Ridley W P, Warren J, Nair R S
Environmental Health Laboratory, Monsanto Agricultural Company, St. Louis, Missouri 63110.
J Toxicol Environ Health. 1988;24(2):217-27. doi: 10.1080/15287398809531155.
The capacity for induction of microsomal metabolic enzymes by tetrachlorophthalic anhydride (TCPA) was evaluated in male Sprague-Dawley rats and male CD-1 mice. The rats were orally dosed for 7 d with TCPA suspended in corn oil at 25, 100, 250, or 500 mg/kg. Following this treatment a dose-dependent reduction in the zoxazolamine paralysis time occurred over the dose range 100-500 mg/kg in the rat. No effect on the hexobarbital sleep time was observed at any test level. TCPA was found to produce statistically significant increases in hepatic aminopyrine N-demethylase, aniline hydroxylase, and cytochrome P-450 in the rat at 500 mg per kg. In addition statistically significant increases were seen in aniline hydroxylase and cytochrome P-450 at 25 mg/kg. Mice were orally dosed with TCPA for 7 d at 250, 500, or 1000 mg/kg. There was no effect in the zoxazolamine paralysis time or the hexobarbital sleep time in this species. Hepatic microsomal enzyme levels were not measured in the mouse. These results suggest that following oral dosage TCPA is a weak inducer of microsomal enzymes in the rat. A similar effect was not observed in the mouse for the parameters tested.
在雄性斯普拉格-道利大鼠和雄性CD-1小鼠中评估了四氯邻苯二甲酸酐(TCPA)诱导微粒体代谢酶的能力。给大鼠口服悬浮于玉米油中的TCPA,剂量分别为25、100、250或500mg/kg,持续7天。经过这种处理后,在100 - 500mg/kg的剂量范围内,大鼠中唑沙宗麻痹时间出现剂量依赖性缩短。在任何测试水平下均未观察到对己巴比妥睡眠时间有影响。发现TCPA在大鼠中以500mg/kg的剂量可使肝脏氨基比林N-脱甲基酶、苯胺羟化酶和细胞色素P-450产生统计学上的显著增加。此外,在25mg/kg时,苯胺羟化酶和细胞色素P-450也出现统计学上的显著增加。给小鼠口服TCPA,剂量为250、500或1000mg/kg,持续7天。该物种的唑沙宗麻痹时间或己巴比妥睡眠时间均未受影响。未对小鼠的肝脏微粒体酶水平进行测量。这些结果表明,经口给药后,TCPA在大鼠中是微粒体酶的弱诱导剂。在所测试的参数方面,未在小鼠中观察到类似效应。