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药物转运体基因多态性对普伐他汀在人体药代动力学的影响。

Influence of drug transporter polymorphisms on pravastatin pharmacokinetics in humans.

作者信息

Kivistö Kari T, Niemi Mikko

机构信息

Department of Pharmacological Sciences, Medical School, University of Tampere, Tampere 33014, Finland.

出版信息

Pharm Res. 2007 Feb;24(2):239-47. doi: 10.1007/s11095-006-9159-2. Epub 2006 Dec 20.

Abstract

The role of drug transporters in pravastatin disposition is underlined by the fact that pravastatin does not undergo significant cytochrome P-450 (CYP)-mediated biotransformation. The organic anion transporting polypeptide 1B1 (OATP1B1), encoded by SLCO1B1, and multidrug resistance-associated protein 2 [MRP2 (ABCC2)], are thought to be the major transporters involved in the pharmacokinetics of pravastatin in humans. Other transporters that may play a role include OATP2B1, organic anion transporter 3 (OAT3), bile salt export pump (BSEP), and the breast cancer resistance protein (BCRP). OATP1B1 and MRP2 mediate the hepatic uptake and biliary excretion of pravastatin, respectively. The SLCO1B1 and ABCC2 polymorphisms probably contribute to the high interindividual variability in pravastatin disposition. Recent small studies have characterized the impact of the SLCO1B1 polymorphism on pravastatin in humans, and especially the c.521T>C single-nucleotide polymorphism (SNP) seems to be an important determinant of pravastatin pharmacokinetics. Pravastatin plasma concentrations may be up to 100% higher in subjects carrying the c.521C variant, as found in the *5, *15, *16, and *17 haplotypes, reflecting diminished OATP1B1-mediated uptake into the major site of pravastatin elimination, the liver. The SLCO1B1 polymorphism seems to have a similar impact on the pharmacokinetics of single- and multiple-dose pravastatin. Overall, 2-5% of individuals in various populations may be expected to show markedly elevated plasma pravastatin concentrations due to the SLCO1B1 polymorphism. Of note, the impact of the SLCO1B1 polymorphism on statins may be dependent on ethnicity. Although individuals with a diminished hepatic uptake of pravastatin might be expected to show reduced cholesterol-lowering efficacy due to lower intracellular pravastatin concentrations, there is preliminary evidence to suggest that the SLCO1B1 polymorphism is not a major determinant of non-response to pravastatin. The possible consequences of drug transporter polymorphisms, especially the SLCO1B1 and ABCC2 polymorphisms, for the lipid-lowering efficacy and tolerability of pravastatin in various ethnic groups warrant further study.

摘要

普伐他汀不经过显著的细胞色素P - 450(CYP)介导的生物转化,这一事实凸显了药物转运体在普伐他汀处置中的作用。由SLCO1B1编码的有机阴离子转运多肽1B1(OATP1B1)和多药耐药相关蛋白2 [MRP2(ABCC2)],被认为是参与普伐他汀在人体内药代动力学的主要转运体。其他可能起作用的转运体包括OATP2B1、有机阴离子转运体3(OAT3)、胆盐输出泵(BSEP)和乳腺癌耐药蛋白(BCRP)。OATP1B1和MRP2分别介导普伐他汀的肝脏摄取和胆汁排泄。SLCO1B1和ABCC2基因多态性可能是导致普伐他汀处置个体间高度变异性的原因。最近的小型研究已明确了SLCO1B1基因多态性对人体内普伐他汀的影响,尤其是c.521T>C单核苷酸多态性(SNP)似乎是普伐他汀药代动力学的一个重要决定因素。在*5、*15、16和17单倍型中发现,携带c.521C变异的受试者的普伐他汀血浆浓度可能高出100%,这反映出OATP1B1介导的普伐他汀向其主要消除部位肝脏的摄取减少。SLCO1B1基因多态性似乎对单剂量和多剂量普伐他汀的药代动力学有类似影响。总体而言,由于SLCO1B1基因多态性,预计不同人群中有2% - 5%的个体血浆普伐他汀浓度会显著升高。值得注意的是,SLCO1B1基因多态性对他汀类药物的影响可能取决于种族。虽然由于细胞内普伐他汀浓度较低,预计肝脏对普伐他汀摄取减少的个体可能会表现出降低胆固醇疗效,但有初步证据表明SLCO1B1基因多态性并非普伐他汀无反应的主要决定因素。药物转运体基因多态性,尤其是SLCO1B1和ABCC2基因多态性,对不同种族人群中普伐他汀降脂疗效和耐受性的可能影响值得进一步研究。

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