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西咪替丁与苯巴比妥联合给药对安替比林消除及代谢物形成的影响。

Effect of concomitant administration of cimetidine and phenobarbital on antipyrine elimination and metabolite formation.

作者信息

Sonne J, Døssing M, Poulsen H E, Pilsgaard H, Rasmussen B, Loft S

出版信息

Int J Clin Pharmacol Ther Toxicol. 1987 Apr;25(4):194-6.

PMID:3583468
Abstract

Cimetidine 1000 mg/day and phenobarbital 100 mg/day were given to five healthy volunteers for 13 days in order to investigate the combined effect and time course of inhibition and induction on hepatic drug metabolism. The one-sample antipyrine saliva clearance (APC) and urinary metabolite profile were measured weekly, once before, two times during and four times after drug administration. On the second day of drug treatment APC was 0.7 fold and the formation clearance of the 3 oxidized metabolites 0.6 fold decreased owing to an early inhibition by cimetidine (p less than 0.05). After 8 days of concomitant drug administration, i.e. when the drug mediated inhibition and induction are supposed to be at maximum, mean APC was 0.85 times the initial value (p greater than 0.05), whereas the formation clearances of nor- and 3-hydroxymethylantipyrine were still significantly depressed. Four and 11 days after drug withdrawal, when phenobarbital, but not cimetidine could be demonstrated in plasma, APC was 1.2 times the initial value (p less than 0.05). The results suggest, that the respective effects of cimetidine and phenobarbital on antipyrine elimination are additive, when given concomitantly, but that cimetidine exerts a relatively greater inhibition in the phenobarbital induced state.

摘要

为研究西咪替丁和苯巴比妥对肝脏药物代谢的抑制和诱导联合效应及时间过程,给予5名健康志愿者每天1000毫克西咪替丁和100毫克苯巴比妥,持续13天。每周测量一次单样本安替比林唾液清除率(APC)和尿代谢物谱,给药前测量一次,给药期间测量两次,给药后测量四次。在药物治疗的第二天,由于西咪替丁的早期抑制作用,APC降低至0.7倍,3种氧化代谢物的生成清除率降低至0.6倍(p<0.05)。联合给药8天后,即药物介导的抑制和诱导作用被认为达到最大时,平均APC为初始值的0.85倍(p>0.05),而去甲安替比林和3-羟甲基安替比林的生成清除率仍显著降低。停药4天和11天后,血浆中可检测到苯巴比妥但未检测到西咪替丁时,APC为初始值的1.2倍(p<0.05)。结果表明,西咪替丁和苯巴比妥同时给药时,对安替比林消除的各自作用是相加的,但西咪替丁在苯巴比妥诱导状态下发挥相对更大的抑制作用。

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