Wong P T, Teo W L
Neurochem Res. 1986 Sep;11(9):1379-82. doi: 10.1007/BF00966131.
Phenytoin was observed to inhibit competitively the sodium dependent high affinity synaptosomal transport of both glutamate (Glu) and gamma-aminobutyric acid (GABA) with Ki values of 66 +/- 10 and 185 +/- 65 microM, respectively. This contrasted with a previous report that the uptakes of Glu and GABA were enhanced by phenytoin. The degree of inhibition is dependent on the concentrations of the competing drug and substrate present. Taking the therapeutic levels of phenytoin and the overall brain Glu and GABA contents, the degrees of inhibition obtainable appear to be negligible. However, as most of the high levels of Glu and GABA in the brain are intracellular, Glu, and GABA concentrations in the microenvironment of the uptake sites may be sufficiently small so that the ability of phenytoin to inhibit Glu and GABA transport may contribute significantly to the anticonvulsant property of this drug.
观察到苯妥英可竞争性抑制谷氨酸(Glu)和γ-氨基丁酸(GABA)依赖钠的高亲和力突触体转运,其抑制常数(Ki)值分别为66±10和185±65微摩尔。这与之前关于苯妥英可增强Glu和GABA摄取的报道形成对比。抑制程度取决于竞争药物和底物的浓度。考虑到苯妥英的治疗水平以及大脑中Glu和GABA的总体含量,可达到的抑制程度似乎可以忽略不计。然而,由于大脑中大多数高水平的Glu和GABA是细胞内的,摄取位点微环境中的Glu和GABA浓度可能足够低,以至于苯妥英抑制Glu和GABA转运的能力可能对该药物的抗惊厥特性有显著贡献。