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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
1977-2-16
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pubmed:abstractText |
Differences in benzo(a)pyrene metabolite pattern have been shown by rodent liver microsomes (Sprague-Dawley) and rodent embryo cells from Syrian hamsters and NIH Swiss mice. Rodent liver induced by methylcholanthrene shows marked quantitative variation between species. Additional pattern changes were found in mouse and hamster embryo secondary cultures with a reduction of the K-region metabolites and a marked increase in 9-hydroxybenzo(a)-pyrene. These results are indicative of a region-specific attack on the carcinogen by the cell monooxygenases which is distinct from the liver attack of microsomal enzymes on benzo(a)pyrene. These results suggest that activation and detoxification of benzo(a)pyrene may be species and tissue variable, and susceptibility and resistence to malignant transformation may be predicted on induction of a fortuitous combination of intermediate metabolic steps.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0008-5472
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
36
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4476-9
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:1000495-Animals,
pubmed-meshheading:1000495-Benzopyrenes,
pubmed-meshheading:1000495-Binding Sites,
pubmed-meshheading:1000495-Cells, Cultured,
pubmed-meshheading:1000495-Cricetinae,
pubmed-meshheading:1000495-Embryo, Mammalian,
pubmed-meshheading:1000495-Male,
pubmed-meshheading:1000495-Mesocricetus,
pubmed-meshheading:1000495-Mice,
pubmed-meshheading:1000495-Mice, Inbred BALB C,
pubmed-meshheading:1000495-Microsomes, Liver,
pubmed-meshheading:1000495-Neoplasms, Experimental,
pubmed-meshheading:1000495-Rats,
pubmed-meshheading:1000495-Species Specificity
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pubmed:year |
1976
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pubmed:articleTitle |
Differences in benzo(a)pyrene metabolism between rodent liver microsomes and embryonic cells.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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