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本文引用的文献

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Cooperative binding of transcription factors promotes bimodal gene expression response.转录因子的协同结合促进了双峰基因表达响应。
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Repression of hepatobiliary transporters and differential regulation of classic and alternative bile acid pathways in mice during pregnancy.妊娠期间小鼠肝肠转运体的抑制作用及经典和替代胆汁酸途径的差异调控。
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Differential expression of extracellular matrix-mediated pathways in single-suture craniosynostosis.细胞外基质介导的途径在单一颅缝早闭中的差异表达。
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The effect of progesterone dose on gene expression after traumatic brain injury.孕激素剂量对创伤性脑损伤后基因表达的影响。
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Repeated developmental exposure of mice to chlorpyrifos oxon is associated with paraoxonase 1 (PON1)-modulated effects on cerebellar gene expression.重复暴露于毒死蜱氧磷会导致小鼠小脑基因表达发生变化,而过氧化物酶 1(PON1)在其中发挥了调节作用。
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Assisted reproduction technologies alter steroid delivery to the mouse fetus during pregnancy.辅助生殖技术改变了妊娠期间类固醇向胎儿的传递。
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Raised hepatic bile acid concentrations during pregnancy in mice are associated with reduced farnesoid X receptor function.在怀孕的小鼠中,升高的肝胆汁酸浓度与法尼醇 X 受体功能降低有关。
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妊娠小鼠代谢酶和转运蛋白基因表达的胎龄依赖性变化。

Gestational age-dependent changes in gene expression of metabolic enzymes and transporters in pregnant mice.

机构信息

Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle, WA 98195-7610, USA.

出版信息

Drug Metab Dispos. 2013 Feb;41(2):332-42. doi: 10.1124/dmd.112.049718. Epub 2012 Nov 21.

DOI:10.1124/dmd.112.049718
PMID:23175668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3558854/
Abstract

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.

摘要

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。