Chang R L, Zampaglione N, Lin C
Drug Metab Dispos. 1975 Nov-Dec;3(6):487-93.
The metabolism of 14C-griseofulvin has been compared in rat liver microsomes, isolated perfused rat livers, and rats with bile duct cannulas. In all three preparations, 4-desmethylgriseofulvin and 6-desmethylgriseofulvin were the major metabolites. The ratio of total 4-desmethylgriseofulvin to 6-desmethylgriseofulvin formed was 1.20, 0.89, and 1.01 in liver microsomes, isolated perfused livers, and rats with bile duct cannulas, respectively. After a 7-min incubation with liver microsomes, most (96%) of the griseofulvin remained unchanged. Only small amounts of 4-desmethylgriseofulvin (1.26%) of dose) and 6-desmethylgriseofulvin (1.05% of dose) were formed. In isolated perfused liver, most of the drug (59% of dose) was excreted into bile within 4 hr, primarily as 4-desmethylgriseofulvin (24% of dose) and 6-methylgriseofulvin (24% of dose). In animals with bile duct cannulas, 65% of the dose was excreted into bile and 18% of the dose into urine within 4 hours. In bile, 32% of the dose was excreted as 4-desmethylgriseofulvin and 20% of the dose as 6-desmethylgriseofulvin, whereas in urine the drug was excreated predominantly as 6-desmethylgriseofulvin (13% of dose) with only a small amount of 4-desmethylgriseofulvin (1% of dose), during the first 4 hr. These results show that there is good correlation in the metabolic fate of 14C-griseofulvin in the liver microsomes, isolated perfused liver, and rats with bile duct cannulas. In addition to the similar ratio of 4-desmethylgriseofulvin to 6-desmethylgriseofulvin, there is also an agreement in the extent of metabolism and biliary excretion in isolated perfused liver and in rats with bile duct cannulas, which suggests that the isolated perfused liver is an important technique for studying drug metabolism in animals.
已对14C-灰黄霉素在大鼠肝微粒体、离体灌注大鼠肝脏以及胆管插管大鼠中的代谢情况进行了比较。在所有这三种制剂中,4-去甲基灰黄霉素和6-去甲基灰黄霉素是主要代谢产物。在肝微粒体、离体灌注肝脏和胆管插管大鼠中,生成的总4-去甲基灰黄霉素与6-去甲基灰黄霉素的比例分别为1.20、0.89和1.01。与肝微粒体孵育7分钟后,大部分(96%)的灰黄霉素保持不变。仅生成少量的4-去甲基灰黄霉素(占剂量的1.26%)和6-去甲基灰黄霉素(占剂量的1.05%)。在离体灌注肝脏中,大部分药物(占剂量的59%)在4小时内排入胆汁,主要为4-去甲基灰黄霉素(占剂量的24%)和6-甲基灰黄霉素(占剂量的24%)。在胆管插管的动物中,65%的剂量在4小时内排入胆汁,18%的剂量排入尿液。在胆汁中,32%的剂量以4-去甲基灰黄霉素形式排出,20%的剂量以6-去甲基灰黄霉素形式排出,而在尿液中,在最初4小时内,药物主要以6-去甲基灰黄霉素(占剂量的13%)形式排出,只有少量的4-去甲基灰黄霉素(占剂量的1%)。这些结果表明,14C-灰黄霉素在肝微粒体、离体灌注肝脏和胆管插管大鼠中的代谢命运具有良好的相关性。除了4-去甲基灰黄霉素与6-去甲基灰黄霉素的比例相似外,离体灌注肝脏和胆管插管大鼠在代谢程度和胆汁排泄方面也一致,这表明离体灌注肝脏是研究动物药物代谢的一项重要技术。