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丙戊酸-乙琥胺相互作用:一项药代动力学研究。

Valproic acid-ethosuximide interaction: a pharmacokinetic study.

作者信息

Pisani F, Narbone M C, Trunfio C, Fazio A, La Rosa G, Oteri G, Di Perri R

出版信息

Epilepsia. 1984 Apr;25(2):229-33. doi: 10.1111/j.1528-1157.1984.tb04180.x.

Abstract

The present pharmacokinetic study was designed to investigate the possible interaction between valproic acid (VPA) and ethosuximide (ESM) in humans. Six drug-free healthy volunteers, four men and two women, 18-42 years of age, received a single oral dose of 500 mg ESM before and during a treatment with VPA at 800- to 1,600-mg daily doses. The second ESM dose was given 9 days after VPA administration was started. In this latter condition, a significant (p less than 0.05) increase in ESM serum half-life, from 44 to 54 h on average, and a significant (p less than 0.05) decrease in total body clearance, from 11.2 to 9.5 ml/min on average, were observed. Other pharmacokinetic parameters were unchanged and showed values similar to those reported in the literature. Serum VPA levels ranged between 66.8 and 95 micrograms/ml. Two subjects showed no evidence of interaction. Although a great interindividual variability in the occurrence of VPA-ESM interaction can be observed, the present study indicates that VPA is able to inhibit the metabolism of ESM. Possible factors affecting this interaction are hypothesized and discussed.

摘要

本药代动力学研究旨在调查丙戊酸(VPA)与乙琥胺(ESM)在人体内可能存在的相互作用。6名健康志愿者,年龄在18至42岁之间,4名男性,2名女性,在未用药状态下,于VPA以每日800至1600毫克剂量治疗前及治疗期间,单次口服500毫克ESM。在开始给予VPA 9天后给予第二次ESM剂量。在后一种情况下,观察到ESM血清半衰期显著(p小于0.05)延长,平均从44小时延长至54小时,全身清除率显著(p小于0.05)降低,平均从11.2毫升/分钟降至9.5毫升/分钟。其他药代动力学参数未发生变化,其值与文献报道的值相似。血清VPA水平在66.8至95微克/毫升之间。两名受试者未显示相互作用的证据。尽管可以观察到VPA-ESM相互作用的发生存在很大的个体差异,但本研究表明VPA能够抑制ESM的代谢。对影响这种相互作用的可能因素进行了假设和讨论。

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