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Interaction between Glutathione and Resveratrol in the Presence of Hydrogen Peroxide: A Kinetic Model

Authors
  • Zinatullina, K. M.1
  • Kasaikina, O. T.1
  • Khrameeva, N. P.2
  • Indeykina, M. I.2
  • Kononikhin, A. S.2
  • 1 Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, 119991, Russia , Moscow (Russia)
  • 2 Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Moscow, 119991, Russia , Moscow (Russia)
Type
Published Article
Journal
Kinetics and Catalysis
Publisher
Pleiades Publishing
Publication Date
Mar 01, 2021
Volume
62
Issue
2
Pages
255–263
Identifiers
DOI: 10.1134/S0023158421020130
Source
Springer Nature
Keywords
License
Yellow

Abstract

AbstractThe kinetics of interaction between glutathione (GSH) and unsaturated phenol resveratrol (RVT) in deionized water in the presence of hydrogen peroxide (H2O2) is studied. At a physiological concentration (0.1–10 mM), GSH containing two carboxyl groups forms acidic solutions (pH of 3–4); the GSH molecules are associated into dimers. Under these conditions, GSH is quite slowly oxidized by atmospheric oxygen, and the reaction between GSH and H2O2 is accompanied by the formation of radicals. The thiyl radical initiation rate (Wi) is a few fractions of a percent of the GSH consumption rate; however, it is sufficient to initiate a thiol–ene chain reaction between GSH and RVT. Using the experimental data on the kinetics and the product composition and the published data on reactions of GSH with H2O2 and thiyl radicals, a kinetic model of the complex interaction between GSH and RVT in the presence of H2O2 in an aqueous medium at 37°C is proposed. The model includes 19 quasi-elementary reactions with respective rate constants, in particular, the formation of intermediate GSH–H2O2 and GSH–GSH complexes, the formation of radicals, and their subsequent transformations into final products in reactions with RVT and GSH. A computer simulation based on the developed model adequately describes the features of the process kinetics in a wide reactant concentration range.

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