Literature DB >> 191070

Benzo[a]yrenedione/benzo[a]pyrenediol oxidation-reduction couples and the generation of reactive reduced molecular oxygen.

R J Lorentzen, P O Ts'o.   

Abstract

The ability of the isomeric quinone metabolites of benzo[a]pyrene, benzo[a]pyrene-6,12-dione, benzo[a]pyrene-1,6-dione, and benzo[a]pyrene-3,6-dione to undergo reversible, univalent oxidation-reduction cycles involving the corresponding benzo[a]pyrenediols and intermediate semiquinone radicals has been characterized. Under anaerobic conditions, all three benzo[a]pyrenediones are easily reduced to benzo[a]pyrenediols, even by mild biological agents such as NAD(P)H, cysteamine, and glutathione. The benzo[a]pyrenediols, in turn, are very rapidly autoxidized to the benzo[a]pyrenediones when exposed to air. Substantial amounts of hydrogen peroxide are produced during these autoxidations, and other reactive reduced oxygen species, such as the superoxide and hydroxyl radicals, are probably formed transiently as well. The benzo[a]pyrenediol-benzo[a]pyrenedione interconversions proceed by one-electron steps; the corresponsing semiquinone radicals can be monitored by electron spin resonance spectroscopy as inter mediates during these reactions carried out at high pH. Benzo[a]pyrenediones induce DNA strand scission when incubated with bacteriophage T7 DNA. This damage is modified by conditions which indicate that reduced oxygen species propagate the free-radical reactions responsible for the strand scission. Benzo[a]pyrenediones are electron-acceptor substrates for NADH dehydrogenase from Clostridium kluyveri. Catalytic amounds of these benzo[a]pyrene metabolites, together with this respiratory enzyme function as cyclic oxidation-reduction couples which link NADH and molecular oxygen in the continuous production of hydrogen peroxide. These data, together with preliminary results with cells in culture, indicate that benzo[a]pyrenediones are potentially harmful metabolites of benzo[a]pyrene, acting by processes which lead to their regeneration rather than depletion; nucleic acid and call damage is probably produced by the reactive reduced oxygen species resulting from such regenerative oxidation-reduction cycles.

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Year:  1977        PMID: 191070     DOI: 10.1021/bi00626a035

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  13 in total

1.  Evidence for the involvement of superoxide in vitamin K-dependent carboxylation of glutamic acid residues of prothrombin.

Authors:  M P Esnouf; M R Green; H A Hill; G B Irvine; S J Walter
Journal:  Biochem J       Date:  1978-07-15       Impact factor: 3.857

2.  Specificity of human aldo-keto reductases, NAD(P)H:quinone oxidoreductase, and carbonyl reductases to redox-cycle polycyclic aromatic hydrocarbon diones and 4-hydroxyequilenin-o-quinone.

Authors:  Carol A Shultz; Amy M Quinn; Jong-Heum Park; Ronald G Harvey; Judy L Bolton; Edmund Maser; Trevor M Penning
Journal:  Chem Res Toxicol       Date:  2011-09-29       Impact factor: 3.739

3.  In utero exposure to benzo(a)pyrene predisposes offspring to cardiovascular dysfunction in later-life.

Authors:  G E Jules; S Pratap; A Ramesh; D B Hood
Journal:  Toxicology       Date:  2012-02-21       Impact factor: 4.221

4.  Mutagenicity of oxygen free radicals.

Authors:  C S Moody; H M Hassan
Journal:  Proc Natl Acad Sci U S A       Date:  1982-05       Impact factor: 11.205

Review 5.  The role of conjugation reactions in detoxication.

Authors:  K W Bock; W Lilienblum; G Fischer; G Schirmer; B S Bock-Henning
Journal:  Arch Toxicol       Date:  1987       Impact factor: 5.153

6.  Mutagenicity of quinones: pathways of metabolic activation and detoxification.

Authors:  P L Chesis; D E Levin; M T Smith; L Ernster; B N Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1984-03       Impact factor: 11.205

7.  Metabolism of benzo[a]pyrene in human bronchoalveolar H358 cells using liquid chromatography-mass spectrometry.

Authors:  Hao Jiang; Stacy L Gelhaus; Dipti Mangal; Ronald G Harvey; Ian A Blair; Trevor M Penning
Journal:  Chem Res Toxicol       Date:  2007-08-17       Impact factor: 3.739

Review 8.  Toxic drug effects associated with oxygen metabolism: redox cycling and lipid peroxidation.

Authors:  H Kappus; H Sies
Journal:  Experientia       Date:  1981-12-15

9.  Genotoxicity of ortho-quinones: reactive oxygen species versus covalent modification.

Authors:  Trevor M Penning
Journal:  Toxicol Res (Camb)       Date:  2017-09-06       Impact factor: 3.524

Review 10.  Pharmacokinetics and molecular detoxication.

Authors:  J R Cashman; B Y Perotti; C E Berkman; J Lin
Journal:  Environ Health Perspect       Date:  1996-03       Impact factor: 9.031

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