Citation: | XU Yue, CHEN Genfu, XIONG Tao, PENG Ying, RUAN Tingting, WANG Guangji, SUN Jianguo. Research progress of P-glycoprotein induction[J]. Journal of China Pharmaceutical University, 2018, 49(1): 26-33. DOI: 10.11665/j.issn.1000-5048.20180104 |
[1] |
Silva R,Vilas-Boas V,Carmo H,et al.Modulation of P-glycoprotein efflux pump:induction and activation as a therapeutic strategy[J].Pharmacol Ther,2015,149:1-123.
|
[2] |
Schinkel AH. P-Glycoprotein, a gatekeeper in the blood-brain barrier[J].Adv Drug Deliv Rev,1999,36(2/3):179-186.
|
[3] |
Zhuo W,Hu L,Lv J,et al.Role of pregnane X receptor in chemotherapeutic treatment[J].Cancer Chemother Pharmacol,2014,74(2):217-227.
|
[4] |
Hennessy M.A primer on themechanics of P-glycoprotein the multidrug transporter[J].Pharmacol Res,2007,55(1):1-15.
|
[5] |
Weiss J,Theile D,Spalwisz A,et al.Influence of sildenafil and tadalafil on the enzyme- and transporter-inducing effects of bosentan and ambrisentan in LS180 cells[J].Biochem Pharmacol,2013,85(2):265-273.
|
[6] |
Naruhashi K, Kurahashi Y, Fujita Y, et al. Comparison of the expression and function of ATP binding cassette transporters in Caco-2 and T84 cells on stimulation by selected endogenous compounds and xenobiotics[J].Drug Metab Pharmacok,2011,26(2):145-153.
|
[7] |
Manceau S,Giraud C,Declèves X,et al.ABC drug transporter and nuclear receptor expression in human cytotrophoblasts:influence of spontaneous syncytialization and induction by glucocorticoids[J].Placenta,2012,33(11):927-932.
|
[8] |
Haslam IS,Jones K,Coleman T,et al.Induction of P-glycoprotein expression and function in human intestinal epithelial cells(T84)[J].Biochem Pharmacol,2008,76(7):850-861.
|
[9] |
Abuznait AH,Kaddoumi A.Role of ABC transporters in the pathogenesis of Alzheimer′s disease[J].ACS Chem Neurosci,2012,3(11):820-831.
|
[10] |
He J, Tang J, Yang WH, et al. P-gp induction by curcumin:an effective antidotal pathway[J].J Bioequiv Bioavail, 2013,5(6):236-241.
|
[11] |
Sérée E,Villard PH,Hevér A.Modulation of MDR1 and CYP3A expression by dexamethasone:evidence for an inverse regulation in adrenals[J].Biochem Biophys Res Commun,1998,252(2):392-395.
|
[12] |
Wen T,Liu YC,Yang HW,et al.Effect of 21-day exposure of phenobarbital,carbamazepine and phenytoin on P-glycoprotein expression and activity in the rat brain[J].J Neurol Sci,2008,271(1):99-106.
|
[13] |
Foti RS.“Target-Site” drug metabolism and transport[J].Drug Metab Dispos,2015,43(8):1156-1168.
|
[14] |
Müller F,Fromm MF.Transporter-mediated drug-drug interactions[J].Pharmacogenomics,2011,12(7):7-21.
|
[15] |
Synold TW,Dussault I,Forman BM.The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux[J].Nat Med,2001,7(5):584-590.
|
[16] |
Liu L,Collier AC,Link JM,et al.Modulation of P-glycoprotein at the human blood-brain barrier by quinidine or rifampin treatment:a positron emission tomography imaging study[J].Drug Metab Dispos,2015,43(11):1795-1804.
|
[17] |
Sager JE,Yu J,Ragueneau-Majlessi I,et al.Physiologically based pharmacokinetic(PBPK)modeling and simulation approaches:a systematic review of published models,applications,and model verification[J].Drug Metab Dispos,2015,43(11):1823-1837.
|
[18] |
Silva R,Carmo H,Dinis-Oliveira R,et al.In vitro study of P-glycoprotein induction as an antidotal pathway to prevent cytotoxicity in Caco-2 cells[J].Arch Toxicol,2011,85(4):315-326.
|
[19] |
Silva R,Carmo H,Vilas-Boas V,et al.Colchicine effect on P-glycoprotein expression and activity:in silico and in vitro studies[J].Chem Biol Interact,2014,218:50-62.
|
[20] |
Zerin T,Kim YS,Hong SY,et al.Protective effect of methylprednisolone on paraquat-induced A549 cell cytotoxicity via induction of efflux transporter,P-glycoprotein expression[J].Toxicol Lett,2012,208(2):101-107.
|
[21] |
Silva R.Pglycoprotein induction in Caco 2 cells by newly synthetized thioxanthones prevents paraquat cytotoxicity[J].Arch Toxicol 2015,89:18.
|
[22] |
Silva R,Sousa E,Carmo H,et al.Induction and activation of P-glycoprotein by dihydroxylated xanthones protect against the cytotoxicity of the P-glycoprotein substrate paraquat[J].Arch Toxicol,2014,88(4):937-951.
|
[23] |
Fenner KS,Troutman MD,Kempshall S,et al.Drug-drug interactions mediated through P-glycoprotein:clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug[J].Clin Pharmacol Ther,2009,85(2):173-181.
|
[24] |
Reitman ML,Chu X,Cai X,et al.Rifampin′s acute inhibitory and chronic inductive drug interactions:experimental and model-based approaches to drug-drug interaction trial design[J].Clin Pharmacol Ther,2011,89(2):234-242.
|
[25] |
Fromm MF.Importance of P-glycoprotein at blood-tissue barriers[J].Trends Pharmacol Sci,2004,25(8):423-429.
|
[26] |
Schwarz UI,Hanso H,Oertel R,et al.Induction of intestinal P-glycoprotein by St John′s wort reduces the oral bioavailability of talinolol[J].Clin Pharmacol Ther,2007,81(5):669-678.
|
[27] |
Liu J,Zhou F,Chen Q,et al.Chronic inflammation up-regulates P-gp in peripheral mononuclear blood cells via the STAT3/Nf-kappab pathway in 2,4,6-trinitrobenzene sulfonic acid-induced colitis mice[J].Sci Rep,2015,5:13558.
|
[28] |
Wen T,Liu YC,Yang HW,et al.Effect of 21-day exposure of phenobarbital,carbamazepine and phenytoin on P-glycoprotein expression and activity in the rat brain[J].J Neurol Sci,2008,270(1):99-106.
|
[29] |
Jin S,Yao D,Liu C,et al.Effect of chronic liver failure on the function and expression of P-GP and MRP2 in rat brain[J].J China Pharm Univ(中国药科大学学报),2012,43(1):64-69.
|
[30] |
Callaghan R,Luk F,Bebawy M.Inhibition of the multidrug resistance P-glycoprotein:time for a change of strategy[J]?Drug Metab Dispos,2014,42(4):623-631.
|
[31] |
Albermann N, Schmitz-Winnenthal FH, Z′graggen K, et al.Expression of the drug transporters MDR1/ABCB1,MRP1/ABCC1,MRP2/ABCC2,BCRP/ABCG2,and PXR in peripheral blood mononuclear cells and their relationship with the expression in intestine and liver[J].Biochem Pharmacol,2005,70(6):949-958.
|
[32] |
Narang VS,Fraga C,Kumar N.Dexamethasone increases expresb>(4):694-705.
|
[33] |
FDA. Guidance for industry, drug interaction studies-study design,data analysis,and implications for dosing and labeling recommendations[S].2012.J,Fuksa L,Brcakova E,et al.Up-regulation of renal Mdr1 and Mrp2 transporters during amiodarone pretreatment in rats[J].Pharmacol Res,2010,61(2):129-135.
|
[34] |
Safa AR.Identification and characterization of the binding sites of P-glycoprotein for multidrug resistance-related drugs and modulators[J].Curr Med Chem Anticancer Agents,2004,4(1):1-17.
|
[35] |
Aller SG, Yu J, Ward A.Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding[J].Science,2009,323(5922):1718-1722.
|
[36] |
Drescher S,Glaeser H,Mürdter T,et al.P-glycoprotein mediated intestinal and biliary digoxin transport in humans[J].Clin Pharmacol Ther,2003,73(3):223-231.
|
[37] |
Greiner B,Eichelbaum M,Fritz P,et al.The role of intestinal P-glycoprotein in the interaction of digoxin and rifampin[J].J Clin Invest,1999,104(2):147-153.
|
[38] |
Gurley BJ,Swain A,Williams DK,et al.Gauging the clinical significance of P-glycoprotein-mediated herb-drug interactions:comparative effects of St.John′s wort,Echinacea,clarithromycin,and rifampin on digoxin pharmacokinetics[J].Mol Nutr Food Res,2008,52(7):772-779.
|
[39] |
Montanari F,Ecker GF.Prediction of drug-ABC-transporter interaction-Recent advances and future challenges[J].Adv Drug Deliv Rev,2015,86:17-26.
|
[40] |
Westphal K,Weinbrenner A,Zschiesche M,et al.Induction of P-glycoprotein by rifampin increases intestinal secretion of talinolol in human beings:a new type of drug-drug interaction[J].Clin Pharmacol Ther,2000,68(4):345-355.
|
[41] |
Schwarz UI,Hanso H,Oertel R.Induction of intestinal P-glycoprotein by St John′s wort reduces the oral bioavailability of talinolol[J].Clin Pharmacol Ther,2007,81(5):669-678.
|
[42] |
Silva R.Induction and activation of P-glycoprotein by dihydroxylated xanthones protect against the cytotoxicity of the P-glycoprotein[J].Arch Toxicol,2014,88(4):15.
|
[43] |
Silva R,Palmeira A,Carmo H,et al.P-glycoprotein induction in Caco-2 cells by newly synthetized thioxanthones prevents paraquat cytotoxicity[J].Arch Toxicol,2015,89(10):1783-1800.
|
[44] |
Dinis-Oliveira RJ, Remiao F, Duarte JA, et al. P-glycoprotein induction:an antidotal pathway for paraquat-induced lung toxicity[J].Free Radic Biol Med,2006,41(8):1213-1224.
|
[45] |
Murgueitio MS,Bermudez M,Mortier J,et al.In silico virtual screening approaches for anti-viral drug discovery[J].Drug Discovery Today:Technologies,2012,9(3):e219-e225.
|
[46] |
Lu JR,Wang FX,Li YM,et al.Synthesis,biological evaluation and 2D-QSAR study of a series of isoflavone derivatives as modulators of multidrug resistance[J].J China Pharm Univ(中国药科大学学报),2013,44(4):296-302.
|
[47] |
Padala AK,Wani A,Vishwakarma RA,et al.Functional induction of P-glycoprotein efflux pump by phenyl benzenesulfonamides:synthesis and biological evaluation of T0901317 analogs[J].Eur J Med Chem,2016,122:744-755.
|
[48] |
Vilas-Boas V,Silva R,Palmeira A.Development of novel rifampicin-derived P-glycoprotein activators/inducers.Synthesis,in silico analysis and application in the RBE4 cell model,using paraquat as substrate[J].PLoS One,2013,8(8):e74425.
|
[49] |
Yamaura Y,Chapron BD,Wang Z,et al.Functional comparison of human colonic carcinoma cell lines and primary small intestinal epithelial cells for investigations of intestinal drug permeability and first-pass metabolism[J].Drug Metab Dispos,2016,44(3):329-335.
|
[50] |
Bourgine J,Billaut-Laden I,Happillon M,et al.Gene expression profiling of systems involved in the metabolism and the disposition of xenobiotics:comparison between human intestinal biopsy samples and colon cell lines[J].Drug Metab Dispos,2012,40(4):694-705.
|
[51] |
FDA. Guidance for industry, drug interaction studies-study design,data analysis,and implications for dosing and labeling recommendations[S].2012.
|
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