Jung B, Graf H, Ullrich V
Biol Chem Hoppe Seyler. 1985 Jan;366(1):23-31. doi: 10.1515/bchm3.1985.366.1.23.
The widely used fluorometric microsomal monooxygenase test for 7-ethoxycoumarin O-dealkylation was reinvestigated with regard to other possible hydroxylation products. By HPLC-analysis no beta-hydroxylation of the ethyl group and no 8-hydroxylation could be detected. Only a small percentage of 6-hydroxylation occurred, but as a new major metabolite 7-ethoxy-3-hydroxycoumarin was found in quantities depending on the microsomal preparation used. The ratio of O-dealkylation to 3-hydroxylation varied according to species, induction, buffer and pH, suggesting that different isozymes of cytochrome P450 were involved. The isozyme mainly responsible for 3-hydroxylation exhibited a great dependence on cytochrome b5 as the donor for the second electron. The fluorometric test does not include 3-hydroxylation due to the virtual absence of an emission spectrum above 450 nm.
针对7-乙氧基香豆素O-脱烷基化广泛使用的荧光微粒体单加氧酶试验,就其他可能的羟基化产物进行了重新研究。通过高效液相色谱分析,未检测到乙基的β-羟基化和8-羟基化。仅发生了少量的6-羟基化,但发现一种新的主要代谢产物7-乙氧基-3-羟基香豆素的量取决于所使用的微粒体制剂。O-脱烷基化与3-羟基化的比例因物种、诱导、缓冲液和pH值而异,这表明涉及细胞色素P450的不同同工酶。主要负责3-羟基化的同工酶对细胞色素b5作为第二个电子供体有很大依赖性。由于在450nm以上几乎没有发射光谱,荧光试验未包括3-羟基化。