Lee Craig R, Pieper John A, Hinderliter Alan L, Blaisdell Joyce A, Goldstein Joyce A
Divisions of Pharmacotherapy and Cardiology, University of North Carolina at Chapel Hill, USA.
Clin Pharmacol Ther. 2002 Nov;72(5):562-71. doi: 10.1067/mcp.2002.127913.
Multiple single-nucleotide polymorphisms in the gene encoding cytochrome P450 (CYP) 2C9 have been identified, but the functional significance of the various putative defective genotypes in humans merits further study.
Using tolbutamide as a probe of CYP2C9 activity, we evaluated CYP2C9 phenotype in 15 healthy individuals expressing the CYP2C9()1/()1, ()1/()2, and ()1/()3 genotypes (n = 5 per group). CYP2C9 genotype was determined by polymerase chain reaction-restriction fragment length polymorphism methods. Subjects received 500 mg of tolbutamide, with plasma and urine collected over a 24-hour period. Plasma tolbutamide and urinary tolbutamide, 4'-hydroxytolbutamide, and carboxytolbutamide concentrations were determined by an HPLC method.
Tolbutamide area under the plasma concentration-time curve from time zero to infinity [AUC(0- infinity )] significantly increased by 1.5-fold and 1.9-fold, respectively, in subjects expressing the CYP2C9()1/()2 and ()1/()3 genotypes compared with ()1/()1 subjects. Statistically significant reductions in tolbutamide oral clearance (29% and 48%) and formation clearance (38% and 56%) were detected in the ()1/()2 and ()1/()3 individuals, respectively, compared with ()1/()1 subjects. The increases in AUC(0- infinity) and decreases in oral clearance observed in the ()1/()3 individuals were also significantly greater than those expressing the ()1/()2 genotype (P <.05). The amount of urinary 4'-hydroxytolbutamide and carboxytolbutamide excreted in the 0- to 12-hour and 6- to 12-hour collection intervals was significantly less in ()1/()2 and ()1/()3 individuals compared with ()1/()1 subjects. With tolbutamide used as a CYP2C9 probe, CYP2C9 genotype was the major determinant of CYP2C9 phenotype (r(2) = 0.77).
CYP2C9 activity was significantly reduced in ()1 heterozygotes compared with ()1 homozygotes, and metabolism was more severely impaired in ()1/()3 individuals compared with those expressing ()1/()2.
细胞色素P450(CYP)2C9编码基因中已鉴定出多个单核苷酸多态性,但各种假定的缺陷基因型在人类中的功能意义值得进一步研究。
使用甲苯磺丁脲作为CYP2C9活性的探针,我们评估了15名表达CYP2C9()1/()1、()1/()2和()1/()3基因型的健康个体(每组n = 5)的CYP2C9表型。通过聚合酶链反应-限制性片段长度多态性方法确定CYP2C9基因型。受试者服用500 mg甲苯磺丁脲,并在24小时内收集血浆和尿液。采用高效液相色谱法测定血浆甲苯磺丁脲、尿甲苯磺丁脲、4'-羟基甲苯磺丁脲和羧基甲苯磺丁脲的浓度。
与()1/()1受试者相比,表达CYP2C9()1/()2和()1/()3基因型的受试者血浆浓度-时间曲线下甲苯磺丁脲面积从0至无穷大[AUC(0-无穷大)]分别显著增加1.5倍和1.9倍。与()1/()1受试者相比,在()1/()2和()1/()3个体中分别检测到甲苯磺丁脲口服清除率(分别降低29%和48%)和生成清除率(分别降低38%和56%)有统计学意义的下降。在()1/()3个体中观察到的AUC(0-无穷大)增加和口服清除率降低也显著大于表达()1/()2基因型的个体(P <.05)。与()1/()1受试者相比,在()1/()2和()1/()3个体中,在0至12小时和6至12小时收集间隔内排泄的尿4'-羟基甲苯磺丁脲和羧基甲苯磺丁脲量显著减少。以甲苯磺丁脲作为CYP2C9探针时,CYP2C9基因型是CYP2C9表型的主要决定因素(r2 = 0.77)。
与()1纯合子相比,()1杂合子中的CYP2C9活性显著降低,与表达()1/()2的个体相比,()1/()3个体的代谢受损更严重。