 months. RESULTS: In females, body and fat mass were proportional to the changes in feeding regime and plasma insulin and glucose tolerance were unaffected by the crossovers. However, in male mice, glucose tolerance and plasma insulin levels were reversed within 6 to 12 weeks. When males returned to AL intake following 5 months DR (AL-DR-AL), body mass was maintained below baseline, proportional to changes in fat mass. Glucose tolerance was also significantly better compared to baseline. CONCLUSIONS: Male mice retained a metabolic memory of 5 months of DR feeding in terms of reduced body mass and improved glucose tolerance. This implies that some of the beneficial effects induced by a period of DR in adult life may be beneficial, even when free feeding is resumed at least in males. However, under continuous DR, lifespan extension was more prominent in females than in males. BioMed Central 2012-09-03 /pmc/articles/PMC3886267/ /pubmed/24764509 http://dx.doi.org/10.1186/2046-2395-1-3 Text en Copyright © 2012 Cameron et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cameron, Kerry M
Miwa, Satomi
Walker, Cornelia
von Zglinicki, Thomas
Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
title Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
title_full Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
title_fullStr Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
title_full_unstemmed Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
title_short Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
title_sort male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3886267/
https://www.ncbi.nlm.nih.gov/pubmed/24764509
http://dx.doi.org/10.1186/2046-2395-1-3
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