Loeser W, Siegers C P
Arch Int Pharmacodyn Ther. 1985 Jun;275(2):180-8.
Rats with cannulated bile ducts excreted 24.6% of an i.v. dose of 100 mg/kg acetaminophen (AA) into bile within 8 hr, 0.9% as unchanged drug, 5.5% as sulfate, 15.1% as glucuronide and 3.1% as the glutathione conjugate. Pretreatment with phenobarbital (0.1% solution for 7 days instead of drinking water) significantly decreased the amount of total AA recovered in bile, to 12.8% mainly as a consequence of reduced glucuronide excretion (3.5%), whereas the GSH-conjugate was augmented to 6.3%. Pretreatment with the GSH-depletor phorone (250 mg/kg i.p. 1 hr prior to AA) slightly reduced the total recovery of AA to 19.2%, due to a diminished excretion of the glucuronide (10.3%). Liver damage due to carbon tetrachloride administration (0.5 ml/kg p.o. 24 hr prior to AA) markedly decreased the total recovery of AA to 8.9% as a consequence of the reduction of the glucuronic acid (5.0%) and the GSH-conjugates (0.2%). These observations are discussed with respect to the effects of phenobarbital, phorone and CCl4 on microsomal and cytosolic GSH-dependent enzymes involved in the metabolism of AA.
胆管插管大鼠在8小时内将静脉注射剂量为100mg/kg的对乙酰氨基酚(AA)的24.6%排泄到胆汁中,其中0.9%为原形药物,5.5%为硫酸盐,15.1%为葡萄糖醛酸苷,3.1%为谷胱甘肽结合物。用苯巴比妥预处理(用0.1%溶液代替饮用水处理7天)显著降低了胆汁中回收的总AA量,降至12.8%,主要是由于葡萄糖醛酸苷排泄减少(3.5%),而谷胱甘肽结合物增加到6.3%。用谷胱甘肽消耗剂佛尔酮预处理(在给予AA前1小时腹腔注射250mg/kg)使AA的总回收率略有降低,降至19.2%,这是由于葡萄糖醛酸苷排泄减少(10.3%)。由于给予四氯化碳(在给予AA前24小时口服0.5ml/kg)导致的肝损伤使AA的总回收率显著降低至8.9%,这是由于葡萄糖醛酸(5.0%)和谷胱甘肽结合物(0.2%)减少所致。针对苯巴比妥、佛尔酮和四氯化碳对参与AA代谢的微粒体和胞质谷胱甘肽依赖性酶的影响对这些观察结果进行了讨论。