TY - JOUR
T1 - Fat maintenance is a predictor of the murine lifespan response to dietary restriction
AU - Liao, Chen Yu
AU - Rikke, Brad A.
AU - Johnson, Thomas E.
AU - Gelfond, Jonathan A.L.
AU - Diaz, Vivian
AU - Nelson, James F.
PY - 2011/8
Y1 - 2011/8
N2 - Dietary restriction (DR), one of the most robust life-extending manipulations, is usually associated with reduced adiposity. This reduction is hypothesized to be important in the life-extending effect of DR, because excess adiposity is associated with metabolic and age-related disease. Previously, we described remarkable variation in the lifespan response of 41 recombinant inbred strains of mice to DR, ranging from life extension to life shortening. Here, we used this variation to determine the relationship of lifespan modulation under DR to fat loss. Across strains, DR life extension correlated inversely with fat reduction, measured at midlife (males, r=-0.41, P<0.05, n=38 strains; females, r=-0.63, P<0.001, n=33 strains) and later ages. Thus, strains with the least reduction in fat were more likely to show life extension, and those with the greatest reduction were more likely to have shortened lifespan. We identified two significant quantitative trait loci (QTLs) affecting fat mass under DR in males but none for lifespan, precluding the confirmation of these loci as coordinate modulators of adiposity and longevity. Our data also provide evidence for a QTL previously shown to affect fuel efficiency under DR. In summary, the data do not support an important role for fat reduction in life extension by DR. They suggest instead that factors associated with maintaining adiposity are important for survival and life extension under DR.
AB - Dietary restriction (DR), one of the most robust life-extending manipulations, is usually associated with reduced adiposity. This reduction is hypothesized to be important in the life-extending effect of DR, because excess adiposity is associated with metabolic and age-related disease. Previously, we described remarkable variation in the lifespan response of 41 recombinant inbred strains of mice to DR, ranging from life extension to life shortening. Here, we used this variation to determine the relationship of lifespan modulation under DR to fat loss. Across strains, DR life extension correlated inversely with fat reduction, measured at midlife (males, r=-0.41, P<0.05, n=38 strains; females, r=-0.63, P<0.001, n=33 strains) and later ages. Thus, strains with the least reduction in fat were more likely to show life extension, and those with the greatest reduction were more likely to have shortened lifespan. We identified two significant quantitative trait loci (QTLs) affecting fat mass under DR in males but none for lifespan, precluding the confirmation of these loci as coordinate modulators of adiposity and longevity. Our data also provide evidence for a QTL previously shown to affect fuel efficiency under DR. In summary, the data do not support an important role for fat reduction in life extension by DR. They suggest instead that factors associated with maintaining adiposity are important for survival and life extension under DR.
KW - Body weight
KW - Dietary restriction
KW - Fat mass
KW - Lean mass
KW - Quantitative trait loci, lifespan
KW - Recombinant inbred mice
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UR - http://www.scopus.com/inward/citedby.url?scp=79960329362&partnerID=8YFLogxK
U2 - 10.1111/j.1474-9726.2011.00702.x
DO - 10.1111/j.1474-9726.2011.00702.x
M3 - Article
C2 - 21388497
AN - SCOPUS:79960329362
SN - 1474-9718
VL - 10
SP - 629
EP - 639
JO - Aging cell
JF - Aging cell
IS - 4
ER -