Association of Antioxidant Systems in the Protection of Human Fibroblasts Against Oxygen Derived Free Radicals

References

• Fridovich I. Superoxide dismutases: regularities and irregularities. The Harvey Lectures 1985; 79: 51–75
   Google Scholar
• Pryor W. A. The role of free radical reactions in biological systems. Free Radicals in Biology, W. Pryor. Academic Press, New York 1976; vol I: 1–49
   Google Scholar
• McCord J. M., Fridovich I. The biology and pathology of oxygen radicals. Annals of Internal Medicine 1978; 89: 122–127
   PubMed Web of Science ®Google Scholar
• Fucci L., Oliver C. N., Coon M. J., Stadtman E. R. Inactivation of key metabolic enzymes by mixed-function oxidation reactions: possible implication in protein turnover and aging. Proceedings of the Natural Sciences 1983; 80: 1521–1525
   PubMed Web of Science ®Google Scholar
• Sestili P., Piedmonte G., Cattabeni F., Cantoni O. Induction of DNA breakage and suppression of DNA synthesis by the OH radical generated in a Fenton-like reaction. Biochemistry International 1986; 12: 493–501
   PubMedGoogle Scholar
• Tappel A. Lipid peroxidation damage to cell components. Federation Proceedings 1973; 32: 1870–1874
   PubMedGoogle Scholar
• Comporti M. Biology of disease. Lipid peroxidation and cellular damage in toxic liver injury. Laboratory Investigation 1985; 53: 599–623
   PubMed Web of Science ®Google Scholar
• Leibovitz B. E., Siegel M. S. Aspects of free radical reactions in biological systems: aging. Journal of Gerontology 1980; 35: 45–56
   PubMed Web of Science ®Google Scholar
• Halliwell B. Biochemical mechanisms accounting for the toxic action of oxygen on living organisms: the key role of superoxide dismutase. Cell Biology of International Reports 1978; 2: 113–124
   PubMedGoogle Scholar
• Fridovich I. Oxygen radicals, hydrogen peroxide and oxygen toxicity. Free Radicals in Biology, W. Pryor. Academic Press, New York 1976; vol I: 239–277
   Google Scholar
• Burton G. W., Cheeseman K. H., Doba T., Ingold K. V., Slater T. F. Vitamin E as an oxidant in vitro and in vivo in Ciba Foundation Symposium. ed Pitman, London 1983; vol 101: 4–14
   Google Scholar
• Doba T., Burtona G. W., Ingold K. V. Antioxidant and coantioxidant activity of vitamin C. The effect of vitamin C either alone or in the presence of vitamin E or a water soluble vitamin E analogue upon the peroxidation of aqueous multilamellar phospholipid liposomes. Biochimica et Biophysica Acta 1985; 835: 298–303
   PubMed Web of Science ®Google Scholar
• Halliwell B., Gutteridge J. M. C. Oxygen toxicity, oxygen radicals transition metals and disease. Biochemical Journal 1984; 219: 1–14
   PubMed Web of Science ®Google Scholar
• Chance B., Sies H., Boveris A. Hydroperoxide metabolism in mammalian organs. Physiological Reviews 1979; 59: 527–605
   PubMed Web of Science ®Google Scholar
• Michiels C., Raes M., Remacle J. A new experiment model to study oxygen toxicity. Archives Internationales de Physiologie et Biochimie 1986; 94: S13–S17
   Google Scholar
• Raes M., Michiels C., Remacle J. Comparative study of the enzymatic defence systems against oxygen-derived free radicals: the key role of glutathione peroxidase. Free Radical in Biology and Medicine 1987; 3: 3–7
   PubMed Web of Science ®Google Scholar
• Michiels C., Raes M., Pigeolet E., Corbisier P., Lambert D., Remacle J. Importance of a threshold level for error accumulation in cell degenerative processes. I. Modulation of the threshold in a model of free radical-induced cell degeneration. Mechanisms of Ageing and development 1990; 51: 41–54
   PubMed Web of Science ®Google Scholar
• Hayflick L., Moorhead P. S. The serial cultivation of human diploid cell strains. Experimental Cell Research 1961; 25: 585–621
   PubMed Web of Science ®Google Scholar
• Ansorge W. Improved system for capillary microinjection in living cells. Experimental Cell Research 1982; 140: 31–37
   PubMed Web of Science ®Google Scholar
• Graessmann A., Graessmann M., Mueller C. Microinjection of tissue culture using capillaries: methods. Methods in Enzymology. Academic Press, New York 1980; vol 65: 4831–4834
   Google Scholar
• Rogers S., Wells R., Rechsteiner M. Amino acid sequences common to rapidly degraded proteins: the PEST hypothesis. Science 1986; 234: 364–368
   PubMed Web of Science ®Google Scholar
• Rechsteiner M., Chin D., Hough R., McGarry T., Rogers S., Rote K., Wu L. What determines the degradation rate of an injected protein?. Ciba Foundation Symposium. ed Pitman, London 1984; vol 103: 181–195
   Google Scholar
• Halliwell B., Gutteridge J. M. C. Oxygen free radicals and iron in relation to biology and medicine some problems and concepts. Archives. Biochemistry and Biophysics 1986; 246: 501–514
   PubMed Web of Science ®Google Scholar
• Balin A. K., Goodman D. B. P., Hasmussen H., Cristofalo V. J. The effect of oxygen tension on the growth and metabolism of WI-38 cells. Journal of Cellular Physiology 1976; 89: 235–250
   PubMed Web of Science ®Google Scholar
• Honda S., Matsuo M. Shortening of the in vitro lifespan of human diploid fibroblasts exposed to hyperbaric oxygen. Experimental Gerontology 1983; 18: 339–345
   PubMed Web of Science ®Google Scholar
• Brosomer R. W., Rutter W. J. The effect of oxygen tension on the growth and metabolism of a mammalian cell. Experimental Cell Research 1961; 25: 103–113
   Web of Science ®Google Scholar
• Michiels C., Remacle J. Quantitative study of natural antioxidant systems for cellular nitrofurantoin toxicity. Biochimica Biophysica Acta 1988; 967: 341–347
   PubMedGoogle Scholar
• Freeman B. A., Turrens J. F., Mirza Z., Crapo J. D., Young S. L. Modulation of oxidant lung injury by using liposome-entrapped superoxide dismutase and catalase. Federation Proceedings 1985; 44: 2591–2595
   PubMedGoogle Scholar
• Ragley A. C., Krall J., Lynch R. E. Superoxide mediated the toxicity of paraquat for chinese hamster ovary cells. Proceedings of the National Academy of Sciences 1986; 83: 3189–3193
   PubMed Web of Science ®Google Scholar
• Finazzi-Agro A., DiGuilo A., Arnicosante G., Crifo C. Photohemolysis of erythrocytes enriched with superoxide dismutase, catalase and glutathione peroxidase. Photochemistry and Photobiology 1986; 43: 409–412
   PubMed Web of Science ®Google Scholar
• Allen R. G., Balin A. K., Reimer R. J., Sohal R. S., Nations C. Superoxide dismutase induces differentiation in microplasmodia of the slime mold Physarum polycephalum. Archives in Biochemistry Biophysics 1988; 261: 205–211
   PubMed Web of Science ®Google Scholar
• Petkau A. Scientific basis for the clinical use of superoxide dismutase. Cancer Treatment Review 1986; 13: 17–44
   PubMed Web of Science ®Google Scholar
• Flohé L. Glutathione peroxidase brought into focus. Free Radicals in Biology, W. Pryor. Academic Press, New York 1982; vol V: 223–254
   Google Scholar
• Hochstein P., Ustley H. Hydrogen peroxide detoxification by glutathione peroxidase and catalase in rat liver homogenates. Molecular Pharmacology 1968; 4: 574–579
   PubMed Web of Science ®Google Scholar
• Simon R. H., Scoggin C. H., Paterson D. Hydrogen peroxide causes the fatal injury to human fibroblasts exposed to oxygen radicals. Journal of Biological Chemistry 1981; 256: 7181–7186
   PubMed Web of Science ®Google Scholar
• Sacks S. T., Moldow C. F., Craddock P. R., Bowers T. K., Jacob M. S. Oxygen radicals mediate endothelial cell damage by complement-stimulated granulocytes. Journal of Clinical Investigation 1978; 61: 1161–1167
   PubMed Web of Science ®Google Scholar
• McCay P. B., Gibson D. D., Fong K. L., Hornbrook K. R. Effect of glutathione peroxidase activity on lipid peroxidation in biological membranes. Biochimica et Biophysica Acta 1976; 431: 459–468
   PubMed Web of Science ®Google Scholar
• Van Kuijk F. J. G. M., Handelmann G. J., Pratz E. A. Consecutive action of phospholipase A2 and glutathione peroxidase is required for reduction of phospholipid hydroperoxides and provides a convenient method to determine peroxide values in membranes. Journal of Free Radicals in Biological Medicine 1985; 1: 421–427
   PubMedGoogle Scholar
• Fong K. L., McCay P. B., Poyer J. L., Keele B. B., Misra M. Evidence that peroxidation of lysomal membranes is initiated by hydroxyl free radicals produced during flavin enzyme activity. Journal of Biological Chemistry 1973; 248: 7792–7797
   PubMed Web of Science ®Google Scholar