Pakuts A P, Parks R J, Paul C J, Bujaki S J, Mueller R W
Health Protection Branch, Bureau of Drug Research, Drug Toxicology Division, Ottawa, Ontario, Canada.
Res Commun Chem Pathol Pharmacol. 1990 Jan;67(1):55-62.
An unusual hepatic phospholipidosis produced by repeated high doses of ketoconazole in the mouse was investigated. This abnormal phospholipid accumulation was dose dependent after seven days of daily oral treatment over a 150-350 mg/kg ketoconazole dose range. The accumulation continued after 21 days at the 250 mg/kg dose level. Ultrastructural and biochemical studies revealed that ketoconazole produced a hepatic lysosomal accumulation of concentric lamellar bodies, as typically produced by many cationic amphiphilic drugs. Ketoconazole administered orally in mice at 250 mg/kg also induced total hepatic protein, microsomal protein, cytochrome p-450, and ethylmorphine N-demethylation. Concurrent phenobarbital and ketoconazole administration appeared to further increase hepatic drug metabolizing parameters and to reduce the extent of the hepatic phospholipid accumulation.
研究了在小鼠中反复高剂量给予酮康唑所产生的一种不寻常的肝磷脂沉积症。在150 - 350mg/kg酮康唑剂量范围内,每日口服治疗7天后,这种异常的磷脂积累呈剂量依赖性。在250mg/kg剂量水平下,21天后积累仍在继续。超微结构和生化研究表明,酮康唑导致肝脏溶酶体中出现同心层状小体的积累,这是许多阳离子两亲性药物典型产生的现象。以250mg/kg口服给予小鼠的酮康唑还诱导了肝脏总蛋白、微粒体蛋白、细胞色素p - 450以及乙基吗啡N - 去甲基化。同时给予苯巴比妥和酮康唑似乎进一步增加了肝脏药物代谢参数,并减少了肝脏磷脂积累的程度。