Literature DB >> 12042467

Living fast, dying when? The link between aging and energetics.

John R Speakman1, Colin Selman, Jane S McLaren, E Jean Harper.   

Abstract

The idea that aging should be linked to energy expenditure has a long history that can be traced to the late 1800s and the industrial revolution. Machines that are run fast wear out more quickly, so the notion was born that humans and animals might experience similar fates: the faster they live (expressed as greater energy expenditure), the sooner they die. Evidence supporting the "rate-of-living" theory was gleaned from the scaling of resting metabolism and life span as functions of body mass. The product of these factors yields a mass-invariant term, equivalent to the "amount of living." There are at least four problems with this evidence, which are summarized and reviewed in this communication: 1) life span is a poor measure of aging, 2) resting metabolism is a poor measure of energy expenditure, 3) the effects are confounded by body mass and 4) the comparisons made are not phylogenetically independent. We demonstrate that there is a poor association between resting metabolic rate (RMR) and daily energy expenditure (DEE) measured using the doubly labeled water (DLW) method at the level of species. Nevertheless, the scaling relation between DEE and body mass still has the same scaling exponent as the RMR and body mass relationship. Thus, if we use DEE rather than RMR in the analysis, the rate-of-living ideas are still supported. Data for 13 species of small mammal were obtained, where energy demands by DLW and longevity were reliably known. In these species, there was a strong negative relationship between residual longevity and residual DEE, both with the effects of body mass removed (r(2) = 0.763, F = 32.1, P < 0.001). Hence, the association of energy demands and life span is not attributed to the confounding effects of body size. We subjected these latter data to an analysis that extracts phylogenetically independent contrasts, and the relationship remained significant (r(2) = 0.815, F = 39.74, P < 0.001). Small mammals that live fast really do die young. However, there are very large differences between species in the amounts of living that each enjoy and these disparities are even greater when other taxa are included in the comparisons. Such differences are incompatible with the "rate-of-living" theory. However, the link between energetics and aging across species is reconcilable within the framework of the "free-radical damage hypothesis" and the "disposable soma hypothesis." Within species one might anticipate the rate-of-living model would be more appropriate. We reviewed data generated from three different sources to evaluate whether this were so, studies in which metabolic rate is experimentally increased and impacts on life span followed, studies of caloric restriction and studies where links between natural variation in metabolism and life span are sought. This review reveals that there might be contrasting effects of resting and nonresting energy expenditure on aging, with increases in the former being protective and increases in the latter being harmful.

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Year:  2002        PMID: 12042467     DOI: 10.1093/jn/132.6.1583S

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  41 in total

1.  Long-term caloric restriction reduces metabolic rate and heart rate under cool and thermoneutral conditions in FBNF1 rats.

Authors:  W David Knight; M M Witte; A D Parsons; M Gierach; J Michael Overton
Journal:  Mech Ageing Dev       Date:  2011-04-12       Impact factor: 5.432

2.  Association between mammalian lifespan and circadian free-running period: the circadian resonance hypothesis revisited.

Authors:  C A Wyse; A N Coogan; C Selman; D G Hazlerigg; J R Speakman
Journal:  Biol Lett       Date:  2010-04-14       Impact factor: 3.703

3.  Tropical birds have a slow pace of life.

Authors:  Popko Wiersma; Agustí Muñoz-Garcia; Amy Walker; Joseph B Williams
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-21       Impact factor: 11.205

4.  A controlled trial of reduced meal frequency without caloric restriction in healthy, normal-weight, middle-aged adults.

Authors:  Kim S Stote; David J Baer; Karen Spears; David R Paul; G Keith Harris; William V Rumpler; Pilar Strycula; Samer S Najjar; Luigi Ferrucci; Donald K Ingram; Dan L Longo; Mark P Mattson
Journal:  Am J Clin Nutr       Date:  2007-04       Impact factor: 7.045

Review 5.  The physiological costs of reproduction in small mammals.

Authors:  John R Speakman
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2008-01-27       Impact factor: 6.237

6.  Alternative types of small mammal ontogeny: Contribution to the radiobiology and radioecology.

Authors:  E B Grigorkina; G V Olenev; O V Tarasov
Journal:  Dokl Biol Sci       Date:  2015-05-05

7.  Physical activity after surgically obtained weight loss: study with a SenseWear armband in subjects undergoing biliopancreatic diversion.

Authors:  Raffaella Gradaschi; Giovanni Camerini; Flavia Carlini; Samyr Sukkar; Nicola Sopinaro; Gian Franco Adami
Journal:  Obes Surg       Date:  2014-02       Impact factor: 4.129

8.  Effect of aging, caloric restriction, and uncoupling protein 3 (UCP3) on mitochondrial proton leak in mice.

Authors:  Danny K Asami; Roger B McDonald; Kevork Hagopian; Barbara A Horwitz; David Warman; Aileen Hsiao; Craig Warden; Jon J Ramsey
Journal:  Exp Gerontol       Date:  2008-09-30       Impact factor: 4.032

9.  Individual responsiveness to exercise-induced fat loss is associated with change in resting substrate utilization.

Authors:  Nicholas D Barwell; Dalia Malkova; Melanie Leggate; Jason M R Gill
Journal:  Metabolism       Date:  2009-06-18       Impact factor: 8.694

10.  The timing of the shrew: continuous melatonin treatment maintains youthful rhythmic activity in aging Crocidura russula.

Authors:  Elodie Magnanou; Joël Attia; Roger Fons; Gilles Boeuf; Jack Falcon
Journal:  PLoS One       Date:  2009-06-15       Impact factor: 3.240

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