Initiating activity of 4-chlorobiphenyl metabolites in the resistant hepatocyte model.
Toxicol Sci, 2004/5;79(1):41-6.
Espandiari P[1], Glauert HP, Lehmler HJ, Lee EY, Srinivasan C, Robertson LW
Affiliations
PMID: 14976334
Impact factor: 4.109
Abstract
We recently reported that several mono- to tetrachlorinated biphenyls have initiating activity in the livers of Fischer 344 rats. In the present study, we investigated the metabolic activation of one of those compounds, 4-chlorobiphenyl (PCB 3). Monohydroxy (400 micromol/kg), dihydroxy (200 micromol/kg), and quinone (100 micromol/kg) metabolites of PCB 3 were evaluated for their initiating activity. Fischer 344 male rats were fasted for 4 days; 24 h after feeding again, they were injected (ip) with metabolites, vehicle, or diethylnitrosamine (DEN, 20 or 40 mg/kg). All animals were treated with selection agents as follows: three daily p.o. doses of 2-acetylaminofluorene (2-AAF, 30 mg/kg), followed by a single p.o. dose of carbon tetrachloride (2 ml/kg) and three additional daily treatments of 2-AAF. Rats were killed 2 weeks after the last 2-AAF intubation. Livers were evaluated for changes in morphology, and the number and volume of gamma-glutamyl transpeptidase-positive foci were measured. Of the metabolites tested, only one monohydroxy and one quinoid metabolite showed initiating activity. The metabolic activation of PCB 3, therefore, proceeds via parahydroxylation and oxidation to the ortho 3,4-quinone, the ultimate carcinogen. This is the first report to demonstrate that specific PCB metabolites possess initiating activity in the rodent liver in vivo. The results support the conclusion that 4-OH PCB 3 and 3,4-BQ PCB 3 act as proximate and ultimate carcinogenic metabolites resulting from the bioactivation of PCB 3 in rat liver.
MeSH terms
2-Acetylaminofluorene; Adenoma, Liver Cell; Administration, Oral; Animals; Biphenyl Compounds; Body Weight; Carbon Tetrachloride; Carcinogens; Diethylnitrosamine; Drug Administration Schedule; Drug Evaluation, Preclinical; Hydroxylation; Injections, Intraperitoneal; Intubation, Intratracheal; Liver; Liver Neoplasms, Experimental; Male; Models, Biological; Organ Size; Quinones; Rats; Rats, Inbred F344; Time Factors; gamma-Glutamyltransferase
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