Dhillon S, Richens A
Br J Clin Pharmacol. 1982 Apr;13(4):553-60. doi: 10.1111/j.1365-2125.1982.tb01421.x.
1 The effect of oral administration of sodium valproate (1500 mg daily) on the distribution and elimination kinetics of intravenously administered diazepam in six healthy volunteers has been studied. 2 During valproate administration the unbound fraction of diazepam in serum increased approximately two fold. This was accompanied by a significant increase in apparent volume of distribution and plasma clearance of diazepam. 3 There was a positive correlation between the change in free fraction and the increase in both apparent volume of distribution and plasma clearance of the drug. 4 The concentration of unbound diazepam in serum (calculated from the percent free diazepam and total serum concentration) was significantly higher during valproate administration. Both the intrinsic clearance and volume of distribution of unbound drug were significantly reduced. 5 Mean serum N-desmethyldiazepam levels were significantly lower during valproate coadministration. 6 These results suggest that valproic acid displaces diazepam from plasma protein binding sites and inhibits its metabolism.
1 研究了口服丙戊酸钠(每日1500毫克)对6名健康志愿者静脉注射地西泮的分布和消除动力学的影响。2 在服用丙戊酸钠期间,血清中地西泮的游离分数增加了约两倍。这伴随着地西泮的表观分布容积和血浆清除率的显著增加。3 游离分数的变化与药物的表观分布容积和血浆清除率的增加之间存在正相关。4 在服用丙戊酸钠期间,血清中游离地西泮的浓度(根据游离地西泮百分比和总血清浓度计算)显著更高。未结合药物的内在清除率和分布容积均显著降低。5 在联合使用丙戊酸钠期间,平均血清N-去甲基地西泮水平显著降低。6 这些结果表明,丙戊酸从血浆蛋白结合位点置换地西泮并抑制其代谢。