Featured Article: Accelerated decline of physical strength in peroxiredoxin-3 knockout mice

Exp Biol Med (Maywood). 2016 Jul;241(13):1395-400. doi: 10.1177/1535370216642039. Epub 2016 Mar 31.

Abstract

As a member of peroxiredoxin family, peroxiredoxin-3 plays a major role in the control of mitochondrial level of reactive oxygen species. During the breeding of experimental mice, we noticed that the peroxiredoxin-3 knockout mice were listless with aging. In the present study, we compared the swimming exercise performance and oxidative status between peroxiredoxin-3 knockout mice (n = 15) and wild-type littermates (n = 15). At the age of 10 months, the physical strength of peroxiredoxin-3 knockout mice was much lower than the wild-type littermates. Increased oxidative damage and decreased mitochondrial DNA copy number of the animal skeletal muscles were observed in peroxiredoxin-3 knockout mice as compared to that in the wild-type littermates. In addition, we found increased apoptotic cells in the brains of peroxiredoxin-3 knockout mice. Our results suggest that the deficiency of peroxiredoxin-3 induces accelerated oxidative stress and mitochondrial impairment, resulting in the decrease of energy supply and cellular activities. Peroxiredoxin-3 might be involved in the inhibition of aging process.

Keywords: Peroxiredoxin; aging; mitochondria; oxidative stress; reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / metabolism
  • Aging / pathology
  • Aging / physiology
  • Animals
  • Apoptosis / genetics
  • Biomarkers / metabolism
  • DNA Copy Number Variations
  • Genotype
  • Mice, Knockout
  • Mitochondria / metabolism
  • Muscle Strength / genetics*
  • Oxidative Stress
  • Peroxiredoxin III / genetics
  • Peroxiredoxin III / metabolism
  • Peroxiredoxin III / physiology*
  • Reactive Oxygen Species / metabolism

Substances

  • Biomarkers
  • Reactive Oxygen Species
  • Peroxiredoxin III