Lemonnier F J, Scotto J M, Thuong-Trieu C
J Natl Cancer Inst. 1975 Nov;55(5):1085-7. doi: 10.1093/jnci/55.5.1085.
Female Wistar rats were given a single oral dose of aflatoxin B1, either alone or with a large amount of riboflavin. Biochemical and histologic studies were performed for 30 months. Nine animals of 19 in the aflatoxin-treated group and only 5 of 18 in the riboflavin-aflatoxin-treated group developed hepatomas. The number of rats was insufficient for tests of statistical significance to be fruitful. Urinary excretion of tryptophan metabolites was studied in aflatoxin- and riboflavin-treated rats after an oral administration of 10 mg tryptophan/100 g rat. Riboflavin did not affect the percentage of aflatoxin-treated animals with abnormal urinary excretion patterns, but did increase the magnitude of the disturbances in elimination of kynurenic and xanthurenic acids. The hepatic tryptophan-oxygenase activity was increased only in the two groups given riboflavin, and the levels of nucleic acids were the same in all groups.
给雌性Wistar大鼠单次口服黄曲霉毒素B1,或单独给药,或与大量核黄素一起给药。进行了30个月的生化和组织学研究。黄曲霉毒素处理组的19只动物中有9只发生了肝癌,而核黄素-黄曲霉毒素处理组的18只动物中只有5只发生了肝癌。大鼠数量不足以进行有意义的统计学检验。在给大鼠口服10 mg色氨酸/100 g体重后,研究了黄曲霉毒素和核黄素处理的大鼠中色氨酸代谢产物的尿排泄情况。核黄素不影响黄曲霉毒素处理动物中尿排泄模式异常的百分比,但确实增加了犬尿酸和黄尿酸消除紊乱的程度。仅在给予核黄素的两组中,肝脏色氨酸加氧酶活性增加,且所有组的核酸水平相同。