Photoaging and chronological aging profile: Understanding oxidation of the skin

J Photochem Photobiol B. 2011 May 3;103(2):93-7. doi: 10.1016/j.jphotobiol.2011.01.019. Epub 2011 Feb 1.

Abstract

The impact of chronological aging and photoaging on the skin is particularly concerning, especially when oxidative stress is involved. This article provides evidence of quantitative and qualitative differences in the oxidative stress generated by chronological aging and photoaging of the skin in HRS/J hairless mice. Analysis of the results revealed an increase in lipid peroxides as the skin gets older and in photoaged skin (10.086 ± 0.70 η MDA/mg and 14.303 ± 1.81 η MDA/mg protein, respectively), although protein oxidation was only verified in chronological aged skin (15.449 ± 0.99 η protein/mg protein). The difference between both skin types is the decay in the capacity of lipid membrane turnover revealed by the dislocation of older skin to the left in the chemiluminescence curve. Imbalance between antioxidant and oxidation processes was verified by the decrease in total antioxidant capacity of chronological and photoaged skins. Although superoxide dismutase remained unchanged, catalase increased in the 18 and 48-week-old skin groups and decreased in irradiated mice, demonstrating that neither enzyme is a good parameter to determine oxidative stress. The differences observed between chronological and photoaging skin represent a potential new approach to understanding the phenomenon of skin aging and a new target for therapeutic intervention.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging*
  • Animals
  • Antioxidants / metabolism
  • Catalase / metabolism
  • Female
  • Lipid Peroxides / metabolism
  • Male
  • Mice
  • Mice, Hairless
  • Oxidation-Reduction
  • Oxidative Stress
  • Skin / metabolism
  • Skin / radiation effects*
  • Skin Aging* / radiation effects
  • Superoxide Dismutase / metabolism
  • Ultraviolet Rays

Substances

  • Antioxidants
  • Lipid Peroxides
  • Catalase
  • Superoxide Dismutase