Kapetanović I M, Kupferberg H J, Porter R J, Theodore W, Schulman E, Penry J K
Clin Pharmacol Ther. 1981 Apr;29(4):480-6. doi: 10.1038/clpt.1981.66.
Valproate effects on phenobarbital biodisposition were examined in a search for the mechanisms of the valproate-induced elevation of plasma phenobarbital during antiepileptic therapy. The study involved patients who were treated with phenobarbital alone and phenobarbital plus valproate. Several kinetic parameters were determined after a pulse dose of stable isotope-labeled phenobarbital, with plasma phenobarbital levels at a steady state. Plasma elimination of labeled phenobarbital was studied by selected ion monitoring. The addition of valproate to the phenobarbital regimen resulted in elevation of plasma phenobarbital and increase in urinary output of unchanged phenobarbital. There was no effect on urinary pH. The rise in plasma phenobarbital was paralleled by lengthening of phenobarbital elimination half-life while the decrease of plasma phenobarbital clearance paralleled the decrease in phenobarbital elimination rate constant. These findings suggest that inhibition of phenobarbital metabolism by valproate is the mechanism for this clinically important drug-drug interaction.
为探寻丙戊酸盐在抗癫痫治疗期间引起血浆苯巴比妥水平升高的机制,研究了丙戊酸盐对苯巴比妥生物转化的影响。该研究纳入了单独接受苯巴比妥治疗以及接受苯巴比妥加丙戊酸盐治疗的患者。在给予一次脉冲剂量的稳定同位素标记苯巴比妥后,测定了几个动力学参数,此时血浆苯巴比妥水平处于稳态。通过选择离子监测研究了标记苯巴比妥的血浆消除情况。在苯巴比妥治疗方案中添加丙戊酸盐导致血浆苯巴比妥水平升高以及未变化苯巴比妥的尿量增加。对尿液pH值无影响。血浆苯巴比妥的升高与苯巴比妥消除半衰期的延长平行,而血浆苯巴比妥清除率的降低与苯巴比妥消除速率常数的降低平行。这些发现表明丙戊酸盐对苯巴比妥代谢的抑制是这种具有临床重要性的药物相互作用的机制。