Medical Journals

Aging in Mouse and Human Systems: a Comparative Study.

Authors:
  • Demetrius Lloyd

From: Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138, USA. ldemetr@fas.harvard.edu

Annals of the New York Academy of Sciences

  • Publish Date: May 2006
  • ISSN: 0077-8923
  • Volume: 1067
  • Issue:
  • Pages: 66-82
  • Medium: Print
  • Language: English
  • Citation (JAMA): Demetrius Lloyd, et al. Aging in Mouse and Human Systems: a Comparative Study.. Ann. N. Y. Acad. Sci. May 2006;1067:66-82

Abstract

This article discusses the significance of mouse models as a basis for elucidating the aging process in humans. We identify certain parallels between mouse and human systems and review the theoretical and empirical support for the claim that the large divergence in the rate of aging between the two species resides in differences in the stability of their metabolic networks. We will show that these differences in metabolic stability have their origin in the different ecological constraints the species experience during their evolutionary history. We exploit these ideas to compare the effect of caloric restriction on murine and human systems. The studies predict that the large increases in mean life span and maximum life-span potential observed in laboratory rodents subject to caloric restriction will not obtain in human populations. We predict that, in view of the different metabolic stability of the two systems, caloric restriction will have no effect on the maximum life-span potential of humans, and a relatively minor effect on the mean life span of nonobese populations. This article thus points to certain intrinsic limitations in the use of mouse models in elucidating the aging process in humans. We furthermore contend the view that these limitations can be mitigated by considering the metabolic stability of the two species.

Mesh Headings (Keywords): Aging, Animals, Basal Metabolism, Caloric Restriction, Entropy, Evolution, Humans, Longevity, Mice


Check for Full Text / PubMed Unique Identifier (PMID): 16803972


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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