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Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice

Dietary restriction (DR) was reported to either have no effect or reduce the lifespan of the majority of the 41‐recombinant inbred (RI) lines studied by Liao et al. (Aging Cell, 2010, 9, 92). In an appropriately power longevity study (n > 30 mice/group), we measured the lifespan of the four RI li...

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Autores principales: Unnikrishnan, Archana, Matyi, Stephanie, Garrett, Karla, Ranjo‐Bishop, Michelle, Allison, David B., Ejima, Keisuke, Chen, Xiwei, Dickinson, Stephanie, Richardson, Arlan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590105/
https://www.ncbi.nlm.nih.gov/pubmed/34713968
http://dx.doi.org/10.1111/acel.13500
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author Unnikrishnan, Archana
Matyi, Stephanie
Garrett, Karla
Ranjo‐Bishop, Michelle
Allison, David B.
Ejima, Keisuke
Chen, Xiwei
Dickinson, Stephanie
Richardson, Arlan
author_facet Unnikrishnan, Archana
Matyi, Stephanie
Garrett, Karla
Ranjo‐Bishop, Michelle
Allison, David B.
Ejima, Keisuke
Chen, Xiwei
Dickinson, Stephanie
Richardson, Arlan
author_sort Unnikrishnan, Archana
collection PubMed
description Dietary restriction (DR) was reported to either have no effect or reduce the lifespan of the majority of the 41‐recombinant inbred (RI) lines studied by Liao et al. (Aging Cell, 2010, 9, 92). In an appropriately power longevity study (n > 30 mice/group), we measured the lifespan of the four RI lines (115‐RI, 97‐RI, 98‐RI, and 107‐RI) that were reported to have the greatest decrease in lifespan when fed 40% DR. DR increased the median lifespan of female RI‐115, 97‐RI, and 107‐RI mice and male 115‐RI mice. DR had little effect (<4%) on the median lifespan of female and male 98‐RI mice and male 97‐RI mice and reduced the lifespan of male 107‐RI mice over 20%. While our study was unable to replicate the effect of DR on the lifespan of the RI mice (except male 107‐RI mice) reported by Liao et al. (Aging Cell, 2010, 9, 92), we found that the genotype of a mouse had a major impact on the effect of DR on lifespan, with the effect of DR ranging from a 50% increase to a 22% decrease in median lifespan. No correlation was observed between the changes in either body composition or glucose tolerance induced by DR and the changes observed in lifespan of the four RI lines of male and female mice. These four RI lines of mice give the research community a unique resource where investigators for the first time can study the anti‐aging mechanism of DR by comparing mice in which DR increases lifespan to mice where DR has either no effect or reduces lifespan.
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spelling pubmed-85901052021-11-19 Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice Unnikrishnan, Archana Matyi, Stephanie Garrett, Karla Ranjo‐Bishop, Michelle Allison, David B. Ejima, Keisuke Chen, Xiwei Dickinson, Stephanie Richardson, Arlan Aging Cell Original Papers Dietary restriction (DR) was reported to either have no effect or reduce the lifespan of the majority of the 41‐recombinant inbred (RI) lines studied by Liao et al. (Aging Cell, 2010, 9, 92). In an appropriately power longevity study (n > 30 mice/group), we measured the lifespan of the four RI lines (115‐RI, 97‐RI, 98‐RI, and 107‐RI) that were reported to have the greatest decrease in lifespan when fed 40% DR. DR increased the median lifespan of female RI‐115, 97‐RI, and 107‐RI mice and male 115‐RI mice. DR had little effect (<4%) on the median lifespan of female and male 98‐RI mice and male 97‐RI mice and reduced the lifespan of male 107‐RI mice over 20%. While our study was unable to replicate the effect of DR on the lifespan of the RI mice (except male 107‐RI mice) reported by Liao et al. (Aging Cell, 2010, 9, 92), we found that the genotype of a mouse had a major impact on the effect of DR on lifespan, with the effect of DR ranging from a 50% increase to a 22% decrease in median lifespan. No correlation was observed between the changes in either body composition or glucose tolerance induced by DR and the changes observed in lifespan of the four RI lines of male and female mice. These four RI lines of mice give the research community a unique resource where investigators for the first time can study the anti‐aging mechanism of DR by comparing mice in which DR increases lifespan to mice where DR has either no effect or reduces lifespan. John Wiley and Sons Inc. 2021-10-29 2021-11 /pmc/articles/PMC8590105/ /pubmed/34713968 http://dx.doi.org/10.1111/acel.13500 Text en © 2021 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Unnikrishnan, Archana
Matyi, Stephanie
Garrett, Karla
Ranjo‐Bishop, Michelle
Allison, David B.
Ejima, Keisuke
Chen, Xiwei
Dickinson, Stephanie
Richardson, Arlan
Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
title Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
title_full Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
title_fullStr Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
title_full_unstemmed Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
title_short Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
title_sort reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590105/
https://www.ncbi.nlm.nih.gov/pubmed/34713968
http://dx.doi.org/10.1111/acel.13500
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