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Biological Chemistry

Editor-in-Chief: Brüne, Bernhard

Editorial Board Member: Buchner, Johannes / Lei, Ming / Ludwig, Stephan / Sies, Helmut / Thomas, Douglas D. / Turk, Boris / Wittinghofer, Alfred

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IMPACT FACTOR 2016: 3.273

CiteScore 2016: 3.01

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Source Normalized Impact per Paper (SNIP) 2016: 0.800

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1437-4315
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Volume 389, Issue 3 (Mar 2008)

Issues

Increased molecular damage and heterogeneity as the basis of aging

Suresh I.S. Rattan
  • 1Laboratory of Cellular Ageing, Department of Molecular Biology, University of Aarhus, DK-8000 Aarhus C, Denmark
  • Other articles by this author:
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Published Online: 2008-03-03 | DOI: https://doi.org/10.1515/BC.2008.030

Abstract

Aging at the molecular level is characterized by the progressive accumulation of molecular damage. The sources of damage act randomly through environmental and metabolically generated free radicals, through spontaneous errors in biochemical reactions, and through nutritional components. However, damage to a macromolecule may depend on its structure, localization and interactions with other macromolecules. Damage to the maintenance and repair pathways comprising homeodynamic machinery leads to age-related failure of homeodynamics, increased molecular heterogeneity, altered cellular functioning, reduced stress tolerance, diseases and ultimate death. Novel approaches for testing and developing effective means of intervention, prevention and modulation of aging involve means to minimize the occurrence and accumulation of molecular damage. Mild stress-induced hormesis by physical, biological and nutritional methods, including hormetins, represents a promising strategy for achieving healthy aging and for preventing age-related diseases.

Keywords: biogerontology; gerontogenes; homeodynamics; homeostasis; reactive oxygen species; stress

About the article


Published Online: 2008-03-03

Published in Print: 2008-03-01


Citation Information: Biological Chemistry, ISSN (Online) 14374315, ISSN (Print) 14316730, DOI: https://doi.org/10.1515/BC.2008.030.

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