Antioxidant actions of plant foods: Use of oxidative DNA damage as a tool for studying antioxidant efficacy

References

• Johnson T., Williamson G., Musk S.R.R. Anticarcinogenic factors in plant foods. A new class of nutrients. Nutrition Research Review 1994; 7: 1–30
   PubMedGoogle Scholar
• Aruoma O.I. Free radicals, oxidative stress and antioxidants in human health and disease. Journal of the American Oil Chemist's Society 1998; 75: 199–212
   PubMed Web of Science ®Google Scholar
• Cook N.C., Samman S. Flavonoids — Chemistry, metabolism, cardio protective effects and dietary sources. Journal of Nutritional Biochemistry 1996; 7: 66–76
   Web of Science ®Google Scholar
• Aruoma O.I. Extracts as antioxidant prophylactic agents. INFORM 1997; 8: 1236–1242
   Google Scholar
• Pezzuto J.M. Plant-derived anticancer agents. Biochemical Pharmacology 1997; 53: 121–133
   PubMed Web of Science ®Google Scholar
• Shahidi F. Natural Antioxidants. Chemistry, Health Effects and Applications. AOCS Press, Champaign 1997
   Google Scholar
• Halliwell B., Gutteridge J.M.C. Free Radicals in Biology and Medicine2nd Edition. Clarendon Press, Oxford 1989
   Google Scholar
• Sies H. Antioxidants in Disease Mechanisms and Therapy. Academic Press, London 1996
   Google Scholar
• Lancaster J. The Biological Chemistry of Nitric Oxide. Academic Press, New York 1996
   Google Scholar
• Moncada S., Higgs H. The L-arginine-nitric oxide pathway. New England Journal of Medicine 1993; 329: 2002–2012
   PubMed Web of Science ®Google Scholar
• Weiss S.J. Tissue destruction by neutrophils. New England Journal of Medicine 1989; 320: 3365–3375
   Google Scholar
• Babior M. Oxidants from phagocytes: agents of defense and destruction. Blood 1984; 64: 959–966
   PubMed Web of Science ®Google Scholar
• Szabo C., Ferrer-Sueta G., Zingarelli B., Southan G.J., Salzman A.L., Radi R. Mercaptoethyl-guanidine and guanidine inhibitors of nitric-oxide synthase react with peroxynitrite and protect against peroxynitrite induced oxidative damage. Journal of Biological Chemistry 1997; 272: 9030–9036
   PubMed Web of Science ®Google Scholar
• Southan G.J., Szabo C. Selective pharmacological inhibition of distinct nitric oxide synthase isoforms. Biochemical Pharmacology 1996; 51: 383–394
   PubMed Web of Science ®Google Scholar
• Aruoma O.I., Halliwell B. DNA and Free Radicals: Techniques, Mechanisms and Applications. OICA International, Saint Lucia 1998
   Google Scholar
• Olanow C.W., Jenner P., Youdim M. Neurodegeneration and Neuroprotection in Parkinson's Disease. Academic Press, London 1996
   Google Scholar
• Aruoma O.I., Evans P.J., Kaur H., Sutcliffe L., Halliwell B. An evaluation of the antioxidant and potential prooxidant properties of food additives and trolox C, vitamin E and probucol. Free Radical Research Communications 1990; 10: 143–157
   PubMed Web of Science ®Google Scholar
• Aruoma O.I. Free radicals, antioxidants and international nutrition. Asia Pacific Journal of Clinical Nutrition February, 1999, 1999 issue in press
   PubMedGoogle Scholar
• Sigman D.S. Nuclease activity of 1,10-phenanthroline copper ion. Accounts in Chemical Research 1986; 19: 180–186
   Web of Science ®Google Scholar
• Thederahn T.B., Kuwabra D.M., Larson T.A., Sigman D.S. Nuclease activity of 1,10-phenanthroline copper: kinetic mechanism. Journal of the American Chemical Society 1989; III: 4941–4946
   Google Scholar
• Dizdaroglu M., Aruoma O.I., Halliwell B. Modification of bases in DNA by copper-ion 1,10-phenanthroline complexes. Biochemistry 1990; 29: 8447–8451
   PubMed Web of Science ®Google Scholar
• Aruoma O.I., Halliwell B., Gajewski E., Dizdaroglu M. Copper-ion dependent damage to the bases in DNA in the presence of hydrogen peroxide. The Biochemical Journal 1991; 273: 601–604
   PubMed Web of Science ®Google Scholar
• Que G., Downey K.M., So A.G. Degradation of deoxyribonucleic acid by a 1,10-phenanthroline-copper complex: the role of hydroxyl radicals. Biochemistry 1980; 19: 5987–5991
   PubMed Web of Science ®Google Scholar
• Reich K.A., Marshall L.E., Graham D.R., Sigman D.S. Cleavage of DNA by the phenanthroline-copper ion complex. Superoxide mediates the reaction dependent on NADH and hydrogen peroxide. Journal of the American Chemical Society 1981; 103: 3582–3584
   Web of Science ®Google Scholar
• Aruoma O.I., Deiana M., Jenner A., Halliwell B., Kaur H., Banni S., Corongiu F.P., Dessi M.A., Aeschbach R. Effect of hydroxytyrosol found in extra virgin olive oil on oxidative DNA damage and on low density lipoprotein oxidation in vitro. Journal of Agricultural and Food Chemistry 1998; 46: 5181–5187
   Web of Science ®Google Scholar
• Spencer J.P.E., Wong J., Jenner A., Aruoma O.I., Cross C.E., Halliwell B. Base modification and strand breakage in isolated calf thymus DNA and in DNA from human skin epidermal keratinocytes exposed to peroxynitrite or 3-morpholinosydnonimine. Chemical Research in Toxicology 1996; 9: 1152–1158
   PubMed Web of Science ®Google Scholar
• Douki T., Cadet J. Peroxynitrite mediated oxidation of purine bases of nucleosides and isolated DNA. Free Radical Research 1996; 24: 369–380
   PubMed Web of Science ®Google Scholar
• Douki T., Cadet J., Ames B.N. An adduct between peroxynitrite and 2′-deoxynitrite and 2′-deoxyguanosine: 4,5-dihydro-5-hydroxy-4-(nitrosooxy)-2′-deoxyguanosine. Chemical Research in Toxicology 1996; 9: 3–7
   PubMed Web of Science ®Google Scholar
• Jocelyn P.C. Biochemistry of the SH Group. Academic Press, New York 1971
   Google Scholar
• Hartman P.E. Ergothioneine as an antioxidant. Methods in Enzymology 1990; 186: 310–318
   PubMed Web of Science ®Google Scholar
• Melville D.B., Horner W.H., Otken C.C., Ludwig M.L. Studies on the origin of ergothioneine. Journal of Biological Chemistry 1955; 213: 61–68
   PubMed Web of Science ®Google Scholar
• Deiana M., Aruoma O.I., Bianchi M.L.P., Spencer J.P.E., Kaur H., Halliwell B., Aeschbach R., Dessi M.A., Banni S., Corongiu F.P. Inhibition of peroxynitrite dependent DNA base modification and tyrosine nitration by the extra virgin olive oil-derived antioxidant hydroxytyrosol. Free Radical Biology and Medicine 1999; 26, in press
   PubMedGoogle Scholar
• Halliwell B., Aruoma O.I. DNA damage by oxygen-derived species. Its mechanism and measurement in mammalian system. FEBS Letters 1991; 281: 9–19
   PubMed Web of Science ®Google Scholar
• Ostling O., Johanson K.J. Microelectrophorectic study of irradiation-induced DNA damage in individual mammalian cells. Biochemical and Biophysical Research Communications 1984; 123: 291–298
   PubMed Web of Science ®Google Scholar
• Singh N.P., McCoy M.T., Tice R.R., Schnieder E.L. A simple technique for quantitation of low level of DNA damage in individual cells. Experimental Cell Research 1988; 123: 184–191
   Google Scholar
• Collins A.R. The comet assay: a novel approach to measuring DNA oxidation. DNA and Free Radicals: Techniques, Mechanisms and Applications, O.I. Aruoma, B. Halliwell. OICA International, Saint Lucia 1998; 241–260, In
   Google Scholar
• McKelvey V.J., Green M., Schmezer P., Pool-Zobel B.L., De-Meo M.P., Collins A. The single cell gel electrophoresis (SCGE) assay (comet assay): A European review. Mutation Research 1993; 288: 47–63
   PubMed Web of Science ®Google Scholar
• Fairbairn D.W., Olive P.L., O'Neill K.L. The comet assay: A comprehensive review. Mutation Research 1995; 339: 37–59
   PubMed Web of Science ®Google Scholar
• Diplock A.T., Charleux J.-L., Crozier-Willi G., Kok F.J., Rice-Evans C., Roberfroid M., Stahl W., Vina-Ribes J. Functional food science and defence against reactive oxidative species. British Journal of Nutrition 1998; 80(Suppl 1)S77–S112
   PubMed Web of Science ®Google Scholar
• Halliwell B. Oxidative stress, nutrition and health. Experimental strategies for optimization of nutritional antioxidant intake in humans. Free Radical Research 1996; 25: 1–32
   PubMed Web of Science ®Google Scholar