Tucker A N, Tang T
J Environ Pathol Toxicol. 1979 Jan-Feb;2(3):613-23.
The effects of the inducers phenobarbital (PB) and 3-methylcholanthrene (MC) on hamster liver mixed-function-oxidase activities were studied. Both inducers increased to content of cytochrome P-450 in the microsomes, aminopyrine demethylase activity, and biphenyl 4-hydroxylase activity when given for 8 days. The ability of liver homogenates from treated animals to activate compounds to mutagens was tested using the Salmonella/microsome test. Neither inducer appreciably altered mutagenicity of 2-acetylaminofluorene, benzidine, benzo(a)pyrene, aflatoxin B1, or sterigmatocystin. Mutagenicity of MC was increased when homogenates from MC-treated hamsters were used as a source of activating enzymes, and this mutagenicity could be correlated with increased biphenyl 2-hydroxylase activity.
研究了诱导剂苯巴比妥(PB)和3-甲基胆蒽(MC)对仓鼠肝脏混合功能氧化酶活性的影响。给予这两种诱导剂8天后,微粒体中细胞色素P-450的含量、氨基比林脱甲基酶活性和联苯4-羟化酶活性均增加。使用沙门氏菌/微粒体试验检测了经处理动物的肝脏匀浆将化合物激活为诱变剂的能力。两种诱导剂均未明显改变2-乙酰氨基芴、联苯胺、苯并(a)芘、黄曲霉毒素B1或杂色曲霉素的诱变性。当使用经MC处理的仓鼠的匀浆作为激活酶的来源时,MC的诱变性增加,且这种诱变性与联苯2-羟化酶活性的增加相关。