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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
77
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pubmed:dateCreated |
1987-7-28
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pubmed:abstractText |
This study compared the ability of hexachlorobenzene (HCB) and of other chlorinated benzenes to induce cytochrome P-450 isozymes in rat liver. HCB (greater than 99% pure) induced both the phenobarbital-inducible forms (cytochrome P-450b and P-450e) and the 3-methylcholanthrene (3-MC)-inducible forms (P-450c and P-450d) of cytochrome P-450. However, HCB differed from many 3-MC-type inducers by inducing P-450d preferentially over P-450c. In contrast to HCB, the lower chlorinated benzenes did not induce significant amounts of P-450c or P-450d in the rat, but were phenobarbital-type inducers, inducing P-450b and P-450e. These data indicate that the hepatic effects of HCB differ markedly from those of other chlorinated benzenes. However, chlorinated dibenzodioxins also induce P-450c and P-450d in the rat, and although chlorinated dibenzodioxins and dibenzofurans contaminate certain commercial products, none were detected by gas chromatography/mass spectrometry (detection limit 0.5 ppm) in the HCB used in this study. The evidence that HCB interacted with the receptor for 2,3,7,8-tetrachlorodibenzo-para-dioxin (TCDD) was equivocal. At a concentration of 10(-6) M, HCB produced a slight decrease (18%) in the binding of 3H-TCDD to this protein in vitro, but had no effect at lower concentrations. However, as an inducer of two 3-MC-inducible isozymes of P-450, HCB was clearly more effective in aromatic-hydrocarbon-responsive mice (C57Bl/6J) than in non-responsive mice (DBA/2J), suggesting that HCB may act through the Ah receptor.
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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/Aryl Hydrocarbon Hydroxylases,
http://linkedlifedata.com/resource/pubmed/chemical/Benzofurans,
http://linkedlifedata.com/resource/pubmed/chemical/Chlorobenzenes,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System,
http://linkedlifedata.com/resource/pubmed/chemical/Hexachlorobenzene,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Polymers,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrachlorodibenzodioxin,
http://linkedlifedata.com/resource/pubmed/chemical/polychlorodibenzo-4-dioxin,
http://linkedlifedata.com/resource/pubmed/chemical/polychlorodibenzofuran
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pubmed:status |
MEDLINE
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pubmed:issn |
0300-5038
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
519-26
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:3596751-Animals,
pubmed-meshheading:3596751-Aryl Hydrocarbon Hydroxylases,
pubmed-meshheading:3596751-Benzofurans,
pubmed-meshheading:3596751-Chlorobenzenes,
pubmed-meshheading:3596751-Cytochrome P-450 Enzyme System,
pubmed-meshheading:3596751-Enzyme Induction,
pubmed-meshheading:3596751-Hexachlorobenzene,
pubmed-meshheading:3596751-Isoenzymes,
pubmed-meshheading:3596751-Liver,
pubmed-meshheading:3596751-Polymers,
pubmed-meshheading:3596751-Rats,
pubmed-meshheading:3596751-Structure-Activity Relationship,
pubmed-meshheading:3596751-Tetrachlorodibenzodioxin
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pubmed:year |
1986
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pubmed:articleTitle |
Structure-activity relationships of chlorinated benzenes as inducers of hepatic cytochrome P-450 isozymes in the rat.
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pubmed:publicationType |
Journal Article
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