Evidence for production of hydroxyl radicals by pentachlorophenol metabolites and hydrogen peroxide: A metal-independent organic Fenton reaction
Autor: | Ben-Zhan Zhu, Mordechai Chevion, Nahum Kitrossky |
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Rok vydání: | 2000 |
Předmět: |
Ethanol
Pentachlorophenol Dimethyl sulfoxide Hydroxyl Radical Radical Iron Biophysics Cell Biology Hydrogen Peroxide Resorcinols Photochemistry Biochemistry Medicinal chemistry Ferrous Hydroquinones Hydroxylation chemistry.chemical_compound Kinetics chemistry Hydroxybenzoates Hydroxyl radical Chelation Hydrogen peroxide Molecular Biology Chelating Agents |
Zdroj: | Biochemical and biophysical research communications. 270(3) |
ISSN: | 0006-291X |
Popis: | The production of hydroxyl radicals by tetrachlorohydroquinone (TCHQ, a major metabolite of the widely used biocide pentachlorophenol) in the presence of H 2 O 2 was studied by salicylate hydroxylation method. HPLC with electrochemical detection was used to measure the levels of 2,3- and 2,5-dihydroxybenzoic acid (DHBA) formed when the hydroxyl radicals react with salicylate. We found that TCHQ and H 2 O 2 could produce both 2,3- and 2,5-DHBA when incubated with salicylate. Their production was markedly inhibited by hydroxyl radical scavenging agents dimethyl sulfoxide and ethanol, as well as by tetrachlorosemiquinone radical scavengers desferrioxamine and other hydroxamic acids. In contrast, their production was not affected by the nonhydroxamate iron chelators diethylenetriaminepentaacetic acid (DTPA), bathophenanthroline disulfonic acid, and phytic acid, as well as the copper-specific chelator bathocuprione disulfonic acid. A comparison of product formation and distribution from the reaction of ferrous iron with hydrogen peroxide (the classic Fenton system) strongly suggests that the same hydroxyl radical adducts are formed as in the TCHQ/H 2 O 2 experiments. Taken together, we propose that hydroxyl radicals were produced by TCHQ in the presence of H 2 O 2 , probably through a metal-independent organic Fenton reaction. |
Databáze: | OpenAIRE |
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