Zeng J Z, Bircher J
Eur J Clin Invest. 1983 Dec;13(6):475-9. doi: 10.1111/j.1365-2362.1983.tb00132.x.
The disposition of clomethiazole was studied in six dogs subjected to pretreatment with cimetidine or saline according to a cross-over design. Pretreated dogs received approximately 20 mg/kg of cimetidine p.o. for 4 days and 30 mg/kg i.v. immediately before an intraduodenal infusion of clomethiazole (117 mumol/kg clomethiazole base within 90 min). Compared to controls, cimetidine had no effect on peak plasma concentrations and on areas under the plasma concentration time curves of clomethiazole or of its metabolite 5-acetyl-4-methylthiazole (P greater than 0.05). Identical pretreatment of the same dogs resulted in a 50% inhibition of aminopyrine demethylation (P less than 0.001) as revealed by the aminopyrine breath test. Clomethiazole may be metabolized in the dog through metabolic routes which cannot be inhibited by cimetidine.
采用交叉设计,在6只预先用西咪替丁或生理盐水处理的犬中研究了氯美噻唑的处置情况。预处理的犬口服约20mg/kg西咪替丁,持续4天,并在十二指肠内输注氯美噻唑(90分钟内输注117μmol/kg氯美噻唑碱)前立即静脉注射30mg/kg。与对照组相比,西咪替丁对氯美噻唑或其代谢产物5-乙酰-4-甲基噻唑的血浆峰浓度和血浆浓度-时间曲线下面积均无影响(P>0.05)。氨基比林呼气试验显示,相同的犬进行相同的预处理后,氨基比林去甲基化受到50%的抑制(P<0.001)。氯美噻唑在犬体内可能通过西咪替丁无法抑制的代谢途径进行代谢。