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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
20
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pubmed:dateCreated |
1986-11-19
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pubmed:abstractText |
Male Sprague-Dawley rats were treated with 4-aminoazobenzene derivatives or other drug metabolizing enzyme inducers such as phenobarbital, 3-methylcholanthrene and isosafrole. The expression of hepatic microsomal cytochrome P-450 of the rats, principally that of a high spin form of cytochrome P-448 (cytochrome P-448H), was assessed by a bacterial mutation test and by immunological methods. The results of the mutation test with use of Salmonella typhimurium TA9 and 3 aromatic amine substrates showed that 2-methoxyl, 3-methoxyl and 2',3-dimethoxyl derivatives of AAB and methyl derivatives of AAB such as o-aminoazotoluene, N-methyl-4-aminoazobenzene and N,N-dimethyl-4-aminoazobenzene have a large capacity for the selective induction of cytochrome P-448H. Activity of the cytochrome increased by 6 hr after an azo dye treatment, reached a maximum after 24 hr, and then declined. In contrast, 4'-methoxy-AAB has a small, and AAB has no, capacity for the cytochrome induction. The aminoazo dye-induced enzymes differ in their substrate specificities from those induced with 3-methylcholanthrene or phenobarbital, and the induced enzyme was identified to be cytochrome P-448H, as determined by an enzyme-linked immunosorbent assay and immunoblotting with use of anti-cytochrome P-448 monoclonal antibodies. These observations indicate that several methoxyl and methyl derivatives of 4-aminoazobenzene are potent and selective inducers of cytochrome P-448H in the rat.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Azo Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Benzoflavones,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochromes,
http://linkedlifedata.com/resource/pubmed/chemical/Methylcholanthrene,
http://linkedlifedata.com/resource/pubmed/chemical/Phenobarbital,
http://linkedlifedata.com/resource/pubmed/chemical/Safrole,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrachlorodibenzodioxin,
http://linkedlifedata.com/resource/pubmed/chemical/beta-Naphthoflavone,
http://linkedlifedata.com/resource/pubmed/chemical/cytochrome P-448,
http://linkedlifedata.com/resource/pubmed/chemical/isosafrole,
http://linkedlifedata.com/resource/pubmed/chemical/p-Aminoazobenzene
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0006-2952
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3565-70
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3768039-Animals,
pubmed-meshheading:3768039-Azo Compounds,
pubmed-meshheading:3768039-Benzoflavones,
pubmed-meshheading:3768039-Cytochromes,
pubmed-meshheading:3768039-Dose-Response Relationship, Drug,
pubmed-meshheading:3768039-Male,
pubmed-meshheading:3768039-Methylcholanthrene,
pubmed-meshheading:3768039-Microsomes, Liver,
pubmed-meshheading:3768039-Phenobarbital,
pubmed-meshheading:3768039-Rats,
pubmed-meshheading:3768039-Rats, Inbred Strains,
pubmed-meshheading:3768039-Safrole,
pubmed-meshheading:3768039-Tetrachlorodibenzodioxin,
pubmed-meshheading:3768039-beta-Naphthoflavone,
pubmed-meshheading:3768039-p-Aminoazobenzene
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pubmed:year |
1986
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pubmed:articleTitle |
Induction of a high spin form of microsomal cytochrome P-448 in rat liver by 4-aminoazobenzene derivatives.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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