Abstract
Treatment of Sprague Dawley rats with 3-methoxy-4-aminoazobenzene (3-MeO-AAB) resulted in striking increase of the activity of hepatic microsomal cytochrome P-450s which could efficiently catalyze the mutagenic activation of hepatocarcinogenic aromatic amines such as a tryptophan-pyrolysate component, Trp P-2, and a glutamic acid-pyrolysate component, Glu P-1. The 3-MeO-AAB-induced cytochrome P-450 (3-MeO-AAB-P-450) was examined for the molecular character by immuno-Western blotting using monoclonal antibody to 3-methylcholanthrene-induced cytochrome P-448 (P-448H; m.w. 54,000).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Azo Compounds / pharmacology*
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Catalysis
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Cytochrome P-450 CYP1A2
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Cytochrome P-450 Enzyme System / biosynthesis
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Cytochromes / biosynthesis*
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Electrophoresis, Polyacrylamide Gel
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Enzyme Induction / drug effects
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Immunochemistry
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Male
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Microsomes, Liver / enzymology*
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Mutagenicity Tests
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Rats
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Rats, Inbred Strains
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p-Aminoazobenzene / analogs & derivatives
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p-Aminoazobenzene / pharmacology*
Substances
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Azo Compounds
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Cytochromes
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p-Aminoazobenzene
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3-methoxy-4-aminoazobenzene
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Cytochrome P-450 Enzyme System
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Cyp1a2 protein, rat
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Cytochrome P-450 CYP1A2