Nitric oxide-donor compounds inhibit lipoxygenase activity

Biochem Biophys Res Commun. 1996 Feb 6;219(1):128-33. doi: 10.1006/bbrc.1996.0193.

Abstract

The nitric oxide (N0-releasing agents sodium nitroprusside (SNP) and S-nitroso-N-acetylpenicillamine (SNAP) inhibit dioxygenase activity of lipoxygenase in human platelets and human CHP100 neuroblastoma cells, leading the latter to necrosis. The effect of both NO-donors on the dioxygenase reaction was investigated by using soybean lipoxygenase type II (LOX-2) as a model for the mammalian enzyme. SNP and SNAP were competitive inhibitors of LOX-2, with inhibition constants of 525 microM and 710 microM, respectively. Both compounds inactivated LOX-2 by reducing the catalytic iron to the inactive Fe(II) form and counteracted the H2O2-mediated activation of the LOX-2 catalyzed dioxygenase reaction. Similarly, the co-oxidative and per-oxidative activities of LOX-2 were also inhibited by the NO-releasing agents. These findings suggest that the biological role played by NO can be mediated, at least in part, by the inactivation of lipoxygenase, a key-enzyme for the arachidonic acid metabolism in human cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Platelets / enzymology*
  • Cell Death / drug effects
  • Cell Line
  • Humans
  • Kinetics
  • Lipoxygenase / blood
  • Lipoxygenase / metabolism*
  • Lipoxygenase Inhibitors / pharmacology*
  • Necrosis
  • Neuroblastoma
  • Nitric Oxide / pharmacology*
  • Nitroprusside / pharmacology*
  • Oxygenases / antagonists & inhibitors*
  • Oxygenases / blood
  • Penicillamine / analogs & derivatives*
  • Penicillamine / pharmacology
  • S-Nitroso-N-Acetylpenicillamine
  • Tumor Cells, Cultured

Substances

  • Lipoxygenase Inhibitors
  • Nitroprusside
  • Nitric Oxide
  • S-Nitroso-N-Acetylpenicillamine
  • Oxygenases
  • Lipoxygenase
  • Penicillamine