Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice. Issue 11 (29th October 2021)
- Record Type:
- Journal Article
- Title:
- Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice. Issue 11 (29th October 2021)
- Main Title:
- Reevaluation of the effect of dietary restriction on different recombinant inbred lines of male and female mice
- Authors:
- Unnikrishnan, Archana
Matyi, Stephanie
Garrett, Karla
Ranjo‐Bishop, Michelle
Allison, David B.
Ejima, Keisuke
Chen, Xiwei
Dickinson, Stephanie
Richardson, Arlan - Abstract:
- Abstract: 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. Abstract : In thisAbstract: 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. Abstract : In this study, we reevaluated the effect of the genotype and sex of recombinant inbred strains of mice on their response to dietary restriction. Out of the eight groups studied, half showed an increase in lifespan when the diet was restricted by 40% and the other half either did not respond or showed a decrease in lifespan. The recombinant inbred lines used in this study are a potentially important resource for aging research to identify pathways and understand the mechanism involved in the anti‐aging action of DR. … (more)
- Is Part Of:
- Aging cell. Volume 20:Issue 11(2021)
- Journal:
- Aging cell
- Issue:
- Volume 20:Issue 11(2021)
- Issue Display:
- Volume 20, Issue 11 (2021)
- Year:
- 2021
- Volume:
- 20
- Issue:
- 11
- Issue Sort Value:
- 2021-0020-0011-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-10-29
- Subjects:
- adiposity -- dietary restriction -- glucose tolerance -- lifespan -- recombinant inbred lines
Cells -- Aging -- Periodicals
571.8783605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1474-9726 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/acel.13500 ↗
- Languages:
- English
- ISSNs:
- 1474-9718
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0736.360500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19827.xml