Siegers C P, Schütt A
Pharmacology. 1979;18(4):175-9. doi: 10.1159/000137249.
In rats, the biliary and renal excretion of paracetamol changed in a dose-dependent manner. After an oral nonhepatotoxic dose of 200 mg/kg paractamol, the drug excreted in the bile amonted to only 5.5% within 24 h, whereas 72% of the dose were excreted into the urine. Following an oral hepatoxic dose (1,000 mg/kg), the biliary excretion of thotal paracetamol was enhanced to 13.5% whereas the renal elimination was reduced to 51% of the dose. After a nontoxic intravenous treatment with paracetamol (25-100-400 mg/kg), both the excretion of paracetamol conjugates into the bile and the elimination of free paracetamol into the urine were augmented in a dose-dependent manner. Hepatic damage due to carbon tetrachloride pretreatment (0.5 ml/kg i.p. 24 h before 100 mg/kg paracetamol i.v.) diminished both the bile flow and the biliary excretion of paracetamol conjugates, whereas the renal elimination was not affected.
在大鼠中,对乙酰氨基酚的胆汁排泄和肾脏排泄呈剂量依赖性变化。口服非肝毒性剂量200mg/kg对乙酰氨基酚后,24小时内胆汁中排泄的药物仅占5.5%,而72%的剂量经尿液排泄。口服肝毒性剂量(1000mg/kg)后,对乙酰氨基酚的总胆汁排泄增加至13.5%,而经肾脏消除的剂量减少至51%。对乙酰氨基酚进行无毒静脉注射治疗(25 - 100 - 400mg/kg)后,对乙酰氨基酚结合物向胆汁中的排泄以及游离对乙酰氨基酚向尿液中的消除均呈剂量依赖性增加。四氯化碳预处理(在静脉注射100mg/kg对乙酰氨基酚前24小时腹腔注射0.5ml/kg)导致的肝损伤使胆汁流量和对乙酰氨基酚结合物的胆汁排泄均减少,而肾脏消除未受影响。