4.7 Article

Biomarkers of aging in Drosophila

Journal

AGING CELL
Volume 9, Issue 4, Pages 466-477

Publisher

WILEY
DOI: 10.1111/j.1474-9726.2010.00573.x

Keywords

biomarkers of aging; demography of aging; Drosophila

Funding

  1. Spanish Ministry of Education and Science [BFU2006-14495/BFI, AGL2006-12433]
  2. Spanish Ministry of Health [RD06/0013/0012, FIS PI081843]
  3. Generalitat of Catalunya [2005SGR00101]
  4. La Caixa Foundation
  5. Max Planck Society
  6. Medical Research Council
  7. National Institutes of Health [P01 AG025901, PL1 AG032118, P30 AG025708]
  8. Wellcome Trust
  9. COST Action [B-35]

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P>Low environmental temperature and dietary restriction (DR) extend lifespan in diverse organisms. In the fruit fly Drosophila, switching flies between temperatures alters the rate at which mortality subsequently increases with age but does not reverse mortality rate. In contrast, DR acts acutely to lower mortality risk; flies switched between control feeding and DR show a rapid reversal of mortality rate. Dietary restriction thus does not slow accumulation of aging-related damage. Molecular species that track the effects of temperatures on mortality but are unaltered with switches in diet are therefore potential biomarkers of aging-related damage. However, molecular species that switch upon instigation or withdrawal of DR are thus potential biomarkers of mechanisms underlying risk of mortality, but not of aging-related damage. Using this approach, we assessed several commonly used biomarkers of aging-related damage. Accumulation of fluorescent advanced glycation end products (AGEs) correlated strongly with mortality rate of flies at different temperatures but was independent of diet. Hence, fluorescent AGEs are biomarkers of aging-related damage in flies. In contrast, five oxidized and glycated protein adducts accumulated with age, but were reversible with both temperature and diet, and are therefore not markers either of acute risk of dying or of aging-related damage. Our approach provides a powerful method for identification of biomarkers of aging.

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