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Reduction in Binding of Aflatoxin B1 to Rat Liver DNA by Vitamin A and E Pretreatment

The Ewha Medical Journal 1984;7(2):71-78. Published online: July 24, 2015

Department of Biochemistry, College of Medicine, Ewha Womans University, Korea.

Corresponding author: Young-Sook Hong. Department of Biochemistry, College of Medicine, Ewha Womans University, Korea.

Copyright © 1984. Ewha Womans University School of Medicine

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • We examined pattern of covalent modification of DNA produced in rat liver after exposure to single dose of aflatoxin B1. DNA-bound aflatoxin B1 adducts obtained from rat liver microsomes were hydrolyzed with weak acid to yield 2, 3-dihydro-3-hydroxy-(N7-guanyl) aflatoxin B1 as major product. This adduct was derived from the aflatoxin B1, 2, 3-dioxide and accounted for approximately 80% of the carcinogen-derived radioactivity incorporated into DNA. Acid hydrolysis of the nucleic acid-aflatoxin B1, adducts also yielded 2,3-dihydro-2,3-dihydroxy-aflatoxin B1 and other minor products. Vitamin A and E pretreatment of rats resulted in reduction in the level of hepatic AFB1-DNA adducts to two-third of the control value. Therefore, administration of vitamin A and E to rats chages in AFB1 metabolism probably decreased modification of DNA during this experiment.

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      Ihwa Ŭidae chi. 1984;7(2):71-78.   Published online July 24, 2015
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      Ihwa Ŭidae chi. 1984;7(2):71-78.   Published online July 24, 2015
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