Toskulkao C, Taycharpipranai S, Glinsukon T
Res Commun Chem Pathol Pharmacol. 1982 Jun;36(3):477-91.
Hepatotoxicity of aflatoxin B1 (2.0 and 4.0 mg/kg i.p.) as determined by plasma enzyme activities (GPT and GOT), liver triglycerides and histopathologic changes was enhanced in rats pretreated with four oral doses of ethanol (4.0 g/kg each) at 48, 45, 24 and 21 hrs prior to aflatoxin B1 administration. Pretreatment with ethanol (4.0 g/kg) slightly increased liver weight without changing hepatic microsomal protein contents. Also it caused an increase in microsomal aniline hydroxylase but a decrease in p-nitroanisole-o-demethylase, 48 hrs after the first ethanol dose. In the rats pretreated with ethanol, aflatoxin B1 was metabolized at a higher extent to aflatoxins M1 and Q1. These results suggest that an increased hepatotoxicity of aflatoxin B1 after pretreatment with ethanol may presumably due to an increase in microsomal formation of active aflatoxin B1 metabolite.
在用黄曲霉毒素B1给药前48、45、24和21小时经口给予四剂乙醇(每剂4.0 g/kg)预处理的大鼠中,通过血浆酶活性(谷丙转氨酶和谷草转氨酶)、肝脏甘油三酯和组织病理学变化测定的黄曲霉毒素B1(2.0和4.0 mg/kg腹腔注射)的肝毒性增强。用乙醇(4.0 g/kg)预处理可使肝脏重量略有增加,而肝微粒体蛋白含量不变。在首次给予乙醇48小时后,它还会导致微粒体苯胺羟化酶增加,但对硝基苯甲醚-O-脱甲基酶减少。在用乙醇预处理的大鼠中,黄曲霉毒素B1更多地代谢为黄曲霉毒素M1和Q1。这些结果表明,乙醇预处理后黄曲霉毒素B1肝毒性增加可能是由于微粒体中活性黄曲霉毒素B1代谢物的形成增加所致。