摘要
采用未成熟SD大鼠肝细胞微粒体为试验材料,以2,3,7,8-四氯-二苯基-并-二哑噁英(2,3,7,8- tetrachlorobenzo-p-dioxin,TCDD)作为参照,利用甲氧基-异酚噁脱甲基酶(methoxyresorufin-O- demethylase,MROD)竞争性抑制动力学和荧光光谱法分析法,测定了5种多溴联苯(polybrominated diphenyl ethers,PBDEs)对7-甲氧基-异酚噁唑脱甲基反应的影响,间接研究了这些PBDEs对CYP1A2 的竞争性抑制作用。结果表明,和TCDD相比,PBDEs对MROD活性的抑制作用较弱,亦即对CYP1A2的 竞争性抑制作用较弱。
The role of a number of polybrominated diphenyl ethers (PBDEs) as inhibitors of the demethylation of 7-methoxyresorufin, a process that is selectively catalyzed by cytochrome P450 1A2 (CYP1A2), was examined, using methoxyresorufin-O-demethylase (MROD) fluorescent assay and competitive inhibition constant Ki determination. It was found that those examined PBDEs showed punier inhibiting effects to MROD / CYPtA2 than that of 2,3,7,8-Tetrachlorobenzo-p-dioxin (TCDD) which is the strongest inhibitor of MROD / CYP1A2 activity in dioxin-like compounds.
出处
《中国农学通报》
CSCD
2005年第12期11-13,共3页
Chinese Agricultural Science Bulletin
基金
教育部留学回国人员科研启动基金(教外司[2003]406号)广东海洋大学SCI源刊作者奖励基金(0412130)