References
- Ames, B. N. (1983) Dietary carcinogens and anticarcinogens. Oxygen radicals and degenerative diseases. Science 221, 1256-1264 https://doi.org/10.1126/science.6351251
- Boveries, A., Oshino, N. and Chance, B. (1972) The cellular production of hydrogen peroxide. Biochem. J. 128, 617-630 https://doi.org/10.1042/bj1280617
- Breen, A. P. and Murphy, J. A. (1995) Reactions of oxyl radicals with DNA Free Radic. Biol. Med. 18, 1033-1077
- Britton, R. S., Bacon, B. R. and Recknagel, R. O. (1987) Lipid peroxidation and associated hepatic organelle dysfunction in iron overload. Chem. Phys. Lipids 45, 207-239 https://doi.org/10.1016/0009-3084(87)90066-1
- Cai, J., Yang, J. and Jones, D. P. (1998) Mitochondrial control of apoptosis: the role of cytochrome c. Biochim. Biophys. Acta 1366, 139-149 https://doi.org/10.1016/S0005-2728(98)00109-1
- Cerruti, P. A. (1994) Oxy-radicals and cancer. Lancet 344, 862-863 https://doi.org/10.1016/S0140-6736(94)92832-0
- Choi, D.-S., Kim, S.-J. and Jung, M. Y. (2001) Inhibitory activity of berberine on DNA strand cleavage induced by hydrogen peroxide and cytochrome c. Biosci. Biotechnol. Biochem. 65, 452-455 https://doi.org/10.1271/bbb.65.452
- Davies, K. J. (1986) Intracellular proteolytic systems may function as secondary antioxidant defenses: a hypothesis. J. Free Radic. Biol. Med. 2, 155-173 https://doi.org/10.1016/S0748-5514(86)80066-6
- Dean, R. T., Fu, S., Stocker, R. and Davies, M. J. (1997) Biochemistry and pathology of radical-mediated protein oxidation. Biochem. J. 324, 1-18 https://doi.org/10.1042/bj3240001
- Frank, H., Thiel, D. and MacLoad, J. (1989) Mass spectrometric detection of cross-linked fatty acids formed during radicalinduced lesion of lipid embranes. Biochem. J. 260, 873-878 https://doi.org/10.1042/bj2600873
- Goldstein, S. and Czapski, G. (1986) The role and mechanism of metal ions and their complexes in enhancing damage in biological systems or in protecting these system. J. Free Radic. Biol. Med. 2, 3-11 https://doi.org/10.1016/0748-5514(86)90117-0
- Halliwell, B. and Gutteridge, J. M. (1981) Formation of thiobarbituric-acid-reactive substance from deoxyribose in the presence of iron salts: the role of superoxide and hydroxyl radicals. FEBS Lett. 128, 347-352 https://doi.org/10.1016/0014-5793(81)80114-7
- Hashimoto, M., Takeda, A., Hsu, L. J., Takenouchi, T. and Masliah, E. (1999) Role of cytochrome c as a stimulator of alpha-synuclein aggregation in Lewy body disease. J. Biol. Chem. 274, 28849-28852 https://doi.org/10.1074/jbc.274.41.28849
- Imlay, J. A., Chin, S. M. and Linn, S. (1988) Toxic DNA damage by hydrogen peroxide through the Fenton reaction in vivo and in vitro. Science 240, 640-642 https://doi.org/10.1126/science.2834821
- Kang, J. H. (2004) Modification of Cu,Zn-superoxide dismutase by oxidized catecholamines. J. Biochem. Mol. Biol. 37, 325-329 https://doi.org/10.5483/BMBRep.2004.37.3.325
- Kang, J. H. and Kim, S. M. (1997) Fragmentation of human Cu,Zn-superoxide dismutase by peroxidative reaction. Mol. Cells 7, 553-558
-
Lawrence, A., Jones, C. M., Wardman, P. and Burkitt, M. J. (2003) Evidence for the role of a peroxidase compound I-type intermediate in the oxidation of glutathione, NADH, ascorbate, and dichlorofluorescin by cytochrome c/H
$_{2}$ O$_{2}$ . Implications for oxidative stress during apoptosis. J. Biol. Chem. 278, 29410-29419 https://doi.org/10.1074/jbc.M300054200 - Oliver, C. N., Levine, R. L. and Stadtman, E. R. (1987) A role of mixed-function oxidation reactions in the accumulation of altered enzyme forms during aging. J. Am. Geriatr. Soc. 35, 947-956 https://doi.org/10.1111/j.1532-5415.1987.tb02297.x
- Park, J.-H. and Kim, T,-H. (2005) Release of cytochrome c from isolated mitochondria by etoposide. J. Biochem. Mol. Biol. 38, 619-623 https://doi.org/10.5483/BMBRep.2005.38.5.619
- Pieroni, L., Khalil, L., Charlotte, F., Poynard, T., Piton, A., Hainque, B. and Imbert-Bismut, F. (2001) Comparison of bathophenanthroline sulfonate and ferene as chromogens in colorimetric measurement of low hepatic iron concentration. Clin. Chem. 47, 2059-2061
-
Prutz, W. A. (1984) Inhibition of DNA-ethidium bromide intercalation due to free radical attack upon DNA. II. Copper(II)-catalysed DNA damage by O
$_{2}$ . Radiat. Environ. Biophys. 23, 7-18 https://doi.org/10.1007/BF01326732 - Radi, R, Thomson, L., Rubbo, H. and Prodanov, E. (1991a) Cytochrome c-catalyzed oxidation of organic molecules by hydrogen peroxide. Arch. Biochem. Biophys. 288, 112-117 https://doi.org/10.1016/0003-9861(91)90171-E
- Radi, R., Sims, S., Cassina, A. and Turrens, J. F. (1993b) Roles of catalase and cytochrome c in hydroperoxide-dependent lipid peroxidation and chemiluminescence in rat heart and kidney mitochondria. Free Radic. Biol. Med. 15, 653-659 https://doi.org/10.1016/0891-5849(93)90169-U
- Sagripanti, J. L., Swicord, M. L. and Davis, C. C. (1987) Microwave effects on plasmid DNA. Radiat. Res. 110, 219-231 https://doi.org/10.2307/3576900
-
Samuni, A., Chevion, M. and Czapski, G. (1984) Roles of copper and O
$_{2}$ in the radiation-induced inactivation of T7 bacteriophage. Radiat. Res. 99, 562-572 https://doi.org/10.2307/3576330 - Schapira, A. H. (1994) Evidence for mitochondrial dysfunction in Parkinson's disease - a critical appraisal. Mov. Disord. 9, 125-138 https://doi.org/10.1002/mds.870090202
-
Tachon, P. (1989) Ferric and cupric ions requirement for DNA single-strand breakage by H
$_{2}$ O$_{2}$ . Free Radic. Res. Commun. 7, 1-10 https://doi.org/10.3109/10715768909088155 - von Sonntag, C. (1987) The Chemical Basis of Radiation Biology, Taylor & Francis, New York, USA
- Wikstrom, M. and Saraste, M. (1984) Cytochrome oxidase; in Bioenegetics, Ernster, L., (ed.) pp. 49-94, Elsevier Science Publishers B. V., Amsterdam, Netherlands
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