Knodell R G, Hall S D, Wilkinson G R, Guengerich F P
J Pharmacol Exp Ther. 1987 Jun;241(3):1112-9.
In vitro investigations suggest the same human liver cytochrome P-450 that catalyzes S-mephenytoin 4-hydroxylation, P-450MP, is responsible for methyl hydroxylation of the oral hypoglycemic agent tolbutamide. Tolbutamide hydroxylase activity copurified with P-450MP; electrophoretically homogenous P-450MP catalyzed both tolbutamide and S-mephenytoin hydroxylation. Each substrate competitively inhibited hydroxylation of the other, and anti-P-450MP inhibited tolbutamide hydroxylation in human liver microsomes. Significant correlation between tolbutamide and S-mephenytoin hydroxylase activities was seen in a set of human liver samples. These findings suggested that subjects with a genetically determined impairment in ability to hydroxylate mephenytoin might also have deficient tolbutamide metabolism. However, plasma tolbutamide concentration-time profiles and urinary excretion of metabolites formed via the hydroxylation pathway were similar in four phenotypically poor and six extensive metabolizers of mephenytoin. We suggest that alteration of a substrate binding site of P-450MP may reduce its ability to hydroxylate S-mephenytoin but not tolbutamide.
体外研究表明,催化S-美芬妥因4-羟化反应的同一种人肝细胞色素P-450,即P-450MP,负责口服降糖药甲苯磺丁脲的甲基羟化反应。甲苯磺丁脲羟化酶活性与P-450MP共纯化;经电泳均一化的P-450MP催化甲苯磺丁脲和S-美芬妥因的羟化反应。每种底物都竞争性抑制另一种底物的羟化反应,抗P-450MP抑制人肝微粒体中甲苯磺丁脲的羟化反应。在一组人肝样本中观察到甲苯磺丁脲和S-美芬妥因羟化酶活性之间存在显著相关性。这些发现表明,因遗传因素导致美芬妥因羟化能力受损的受试者,其甲苯磺丁脲代谢可能也存在缺陷。然而,在4名美芬妥因表型慢代谢者和6名快代谢者中,甲苯磺丁脲的血浆浓度-时间曲线以及经羟化途径生成的代谢产物的尿排泄情况相似。我们认为,P-450MP底物结合位点的改变可能会降低其羟化S-美芬妥因的能力,但不会影响甲苯磺丁脲的羟化能力。