Age-related changes in rat prostate tissue; perspective of protein oxidation

Aging Male. 2015 Mar;18(1):54-9. doi: 10.3109/13685538.2014.951921. Epub 2014 Aug 28.

Abstract

Background: Increased systemic oxidative stress is considered as an important risk factor for prostate cancer occurrence; however, the relationship between impaired redox homeostasis of prostate tissue and aging remains unclear.

Objective: In our study, we hypothesized that age-related deterioration of redox homeostasis in prostate tissue may be considered as a predisposing factor for prostate cancer occurrence.

Methods: Sprague-Dawley rats were divided into two groups as young control (5 months) and naturally aged (24 months). We investigated the levels of oxidant and antioxidant parameters in prostate tissue.

Results: Advanced oxidation protein products, protein carbonyl, non-protein thiol and lipid hydroperoxides levels of aged rats were significantly higher than in the young control rats (p < 0.01, p < 0.05, p < 0.001, p < 0.05, respectively). Additionally, antioxidant activity of Cu-Zn-superoxide dismutase in elderly group was significantly lower than young controls (p < 0.05).

Conclusions: We suggest that increased non-protein thiol levels found in aged rats may prevent further dissemination of oxidative protein damage. We also propose that the increased levels of oxidative protein damage markers and decreased Cu-Zn superoxide dismutase activity in aged prostate may be considered as a predisposing factor for prostate cancer. Further studies are warranted to clarify all these oxidative changes as initiation factors for prostate cancer in the association of aging with prostate cancer.

Keywords: Aging; antioxidant capacity; lipid peroxidation; prostate; protein oxidation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / physiology*
  • Animals
  • Biomarkers
  • Lipid Peroxidation*
  • Male
  • Malondialdehyde / metabolism
  • Oxidation-Reduction
  • Oxidative Stress / physiology*
  • Prostate / metabolism*
  • Protein Carbonylation
  • Rats
  • Rats, Sprague-Dawley
  • Sulfhydryl Compounds / metabolism
  • Superoxide Dismutase / metabolism

Substances

  • Biomarkers
  • Sulfhydryl Compounds
  • Malondialdehyde
  • Superoxide Dismutase