Latour, I
Pregaldien, J L
Buc Calderon, Pedro
[UCL]
The incubation of isolated hepatocytes in the presence of glucose plus glucose oxidase, a H2O2-generating system, resulted in extensive loss of cell viability, as expressed by the release of lactate dehydrogenase (LDH). Disturbance of metabolic functions such as glycogen and protein synthesis was also caused by H2O2, but in no case was malondialdehyde (MDA)-like products detected. The lytic effect of H2O2 was significantly enhanced by incubating hepatocytes in the presence of iron salts. Under these conditions, MDA-like products were detected, but lipid peroxidation and cell injury did not correlate. Iron chelators modulated the cytotoxicity of H2O2 in different (and opposite) ways: when iron was complexed with ADP, increased cell lysis was observed compared to uncomplexed iron plus H2O2. Iron-DTPA, on the contrary, decreased such a lytic effect. The preincubation of hepatocytes with desferrioxamine mesylate (Desferal; a strong iron chelator) abolished the cytolytic effects produced by the association of iron salts and H2O2, as well as the membrane oxidative injury due to H2O2 alone, thus suggesting the existence of an intracellular source of iron. This kind of mechanism (metal chelation rather than radical scavenging) is supported by the absence of any protective effect by some free radical scavengers against the oxidative injury induced by the association iron H2O2. Nevertheless, the glycogenolytic effects observed in the presence of H2O2 were not modified by Desferal. In our opinion, the cytotoxicity of the association H2O2 plus iron salts involves at least two different and independent mechanisms.
- Berry MN, Friend DS (1969) High-yield preparation of isolated rat liver parenchymal cells. A biochemical and fine structural study. J Cell Biol 43: 506–520
- Braughler JM, Duncan LA, Chase RL (1986) The involvement of iron in lipid peroxidation. Importance of ferric to ferrous ratios in initiation. J Biol Chem 261: 10282–10289
- Cantoni O, Cattabeni F, Stocchi V, Meyn RE, Cerutti P, Murray D (1989) Hydrogen peroxide insult in cultured mammalian cells: relationships between DNA single-strands breakage, poly(ADP-ribose) metabolism and cell killing. Biochim Biophys Acta 1014: 1–7
- Floyd RA (1983) Direct demonstration that ferrous ion complexes of di- and triphosphate nucleotides catalyze hydroxyl free radical formation from hydrogen peroxide. Arch Biochem Biophys 225: 263–270
- Goethals F, Krack G, Deboyser D, Vossen P, Roberfroid M (1984) Critical biochemical functions of isolated hepatocytes as sensitive indicators of chemical toxicity. Fundam Appl Toxicol 4: 441–450
- Halliwell B (1989) Protection against tissue damage in vivo by desferrioxiamine: what is its mechanism of action? Free Rad Biol Med 7: 645–651
- Halliwell B, Gutteridge J M C, Oxygen toxicity, oxygen radicals, transition metals and disease, 10.1042/bj2190001
- Halliwell B, Gutteridge JMC (1986) Oxygen free radicals and iron in relation to biology and medicine: some problems and concepts. Arch Biochem Biophys 246: 501–514
- Hyslop PA, Hinshaw DB, Halsey Jr. WA, Schraufstätter IU, Sauerheber RD, Spragg RG, Jackson JH, Cochrane CG (1988) Mechanisms of oxidant-mediated cell injury. The glycolytic and mitochondrial pathways of ADP phosphorylation are major intracellular targets inactivated by hydrogen peroxide. J Biol Chem 263: 1665–1675
- Innes GK, Fuller BJ, Hobbs KE (1988) Lipid peroxidation in hepatocyte cell cultures: modulation by free radical scavengers and iron. In Vitro Cell Dev Bio 24: 126–132
- Jonas S K, Riley P A, Willson R L, Hydrogen peroxide cytotoxicity. Low-temperature enhancement by ascorbate or reduced lipoate, 10.1042/bj2640651
- Kirkland JB (1991) Lipid peroxidation, protein thiol oxidation and DNA damage in hydrogen peroxide-induced injury to endothelial cells: role of activation of poly(ADP-ribose) polymerase. Biochim Biophys Acta 1092: 319–325
- Krack Geneviève, Gravier Odette, Roberfroid Marcel, Mercier Michel, Subcellular fractionation of isolated rat hepatocytes a comparison with liver homogenate, 10.1016/0304-4165(80)90338-4
- Kyle ME, Nakae D, Sakaida I, Serroni A, Farber JL (1989) Protein thiol depletion and the killing of cultured hepatocytes by hydrogen peroxide. Biochem Pharmacol 38: 3797–3805
- Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin reagent. J Biol Chem 193: 265–273
- Masini A, Ceccarelli D, Trenti T, Corongiu FP, Muscatello U (1989) Perturbation in liver mitochondrial Ca+2 homeostasis in experimental iron overload: a possible factor in cell injury. Biochim Biophys Acta 1014: 133–140
- McCORD JOE M., The Biology and Pathology of Oxygen Radicals, 10.7326/0003-4819-89-1-122
- Minotti G, Aust SD (1987) The requirement for iron(III) in the initiation of lipid peroxidation by iron(II) and hydrogen peroxide. J Biol chem 262: 1098–1104
- Minotti G, Aust SD (1989) The role of iron in oxygen radical mediated lipid peroxidation. Chem Biol Interact 71: 1–19
- Morehouse LA, Tien M, Bucher JR, Aust AD (1983) Effect of hydrogen peroxide on the initiation of microsomal lipid peroxidation. Biochem Pharmacol 32: 123–127
- Morel I, Lescoat G, Cillard J, Pasdeloup N, Brissot P, Cillard P (1990) Kinetic evaluation of free malondialdehyde and enzyme leakage as indices of iron damage in rat hepatocytes cultures. Biochem Pharmacol 39: 1647–1655
- Mouret JF, Polverelli M, Sarrazini F, Cadet J (1991) Ionic and radical oxidations of DNA by hydrogen peroxide. Chem Biol Interact 77: 187–201
- Pryor WA (1986) Oxy-radicals and related species: their formation, lifetimes, and reactions. Annu Rev Physiol 48: 657–667
- Rubin R, Farber JL (1984) Mechanisms of the killing of cultured hepatocytes by hydrogen peroxide. Arch Biochem Biophys 228: 450–459
- Schraufstatter IU, Hyslop PA, Hinshaw DB, Spragg RG, Sklar LA, Cochrane CG (1986) hydrogen peroxide-induced injury of cells and its prevention by inhibitors of poly(ADP-ribose) polymerase. Proc Natl Acad Sci USA 83: 4908–4912
- Schraufstatter IU, Hyslop PA, Pakson JH, Cochrane CG (1988) Oxidant-induced DNA damage of target cells. J Clin Invest 82: 1040–1050
- Seglen Per O., Incorporation of radioactive amino acids into protein in isolated rat hepatocytes, 10.1016/0005-2787(76)90313-0
- Sharma BP, Bacon BR, Britton RS, Park CH, Magiera CJ, O'Neill R, Dalton N, Smanik P, Speroff T (1990) Prevention of hepatocyte injury and lipid peroxidation by iron chelators and a-tocopherol in isolated iron-loaded rat hepatocytes. Hepatology 12: 31–39
- Slivka A, Kang J, Cohen G (1986) Hydroxyl radicals and the toxicity of oral iron. Biochem Pharmacol 35: 553–556
- Stacey NH, Cantilena LR, Klaassen CD (1980) Cadmium toxicity and lipid peroxidation in isolated rat hepatocytes. Toxicol Appl Pharmacol 53: 470–480
- Starke PE, Farber JL (1985) Ferric iron and superoxide ions are required for the killing of cultured hepatocytes by hydrogen peroxide. Evidence for the participation of hydroxyl radicals formed by an iron-catalyzed Haber-Weiss reaction. J Biol Chem 260: 10099–10104
- Weinberg ED (1990) Cellular iron metabolism in health and disease. Drug Metab Rev 22: 531–579
- Wroblewski F., Ladue J. S., Lactic Dehydrogenase Activity in Blood., 10.3181/00379727-90-21985
Bibliographic reference |
Latour, I ; Pregaldien, J L ; Buc Calderon, Pedro. Cell death and lipid peroxidation in isolated hepatocytes incubated in the presence of hydrogen peroxide and iron salts.. In: Archives of toxicology, Vol. 66, no. 10, p. 743-9 (1992) |
Permanent URL |
http://hdl.handle.net/2078.1/9545 |