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西咪替丁与卡马西平:一种复杂的药物相互作用。

Cimetidine and carbamazepine: a complex drug interaction.

作者信息

Dalton M J, Powell J R, Messenheimer J A, Clark J

出版信息

Epilepsia. 1986 Sep-Oct;27(5):553-8. doi: 10.1111/j.1528-1157.1986.tb03583.x.

Abstract

Cimetidine has been shown to inhibit the elimination of carbamazepine after a single oral dose. The mechanism of this interaction is thought to be inhibition of carbamazepine metabolism by the hepatic microsomal enzyme system. Because carbamazepine metabolism undergoes autoinduction with chronic administration, it is not known whether or not the clinical significance of this interaction can be predicted from the results of a single-dose study. The purpose of this study was to evaluate the presence of an interaction under steady-state enzyme-induced conditions. Using an open treatment design, carbamazepine, 300 mg b.i.d., was taken by eight healthy volunteers for 42 days (days 1-42). Cimetidine, 400 mg t.i.d., was taken for 7 days (days 29-35). Steady-state carbamazepine increased 17% after 2 days of cimetidine treatment (from 4.7 +/- 0.8 to 5.5 +/- 1.4 micrograms/ml; p less than 0.05). Six of the eight subjects noted side effects shortly after starting cimetidine treatment. Carbamazepine returned to the pre-cimetidine level and the side effects diminished by the 7th day of cimetidine administration. Therefore, the clinical significance of this interaction appears to be time dependent, and could not be predicted from the results of single-dose studies.

摘要

已证明西咪替丁可抑制卡马西平单次口服给药后的消除。这种相互作用的机制被认为是肝微粒体酶系统对卡马西平代谢的抑制。由于卡马西平代谢在长期给药后会发生自身诱导,因此尚不清楚这种相互作用的临床意义是否可以从单剂量研究的结果中预测。本研究的目的是评估在稳态酶诱导条件下是否存在相互作用。采用开放治疗设计,8名健康志愿者每日两次服用300mg卡马西平,共42天(第1 - 42天)。每日三次服用400mg西咪替丁,共7天(第29 - 35天)。西咪替丁治疗2天后,稳态卡马西平升高了17%(从4.7±0.8微克/毫升升至5.5±1.4微克/毫升;p<0.05)。8名受试者中有6名在开始西咪替丁治疗后不久出现了副作用。卡马西平恢复到西咪替丁治疗前的水平,且副作用在西咪替丁给药第7天时减轻。因此,这种相互作用的临床意义似乎与时间有关,且无法从单剂量研究的结果中预测。

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