The Effects of Selenium on the Emergence of Aflatoxin B1-Induced Enzyme-Altered Foci in Rat Liver

The Effects of Selenium on the Emergence of Aflatoxin B1-Induced Enzyme-Altered Foci in Rat Liver. MILKS, M. M., WILT, S. R., ALI, I. I., and COURI, D. (1985). Fundam. Appl. Toxicol. 5, 320–326. The effects of selenium on the emergence of aflatoxin B1 (AFB1)-induced enzyme-altered foci were studied...

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Veröffentlicht in:Toxicological sciences 1985-04, Vol.5 (2), p.320-326
Hauptverfasser: MILKS, MICHAEL M., WILT, STEPHEN R., ALI, IBRAHIM I., COURI, DANIEL
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Sprache:eng
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Zusammenfassung:The Effects of Selenium on the Emergence of Aflatoxin B1-Induced Enzyme-Altered Foci in Rat Liver. MILKS, M. M., WILT, S. R., ALI, I. I., and COURI, D. (1985). Fundam. Appl. Toxicol. 5, 320–326. The effects of selenium on the emergence of aflatoxin B1 (AFB1)-induced enzyme-altered foci were studied in male Sprague-Dawley rats. Animals were fed a selenium-deficient diet and supplemented with 5.0, 2.0, and 0.2, or 0 ppm selenium in drinking water for 3 weeks prior to initiation with 2.0 μmol/kg AFB1. After a 1-week period of selenium normalization, the animals were placed on a diet of ordinary rat chow, and were administered a promoting regimen of 500 ppm phenobarbital in drinking water for 1 week, after which time each rat received a two-thirds partial hepatectomy. The promoting regimen of phenobarbital in tap water was then reduced to 100 ppm and continued for 7 weeks. Subsequently, the rats were sacrificed, their livers excised, and fresh frozen sections prepared and stained histochemically to demonstrate areas of γ-glutamyl transpeptidase (GGT) activity. Selenium supplementation was observed to diminish the induction of GGT-positive foci, especially at the 5.0-ppm level. These data suggest that selenium is able to protect against the hepatocarcinogenic effects of AFB1 in the rat, and that the enzyme-altered foci bioassay may be a useful technique in assessing the interaction of selenium on the process of hepatocarcinogenesis.
ISSN:1096-6080
1096-0929
DOI:10.1093/toxsci/5.2.320