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dc.contributor.authorAruoma, O I
dc.contributor.authorHalliwell, B
dc.contributor.authorHoey, Brigid M
dc.contributor.authorButler, John
dc.date.accessioned2010-11-03T15:46:24Z
dc.date.available2010-11-03T15:46:24Z
dc.date.issued1988-11-15
dc.identifier.citationThe antioxidant action of taurine, hypotaurine and their metabolic precursors. 1988, 256 (1):251-5 Biochem. J.en
dc.identifier.issn0264-6021
dc.identifier.pmid2851980
dc.identifier.urihttp://hdl.handle.net/10541/114629
dc.description.abstractIt has been suggested that taurine, hypotaurine and their metabolic precursors (cysteic acid, cysteamine and cysteinesulphinic acid) might act as antioxidants in vivo. The rates of their reactions with the biologically important oxidants hydroxyl radical (.OH), superoxide radical (O2.-), hydrogen peroxide (H2O2) and hypochlorous acid (HOCl) were studied. Their ability to inhibit iron-ion-dependent formation of .OH from H2O2 by chelating iron ions was also tested. Taurine does not react rapidly with O2.-, H2O2 or .OH, and the product of its reaction with HOCl is still sufficiently oxidizing to inactivate alpha 1-antiproteinase. Thus it seems unlikely that taurine functions as an antioxidant in vivo. Cysteic acid is also poorly reactive to the above oxidizing species. By contrast, hypotaurine is an excellent scavenger of .OH and HOCl and can interfere with iron-ion-dependent formation of .OH, although no reaction with O2.- or H2O2 could be detected within the limits of our assay techniques. Cysteamine is an excellent scavenger of .OH and HOCl; it also reacts with H2O2, but no reaction with O2.- could be measured within the limits of our assay techniques. It is concluded that cysteamine and hypotaurine are far more likely to act as antioxidants in vivo than is taurine, provided that they are present in sufficient concentration at sites of oxidant generation.
dc.language.isoenen
dc.subject.meshAntioxidants
dc.subject.meshAscorbic Acid
dc.subject.meshBlood Proteins
dc.subject.meshCysteamine
dc.subject.meshFree Radicals
dc.subject.meshHydrogen Peroxide
dc.subject.meshHydroxides
dc.subject.meshHydroxyl Radical
dc.subject.meshHypochlorous Acid
dc.subject.meshIron
dc.subject.meshPulse Radiolysis
dc.subject.meshSuperoxides
dc.subject.meshTaurine
dc.subject.meshalpha 1-Antitrypsin
dc.titleThe antioxidant action of taurine, hypotaurine and their metabolic precursors.en
dc.typeArticleen
dc.contributor.departmentDepartment of Biochemistry, University of London King's College, London, U.K.en
dc.identifier.journalThe Biochemical Journalen
html.description.abstractIt has been suggested that taurine, hypotaurine and their metabolic precursors (cysteic acid, cysteamine and cysteinesulphinic acid) might act as antioxidants in vivo. The rates of their reactions with the biologically important oxidants hydroxyl radical (.OH), superoxide radical (O2.-), hydrogen peroxide (H2O2) and hypochlorous acid (HOCl) were studied. Their ability to inhibit iron-ion-dependent formation of .OH from H2O2 by chelating iron ions was also tested. Taurine does not react rapidly with O2.-, H2O2 or .OH, and the product of its reaction with HOCl is still sufficiently oxidizing to inactivate alpha 1-antiproteinase. Thus it seems unlikely that taurine functions as an antioxidant in vivo. Cysteic acid is also poorly reactive to the above oxidizing species. By contrast, hypotaurine is an excellent scavenger of .OH and HOCl and can interfere with iron-ion-dependent formation of .OH, although no reaction with O2.- or H2O2 could be detected within the limits of our assay techniques. Cysteamine is an excellent scavenger of .OH and HOCl; it also reacts with H2O2, but no reaction with O2.- could be measured within the limits of our assay techniques. It is concluded that cysteamine and hypotaurine are far more likely to act as antioxidants in vivo than is taurine, provided that they are present in sufficient concentration at sites of oxidant generation.


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