Chez M G, Bourgeois B F, Pippenger C E, Knowles W D
Department of Neurology, Cleveland Clinic Foundation, Ohio.
Clin Neuropharmacol. 1994 Feb;17(1):32-7. doi: 10.1097/00002826-199402000-00003.
Although the current trend is to use monotherapy in the treatment of epilepsy, combination therapy is still employed in patients who have failed to respond to monotherapy. There is little clinical or experimental documentation of evidence against or in favor of anticonvulsant combination therapy. In this context, anticonvulsant and neurotoxic pharmacodynamic interactions between phenytoin (PHT) and valproate (VPA) were assessed in an experimental model in mice. All results were expressed in terms of brain drug concentrations for eliminating any pharmacokinetic interaction from the analysis. Both the median neurotoxic and the median anticonvulsant brain concentrations were determined for each drug used alone and for the combination. The interaction for the combination of PHT and VPA was shown to be supraadditive for the anticonvulsant activity, indicating an antiepileptic potentiation, whereas neurotoxicity was simply additive. These results suggest a potential benefit in terms of overall efficacy versus toxicity for the combination of PHT and VPA, as compared with PHT or VPA used alone.
尽管目前的趋势是在癫痫治疗中使用单一疗法,但对于单一疗法无反应的患者仍采用联合疗法。几乎没有临床或实验文献能证明抗惊厥联合疗法的利弊。在此背景下,在小鼠实验模型中评估了苯妥英(PHT)和丙戊酸盐(VPA)之间的抗惊厥和神经毒性药效学相互作用。所有结果均以脑内药物浓度表示,以便在分析中消除任何药代动力学相互作用。分别测定了每种单独使用的药物以及联合使用时的神经毒性中位数和抗惊厥脑内浓度中位数。结果表明,PHT和VPA联合使用时,抗惊厥活性表现为超相加作用,提示有抗癫痫增效作用,而神经毒性则只是相加作用。这些结果表明,与单独使用PHT或VPA相比,PHT和VPA联合使用在总体疗效与毒性方面可能具有优势。