Metabolism of di-, tri-, tetra-, penta- and hexachlorobiphenyls by hepatic microsomes isolated from control animals and animals treated with Aroclor 1254, a commercial mixture of polychlorinated biphenyls (PCBs).

J T Borlakoglu, J P Wilkins
Author Information
  1. J T Borlakoglu: Department of Biochemistry & Physiology, School of Animal and Microbial Sciences, University of Reading, Whiteknights, U.K.

Abstract

1. The metabolism of a wide range of di-, tri-, tetra-, penta- and hexachlorobiphenyls by hepatic microsomes isolated from control animals and animals treated with Aroclor 1254 was studied. 2. Hepatic microsomes isolated from control rats expressed higher rates of oxidations than avians. 3. Treatment of rats and pigeons with Aroclor 1254 induced cytochrome P450 dependent monooxygenases leading to an increased regioselective metabolism of PCB isomer and congeneres. 4. There was an inverse relationship between the degree of halosubstitution and microsomal oxidation. Meta-para carbon atoms free of halosubstitution were the preferred side for oxidation. 5. A good correlation was found between the in vitro metabolism of PCBs and their relative abundance in tissue extracts, thus suggesting oxidative metabolism to be the major route of metabolic disposal.

MeSH Term

Animals
Aroclors
Carcinogens
Chlorodiphenyl (54% Chlorine)
Columbidae
Cytochrome P-450 Enzyme System
Female
Hydroxylation
Isomerism
Microsomes, Liver
Oxidation-Reduction
Oxygenases
Polychlorinated Biphenyls
Rats
Rats, Sprague-Dawley
Structure-Activity Relationship

Chemicals

Aroclors
Carcinogens
Chlorodiphenyl (54% Chlorine)
Cytochrome P-450 Enzyme System
Polychlorinated Biphenyls
Oxygenases

Word Cloud

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