Literature DB >> 9056248

Inhibition of peroxynitrite-mediated oxidation of glutathione by carbon dioxide.

H Zhang1, G L Squadrito, R M Uppu, J N Lemercier, R Cueto, W A Pryor.   

Abstract

Peroxynitrite reacts with CO2 to from an adduct containing a weak O--O bond that can undergo homolytic and/or heterolytic cleavage to give other reactive intermediates. Because the peroxynitrite/CO2 reaction is fast and physiological concentrations of CO2 are relatively high, peroxynitrite-mediated oxidations of biological species probably involve the peroxynitrite-CO2 adduct and its subsequent reactive intermediates. We have examined the reaction of glutathione with peroxynitrite in the presence and absence of added bicarbonate. In the presence of added bicarbonate, CO2 competes with glutathione for peroxynitrite, resulting in a markedly decreased consumption of glutathione compared with that observed in the absence of added bicarbonate. However, the consumption of glutathione still is much higher than predicted from the assumption that the glutathione-peroxynitrite reaction is the only reaction that can consume glutathione in this system. These results suggest that glutathione partially, but not completely, traps intermediate(s) derived from the peroxynitrite and CO2 reaction. Some rate constants for the trapping of the intermediates are estimated by simulating the reactions, and possible mechanisms for the reaction of peroxynitrite with glutathione in the presence of added bicarbonate are discussed.

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Year:  1997        PMID: 9056248     DOI: 10.1006/abbi.1996.9863

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  7 in total

1.  Peroxynitrite inactivation of tyrosine hydroxylase: mediation by sulfhydryl oxidation, not tyrosine nitration.

Authors:  D M Kuhn; C W Aretha; T J Geddes
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Assessment at the single-cell level identifies neuronal glutathione depletion as both a cause and effect of ischemia-reperfusion oxidative stress.

Authors:  Seok Joon Won; Ji-Eun Kim; Giordano Fabricio Cittolin-Santos; Raymond A Swanson
Journal:  J Neurosci       Date:  2015-05-06       Impact factor: 6.167

3.  Peroxynitrite toxicity in Escherichia coli K12 elicits expression of oxidative stress responses and protein nitration and nitrosylation.

Authors:  Samantha McLean; Lesley A H Bowman; Guido Sanguinetti; Robert C Read; Robert K Poole
Journal:  J Biol Chem       Date:  2010-04-28       Impact factor: 5.157

4.  Global profiling of reactive oxygen and nitrogen species in biological systems: high-throughput real-time analyses.

Authors:  Jacek Zielonka; Monika Zielonka; Adam Sikora; Jan Adamus; Joy Joseph; Micael Hardy; Olivier Ouari; Brian P Dranka; Balaraman Kalyanaraman
Journal:  J Biol Chem       Date:  2011-12-04       Impact factor: 5.157

5.  One-electron oxidation pathway of thiols by peroxynitrite in biological fluids: bicarbonate and ascorbate promote the formation of albumin disulphide dimers in human blood plasma.

Authors:  G Scorza; M Minetti
Journal:  Biochem J       Date:  1998-01-15       Impact factor: 3.857

6.  Bioluminescent detection of peroxynitrite with a boronic acid-caged luciferin.

Authors:  Nathan A Sieracki; Benjamin N Gantner; Mao Mao; John H Horner; Richard D Ye; Asrar B Malik; Martin E Newcomb; Marcelo G Bonini
Journal:  Free Radic Biol Med       Date:  2013-03-07       Impact factor: 7.376

7.  Indomethacin potentiates acetylcholine-induced vasodilation by increasing free radical production.

Authors:  Antonella De Angelis; Barbara Rinaldi; Annalisa Capuano; Francesco Rossi; Amelia Filippelli
Journal:  Br J Pharmacol       Date:  2004-07-20       Impact factor: 8.739

  7 in total

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