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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0001975,
umls-concept:C0010762,
umls-concept:C0026029,
umls-concept:C0030011,
umls-concept:C0048504,
umls-concept:C0072662,
umls-concept:C0205054,
umls-concept:C0456205,
umls-concept:C1167622,
umls-concept:C1280500,
umls-concept:C1550605,
umls-concept:C1704675,
umls-concept:C1979928,
umls-concept:C2827424
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pubmed:issue |
5
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pubmed:dateCreated |
1985-12-18
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pubmed:abstractText |
Microsomes isolated from rats treated with either pyrazole or 4-methylpyrazole, potent inhibitors of alcohol dehydrogenase, catalyzed the oxidation of ethanol and 2-butanol at rates 2-3-fold higher than saline controls. Time course experiments and dose-response experiments indicated that an increase in the microsomal oxidation of alcohols could be observed 24 hr after a single treatment with 200 mg/kg body weight of either pyrazole or 4-methylpyrazole, and after 2 or 3 days of treatment with 50 mg/kg of either of these compounds. The pyrazole treatment did not change the activity of NADPH-cytochrome P-450 reductase, the content of cytochrome P-450, or the oxidation of aminopyrine. Hence, microsomal oxidation of alcohols was increased by the pyrazole treatment whether results were expressed "per mg of protein" or "per nmol of P-450." Microsomes from the pyrazole-treated rats displayed an increase in binding spectrum with ethanol as the substrate as compared to controls, as well as type 2 binding spectrum with dimethyl sulfoxide and 2-butanol. These results suggest the possibility that pyrazole may induce an alcohol-preferring P-450 isozyme. By contrast, the 4-methylpyrazole treatment, besides increasing the oxidation of alcohols, also increased the oxidation of aminopyrine and the content of cytochrome P-450. The increase in the oxidation of alcohols and aminopyrine was primarily due to the increase in content of P-450 produced by the 4-methylpyrazole treatment. Binding spectra with dimethyl sulfoxide and 2-butanol were also observed after 4-methylpyrazole treatment; however, the 2-butanol-binding spectrum was a modified type 1 spectrum, not type 2.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2-butanol,
http://linkedlifedata.com/resource/pubmed/chemical/Alcohols,
http://linkedlifedata.com/resource/pubmed/chemical/Aminopyrine,
http://linkedlifedata.com/resource/pubmed/chemical/Butanols,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System,
http://linkedlifedata.com/resource/pubmed/chemical/Dimethyl Sulfoxide,
http://linkedlifedata.com/resource/pubmed/chemical/Ethanol,
http://linkedlifedata.com/resource/pubmed/chemical/NADPH-Ferrihemoprotein Reductase,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrazoles,
http://linkedlifedata.com/resource/pubmed/chemical/fomepizole
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pubmed:status |
MEDLINE
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pubmed:issn |
0145-6008
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
421-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3933374-Alcohols,
pubmed-meshheading:3933374-Aminopyrine,
pubmed-meshheading:3933374-Animals,
pubmed-meshheading:3933374-Butanols,
pubmed-meshheading:3933374-Cytochrome P-450 Enzyme System,
pubmed-meshheading:3933374-Dimethyl Sulfoxide,
pubmed-meshheading:3933374-Ethanol,
pubmed-meshheading:3933374-Male,
pubmed-meshheading:3933374-Microsomes, Liver,
pubmed-meshheading:3933374-NADPH-Ferrihemoprotein Reductase,
pubmed-meshheading:3933374-Pyrazoles,
pubmed-meshheading:3933374-Rats,
pubmed-meshheading:3933374-Rats, Inbred Strains
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pubmed:articleTitle |
Interaction of pyrazole and 4-methylpyrazole with hepatic microsomes: effect on cytochrome P-450 content, microsomal oxidation of alcohols, and binding spectra.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.
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