Effects of Endurance Training on the Coenzyme Q Redox State in Rat Heart, Liver, and Brain at the Tissue and Mitochondrial Levels: Implications for Reactive Oxygen Species Formation and Respiratory Chain Remodeling

Int J Mol Sci. 2022 Jan 14;23(2):896. doi: 10.3390/ijms23020896.

Abstract

Sixteen adult, 4-month-old male Wistar rats were randomly assigned to the training group (n = 8) or the control group (n = 8). We elucidated the effects of 8 weeks of endurance training on coenzyme Q (Q) content and the formation of reactive oxygen species (ROS) at the tissue level and in isolated mitochondria of the rat heart, liver and brain. We demonstrated that endurance training enhanced mitochondrial biogenesis in all tested organs, while a significant increase in the Q redox state was observed in the heart and brain, indicating an elevated level of QH2 as an antioxidant. Moreover, endurance training increased the mQH2 antioxidant pool in the mitochondria of the heart and liver, but not in the brain. At the tissue and isolated mitochondria level, an increase in ROS formation was only observed in the heart. ROS formation observed in the mitochondria of individual rat tissues after training may be associated with changes in the activity/amount of individual components of the oxidative phosphorylation system and its molecular organization, as well as with the size of the oxidized pool of mitochondrial Q acting as an electron carrier in the respiratory chain. Our results indicate that tissue-dependent changes induced by endurance training in the cellular and mitochondrial QH2 pool acting as an antioxidant and in the mitochondrial Q pool serving the respiratory chain may serve important roles in energy metabolism, redox homeostasis and the level of oxidative stress.

Keywords: coenzyme Q; endurance training; mitochondrial energetics; reactive oxygen species.

MeSH terms

  • Animals
  • Brain / metabolism
  • Electron Transport*
  • Endurance Training
  • Heart
  • Hydrogen Peroxide / metabolism
  • Liver / metabolism
  • Mitochondria / physiology*
  • Myocardium / metabolism
  • Organ Specificity
  • Oxidation-Reduction*
  • Oxidative Phosphorylation*
  • Oxidative Stress
  • Rats
  • Reactive Oxygen Species / metabolism*
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / metabolism

Substances

  • Reactive Oxygen Species
  • Ubiquinone
  • Hydrogen Peroxide
  • coenzyme Q10