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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1988-4-14
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pubmed:abstractText |
DNA binding and metabolism patterns of 3H-labeled aflatoxin B1 (AFB1) and its phase I metabolites, aflatoxicol (AFL), aflatoxin M1 (AFM1), and aflatoxicol-M1 (AFL-M1), were compared in freshly prepared rainbow trout (Salmo gairdneri) hepatocytes. Aflatoxins were incubated with hepatocytes for periods up to 1 h, cellular DNA was isolated and specific activities determined by scintillation counting and Burton analysis. Data for (pmol bound aflatoxin/micrograms DNA)/(mumol dose) versus time fit a linear function (P less than 0.002) passing nearly through the origin for each aflatoxin. DNA binding at 1 h relative to AFB1 was: AFL, 0.53 +/- 0.07; AFM1, 0.81 +/- 0.20 AFL-M1, 0.83 +/- 0.24. Statistical analysis indicated that binding of AFL, AFM1 and AFL-M1 were significantly less than that of AFB1. HPLC analysis of the cellular supernatants indicated that the major metabolites were AFL, AFB1, AFL-M1, and AFM1 from AFB1, AFL, AFM1 and AFL-M1 substrates, respectively. Small quantities of hydroxylated metabolites and glucuronides also were detected in some of the incubations. The time-course data suggested that initial formation of major metabolites was rapid and that, by 20-30 min, net changes in metabolite levels decreased or approached zero. Because the four compounds possess a 8,9-double bond, DNA binding could be due to activation of the parent substrates as well as of their phase I metabolites. Based on current mutagenicity data and limited carcinogenicity studies, AFM1 and AFL-M1 have binding levels which are higher than expected compared to AFB1 and AFL.
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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/Aflatoxin B1,
http://linkedlifedata.com/resource/pubmed/chemical/Aflatoxin M1,
http://linkedlifedata.com/resource/pubmed/chemical/Aflatoxins,
http://linkedlifedata.com/resource/pubmed/chemical/Carcinogens,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Mutagens,
http://linkedlifedata.com/resource/pubmed/chemical/aflatoxicol,
http://linkedlifedata.com/resource/pubmed/chemical/aflatoxicol M1
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0143-3334
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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 |
441-6
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3125996-Aflatoxin B1,
pubmed-meshheading:3125996-Aflatoxin M1,
pubmed-meshheading:3125996-Aflatoxins,
pubmed-meshheading:3125996-Animals,
pubmed-meshheading:3125996-Carcinogens,
pubmed-meshheading:3125996-DNA,
pubmed-meshheading:3125996-Liver,
pubmed-meshheading:3125996-Mutagens,
pubmed-meshheading:3125996-Trout
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pubmed:year |
1988
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pubmed:articleTitle |
Comparative metabolism and DNA binding of aflatoxin B1, aflatoxin M1, aflatoxicol and aflatoxicol-M1 in hepatocytes from rainbow trout (Salmo gairdneri).
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pubmed:affiliation |
Department of Food Science and Technology, Oregon State University, Corvallis 97331.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro,
Research Support, U.S. Gov't, P.H.S.
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