Proton leak modulation in testicular mitochondria affects reactive oxygen species production and lipid peroxidation

Cell Biochem Funct. 2010 Apr;28(3):224-31. doi: 10.1002/cbf.1644.

Abstract

Mitochondrial proton leak can account for almost 20% of oxygen consumption and it is generally accepted that this process contributes to basal metabolism. In order to clarify the role of basal proton leak in testicular mitochondria, we performed a comparative study with kidney and liver mitochondrial fractions. Proton leak stimulated by linoleic acid and inhibited by guanosine diphosphate (GDP) was detected, in a manner that was correlated with protein levels for uncoupling protein 2 (UCP2) in the three fractions. Modulation of proton leak had an effect on reactive oxygen species production as well as on lipid peroxidation, and this effect was also tissue-dependent. However, a possible role for the adenine nucleotide transporter (ANT) in testicular mitochondria proton leak could not be excluded. The modulation of proton leak appears as a possible and attractive target to control oxidative stress with implications for male gametogenesis.

MeSH terms

  • Animals
  • Guanosine Diphosphate / metabolism
  • Hydrogen Peroxide / metabolism
  • Ion Channels / metabolism
  • Kidney / cytology
  • Linoleic Acid / metabolism
  • Lipid Peroxidation*
  • Male
  • Membrane Potential, Mitochondrial / physiology
  • Mitochondria / metabolism*
  • Mitochondria, Liver / metabolism
  • Mitochondrial Proteins / metabolism
  • Oxidants / metabolism
  • Oxidative Phosphorylation
  • Oxidative Stress
  • Oxygen Consumption
  • Protons*
  • Rats
  • Rats, Wistar
  • Reactive Oxygen Species / metabolism*
  • Testis / cytology*
  • Uncoupling Protein 2

Substances

  • Ion Channels
  • Mitochondrial Proteins
  • Oxidants
  • Protons
  • Reactive Oxygen Species
  • Ucp2 protein, rat
  • Uncoupling Protein 2
  • Guanosine Diphosphate
  • Linoleic Acid
  • Hydrogen Peroxide