Piekoszewski W, Brandys J, Lipniak M
Akademii Medycznej im. M. Kopernika w Krakowie.
Folia Med Cracov. 1990;31(3):201-7.
The pharmacokinetics of antipyrine in a dose of 20 mg/kg i.v. and cytochrome P-450 level in liver, were studied in control and pretreated rats with 1, 5, 25 ppm polychlorinated biphenyls in food for up to 120 days. The objective of this work was to quantitate the effects of low environmental levels of the contaminant and enzyme inducer (PCB) on the pharmacokinetics of antipyrine, a drug whose primary elimination route is liver metabolism. After 30 days of pretreatment only the 25 ppm treated rats showed any significant acceleration of antipyrine elimination. At the 60 and 120 days samplings, both the 5 and 25 ppm pretreatments show significant acceleration of antipyrine elimination. The changes in cytochrome P-450 lever were similar and no significant effects on body weight and volume of distribution was observed.
研究了静脉注射20mg/kg剂量安替比林的药代动力学以及肝脏中细胞色素P-450水平,实验对象为对照组大鼠和在食物中添加1、5、25ppm多氯联苯预处理长达120天的大鼠。这项研究的目的是量化低环境水平的污染物和酶诱导剂(多氯联苯)对安替比林药代动力学的影响,安替比林是一种主要通过肝脏代谢消除的药物。预处理30天后,只有接受25ppm多氯联苯处理的大鼠显示出安替比林消除有任何显著加速。在60天和120天取样时,5ppm和25ppm预处理均显示安替比林消除显著加速。细胞色素P-450水平的变化相似,且未观察到对体重和分布容积有显著影响。