[1] Evans RM. The steroid and thyroid hormone receptor superfamily[J]. Science, 1988, 240 (4854): 889-895. [2] Bourguet W, Ruff M, Chambon P, et al. Crystal structure of the ligand-binding domain of the human nuclear receptor RXR-alpha[J]. Nature,1995, 375 (6530): 377-382. [3] Lehmann M, McKee DD, Watson MA, et al. The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions[J]. Clin Investig,1998,102(5):1016-1023. [4] Ekins S, Kortagere S, Iyer M, et al. Challenges predicting ligand-receptor interactions of promiscuous proteins: the nuclear receptor PXR[J]. PLoS Comput Biol, 2009,5(12):e1000594. [5] Kliewer SA, Moore JT, Wade L,et al. An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway[J]. Cell, 1998, 92(1): 73-82. [6] Bertilsson GR, Heidrich J, Svensson K, et al. Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction[J]. Proc Natl Acad Sci USA,1998, 95(21): 12208-12213. [7] Blumberg B, Sabbagh W, Juguilon H, et al.SXR, a novel steroid and xenobioticsensing nuclear receptor[J]. Genes Dev,1998,12(20):3195-3205. [8] Goodwin B, Hodgson E, Liddle C. The orphan human pregnane X receptor mediates the transcriptional activation of CYP3A4 by rifampicin through a distal enhancer module[J].Mol Pharmacol, 1999, 56(6):1329-1339. [9] Chen Y, Ferguson SS, Negishi M, et al. Identification of constitutive androstane receptor and glucocorticoid receptor binding sites in the CYP2C19 promoter[J]. Mol Pharmacol, 2003,64(2): 316-324. [10] Ferguson SS, Chen Y, LeCluyse EL, et al. Human CYP2C8 is transcriptionally regulated by the nuclear receptors constitutive androstane receptor, pregnane X receptor,glucocorticoid receptor, and hepatic nuclear factor 4alpha[J]. Mol Pharmacol, 2005, 68(3):747-757. [11] Schipani A, Siccardi M, D'Avolio A, et al.Population pharmacokinetic modeling of the association between 63396C->T pregnane X receptor polymorphism and unboosted atazanavir clearance[J]. Antimicrob Agents Chemother, 2010, 54(12):5242-5250. [12] Yang J, Luan X, Gui H, et al.Byakangelicin induces cytochrome P450 3A4 expression via transactivation of pregnane X receptors in human hepatocytes[J].Brit J of Pharmacol,2011,162(2):441-451. [13] Li Y, Wang Q, Yao X, et al.Induction of CYP3A4 and MDR1 gene expression by baicalin, baicalein, chlorogenic acid, and ginsenoside Rf through constitutive androstane receptor- and pregnane X receptor-mediated pathways[J].Eur J Pharmacol,2010,640(1/2/3):46-54. [14] Liu CL, Lim YP, Hu ML.Fucoxanthin attenuates rifampin-induced cytochrome P450 3A4 (CYP3A4) and multiple drug resistance 1 (MDR1) gene expression through pregnane X receptor (PXR)-mediated pathways in human hepatoma HepG2 and colon adenocarcinoma LS174T cells [J].Mar Drugs,2012, 10(1):242-257. [15] Moriya N, Kataoka H, Fujino H, et al.Effect of lipopolysaccharide on the xenobiotic-induced expression and activity of hepatic cytochrome P450 in mice[J].Biol Pharm Bull, 2012,35(4):473-480. [16] Satoh T, Hosokawa H. Structure, function and regulation of carboxylesterases[J].Chem Biol Interact, 2006,162(3): 195-211. [17] Xu C, Wang X, Staudinger JL. Regulation of tissue-specific carboxylesterase expression by pregnane X receptor and constitutive androstane receptor[J]. Drug Metab Dispos, 2009,37(7): 1539-1547. [18] Shi D, Yang J, Yang D, et al.Dexamethasone suppresses the expression of multiple rat carboxylesterases through transcriptional repression: evidence for an involvement of the glucocorticoid receptor[J]. Toxicology, 2008,254(1/2):97-105. [19] 张利,周宏灏.孤儿核受体对尿苷二磷酸葡萄糖醛酸转移酶基因转录调节的研究进展[J].中国临床药理学与治疗学, 2007, 12(9): 974-979. [20] Tukey RH, Strassburg CP. Human UDP-glucuronosyltransferases: metabolism,expression, and disease[J]. Annu Rev Pharmacol Toxicol, 2000,40: 581-616. [21] Sugatani J, Uchida T, Kurosawa M, et al. Regulation of PXR function and UGT1A1 gene expression by post-translational modification of PXR protein [J]. Drug Metab Dispos,2012,40(10) :2031-2040. [22] Xie W, Yeuh MF, Radominska-Pandya A, et al. Control of steroid, heme, and carcinogen metabolism by nuclear pregnane X receptor and constitutive androstane receptor[J]. Proc Natl Acad Sci USA, 2003, 100(7):4150-4155. [23] Duanmu Z, Locke D, Smigelski J, et al. Effects of dexamethasone on aryl (SULT1A1)- and hydroxysteroid (SULT2A1)-sulfotransferase gene expression in primary cultured human hepatocytes[J]. Drug Metab Dispos, 2002,30(9): 997-1004. [24] Sonoda J, Xie W, Rosenfeld JM, et al. Regulation of a xenobiotic sulfonation cascade by nuclear pregnane X receptor(PXR)[J]. Proc Natl Acad Sci USA, 2002,99(21): 13801-13806. [25] Zhang B,Cheng Q, Ou Z. Pregnane X receptor as a therapeutic target to inhibit androgen activity[J].Gen Endocrinol,2010, 151(12):5721-5729. [26] Falkner KC, Pinaire JA, Xiao GH, et al. Regulation of the rat glutathione S-transferase A2 gene by glucocorticoids: involvement of both the glucocorticoid and pregnane X receptors[J]. Mol Pharmacol, 2001, 60(3): 611-619. [27] El-Sayed WM. Effect of pregnane X receptor (PXR) prototype agonists on chemoprotective and drug metabolizing enzymes in mice[J]. Eur J Pharmacol, 2011,660(2/3): 291-297. [28] Cui JY, Choudhuri S, Knight TR, et al. Genetic and Epigenetic Regulation and Expression Signatures of Glutathione S-Transferases in Developing Mouse Liver[J]. Toxicol Sci, 2010,116(1):32-43. [29] Naspinski C, Gu X, Zhou GD,et al. Pregnane X Receptor Protects HepG2 Cells from BaP-Induced DNA Damage[J].Toxicol Sci, 2008, 104(1): 67-73. [30] 许茜,许景峰.药物转运体介导的肿瘤细胞多药耐药研究进展[J].中华临床医师杂志,2010,4(9):1643-1645. [31] 张伟,贺毅憬,周宏灏.有机阴离子转运多肽1B1的遗传药理学进展[J]. 中国临床药理学与治疗学,2008,13(7):721-729. [32] Shugarts S, Benet LZ.The Role of transporters in the pharmacokinetics of orally administered drugs[J].Pharm Res, 2009, 26(9):2039-2054. [33] Gui C, Miao Y, Thompson L,et al. Effect of pregnane X receptor ligands on transport mediated by human OATP1B1 and OATP1B3[J].Eur J Pharmacol, 2008,584(1): 57-65. [34] Schwabedissen HE, KimHepatic RB. OATP1B transporters and nuclear receptors PXR and CAR: Interplay, regulation of drug disposition genes, and single nucleotide polymorphisms[J].Mol Pharmacol, 2009,6(6): 1644-1661. [35] Geick A, Eichelbaum M, Burk O. Nuclear receptor response elements mediate induction of intestinal MDR1 by rifampin[J]. J Biol Chem,2001, 276(18): 14581-14587. [36] Kotaa BP, Trana VH, Allen J,et al. Characterization of PXR mediated P-glycoprotein regulation in intestinal LS174T cells[J].Pharmacol Res, 2010,62(5): 426-431. |