Effects of thyroid state on H2O2 production by rat heart mitochondria: sites of production with complex I- and complex II-linked substrates

Horm Metab Res. 2003 Jan;35(1):55-61. doi: 10.1055/s-2003-38392.

Abstract

This work was designed to determine possible effects of altered thyroid states on rates and sites of H 2 O 2 production by rat heart mitochondria. Rates of O 2 consumption and H 2 O 2 release, capacities to remove the peroxide, lipid peroxidation, cytochrome oxidase activities and ubiquinone levels were determined in heart mitochondria from euthyroid, hypothyroid, and hyperthyroid rats. Hypothyroidism decreased, whereas hyperthyroidism increased the rates of O 2 consumption and H 2 O 2 release during both state 4 and state 3 respiration with Complex I- or Complex II-linked substrates. The percentage of O 2 released as H 2 O 2 was not significantly affected by thyroid state. However, the mitochondrial capacity to remove H 2 O 2 increased in the transition from hypothyroid to hyperthyroid state, which indicates that H 2 O 2 production did not modify in proportion to the rate of O 2 consumption. The thyroid-state-linked changes in H 2 O 2 production were well correlated with the levels of hydroperoxides. Rates of H 2 O 2 release in the presence of respiratory inhibitors indicated that changes in the H 2 O 2 production occurred at both sites at which H 2 O 2 was generated in euthyroid state. This result and the observation that ubiquinol levels and cytochrome oxidase activities increase in the transition from hypothyroid to hyperthyroid state suggest that the modifications of H 2 O 2 production are due to a modulation by thyroid hormone of mitochondrial content of autoxidisable electron carriers.

MeSH terms

  • Animals
  • Electron Transport / physiology
  • Electron Transport Complex I / metabolism*
  • Electron Transport Complex II / metabolism*
  • Hydrogen Peroxide / metabolism*
  • Hyperthyroidism / metabolism
  • Hypothyroidism / metabolism
  • Kinetics
  • Lipid Peroxidation / physiology
  • Male
  • Mitochondria, Heart / enzymology
  • Mitochondria, Heart / metabolism*
  • Oxygen Consumption / drug effects
  • Rats
  • Rats, Wistar
  • Thyroid Gland / physiology*
  • Ubiquinone / analogs & derivatives*
  • Ubiquinone / metabolism

Substances

  • Ubiquinone
  • Hydrogen Peroxide
  • Electron Transport Complex II
  • Electron Transport Complex I
  • ubiquinol