Literature DB >> 6311105

Superoxide-dependent and ascorbate-dependent formation of hydroxyl radicals in the presence of copper salts: a physiologically significant reaction?

D A Rowley, B Halliwell.   

Abstract

Copper (Cu2+) ions at physiological concentrations can promote the formation of hydroxyl radical (OH) or a species of equivalent reactivity. The reaction requires H2O2 and a reducing agent. Reduction of Cu2+ can be achieved by superoxide ion generated by a mixture of hypoxanthine and xanthine oxidase or added directly as its potassium salt. Reduction of Cu2+ can also be achieved by ascorbic acid. Hence both O2- -dependent and ascorbate-dependent formation of OH from H2O2 in the presence of Cu2+ can be observed. Only the former reaction is significantly inhibited by superoxide dismutase. The binding of Cu2+ to histidine or albumin at physiological concentrations decreases the formation of OH radicals in free solution in the presence of either ascorbate or an (O2- -generating system. It is suggested that OH is still formed but reacts immediately with the binding molecule.

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Year:  1983        PMID: 6311105     DOI: 10.1016/0003-9861(83)90031-0

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


  26 in total

1.  Structural changes of proteins in fish red blood cells after copper and mercury treatment.

Authors:  K Gwozdzinski
Journal:  Arch Environ Contam Toxicol       Date:  1992-11       Impact factor: 2.804

2.  Polynitroxyl albumin and albumin therapy after pediatric asphyxial cardiac arrest: effects on cerebral blood flow and neurologic outcome.

Authors:  Mioara D Manole; Patrick M Kochanek; Lesley M Foley; T Kevin Hitchens; Hülya Bayır; Henry Alexander; Robert Garman; Li Ma; Carleton J C Hsia; Chien Ho; Robert S B Clark
Journal:  J Cereb Blood Flow Metab       Date:  2011-11-30       Impact factor: 6.200

3.  Degradation of methyl and ethyl mercury into inorganic mercury by oxygen free radical-producing systems: involvement of hydroxyl radical.

Authors:  I Suda; S Totoki; H Takahashi
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

4.  Chemical pathways of peptide degradation. X: effect of metal-catalyzed oxidation on the solution structure of a histidine-containing peptide fragment of human relaxin.

Authors:  M Khossravi; R T Borchardt
Journal:  Pharm Res       Date:  2000-07       Impact factor: 4.200

Review 5.  Role of metal ions in oxidant cell injury.

Authors:  O Cantoni; M Fumo; F Cattabeni
Journal:  Biol Trace Elem Res       Date:  1989 Jul-Sep       Impact factor: 3.738

Review 6.  Polyphenols as Potential Metal Chelation Compounds Against Alzheimer's Disease.

Authors:  Johant Lakey-Beitia; Andrea M Burillo; Giovanni La Penna; Muralidhar L Hegde; K S Rao
Journal:  J Alzheimers Dis       Date:  2021       Impact factor: 4.472

7.  Chemical pathways of peptide degradation. VIII. Oxidation of methionine in small model peptides by prooxidant/transition metal ion systems: influence of selective scavengers for reactive oxygen intermediates.

Authors:  S Li; C Schöneich; R T Borchardt
Journal:  Pharm Res       Date:  1995-03       Impact factor: 4.200

8.  A copper sulfate and hydroxylysine treatment regimen for enhancing collagen cross-linking and biomechanical properties in engineered neocartilage.

Authors:  Eleftherios A Makris; Regina F MacBarb; Donald J Responte; Jerry C Hu; Kyriacos A Athanasiou
Journal:  FASEB J       Date:  2013-03-01       Impact factor: 5.191

Review 9.  Is copper pro- or anti-inflammatory? A reconciling view and a novel approach for the use of copper in the control of inflammation.

Authors:  G Berthon
Journal:  Agents Actions       Date:  1993-07

10.  Chemical pathways of peptide degradation: IX. Metal-catalyzed oxidation of histidine in model peptides.

Authors:  M Khossravi; R T Borchardt
Journal:  Pharm Res       Date:  1998-07       Impact factor: 4.200

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