Source:http://linkedlifedata.com/resource/pubmed/id/17316587
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-3
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pubmed:dateCreated |
2007-3-20
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pubmed:abstractText |
Studies were performed to determine if the detoxification pathway of 1,3-butadiene (BD) through 3-butene-1,2-diol (BD-diol) is a major contributor to mutagenicity in BD-exposed mice and rats. First, female and male mice and rats (4-5 weeks old) were exposed by nose-only for 6h to 0, 62.5, 200, 625, or 1250 ppm BD or to 0, 6, 18, 24, or 36 ppm BD-diol primarily to establish BD and BD-diol exposure concentrations that yielded similar plasma levels of BD-diol, and then animals were exposed in inhalation chambers for 4 weeks to BD-diol to determine the mutagenic potency estimates for the same exposure levels and to compare these estimates to those reported for BD-exposed female mice and rats where comparable blood levels of BD-diol were achieved. Measurements of plasma levels of BD-diol (via GC/MS methodology) showed that (i) BD-diol accumulated in a sub-linear fashion during single 6-h exposures to >200 ppm BD; (ii) BD-diol accumulated in a linear fashion during single or repeated exposures to 6-18 ppm BD and then in a sub-linear fashion with increasing levels of BD-diol exposure; and (iii) exposures of mice and rats to 18 ppm BD-diol were equivalent to those produced by 200 ppm BD exposures (with exposures to 36 ppm BD-diol yielding plasma levels approximately 25% of those produced by 625 ppm BD exposures). Measurements of Hprt mutant frequencies (via the T cell cloning assay) showed that repeated exposures to 18 and 36 ppm BD-diol were significantly mutagenic in mice and rats. The resulting data indicated that BD-diol derived metabolites (especially, 1,2-dihydroxy-3,4-epoxybutane) have a narrow range of mutagenic effects confined to high-level BD (>or=200 ppm) exposures, and are responsible for nearly all of the mutagenic response in the rat and for a substantial portion of the mutagenic response in the mouse following high-level BD exposures.
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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/1,3-butadiene,
http://linkedlifedata.com/resource/pubmed/chemical/3,4-epoxybutane-1,2-diol,
http://linkedlifedata.com/resource/pubmed/chemical/3-butene-1,2-diol,
http://linkedlifedata.com/resource/pubmed/chemical/Butadienes,
http://linkedlifedata.com/resource/pubmed/chemical/Epoxy Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Hemoglobins,
http://linkedlifedata.com/resource/pubmed/chemical/Hypoxanthine...
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0009-2797
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
166
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
191-206
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pubmed:meshHeading |
pubmed-meshheading:17316587-Animals,
pubmed-meshheading:17316587-Butadienes,
pubmed-meshheading:17316587-Dose-Response Relationship, Drug,
pubmed-meshheading:17316587-Epoxy Compounds,
pubmed-meshheading:17316587-Female,
pubmed-meshheading:17316587-Glycols,
pubmed-meshheading:17316587-Hemoglobins,
pubmed-meshheading:17316587-Hypoxanthine Phosphoribosyltransferase,
pubmed-meshheading:17316587-Inhalation Exposure,
pubmed-meshheading:17316587-Male,
pubmed-meshheading:17316587-Mice,
pubmed-meshheading:17316587-Mutation,
pubmed-meshheading:17316587-Rats,
pubmed-meshheading:17316587-Rats, Inbred F344,
pubmed-meshheading:17316587-Reproducibility of Results,
pubmed-meshheading:17316587-Spleen,
pubmed-meshheading:17316587-T-Lymphocytes,
pubmed-meshheading:17316587-Time Factors
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pubmed:year |
2007
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pubmed:articleTitle |
Measurement of plasma or urinary metabolites and Hprt mutant frequencies following inhalation exposure of mice and rats to 3-butene-1,2-diol.
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pubmed:affiliation |
Lovelace Respiratory Research Institute, Albuquerque, NM 87108, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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