Dahms R, Gurtoo H L
Res Commun Chem Pathol Pharmacol. 1976 Sep;15(1):11-20.
We have used a microtechnique to study (a) the metabolism of aflatoxin (AF)B1 by rat and mouse, and (b) the effect of phenobarbital treatment in vivo on the in vitro metabolism of AFB1 by hepatic microsomes from rat and mouse. The results indicate and AFP1, the O-demethylated product of AFB1, is a major metabolite produced by the mouse. Although it is detectable in rat, the amount produced is negligible and was calculated to be at least 10 times less than that produced by the mouse. Using several microincubations, AFP1 was prepared in sufficient quantities to verify its identity by UV spectroscopy and by thin layer chromatography against an authentic standard in six different solvent systems. Phenobarbital pretreatment resulted in an enhancement in the total metabolism of AFB1 as well as in the formation of AFM1, AFQ1 and AFP1.
(a)大鼠和小鼠对黄曲霉毒素(AF)B1的代谢;(b)体内苯巴比妥处理对大鼠和小鼠肝微粒体体外代谢AFB1的影响。结果表明,AFB1的O-去甲基化产物AFP1是小鼠产生的主要代谢物。虽然在大鼠中可检测到,但产生的量可忽略不计,经计算至少比小鼠产生的量少10倍。通过多次微量孵育,制备了足够量的AFP1,以通过紫外光谱法以及在六种不同溶剂系统中与 authentic标准品进行薄层色谱分析来验证其身份。苯巴比妥预处理导致AFB1的总代谢以及AFM1、AFQ1和AFP1的形成增强。