Hubálek F
Laboratory of Developmental Toxicology, Czechoslovak Academy of Sciences, Olesnice v Orlických horách.
Drug Metabol Drug Interact. 1991;9(3-4):241-53. doi: 10.1515/dmdi.1991.9.3-4.241.
The effect of aflatoxin B1 (AFB1) on the liver microsomal and nuclear mixed function oxidase system (MFO) of adult male rats was studied at oral doses of 1 and 3 mg/kg. At first both doses increased the activities and concentrations of all P450 components followed. The maximum values were observed between 24 and 48 h and were dose- and enzyme-dependent. After 72 h the values dropped to 15-55% of the initial values. Inhibition of the MFO system lasted even after 120 h, when a trend to return to the normal values was already noticeable. We assume that AFB1 acts as an inductor of the monooxygenase system and the reactive electrophilic intermediate(s) bind irreversibly to or autocatalytically inactivate P450.
研究了黄曲霉毒素B1(AFB1)以1毫克/千克和3毫克/千克的口服剂量对成年雄性大鼠肝脏微粒体和细胞核混合功能氧化酶系统(MFO)的影响。起初,这两种剂量均使所有P450组分的活性和浓度随之增加。在24至48小时之间观察到最大值,且这些值具有剂量和酶依赖性。72小时后,这些值降至初始值的15%至55%。即使在120小时后,MFO系统的抑制作用仍然存在,此时已经明显出现恢复到正常值的趋势。我们假设AFB1作为单加氧酶系统的诱导剂,反应性亲电中间体与P450不可逆地结合或自催化使其失活。