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Formation of glucuronide, sulphate and glutathione conjugates of benzo(a)pyrene metabolites in hepatocytes isolated from inbred strains of mice

Journal Article · · Carcinogenesis (N.Y.); (United States)

Metabolism of benzo(a)pyrene (BP) was studied in mouse hepatocytes isolated from uninduced animals of C57BL/6 Jacobs (B6) and C/sub 3/Hf/HeHa (C3) inbred strains. Conjugates with sulfhate, glucuronate and glutathione were the major products of BP biotransformation in the intact cells. Their formation was measured by determining the radioactivity incorporated from (/sub 3/H)BP into the appropriate metabolite, after separation on silica gel TLC plates. The conjugates were identified by their susceptibility to the action of specific degrading enzymes, arylsulphatase, beta-glucuronidase and gamma-glutamyltransferase. Effects of inhibitors of conjugation galactosamine, diethyl maleate, salicylamide were also examined. Despite quantitative differences between B6 and C3 strains of mice in BP metabolism, the same degree of covalent binding of BP metabolites to cellular DNA, was observed. The results indicate a relatively high capacity of hepatocytes from uninduced mice for conjugation of BP metabolites.

Research Organization:
New York State Dept. of Health, Buffalo
OSTI ID:
6748104
Journal Information:
Carcinogenesis (N.Y.); (United States), Journal Name: Carcinogenesis (N.Y.); (United States) Vol. 4:11; ISSN CRNGD
Country of Publication:
United States
Language:
English