Thyroxine-supported oxidation in the myeloperoxidase system

Horm Metab Res. 1993 Nov;25(11):569-72. doi: 10.1055/s-2007-1002179.

Abstract

Thyroxine and other iodothyronines (concentrations in the nanomolar range) stimulated the oxidation of NADH in the myeloperoxidase-H2O2-Cl- system. In the absence of chloride, thyroxine had only a marginal effect. This suggests that thyroxine increased the generation of chlorinating oxidants. A peroxidase-catalysed oxidation product of thyroxine, 3,5-diiodotyrosine, was inactive. Pre-incubation of thyroxine in the myeloperoxidase system showed that thyroxine was oxidized to a product capable of stimulating NADH oxidation. Reduction and alkylation of myeloperoxidase under nondenaturing conditions also increased the oxidative activity of the enzyme. It is postulated that both iodoacetamide and a thyroxine-derived oxidation product (presumably a quinone) alkylate sulphydryl groups near the active centre of myeloperoxidase making it more accessible for its substrate.

MeSH terms

  • Alkylation
  • Chlorides / pharmacology
  • Electrophoresis, Polyacrylamide Gel
  • Humans
  • Hydrogen Peroxide / metabolism
  • Kinetics
  • NAD / metabolism*
  • Oxidation-Reduction
  • Peroxidase / metabolism*
  • Thyroxine / metabolism
  • Thyroxine / pharmacology*

Substances

  • Chlorides
  • NAD
  • Hydrogen Peroxide
  • Peroxidase
  • Thyroxine