Source:http://linkedlifedata.com/resource/pubmed/id/12030840
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2002-5-28
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pubmed:abstractText |
Methemoglobin formation, as well as hemoglobin or DNA adducts, are useful biomarkers of occupational exposure to certain arylamines. It has been suggested that, in liver from animals not treated with a cytochrome P450 (CYP) inducer, hepatic CYP1A2 is the major P450 involved in N-hydroxylation. This is the first step in the metabolic activation of many arylamines, such as the human urinary bladder carcinogen 4-aminobiphenyl (ABP). The product of this catalytic step, N-hydroxy-4-ABP, reacts in the blood with oxyhemoglobin to form methemoglobin and nitrosobiphenyl. We therefore examined the role of CYP1A2 in causing methemoglobinemia in ABP-treated Cyp1a2(-/-) knockout mice. Application of ABP (100 micromol/kg body wt) to the skin resulted in a marked depletion in the levels of the hepatic thiols (reduced glutathione and cysteine) after 2 h, which rebounded to basal levels 24 h later, and we found no differences between the Cyp1a2(-/-) and wild-type Cyp1a2(+/+) animals. Unexpectedly, the methemoglobin levels were significantly (p < 0.05) higher in Cyp1a2(-/-) than Cyp1a2(+/+) mice at 2, 7, and 24 h following topical ABP. Treatment with dioxin, 24 h prior to ABP, decreased methemoglobin levels by about half at each of the time points in both the Cyp1a2(-/-) and Cyp1a2(+/+) mice. These data suggest that CYP1A2 does not play a positive role in methemoglobin formation via the activation of ABP; rather, the absence of CYP1A2 enhances ABP-induced methemoglobinemia. Because liver CYP1A2 levels are known to vary more than 60-fold between humans, our findings may be relevant to patients who are exposed to arylamines in the workplace.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/4-biphenylamine,
http://linkedlifedata.com/resource/pubmed/chemical/Aminobiphenyl Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens,
http://linkedlifedata.com/resource/pubmed/chemical/Cysteine,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 CYP1A2,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrachlorodibenzodioxin
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0041-008X
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pubmed:author | |
pubmed:copyrightInfo |
(c) 2002 Elsevier Science (USA).
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
181
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
32-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12030840-Administration, Topical,
pubmed-meshheading:12030840-Aminobiphenyl Compounds,
pubmed-meshheading:12030840-Animals,
pubmed-meshheading:12030840-Biological Markers,
pubmed-meshheading:12030840-Biotransformation,
pubmed-meshheading:12030840-Carcinogens,
pubmed-meshheading:12030840-Cysteine,
pubmed-meshheading:12030840-Cytochrome P-450 CYP1A2,
pubmed-meshheading:12030840-Disease Models, Animal,
pubmed-meshheading:12030840-Glutathione,
pubmed-meshheading:12030840-Liver,
pubmed-meshheading:12030840-Methemoglobinemia,
pubmed-meshheading:12030840-Mice,
pubmed-meshheading:12030840-Mice, Inbred C57BL,
pubmed-meshheading:12030840-Mice, Knockout,
pubmed-meshheading:12030840-Occupational Exposure,
pubmed-meshheading:12030840-Tetrachlorodibenzodioxin
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pubmed:year |
2002
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pubmed:articleTitle |
Decrease in 4-aminobiphenyl-induced methemoglobinemia in Cyp1a2(-/-) knockout mice.
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pubmed:affiliation |
Department of Environmental Health, Center for Environment Genetics, University of Cincinnati Medical Center, Cincinnati, Ohio 45267-0056, USA. shertzhg@ucmail.uc.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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