Abramson F P, Lutz M P
Eur J Drug Metab Pharmacokinet. 1986 Apr-Jun;11(2):135-43. doi: 10.1007/BF03189839.
Doses of phenytoin from 90 to 800 mg/d were used to study induction of hepatic cytochrome P-450 and plasma alpha 1-acid glycoprotein in dogs. The antipyrine clearance was increased by 80%, which is equivalent to an increase in cytochrome P-450 of 140%, and the plasma glycoprotein concentration rose 200% at the highest dose of phenytoin used. Plasma concentrations of phenytoin were measured at each dose level to provide a definitive value for the amount of inducer present. These data were used to assess the concentration-response relationship for phenytoin inducing either cytochrome P-450 or the glycoprotein. A simple relationship between concentration and effect was not observed, suggesting a complex mechanism of induction.
使用90至800毫克/天的苯妥英剂量来研究犬肝脏细胞色素P - 450的诱导以及血浆α1 - 酸性糖蛋白的变化。安替比林清除率提高了80%,这相当于细胞色素P - 450增加了140%,并且在所用苯妥英的最高剂量下,血浆糖蛋白浓度上升了200%。在每个剂量水平测量苯妥英的血浆浓度,以确定诱导剂的存在量。这些数据用于评估苯妥英诱导细胞色素P - 450或糖蛋白的浓度 - 反应关系。未观察到浓度与效应之间的简单关系,提示存在复杂的诱导机制。