Article

Fat maintenance is a predictor of the murine lifespan response to dietary restriction.

Department of Physiology, University of Texas Health Science Center, San Antonio, TX 78229, USA.
Aging cell (impact factor: 7.55). 03/2011; 10(4):629-39. DOI:10.1111/j.1474-9726.2011.00702.x pp.629-39
Source: PubMed

ABSTRACT 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.

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Keywords

41 recombinant inbred strains
 
age-related disease
 
Dietary restriction
 
DR life extension correlated
 
excess adiposity
 
fat loss
 
fat reduction
 
females
 
fuel efficiency
 
greatest reduction
 
life extension
 
life-extending effect
 
lifespan modulation
 
lifespan response
 
metabolic
 
mice
 
midlife
 
remarkable variation
 
robust life-extending manipulations
 
significant quantitative trait loci