Inhibition of lipoxygenase by soy isoflavones: evidence of isoflavones as redox inhibitors

Arch Biochem Biophys. 2007 May 15;461(2):176-85. doi: 10.1016/j.abb.2007.02.013. Epub 2007 Mar 8.

Abstract

Hydroperoxides, the products of lipoxygenase mediated pathways, play a major role in the manifestation of chronic inflammatory diseases. Soy isoflavones act as antioxidants due to their ability to scavenge free radicals. Isoflavones inhibit the activity of soy lipoxygenase-1 and 5-lipoxygenase, from human polymorph nuclear lymphocyte in a concentration dependent manner. Spectroscopic and enzyme kinetic measurements have helped to understand the nature and mechanism of inhibition. Genistein is the most effective inhibitor of soy lipoxygenase 1 and 5-lipoxygenase with IC(50) values of 107 and 125 microM, respectively. Genistein and daidzein are noncompetitive inhibitors of soy lipoxygenase 1 with inhibition constants, K(i), of 60 and 80 microM, respectively. Electron paramagnetic resonance and spectroscopic studies confirm that isoflavones reduce active state iron to ferrous state and prevent the activation of the resting enzyme. A model for the inhibition of lipoxygenase by isoflavones is suggested.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Glycine max / enzymology*
  • Humans
  • Isoflavones / physiology*
  • Lipoxygenase Inhibitors / pharmacology*
  • Oxidation-Reduction

Substances

  • Isoflavones
  • Lipoxygenase Inhibitors