The broad long term objectives of the project are to contribute to the knowledge about how chemicals cause cell injury by studying the model system CC14 hepatotoxicity. That objective includes the attempt to develop treatments based on the knowledge gained. The present project specific aims is to challenge the working hypothesis that CC14- induced liver necrosis might be related to damage to Ca++ pumps to lead to alterations in Ca++ homeostasis which might enhance phospholipid/protein/DNA degradative processes to cause cell injury. Experiments planed to be made include: 1) Studies on the role of .CC1 covalent binding (CB) and of lipid peroxidation (LP) in the """"""""in vivo"""""""" damage by CC14 to endoplasmic reticulum, mitochondrial and nuclear Ca++ pumps. Specific inhibitors of either CB or LP are going to be used to discriminate CB or LP contribution. Use of agents potentially able to revert damage caused by LP or .CC13-mediated H abstraction from Ca++ pumps would also be made to attempt prevention of damage to them and on CC14-induced liver necrosis; 2) The potential preventive effects of Ca++ chelators and on non-phenothiazinic anticalmodulin drugs would be tested as late preventive agents against CC14-induced liver necrosis; 3) The potential preventive effects of specific and potent inhibitors of proteases, phospholipase A2 and endonuclease are going to be tested as late preventive agents against CC14- induced liver necrosis. To achieve these goals we plan to perform the necessary studies evidencing that treatments reached liver tissue (GLC; HPLC; spectrophotometry) and/or performed their expected effects (eg. inhibited CB or LP; reverted damage to Ca++ pumps; prevented protein/phospholipid/DNA degradation; prevented damage as observable by histology, electron microscopy and blood increases in isocitric acid dehydrogenase) and that preventive effects can not be attributable to actions on other parameters influencing the course of CC14-induced liver damage of non-specific nature (CC14 levels in liver, body temperature).4 The major health implication of the project is the potential development of treatments of general value able to operate at late stages of poisoning by CC14 and other chemicals not previously amenable to modulation and potentially useful to many pathologies where changes in calcium homeostasis and enhancement of degradative processes might be relevant.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK013195-19A2
Application #
3224975
Study Section
Toxicology Subcommittee 2 (TOX)
Project Start
1979-01-01
Project End
1994-06-30
Budget Start
1991-08-08
Budget End
1992-06-30
Support Year
19
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Instituto de Investigaciones Cientificas
Department
Type
DUNS #
City
Buenos Aires
State
Country
Argentina
Zip Code
de Mecca, M M; Castro, G D; Diaz Gomez, M I et al. (1995) Dithiothreitol inhibitory effects on carbon tetrachloride-promoted NADPH-dependent lipid peroxidation in liver microsomal suspensions. Res Commun Mol Pathol Pharmacol 88:205-13
de Ferreyra, E C; Bernacchi, A S; San Martin, M F et al. (1995) Late protective effects of the anticalmodulin drug fluphenazine on carbon tetrachloride-induced liver necrosis. Biomed Environ Sci 8:218-25
de Ferreyra, E C; Bernacchi, A S; San Martin, M F et al. (1995) Trifluopromazine late preventive effects on carbon tetrachloride-induced liver necrosis. Exp Mol Pathol 62:75-82
Valles, E G; de Castro, C R; Castro, J A (1994) N-acetyl cysteine is an early but also a late preventive agent against carbon tetrachloride-induced liver necrosis. Toxicol Lett 71:87-95
de Toranzo, E G; Castro, J A (1994) Reaction of 4-hydroxynonenal with some thiol-containing radioprotective agents or their active metabolites. Free Radic Biol Med 17:605-7
de Ferreyra, E C; Bernacchi, A S; San Martin, M F et al. (1994) Nicotinamide late protective effects against carbon tetrachloride-induced liver necrosis. Exp Mol Pathol 60:214-23
de Ferreyra, E C; Bernacchi, A S; Villarruel, M C et al. (1993) Prevention of CCl4-induced liver necrosis by the calcium chelator arsenazo III. Exp Mol Pathol 58:194-204
de Mecca, M M; Castro, G D; Castro, J A (1993) Antioxidative stress therapy with dithiothreitol tetraacetate. I. Protection against carbon tetrachloride induced liver necrosis. Arch Toxicol 67:547-51
de Mecca, M M; Castro, G D; Castro, J A (1993) Dithiothreitol tetraacetate S-acetyl esterase activity in blood and in different tissues of male rats. Arch Int Pharmacodyn Ther 326:101-8
Gonzalez Padron, A; de Toranzo, E G; Castro, J A (1993) Late preventive effects of quinacrine on carbon tetrachloride induced liver necrosis. Arch Toxicol 67:386-91

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