Superoxide dismutase enhances chain-breaking antioxidant capability of hydroquinones

References

• O'Brien P.J. Molecular mechanisms of quinone cytotoxicity. Chemico-Biological Interactions 1991; 80: 1–41
   PubMed Web of Science ®Google Scholar
• Brunmark A., Cadenas E. Redox and addition chemistry of quinoid compounds and its biological implications. Free Radical Biology and Medicine 1989; 7: 435–477
   PubMed Web of Science ®Google Scholar
• Roginsky V.A., Barsukova T.A. Kinetics of the oxidation of hydroquinones by molecular oxygen. Effect of SOD. Journal of the Chemical Society, Perkin Transactions 2000; 2: 1575–1582
   Google Scholar
• Burton G.A., Doba T., Gabe E.G., Lee F.L., Passad L., Ingold K.U. Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols. Journal of American Chemical Society 1985; 107: 7053–7056
   Web of Science ®Google Scholar
• Barclay L.R.C., Vinqvist M.R., Mukai K., Itoh S., Marinoto H. Chain-breaking phenolic antioxidants: steric and electronic effects in polyalkylchromanols, tocopherol analogs, hydroquinones, and superior antioxidants of the polyalkylbenzochromanol and naphtofuran class. Journal of Organic Chemistry 1993; 58: 7416–7420
   Web of Science ®Google Scholar
• Xi F., Barclay L.R.C. Cooperative antioxidant effects of ascorbate with di-tert-butylcatechol during lipid peroxidation in solution and in sodium dodecyl sulfate (SDS) micelles. Canadian Journal of Chemistry 1997; 76: 171–182
   Google Scholar
• Florenti D., Cabrini L., Landi L. Ubiquinol-3 and ubiquinol-7 exhibit similar antioxidant activity in model membranes. Free Radical Research Communications 1993; 18: 201–209
   PubMedGoogle Scholar
• Shi H., Noguchi N., Niki E. Comparative study on dynamics of antioxidative action of α-tocopheryl hydroquinone, ubiquinol, and α-tocopherol against lipid peroxidation. Free Radical Biology and Medicine 1999; 27: 334–346
   PubMed Web of Science ®Google Scholar
• Castle L., Perkins M.J. Inhibition kinetics of chain-breaking phenolic antioxidants in SDS micelles. Evidence that intermolecular diffusion rates may be rate-limiting for hydrophobic inhibitors such as α-tocopherol. Journal of American Chemical Society 1986; 108: 6381–6382
   Web of Science ®Google Scholar
• Pryor W.A., Shricland T., Church D.F. Comparison of the efficiencies of several natural and synthetic antioxidants in aqueous sodium dodecyl sulfate micelle solutions. Journal of American Chemical Society 1988; 110: 2224–2229
   Web of Science ®Google Scholar
• Roginsky V.A. The inhibiting ability of lipid-soluble and water-soluble phenols at lipid peroxidation in micro-heterogeneous systems. Biological Membranes (Translated from Russian) 1990; 4: 437–451
   Google Scholar
• Barclay L.R.C., Baskin K.A., Dakin K.A., Locke S.J., Vinqvist M.R. The antioxidant activities of phenolic antioxidants in free radical peroxidation of phospholipid membranes. Canadian Journal of Chemistry 1990; 68: 2258–2269
   Web of Science ®Google Scholar
• Roginsky V.A., Barsukova T.K., Bruchelt G., Stegmann H.B. Kinetics of redox interactions between some substituted 1,4-benzoquinones and ascorbate under aerobic conditions. Critical phenomena. Free Radical Research 1998; 29: 115–125
   PubMed Web of Science ®Google Scholar
• Roginsky V.A., Barsukova T.K., Stegmann H.B. Kinetics of redox interaction between substituted quinones and ascorbate under aerobic conditions. Chemico-Biological Interactions 1999; 121: 177–197
   PubMed Web of Science ®Google Scholar
• Roginsky V.A., Remorova A.A., Barsukova T.K., Bors W. A moderate antioxidative activity of flavonoids as lipid stabilisers. Journal of American Oil Chemical Society 1996; 73: 777–786
   Google Scholar
• Roginsky V.A. Kinetics of the chain oxidation of methyl linoleate in aqueous micellar solutions of sodium dodecyl sulfate. Kinetics and Catalysis (Translated from Russian) 1996; 37: 488–494
   Web of Science ®Google Scholar
• Roginsky V.A. Kinetics of oxidation of polyunsaturated fatty acid esters inhibited by substituted phenols. Kinetics and Catalysis (Translated from Russian) 1990; 31: 475–481
   Google Scholar
• Landolt-Börnstein. Numerical Data and Functional Relationships in Science and Technology, New Series, Group II. Springer-Verlag, Berlin, Heidelberg, New York, London, Paris, Tokyo and Hong Kong 1984; 13e
   Google Scholar
• Dohrman J.K., Bergmann B. Equilibria and rates of redox reactions involving the tert-butyl-1,4-benzosemiquinone radical in aqueous solution. An investigation by potentiometry, ESR and pulse radiolysis. Journal of Physical Chemistry 1995; 99: 1218–1227
   Google Scholar
• Wardman P. Bioreductive activation of quinones: redox properties and thiol reactivity. Free Radical Research Communications 1990; 8: 219–229
   PubMed Web of Science ®Google Scholar
• Wardman P. Reduction potentials of one-electron couples involving free radicals in aqueous solution. Journal of Physical and Chemical Reference Data 1989; 18: 1637–1756
   Web of Science ®Google Scholar
• Roginsky V.A., Pisarenko L.M., Bors W., Michel C. The kinetics and thermodynamics of quinone-semiquinone-hydroquinone systems under physiological conditions. Journal of Chemical Society, Perkin Transaction 1999; 2: 871–876
   Google Scholar
• Bielski B.H.J., Cabelli R.L., Arudi R.L., Ross A.B. Reactivity of HO·2/O·-2 radicals in aqueous solution. Journal of Physical and Chemical Reference Data 1985; 14: 1041–1041
   Web of Science ®Google Scholar
• Afanas'ev I.B. Superoxide Ion: Chemistry and Biological Implications. CRC Press Inc., Boca Raton, Florida 1991; 2
   Google Scholar
• Marklund S.K. Mammalian superoxide dismutase. Oxygen Radicals in Chemistry and Biology, W. Bors, M. Saran, D. Tait. de Gruyeler, Berlin and New York 1984; 765–783, In
   Google Scholar