Yamazaki H, Tanaka M, Shimada T
Osaka Prefectural Institute of Public Health, Japan.
J Chromatogr B Biomed Sci Appl. 1999 Jan 8;721(1):13-9. doi: 10.1016/s0378-4347(98)00472-1.
A highly sensitive method for the determination of coumarin 7-hydroxylation and 7-ethoxycoumarin O-deethylation by human cytochrome P450 (P450 or CYP) enzymes was developed using high-performance liquid chromatography (HPLC). The newly developed HPLC method was found to be about 100-fold more sensitive than the previous spectrofluorimetric method in detecting the metabolite 7-hydroxycoumarin (umbelliferone). With this high sensitivity, the kinetics of coumarin 7-hydroxylation and 7-ethoxycoumarin O-deethylation catalyzed by human liver microsomal and recombinant P450 enzymes were determined more precisely. With 36 different substrate concentrations in these two reactions, coumarin 7-hydroxylation was found to be catalyzed mainly by a single enzyme CYP2A6 and 7-ethoxycoumarin was oxidized by at least two enzymes CYP2E1 and CYP1A2 in human liver microsomes.
利用高效液相色谱法(HPLC)开发了一种高灵敏度的方法,用于测定人细胞色素P450(P450或CYP)酶对香豆素的7-羟基化作用以及7-乙氧基香豆素的O-脱乙基作用。新开发的HPLC方法在检测代谢产物7-羟基香豆素(伞形酮)方面比以前的荧光分光光度法灵敏约100倍。凭借这种高灵敏度,能更精确地测定人肝微粒体和重组P450酶催化的香豆素7-羟基化作用以及7-乙氧基香豆素O-脱乙基作用的动力学。在这两个反应中采用36种不同的底物浓度,结果发现人肝微粒体中香豆素的7-羟基化作用主要由单一酶CYP2A6催化,而7-乙氧基香豆素至少被两种酶CYP2E1和CYP1A2氧化。