Formation of Irreversible Protein-Binding Metabolites during Microsomal Metabolism of 14c-Bromobenzene and 14c-Bromophenol

  • Sigrun Hesse
  • Thomas Wolff
  • Margot Mezger
Part of the Advances in Experimental Medicine and Biology book series (AEMB)

Abstract

Among hepatotoxic chemicals, bromobenzene is a well known example of a compound thought to induce liver cell necrosis via metabolic activation to protein-binding reactive species. The primarily formed 3,4-epoxide has been suggested to be the reactive metabolite causing hepatotoxicity (Jollow et al., 1974). However, previous studies on the microsomal metabolism of other aromatic hydrocarbons, like 2,2′-dichlorobiphenyl (Hesse et al., 1978), naphthalene (Hesse and Mezger, 1979) and benzene (Tunek et al., 1978), have shown that the major part of covalent binding in vitro originates from reactive intermediates other than the primary epoxides. Studies on the metabolism and binding of naphthol (Hesse and Mezger, 1979) and phenol (Tunek et al., 1978) have demonstrated the high binding capacity of metabolites formed during oxidative metabolism of these phenols. Further, benzene epoxide turned out to be only a weak binding species.

Keywords

Covalent Binding Microsomal Protein Reactive Metabolite Mushroom Tyrosinase Irreversible Binding 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 1982

Authors and Affiliations

  • Sigrun Hesse
    • 1
  • Thomas Wolff
    • 1
  • Margot Mezger
    • 1
  1. 1.Institut für Toxikologie und BiochemieGesellschaft f. Strahlen- und UmweltforschungNeuherberg/MünchenGermany

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