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癫痫患者血浆中丙戊酸代谢物的浓度。

Concentration of metabolites of valproic acid in plasma of epileptic patients.

作者信息

Löscher W

出版信息

Epilepsia. 1981 Apr;22(2):169-78. doi: 10.1111/j.1528-1157.1981.tb04098.x.

Abstract

With the help of synthetic reference substances, five metabolites of valproic acid (VPA) could be quantitated by gas chromatography in the plasma of 26 epileptic patients undergoing chronic therapy with sodium valproate. The products of beta-oxidation, i.e., 2-en-VPA, 3-hydroxy-VPA, and 3-keto-VPA were found to be the major metabolites of VPA in plasma, whereas the intermediates of omega-oxidation, 4-hydroxy-VPA and 5-hydroxy-VPA, were present only in markedly lower concentrations. It was thus confirmed that in addition to the excretion of VPA as the glucuronide, beta-oxidation is the preferred metabolic pathway of VPA in man. However, taking the anticonvulsant activity of the metabolites as derived from animal experiments into consideration, none of the metabolites found in human plasma seems to contribute markedly to the therapeutic effect of VPA. Thus, in most patients, VPA seems responsible for more than 90% of the antiepileptic activity during continued medication in man.

摘要

借助合成参考物质,气相色谱法可对26例接受丙戊酸钠长期治疗的癫痫患者血浆中的5种丙戊酸(VPA)代谢物进行定量分析。β-氧化产物,即2-烯丙戊酸、3-羟基丙戊酸和3-酮基丙戊酸,被发现是血浆中VPA的主要代谢物,而ω-氧化中间体4-羟基丙戊酸和5-羟基丙戊酸仅以明显较低的浓度存在。由此证实,除了以葡萄糖醛酸苷形式排泄VPA外,β-氧化是人中VPA的主要代谢途径。然而,考虑到动物实验得出的代谢物的抗惊厥活性,在人血浆中发现的代谢物似乎均未对VPA的治疗效果有显著贡献。因此,在大多数患者中,在人持续用药期间,VPA似乎负责超过90%的抗癫痫活性。

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