Plummer S, Boobis A R, Davies D S
Xenobiotica. 1987 Feb;17(2):199-208. doi: 10.3109/00498258709043929.
It has been reported that female Fischer rats are much more susceptible to the hepatocarcinogenic effects of aflatoxin B1 than female DA rats. Female Fischer rats are approximately twice as active as female DA rats in producing adducts of aflatoxin B1 with DNA in vivo, in freshly isolated hepatocytes and with hepatic microsomal fractions. There was no difference between the hepatic microsomal fractions from Fischer and DA rats in the production of adducts between aflatoxin B1 and microsomal protein. The difference between the strains in the formation of adducts with DNA was not due to either the activity of glutathione S-transferases or to the selective destruction of cytochrome P-450 in the DA strain. None of the differences reported here was of sufficient magnitude to explain the difference in susceptibility of the rat strains to the hepatocarcinogenic effects of aflatoxin B1.
据报道,雌性Fischer大鼠比雌性DA大鼠对黄曲霉毒素B1的致癌作用更敏感。在体内、新鲜分离的肝细胞以及肝微粒体组分中,雌性Fischer大鼠产生黄曲霉毒素B1与DNA加合物的活性约为雌性DA大鼠的两倍。Fischer大鼠和DA大鼠的肝微粒体组分在黄曲霉毒素B1与微粒体蛋白形成加合物方面没有差异。不同品系在与DNA形成加合物方面的差异既不是由于谷胱甘肽S-转移酶的活性,也不是由于DA品系中细胞色素P-450的选择性破坏。这里报道的差异均不足以解释大鼠品系对黄曲霉毒素B1致癌作用易感性的差异。