Suppression of superoxide anion generation catalyzed by xanthine oxidase with alkyl caffeates and the scavenging activity

Int J Food Sci Nutr. 2016;67(3):283-7. doi: 10.3109/09637486.2016.1153609. Epub 2016 Mar 3.

Abstract

Alkyl caffeates are strong antioxidants and inhibitors of xanthine oxidase. However, it is unclear about the effect of caffeic acid and alkyl caffeates on superoxide anion (O2(-)) generation catalyzed by xanthine oxidase. Effects of caffeic acid and alkyl caffeates on the uric acid formation and O2(-) generation catalyzed by xanthine oxidase were analyzed. The scavenging activities of 1,1-diphenyl-2-picryhydrazyl (DPPH) radical and O2(-) generated with phenazine methosulfate (PMS) and NADH were examined. Caffeic acid derivatives equally suppressed O2(-) generation, and the suppression is stronger than inhibition of xanthine oxidase. Scavenging activity of O2(-) is low compared to the suppression of O2(-) generation. Suppression of O2(-) generation catalyzed by xanthine oxidase with caffeic acid derivatives was not due to enzyme inhibition or O2(-) scavenging but due to the reduction of xanthine oxidase molecules. Alkyl caffeates are effective inhibitors of uric acid and O2(-) catalyzed by xanthine oxidase as well as antioxidants for edible oil.

Keywords: Caffeic acid; enzyme inhibition; enzyme reduction; phenazine methosulfate-NADH.

MeSH terms

  • Caffeic Acids / chemistry*
  • Free Radical Scavengers*
  • Molecular Structure
  • Reactive Oxygen Species
  • Superoxides / chemistry
  • Superoxides / metabolism*
  • Uric Acid / chemistry
  • Uric Acid / metabolism
  • Xanthine Oxidase / chemistry
  • Xanthine Oxidase / metabolism*

Substances

  • Caffeic Acids
  • Free Radical Scavengers
  • Reactive Oxygen Species
  • Superoxides
  • Uric Acid
  • Xanthine Oxidase
  • caffeic acid