Mayer D G, Beyhl F E
Toxicol Lett. 1983 Apr;16(1-2):89-94. doi: 10.1016/0378-4274(83)90015-2.
The effect of bromobenzene on hepatic microsomal drug-metabolizing enzymes was investigated in hamsters after oral applications of 1.5 and 3.0 g/kg body weight. After 1.5 g/kg a decrease of aminopyrine N-demethylase as well as an increase of hepatic hydroperoxide formation occurred. At 3.0 g/kg, most mixed-function oxidases were inhibited with the exception of ketamine N-demethylase, methylayapanine O-demethylase, and coumarin 7-hydroxylase. Hydroperoxide formation was increased but lipoperoxidation was reduced. Neither glucuronyltransferase I nor glucuronyltransferase II were affected by bromobenzene treatment.
在仓鼠口服1.5克/千克和3.0克/千克体重的溴苯后,研究了溴苯对肝微粒体药物代谢酶的影响。给予1.5克/千克后,氨基比林N-脱甲基酶活性降低,同时肝过氧化氢生成增加。给予3.0克/千克时,除氯胺酮N-脱甲基酶、甲基阿亚帕宁O-脱甲基酶和香豆素7-羟化酶外,大多数混合功能氧化酶均受到抑制。过氧化氢生成增加,但脂质过氧化减少。溴苯处理对葡糖醛酸转移酶I和葡糖醛酸转移酶II均无影响。