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Inhibition of monocarboxylate transporter-mediated absorption of valproic acid by Gegen-Qinlian-Tang

机译:葛根-秦联-唐抑制单羧酸盐转运蛋白介导的丙戊酸吸收

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摘要

Valproic acid (VPA), an anti-epileptic drug with a narrow therapeutic index, is a substrate of the monocarboxylate transporter (MCT). In this study, we investigated the effect of Gegen-Qinlian-Tang (GQT), a Chinese Medicine prescription containing Puerariae Radix (PR), Scutellariae Radix (SR), Coptidis Rhizoma (CR) and Glycyrrhizae Radix (GR), on the pharmacokinetics of VPA, as a probe drug of MCT, in rats and the underlying mechanism. Sprague-Dawley rats were orally administered VPA with and without GQT in crossover design. The serum concentrations of VPA were determined by a fluorescence polarization immunoassay. The results showed that coadministration with 2.0 and 4.0 g/kg of GQT remarkably decreased the Cmax of VPA by 72% and 74% and reduced the AUC0-t by 63% and 53%, respectively. The mechanism study using Caco-2 cells revealed that the uptake function of MCT was inhibited by GQT and each component herb. In conclusion, the MCT-mediated absorption of VPA was significantly decreased by GQT and its component herbs.
机译:丙戊酸(VPA)是一种抗癫痫药,具有较窄的治疗指数,是单羧酸盐转运蛋白(MCT)的底物。在这项研究中,我们调查了葛根-秦lian汤(GQT),这是一种含有葛根(PR),黄S(SR),黄连(CR)和甘草基(GR)的中药处方,对药代动力学的影响作为MCT的探针药物的VPA在大鼠中的表达及其潜在机制。在交叉设计中,对Sprague-Dawley大鼠口服GPA或不加GQT的VPA。通过荧光偏振免疫测定法测定VPA的血清浓度。结果表明,与2.0和4.0 g / kg的GQT共同给药显着降低VPA的Cmax分别为72%和74%,并将AUC0-t分别降低63%和53%。使用Caco-2细胞的机理研究表明,MCT的摄取功能受到GQT和每种成分药草的抑制。总之,GQT及其组成成分的草药显着降低了MCT介导的VPA吸收。

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