Shaw P N, Houston J B
Toxicol Appl Pharmacol. 1986 Jun 30;84(2):232-40. doi: 10.1016/0041-008x(86)90130-4.
The in vivo consequences of a single dose of Aroclor 1254 (50 mg/kg) on the drug metabolizing capacity of rats were investigated. A noninvasive method, employing [N-methyl-14C]-antipyrine where both 14CO2 exhalation and urinary excretion of 4-hydroxy-, 3-hydroxymethyl-, and norantipyrine were monitored, was used. A group of rats were sequentially tested over a 3-week period to characterize temporal patterns. The antipyrine metabolite kinetic approach demonstrated that induction of hepatic cytochrome P-450 is maximal 3-6 days after Aroclor 1254 administration and the effects were apparent for at least a further 14-17 days. Evidence is presented to suggest selective effects of Aroclor 1254 on different cytochromes P-450 are apparent in vivo.
研究了单剂量的多氯联苯混合物Aroclor 1254(50毫克/千克)对大鼠药物代谢能力的体内影响。采用了一种非侵入性方法,使用[甲基-14C]安替比林,监测14CO2呼出量以及4-羟基安替比林、3-羟甲基安替比林和去甲安替比林的尿排泄量。一组大鼠在3周内进行了连续测试,以表征时间模式。安替比林代谢物动力学方法表明,在给予Aroclor 1254后3至6天,肝细胞色素P-450的诱导作用达到最大,并且这种影响至少在接下来的14至17天内仍然明显。有证据表明,Aroclor 1254对不同细胞色素P-450的选择性作用在体内是明显的。