[1]Smolen JS, Aletaha D, Mcinnes IB. Rheumatoid arthritis[J]. Lancet, 2016, 388(10055): 2023.
[2]Okada M, Fujii H, Suga Y, et al. Drug interaction between methotrexate and salazosulfapyridine in Japanese patients with rheumatoid arthritis[J]. J Pharm Health Care Sci, 2017, 3(1): 7.
[3]Lee SW, Kim JH, Park MC, et al. Alleviation of rheumatoid arthritis by cell-transducible methotrexate upon transcutaneous delivery[J]. Biomaterials, 2012, 33(5): 1563-1572.
[4]Pavkova GM, Lipkova J, Pavek N, et al. RANTES, MCP-1 chemokines and factors describing rheumatoid arthritis[J]. Mol Immunol, 2012, 52(3-4): 273-278.
[5]Kokkonen H, Sderstrm I, Rocklv J, et al. Up-regulation of cytokines and chemokines predates the onset of rheumatoid arthritis[J]. Arthritis & Rheum, 2010, 62(2): 383-391.
[6]Morgan ET. Impact of infectious and inflammatory disease on cytochrome P450-mediated drug metabolism and pharmacokinetics[J]. Clin Pharmacol Ther, 2009, 85(4): 434-438.
[7]Markova S, Nakamura T, Sakaeda T, et al. Genotype-dependent down-regulation of gene expression and function of MDR1 in human peripheral blood mononuclear cells under acute inflammation[J]. Drug Metab Pharmacokinet, 2006, 21(3): 194-200.
[8]Shitara Y, Horie T, Sugiyama Y. Transporters as a determinant of drug clearance and tissue distribution[J]. Eur J Pharm Sci, 2006, 27(5): 425-446.
[9]Morris ME, Rodriguez-Cruz V, Felmlee MA. SLC and ABC transporters: expression, localization, and species differences at the blood-brain and the blood-cerebrospinal fluid barriers[J]. AAPS J, 2017, 19(5):1317-1331
[10]Koepsell H, Endou H. The SLC22 drug transporter family[J]. Pflügers Archiv - European Journal of Physiology, 2004, 447(5): 666-676.
[11]李聃, 盛莉, 李燕. 药物转运体的研究方法[J]. 药学学报, 2014, 49(7): 963-970.
[12]马莉, 饶志, 武新安. 药物转运体在药物排泄中的作用[J]. 中国药学杂志, 2013, 48(8): 582-586.
[13]Mizuno N, Niwa T, Yotsumoto Y, et al. Impact of drug transporter studies on drug discovery and development[J]. Pharmacol Rev, 2003, 55(3): 425-461.
[14]Koepsell H, Lips K, Volk C. Polyspecific organic cation transporters: structure, function, physiological roles, and biopharmaceutical implications[J]. Pharm Res, 2007, 24(7): 1227-1251.
[15]Sai Y. Biochemical and molecular pharmacological aspects of transporters as determinants of drug disposition[J]. Drug Metab Pharmacokinet, 2005, 20(2): 91-99.
[16]Tyden E, Bjornstrom H, Tjalve H, et al. Expression and localization of BCRP, MRP1 and MRP2 in intestines, liver and kidney in horse[J]. J Vet Pharmacol Ther, 2010, 33(4): 332-340.
[17]Grube M, Kck K, Karner S, et al. Modification of OATP2B1-mediated transport by steroid hormones[J]. Molecular Pharmacology, 2006, 70(5): 1735-1741.
[18]Ronaldson PT, Ashraf T, Bendayan R. Regulation of multidrug resistance protein 1 by tumor necrosis factor alpha in cultured glial cells: involvement of nuclear factor-kappaB and c-Jun N-terminal kinase signaling pathways[J]. Mol Pharmacol, 2010, 77(4): 644-659.
[19]Qiang F, Lee B J, Lee W, et al. Pharmacokinetic drug interaction between fexofenadine and fluvastatin mediated by organic anion-transporting polypeptides in rats[J]. Eur J Pharm Sci, 2009, 37(3-4): 413-417.
[20]Morgan ET, Lee CM, Nyagode BA. Regulation of drug metabolizing enzymes and transporters in infection, inflammation, and cancer[M]. John Wiley & Sons, Inc., 2008: 123-149.
[21]Harvey RD, Morgan ET. Cancer, inflammation, and therapy: effects on cytochrome p450-mediated drug metabolism and implications for novel immunotherapeutic agents[J]. Clin Pharmacol Ther, 2014, 96(4): 449-457.
[22]Le Vee M, Jouan E, Stieger B, et al. Regulation of drug transporter expression by oncostatin M in human hepatocytes[J]. Biochem Pharmacol, 2011, 82(3): 304-311.
[23]Geier A, Wagner M, Dietrich CG, et al. Principles of hepatic organic anion transporter regulation during cholestasis, inflammation and liver regeneration[J]. Biochim Biophys Acta, 2007, 1773(3): 283-308.
[24]Tazoe Y, Hayashi H, Tsuboi S, et al. Reduced folate carrier 1 gene expression levels are correlated with methotrexate efficacy in Japanese patients with rheumatoid arthritis[J]. Drug Metab Pharmacokinet, 2015, 30(3): 227-230.
[25]Lin L, Yee SW, Kim RB, et al. SLC transporters as therapeutic targets: emerging opportunities[J]. Nat Rev Drug Discov, 2015, 14(8):543-560.
[26]Feldmann M, Maini SR. Role of cytokines in rheumatoid arthritis: an education in pathophysiology and therapeutics[J]. Immunol Rev, 2008, 223: 7-19.
[27]Shitara Y, Horie T, Sugiyama Y. Transporters as a determinant of drug clearance and tissue distribution[J]. Eur J Pharm Sci, 2006, 27(5): 425-446.
[28]Fisher CD, Lickteig AJ, Augustine LM, et al. Experimental non-alcoholic fatty liver disease results in decreased hepatic uptake transporter expression and function in rats[J]. Eur J Pharmcol, 2009, 613(1-3): 119-127.
[29]Renton KW. Cytochrome P450 regulation and drug biotransformation during inflammation and infection[J]. Curr Drug Metab, 2004, 5(3): 235-243.
[30]Maeda T, Hirayama M, Kobayashi D, et al. Mechanism of the regulation of organic cation/carnitine transporter 1 (SLC22A4) by rheumatoid arthritis-associated transcriptional factor RUNX1 and inflammatory cytokines[J]. Drug MetabDispos, 2007, 35(3): 394-401.
[31]Uno S, Uraki M, Ito A, et al. Changes in mRNA expression of ABC and SLC transporters in liver and intestines of the adjuvant-induced arthritis rat[J]. Biopharm Drug Dispos, 2009, 30(1): 49.
[32]Han HK. Role of transporters in drug interactions[J]. Archiv Pharmacal Res, 2011, 34(11): 501-517.
[33]Momper JD, Tsunoda SM, Ma JD. Evaluation of proposed in vivo probe substrates and inhibitors for phenotyping transporter activity in humans[J]. J Clin Pharmacol, 2016, 56 Suppl 7(S7): S82-98.
[34]Murakami T, Mori N. Involvement of multiple transporters-mediated transports in mizoribine and methotrexate pharmacokinetics[J]. Pharmaceuticals (Basel), 2012, 5(8): 802-836.
[35]Feng Y, Wang C, Liu Q, et al. Bezafibrate-mizoribine interaction: Involvement of organic anion transporters OAT1 and OAT3 in rats[J]. Eur J Pharm Sci, 2016, 81: 119-128.
[36]Ren TL, Han ZJ, Yang CJ, et al. Association of SLC22A4 gene polymorphism with rheumatoid arthritis in the Chinese population[J]. J Biochem Mol Toxicol, 2014, 28(5): 206-210.
[37]Lima A, Bernardes M, Azevedo R, et al. SLC19A1, SLC46A1 and SLCO1B1 polymorphisms as predictors of methotrexate-related toxicity in Portuguese rheumatoid arthritis patients[J]. Toxicol Sci, 2014, 142(1): 196-209.
[38]Hediger MA, Clémenon B, Burrier RE, et al. The ABCs of membrane transporters in health and disease (SLC series): Introduction[J]. Mol Aspects Med, 2013, 34(2-3): 95-107.
[39]Neumann J, Rose-Sperling D, Hellmich UA. Diverse relations between ABC transporters and lipids: An overview[J]. Biochim Biophys Acta, 2017, 1859(4): 605-618.
[40]Doerks T, Copley RR, Schultz J, et al. Systematic identification of novel protein domain families associated with nuclear functions[J]. Genome Res, 2002, 12(1): 47-56.
[41] Kawase A, Norikane S, Okada A, et al. Distinct alterations in ATP-Binding cassette transporter expression in liver, kidney, small intestine, and brain in adjuvant-induced arthritic rats[J]. J Pharm Sci, 2014, 103(8): 2556-2264.
[42]Kawase A, Yoshida I, Tsunokuni Y, et al. Decreased PXR and CAR inhibit transporter and CYP mRNA Levels in the liver and intestine of mice with collagen-induced arthritis[J]. Xenobiotica, 2007, 37(4): 366-374.
[43]Uno S, Kawase A, Tsuji A, et al. Decreased intestinal CYP3A and P-glycoprotein activities in rats with adjuvant arthritis[J]. Drug Metab Pharmacokinet, 2007, 22(4): 313-321.
[44]Marquez B, Van BF. ABC multidrug transporters: target for modulation of drug pharmacokinetics and drug-drug interactions[J]. Curr Drug Targets, 2011, 12(5): 600-620.
[45]Tsujimura S, Saito K, Nawata M, et al. Overcoming drug resistance induced by P-glycoprotein on lymphocytes in patients with refractory rheumatoid arthritis[J]. Ann Rheum Dis, 2008, 67(3): 380-388.
[46]Schwarz UI, Meyer zu Schwabedissen HE, Tirona RG, et al. Identification of novel functional organic anion-transporting polypeptide 1B3 polymorphisms and assessment of substrate specificity[J]. Pharmacogenet Genomics, 2011, 21(3): 103-114.
[47]García-Carrasco M, Mendoza-Pinto C, Macias DS, et al. P-glycoprotein in autoimmune rheumatic diseases[J]. Autoimmun Rev, 2015, 14(7): 594-600.
[48]Lima A, Bernardes M, Azevedo R, et al. Pharmacogenomics of methotrexate membrane transport pathway: can clinical response to methotrexate in rheumatoid arthritis be predicted[J]? Int J Mol Sci, 2015, 16(6): 13760-13780.
[49]Mazerska Z, Mroz A, Pawlowska M, et al. The role of glucuronidation in drug resistance[J]. Pharmacol Ther, 2016, 159: 35-55.
[50]Agarwal V, Mittal SK, Misra R. Expression of multidrug resistance-1 protein correlates with disease activity rather than the refractoriness to methotrexate therapy in rheumatoid arthritis[J]. Clin Rheumatol, 2009, 28(4): 427-433.
[51]Rodriguez JM, Monsalves-Alvarez M, Henriquez S, et al. Glucocorticoid resistance in chronic diseases[J]. Steroids, 2016, 115: 182-192.
[52]Liu YM, Chen JW, Chen LX, et al. Overexpression of P-glycoprotein on fibroblast-like synoviocytes in refractory rheumatoid arthritis patients: a potential mechanism for multidrug resistance in rheumatoid arthritis treatment[J]. Genet Mol Res, 2016, 15(2).
[53]Marki-Zay J, Tauberne Jakab K, Szeremy P, et al. MDR-ABC transporters: biomarkers in rheumatoid arthritis[J]. Clin Exp Rheumatol, 2013, 31(5): 779-787.
[54]Chen QX, Hu HH, Zhou Q, et al. An overview of ABC and SLC drug transporter gene regulation[J]. Curr Drug Metab, 2013, 14(2): 253-264.
[55]Sissung TM, Troutman SM, Campbell TJ, et al. Transporter pharmacogenetics: transporter polymorphisms affect normal physiology, diseases, and pharmacotherapy[J]. Discov Med, 2012, 13(68): 19-34. |