Citation

Azri-Meehan S, Mata HP, Gandolfi AJ, Brendel K. Fundam. Appl. Toxicol. 1994; 22(2): 172-177.

Copyright

(Copyright © 1994, Elsevier Publishing)

DOI

10.1006/faat.1994.1021

PMID

8005369

Abstract

The interactive toxicity of two nontoxic concentrations of chloroform (CHCl3) and bromotrichloromethane (BrCCl3) was examined in precision-cut rat liver slices. Liver slices were prepared from male Sprague-Dawley rats (220-250 g) pretreated with phenobarbital for 4 days. Toxicants were administered 1 hr apart. Intracellular K+ levels were similar to untreated controls in slices treated with 0.2 mM CHCl3 or 0.125 microliters (0.25 mg, 1.26 mumol) BrCCl3 alone, indicating that these concentrations were nontoxic. However, addition of both toxicants, irrespective of order, resulted in a time-dependent loss of intracellular K+ which was significant at 9 hr following administration. This was interpreted as evidence of synergistic toxicity. Cytochrome P450 loss was significant as early as 3 hr following exposure to BrCCl3, alone or when added with CHCl3. This loss may be attributed to BrCCl3-induced suicide inactivation of cytochrome P450. Centrilobular hepatocytes may be more susceptible to the interactive toxicity of CHCl3 and BrCCl3. Activity of enzymes found predominantly in this area was significantly decreased in slices exposed to both toxicants relative to controls. Conversely, activity of enzymes found predominantly in the periportal region was similar to that of untreated and treated controls. Interactive toxicity of BrCCl3 and CHCl3 was not a consequence of increased lipid peroxidation or depletion of slice glutathione content. Further studies need to be conducted to elucidate the mechanisms mediating the interactive toxicity of BrCCl3 and CHCl3.

Language: en

Keywords

Animals; Biomarkers; Bromotrichloromethane; Chemical and Drug Induced Liver Injury; Chloroform; Cytochrome P-450 Enzyme System; Drug Interactions; Electrolytes; Glucosephosphate Dehydrogenase; Glutathione; In Vitro Techniques; Isocitrate Dehydrogenase; Lipid Peroxidation; Liver; Male; Potassium; Rats; Rats, Sprague-Dawley