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[Cancer Research 37, 1649-1656, June 1, 1977]
© 1977 American Association for Cancer Research

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Species Comparison of in Vitro Metabolism of Aflatoxin B11

Bill D. Roebuck2 and Gerald N. Wogan3

Department of Nutrition and Food Science, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139

The metabolism of [14C]aflatoxin B1 by 9000 x g supernatant fraction of livers of duck, rat, mouse, monkey, and humans was compared by incubating the compound and liver fractions in the presence of cofactors and air for 30 min. The incubation medium was extracted with chloroform, and the soluble metabolites were separated on thin-layer plates and quantified; radioactivity remaining in the aqueous phase was determined in order to quantify metabolism to water-soluble derivatives. Duck, monkey, and human livers were most active in total conversion, each metabolizing approximately 80% of available substrate in 30 min. Rat and mouse livers had lower activities, metabolizing 15 to 20%. Duck liver produced mainly (60%) chloroform-insoluble derivatives, but all other species produced larger quantities of chloroform-soluble than insoluble metabolites. Aflatoxin Q1 was the principal chloroform-soluble metabolite produced by monkey, human, and rat liver, whereas duck liver produced mainly aflatoxicol in that fraction. Aflatoxin P1 was produced by monkey, human, and mouse liver, but not by duck and rat. The chromatographic region containing M1 and B2a contained low levels of radioactivity in all species except human. No consistent pattern of metabolism emerged which could be correlated with species differences in response to aflatoxin B1 toxicity or carcinogenicity.

1 Financial support was provided by Grants NIH 5 PO1 ES 00597 and 5 TO1 ES 00056, and Contract NIH NO1 CP 43265. Preliminary accounts of this work were presented at the 1975 Annual Meeting of the American Association for Cancer Research (18).

2 Present address: Department of Pathology, Dartmouth Medical School, Hanover, N. H. 03755.

3 To whom requests for reprints should be addressed, at Room 56-215, MIT, Cambridge, Mass. 02139.

Received 5/26/76. Accepted 3/ 8/77.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1977 by the American Association for Cancer Research.