[1] 陈卿, 吴健, 伍建红, 等.高血压患者长期服用氨氯地平对动脉弹性和左心室肥大的影响[J]. 中国动脉硬化杂志, 2007, 15(7): 503-505. [2] Park JY, Kim KA, Lee GS, et al. Randomized, open-label, two-period crossover comparison of the pharmacokinetic and pharmacodynamic properties of two amlodipine formulations in healthy adult male Korean subjects[J]. Clin Ther, 2004, 26(5): 715-723. [3] Kim KA, Park PW, Lee OJ, et al. Effect of CYP3A5*3 genotype on the pharmacokinetics and pharmacodynamics of amlodipine in healthy Korean subjects[J]. Clin Pharmacol Ther, 2006, 80(6): 646-656. [4] Kuehl P, Zhang J, Lin Y, et al. Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression[J]. Nat Genet, 2001, 27(4): 383-391. [5] Kim KA, Park PW, Park JY. Effect of ABCB1(MDR1) haplotypes derived from G2677T/C3435T on the pharmacokinetics of amlodipine in healthy subjects[J]. Br J Clin Pharmacol, 2007, 63(1): 53-58. [6] Fukuen S, Fukuda T, Matsuda H, et al.Identification of the novel splicing variants for the hPXR in human livers[J]. Biochem Biophys Res Commun, 2002, 298(3): 433-438. [7] Uno Y, Sakamoto Y, Yoshida K, et al. Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoter[J]. J Hum Genet,2003, 48(11): 594-597. [8] 刘国仗, 胡大一, 陶萍, 等.心血管药物临床试验评价方法的建议[J].中华心血管病杂志, 1998, 26(1): 5-1l. [9] Oleson L, von Moltke LL, Greenblatt DJ, et al. Identification of polymorphisms in the 3'-untranslated region of the human pregnane X receptor(PXR) gene associated with variability in cytochrome P450 3A(CYP3A) metabolism[J]. Xenobiotica, 2010, 40(2): 146-162. [10] Miura M, Satoh S, Inoue K, et al. Influence of CYP3A5, ABCB1 and NR1I2 polymorphisms on prednisolone pharmacokinetics in renal transplant recipients[J]. Steroids, 2008, 73(11): 1052-1059. [11] Qiu H, Mathäs M, Nestler S, et al. The unique complexity of the CYP3A4 upstream region suggests a nongenetic explanation of its expression variability[J]. Pharmacogenet Genomics, 2010, 20(3): 167-178. |