Acetylation of prostaglandin H2 synthases by aspirin is inhibited by redox cycling of the peroxidase

Biochem Pharmacol. 2008 Apr 1;75(7):1472-81. doi: 10.1016/j.bcp.2007.12.005. Epub 2007 Dec 27.

Abstract

Aspirin exerts its unique pharmacological effects by irreversibly acetylating a serine residue in the cyclooxygenase site of prostaglandin-H2-synthases (PGHSs). Despite the irreversibility of the inhibition, the potency of aspirin varies remarkably between cell types, suggesting that molecular determinants could contribute to cellular selectivity. Using purified enzymes, we found no evidence that aspirin is selective for either of the two PGHS isoforms, and we showed that hydroperoxide substrates of the PGHS peroxidase inhibited the rate of acetylation of PGHS-1 by 68%. Using PGHS-1 reconstituted with cobalt protoporphyrin, a heme devoid of peroxidase activity, we demonstrated that reversal by hydroperoxides of the aspirin-mediated acetylation depends upon the catalytic activity of the PGHS peroxidase. We demonstrated that inhibition of PGHS-2 by aspirin in cells in culture is reversed by 12-hydroperoxyeicosatetraenoic acid dose-dependently (ED50=0.58+/-0.15 microM) and that in cells with high levels of hydroperoxy-fatty acids (RAW264.7) the efficacy of aspirin is markedly decreased as compared to cells with low levels of hydroperoxides (A549; IC50s=256+/-22 microM and 11.0+/-0.9 microM, respectively). Together, these findings indicate that acetylation of the PGHSs by aspirin is regulated by the catalytic activity of the peroxidase, which yields a higher oxidative state of the enzyme.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation / drug effects
  • Animals
  • Aspirin / pharmacology*
  • Blood Platelets / drug effects
  • Blood Platelets / enzymology
  • Cattle
  • Cells, Cultured
  • Cyclooxygenase 2 / metabolism*
  • Enzyme Activation / drug effects
  • Enzyme Activation / physiology
  • Humans
  • Mice
  • Oxidation-Reduction / drug effects
  • Peroxidase / metabolism*
  • Sheep

Substances

  • Peroxidase
  • Cyclooxygenase 2
  • Aspirin