Literature DB >> 12763053

Radical-radical reactions of superoxide: a potential route to toxicity.

Christine C Winterbourn1, Anthony J Kettle.   

Abstract

Superoxide reacts with many radicals, such as phenoxyl radicals, at near diffusion-controlled rates. These reactions are usually considered to be repair processes and have received little biological attention. However, addition of superoxide to give hydroperoxides and secondary oxidation products can also occur. The relative contributions of addition and repair vary depending on the properties of the phenol. With tyrosine, addition to give tyrosine hydroperoxide predominates, but in peptides the efficiency of hydroperoxide formation depends on the proximity of free amine groups. Radicals from other phenolic compounds, such as alpha-tocopherol and serotonin, also undergo addition reactions with superoxide. Physiologically, these reactions are likely to be more significant than dimerization when both radicals are generated together. They warrant attention as potential contributors to superoxide toxicity.

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Year:  2003        PMID: 12763053     DOI: 10.1016/s0006-291x(03)00810-6

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  16 in total

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Journal:  Free Radic Res       Date:  2012-02-22

2.  Cytokine toxicity in insulin-producing cells is mediated by nitro-oxidative stress-induced hydroxyl radical formation in mitochondria.

Authors:  Ewa Gurgul-Convey; Ilir Mehmeti; Stephan Lortz; Sigurd Lenzen
Journal:  J Mol Med (Berl)       Date:  2011-04-13       Impact factor: 4.599

3.  Mechanism of nitrite oxidation by eosinophil peroxidase: implications for oxidant production and nitration by eosinophils.

Authors:  Christine J van Dalen; Christine C Winterbourn; Anthony J Kettle
Journal:  Biochem J       Date:  2006-03-15       Impact factor: 3.857

4.  Uric acid and thiocyanate as competing substrates of lactoperoxidase.

Authors:  Antonia Seidel; Heather Parker; Rufus Turner; Nina Dickerhof; Irada S Khalilova; Sigurd M Wilbanks; Anthony J Kettle; Guy N L Jameson
Journal:  J Biol Chem       Date:  2014-06-13       Impact factor: 5.157

5.  Urate as a physiological substrate for myeloperoxidase: implications for hyperuricemia and inflammation.

Authors:  Flavia C Meotti; Guy N L Jameson; Rufus Turner; D Tim Harwood; Samantha Stockwell; Martin D Rees; Shane R Thomas; Anthony J Kettle
Journal:  J Biol Chem       Date:  2011-01-25       Impact factor: 5.157

6.  Superoxide-mediated formation of tyrosine hydroperoxides and methionine sulfoxide in peptides through radical addition and intramolecular oxygen transfer.

Authors:  Péter Nagy; Anthony J Kettle; Christine C Winterbourn
Journal:  J Biol Chem       Date:  2009-03-18       Impact factor: 5.157

7.  Theoretical and experimental studies of tyrosyl hydroperoxide formation in the presence of H-bond donors.

Authors:  Steven M Field; Frederick A Villamena
Journal:  Chem Res Toxicol       Date:  2008-09-25       Impact factor: 3.739

8.  Protein tyrosine nitration: biochemical mechanisms and structural basis of functional effects.

Authors:  Rafael Radi
Journal:  Acc Chem Res       Date:  2012-11-16       Impact factor: 22.384

9.  Human indoleamine 2,3-dioxygenase is a catalyst of physiological heme peroxidase reactions: implications for the inhibition of dioxygenase activity by hydrogen peroxide.

Authors:  Mohammed Freewan; Martin D Rees; Tito S Sempértegui Plaza; Elias Glaros; Yean J Lim; Xiao Suo Wang; Amanda W S Yeung; Paul K Witting; Andrew C Terentis; Shane R Thomas
Journal:  J Biol Chem       Date:  2012-12-03       Impact factor: 5.157

10.  Kinetics of serotonin oxidation by heme-Aβ relevant to Alzheimer's disease.

Authors:  Soumya Mukherjee; Manas Seal; Somdatta Ghosh Dey
Journal:  J Biol Inorg Chem       Date:  2014-09-24       Impact factor: 3.358

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