Differences in Rat Liver Enzyme-Altered Foci Produced By Chlorinated Aliphatics and Phenobarbital
- 1 October 1986
- journal article
- review article
- Published by SAGE Publications in Toxicology and Industrial Health
- Vol. 2 (4) , 351-362
- https://doi.org/10.1177/074823378600200402
Abstract
Nine chlorinated aliphatics (CAs)—1,1-dichloroethane, 1,2-dichloro ethane, 1,1,1-trichloroethane, 1,1,2-trichloroethane, trichloro ethylene, tetrachloroethylene, 1,1,1,2-tetrachloroethane, 1,1,2,2- tetrachloroethane, and hexachloroethane—were examined in a rat liver foci assay for evidence of initiating and promoting potential. Young adult male Osborne-Mendel rats (ten/group) were given partial hepa tectomies, followed 24 hr later by a single i.p. dose of either diethyl nitrosamine (30 mg/kg body weight) or CA, 1 wk later either a diet containing 0.05% (w/w) phenobarbital or daily oral gavage (5 × /wk) of CA in corn oil for 7 weeks, and sacrificed 1 wk later. Putative preneo plastic markers monitored were foci with increased γ-glutamyltrans peptidase activity [GGT( + )]. CAs were without significant effect in the initiation protocol at the maximum tolerated dose. In the promotion protocol, 1,1-dichloroethane, 1,1,2-trichloroethane, tetrachloro ethylene, 1,1,2,2-tetrachloroethane, and hexachloroethane induced significant increases in GGT( + ) foci above control levels. Two variants of GGT( + ) foci were distinguishable, one associated predominantly with phenobarbital promotion, resembling preneoplastic foci in other models, and the other associated with CA promotion, which was less intensely stained and exhibited branching, resemblingfoci undergoing redifferentiation. The marked differences in response may relate to differences in cytotoxic potential or mechanism of action of the two types of agents.Keywords
This publication has 22 references indexed in Scilit:
- The phenotypic stability of altered hepatic foci: effect of the shortterm withdrawal of phenobarbital and of the long-term feeding of purified diets after the withdrawal of phenobarbitalCarcinogenesis: Integrative Cancer Research, 1986
- Regulation and expression of four cytochrome P-450 isoenzymes, NADPH-cytochrome P-450 reductase, the glutathione transferases B and C and microsomal epoxide hydrolase in preneoplastic and neoplastic lesions in rat liverCarcinogenesis: Integrative Cancer Research, 1985
- Metabolic Disposition Study of Chlorinated Hydrocarbons in Rats and MiceDrug and Chemical Toxicology, 1985
- Gamma-glutamyl transpeptidase – its role in hepatocarcinogenesisCarcinogenesis: Integrative Cancer Research, 1985
- Controlled death (apoptosis) of normal and putative preneoplastic cells in rat liver following withdrawal of tumor promotersCarcinogenesis: Integrative Cancer Research, 1984
- Induction by butylated hydroxytoluene of rat liver γ-glutamyl transpeptidase activity in comparison to expression in carcinogen-induced altered lesionsChemico-Biological Interactions, 1984
- Tumor promotion in rat liver.Environmental Health Perspectives, 1983
- Phenotypic instability in focal and nodular lesions induced in a short term system in the rat liverCarcinogenesis: Integrative Cancer Research, 1983
- Dibromoethane effects on the induction of ?-glutamyl-transpeptidase positive foci in rat liverArchives of Toxicology, 1982
- Comparison of hepatic carcinogen initiation-promotion systemsCarcinogenesis: Integrative Cancer Research, 1982