Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA 98195-7610, USA.
Drug Metab Dispos. 2013 Feb;41(2):332-42. doi: 10.1124/dmd.112.049718. Epub 2012 Nov 21.
Pregnancy-induced changes in drug pharmacokinetics can be explained by changes in expression of drug-metabolizing enzymes and transporters and/or normal physiology. In this study, we determined gestational age-dependent expression profiles for all metabolic enzyme and transporter genes in the maternal liver, kidney, small intestine, and placenta of pregnant mice by microarray analysis. We specifically examined the expression of genes important for xenobiotic, bile acid, and steroid hormone metabolism and disposition, namely, cytochrome P450s (Cyp), UDP-glucuronosyltranserases (Ugt), sulfotransferases (Sult), and ATP-binding cassette (Abc), solute carrier (Slc), and solute carrier organic anion (Slco) transporters. Few Ugt and Sult genes were affected by pregnancy. Cyp17a1 expression in the maternal liver increased 3- to 10-fold during pregnancy, which was the largest observed change in the maternal tissues. Cyp1a2, most Cyp2 isoforms, Cyp3a11, and Cyp3a13 expression in the liver decreased on gestation days (gd) 15 and 19 compared with nonpregnant controls (gd 0). In contrast, Cyp2d40, Cyp3a16, Cyp3a41a, Cyp3a41b, and Cyp3a44 in the liver were induced throughout pregnancy. In the placenta, Cyp expression on gd 10 and 15 was upregulated compared with gd 19. Notable changes were also observed in Abc and Slc transporters. Abcc3 expression in the liver and Abcb1a, Abcc4, and Slco4c1 expression in the kidney were downregulated on gd 15 and 19. In the placenta, Slc22a3 (Oct3) expression on gd 10 was 90% lower than that on gd 15 and 19. This study demonstrates important gestational age-dependent expression of metabolic enzyme and transporter genes, which may have mechanistic relevance to drug disposition in human pregnancy.
妊娠引起的药物药代动力学变化可以用药物代谢酶和转运体的表达变化和/或正常生理来解释。在这项研究中,我们通过微阵列分析确定了妊娠小鼠母体肝脏、肾脏、小肠和胎盘内所有代谢酶和转运体基因的与妊娠相关的表达谱。我们特别研究了对外源化学物、胆汁酸和甾体激素代谢和处置重要的基因的表达,包括细胞色素 P450(Cyp)、UDP-葡糖醛酸基转移酶(Ugt)、磺基转移酶(Sult)和 ATP 结合盒(Abc)、溶质载体(Slc)和溶质载体有机阴离子(Slco)转运体。妊娠对少数 Ugt 和 Sult 基因有影响。母体肝脏 Cyp17a1 的表达在妊娠期间增加了 3 到 10 倍,这是母体组织中观察到的最大变化。Cyp1a2、大多数 Cyp2 同工酶、Cyp3a11 和 Cyp3a13 的表达在妊娠第 15 和 19 天与非妊娠对照组(妊娠第 0 天)相比下降。相比之下,Cyp2d40、Cyp3a16、Cyp3a41a、Cyp3a41b 和 Cyp3a44 在肝脏中整个妊娠期间被诱导。在胎盘,Cyp 的表达在妊娠第 10 和 15 天与妊娠第 19 天相比上调。Abc 和 Slc 转运体也观察到显著变化。Cyp 在肝脏中的表达和 Cyp3a44 在胎盘中的表达在妊娠第 15 和 19 天下调。在肾脏,Abcc3 的表达在第 15 和 19 天下降。在胎盘,Slc22a3(Oct3)在妊娠第 10 天的表达比妊娠第 15 和 19 天低 90%。这项研究表明,代谢酶和转运体基因的表达具有重要的妊娠相关依赖性,这可能对人类妊娠期间的药物处置具有机制相关性。