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Volumn 65, Issue 2, 2012, Pages 64-74

Determining P-glycoprotein-drug interactions: Evaluation of reconstituted P-glycoprotein in a liposomal system and LLC-MDR1 polarized cell monolayers

Author keywords

ABCB1; Drug transport; Fluorescence; Inhibitor; Liposome; Polarized cell monolayer; Reconstitution

Indexed keywords

ADENOSINE TRIPHOSPHATE; AMIODARONE; CAPTOPRIL; CARVEDILOL; CYCLOSPORIN A; DIGOXIN; ELACRIDAR; GLYCOPROTEIN P; INDINAVIR; ISRADIPINE; IVERMECTIN; KETOCONAZOLE; LIPOSOME; MIBEFRADIL; NELFINAVIR; NICARDIPINE; NIFEDIPINE; NITRENDIPINE; PACLITAXEL; PROGESTERONE; QUINIDINE; RESERPINE; RITONAVIR; TAMOXIFEN; TARIQUIDAR; TELMISARTAN; TROGLITAZONE; UNINDEXED DRUG; VALSPODAR; VERAPAMIL;

EID: 84859435363     PISSN: 10568719     EISSN: 1873488X     Source Type: Journal    
DOI: 10.1016/j.vascn.2012.02.002     Document Type: Article
Times cited : (28)

References (38)
  • 1
    • 38749113348 scopus 로고    scopus 로고
    • Kinetic identification of membrane transporters that assist P-glycoprotein-mediated transport of digoxin and loperamide through a confluent monolayer of MDCKII-hMDR1 cells
    • Acharya P., O'Connor M.P., Polli J.W., Ayrton A., Ellens H., Bentz J. Kinetic identification of membrane transporters that assist P-glycoprotein-mediated transport of digoxin and loperamide through a confluent monolayer of MDCKII-hMDR1 cells. Drug Metabolism and Disposition: The Biological Fate of Chemicals 2008, 36:452-460.
    • (2008) Drug Metabolism and Disposition: The Biological Fate of Chemicals , vol.36 , pp. 452-460
    • Acharya, P.1    O'Connor, M.P.2    Polli, J.W.3    Ayrton, A.4    Ellens, H.5    Bentz, J.6
  • 2
    • 63449139456 scopus 로고    scopus 로고
    • Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding
    • Aller S.G., Yu J., Ward A., Weng Y., Chittaboina S., Zhuo R., et al. Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding. Science 2009, 323:1718-1722.
    • (2009) Science , vol.323 , pp. 1718-1722
    • Aller, S.G.1    Yu, J.2    Ward, A.3    Weng, Y.4    Chittaboina, S.5    Zhuo, R.6
  • 3
    • 33745653136 scopus 로고    scopus 로고
    • Development and characterization of LLC-PK1 cells containing Sprague-Dawley rat Abcb1a (Mdr1a): comparison of rat P-glycoprotein transport to human and mouse
    • Booth-Genthe C.L., Louie S.W., Carlini E.J., Li B., Leake B.F., Eisenhandler R., et al. Development and characterization of LLC-PK1 cells containing Sprague-Dawley rat Abcb1a (Mdr1a): comparison of rat P-glycoprotein transport to human and mouse. Journal of Pharmacological and Toxicological Methods 2006, 54:78-89.
    • (2006) Journal of Pharmacological and Toxicological Methods , vol.54 , pp. 78-89
    • Booth-Genthe, C.L.1    Louie, S.W.2    Carlini, E.J.3    Li, B.4    Leake, B.F.5    Eisenhandler, R.6
  • 4
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 1976, 72:248-254.
    • (1976) Analytical Biochemistry , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 5
    • 31844448665 scopus 로고    scopus 로고
    • The translocation mechanism of P-glycoprotein
    • Callaghan R., Ford R.C., Kerr I.D. The translocation mechanism of P-glycoprotein. FEBS Letters 2006, 580:1056-1063.
    • (2006) FEBS Letters , vol.580 , pp. 1056-1063
    • Callaghan, R.1    Ford, R.C.2    Kerr, I.D.3
  • 6
    • 0023874147 scopus 로고
    • A method for the determination of inorganic phosphate in the presence of labile organic phosphate and high concentrations of protein: application to lens ATPases
    • Chifflet S., Torriglia A., Chiesa R., Tolosa S. A method for the determination of inorganic phosphate in the presence of labile organic phosphate and high concentrations of protein: application to lens ATPases. Analytical Biochemistry 1988, 168:1-4.
    • (1988) Analytical Biochemistry , vol.168 , pp. 1-4
    • Chifflet, S.1    Torriglia, A.2    Chiesa, R.3    Tolosa, S.4
  • 7
    • 84859430407 scopus 로고    scopus 로고
    • Determination of the inhibitory potencies of p-glycoprotein inhibitors by transcellular permeability of Caco-2 cells
    • Dickens D., Owen A., Alfirevic A., Pirmohamed M. Determination of the inhibitory potencies of p-glycoprotein inhibitors by transcellular permeability of Caco-2 cells. Proceedings of the British Pharmacological Society 2009, http://pa2online.org/abstracts/Vol7Issue4abst092P.pdf.
    • (2009) Proceedings of the British Pharmacological Society
    • Dickens, D.1    Owen, A.2    Alfirevic, A.3    Pirmohamed, M.4
  • 8
    • 33947401100 scopus 로고    scopus 로고
    • P-glycoprotein (ABCB1) interacts directly with lipid-based anti-cancer drugs and platelet-activating factors
    • Eckford P.D., Sharom F.J. P-glycoprotein (ABCB1) interacts directly with lipid-based anti-cancer drugs and platelet-activating factors. Biochemistry and Cell Biology 2006, 84:1022-1033.
    • (2006) Biochemistry and Cell Biology , vol.84 , pp. 1022-1033
    • Eckford, P.D.1    Sharom, F.J.2
  • 9
    • 67650685020 scopus 로고    scopus 로고
    • ABC efflux pump-based resistance to chemotherapy drugs
    • Eckford P.D., Sharom F.J. ABC efflux pump-based resistance to chemotherapy drugs. Chemical Reviews 2009, 109:2989-3011.
    • (2009) Chemical Reviews , vol.109 , pp. 2989-3011
    • Eckford, P.D.1    Sharom, F.J.2
  • 11
    • 58549088199 scopus 로고    scopus 로고
    • Drug-drug interactions mediated through P-glycoprotein: clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug
    • Fenner K.S., Troutman M.D., Kempshall S., Cook J.A., Ware J.A., Smith D.A., et al. Drug-drug interactions mediated through P-glycoprotein: clinical relevance and in vitro-in vivo correlation using digoxin as a probe drug. Clinical Pharmacology and Therapeutics 2009, 85:173-181.
    • (2009) Clinical Pharmacology and Therapeutics , vol.85 , pp. 173-181
    • Fenner, K.S.1    Troutman, M.D.2    Kempshall, S.3    Cook, J.A.4    Ware, J.A.5    Smith, D.A.6
  • 13
    • 84859429838 scopus 로고    scopus 로고
    • New tariquidar-like ABCB1 modulators in cancer chemotherapy: Preclinical pharmacokinetic/pharmacodynamic investigations and computational studies. Ph.D. Dissertation: Universität Regensburg.
    • Höcheri, P. (2010). New tariquidar-like ABCB1 modulators in cancer chemotherapy: Preclinical pharmacokinetic/pharmacodynamic investigations and computational studies. Ph.D. Dissertation: Universität Regensburg.
    • (2010)
    • Höcheri, P.1
  • 14
    • 62149110091 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators
    • Klinkhammer W., Muller H., Globisch C., Pajeva I.K., Wiese M. Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators. Bioorganic and Medicinal Chemistry 2009, 17:2524-2535.
    • (2009) Bioorganic and Medicinal Chemistry , vol.17 , pp. 2524-2535
    • Klinkhammer, W.1    Muller, H.2    Globisch, C.3    Pajeva, I.K.4    Wiese, M.5
  • 16
    • 17544368685 scopus 로고    scopus 로고
    • Multidrug resistance proteins: role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense
    • Leslie E.M., Deeley R.G., Cole S.P.C. Multidrug resistance proteins: role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense. Toxicology and Applied Pharmacology 2005, 204:216-237.
    • (2005) Toxicology and Applied Pharmacology , vol.204 , pp. 216-237
    • Leslie, E.M.1    Deeley, R.G.2    Cole, S.P.C.3
  • 17
    • 0029840320 scopus 로고    scopus 로고
    • Site-directed fluorescence labeling of P-glycoprotein on cysteine residues in the nucleotide binding domains
    • Liu R., Sharom F.J. Site-directed fluorescence labeling of P-glycoprotein on cysteine residues in the nucleotide binding domains. Biochemistry 1996, 35:11865-11873.
    • (1996) Biochemistry , vol.35 , pp. 11865-11873
    • Liu, R.1    Sharom, F.J.2
  • 18
    • 0034610402 scopus 로고    scopus 로고
    • Intrinsic fluorescence of the P-glycoprotein multidrug transporter: sensitivity of tryptophan residues to binding of drugs and nucleotides
    • Liu R., Siemiarczuk A., Sharom F.J. Intrinsic fluorescence of the P-glycoprotein multidrug transporter: sensitivity of tryptophan residues to binding of drugs and nucleotides. Biochemistry 2000, 39:14927-14938.
    • (2000) Biochemistry , vol.39 , pp. 14927-14938
    • Liu, R.1    Siemiarczuk, A.2    Sharom, F.J.3
  • 19
    • 0141994817 scopus 로고    scopus 로고
    • Simultaneous binding of two different drugs in the binding pocket of the human multidrug resistance P-glycoprotein
    • Loo T.W., Bartlett M.C., Clarke D.M. Simultaneous binding of two different drugs in the binding pocket of the human multidrug resistance P-glycoprotein. Journal of Biological Chemistry 2003, 278:39706-39710.
    • (2003) Journal of Biological Chemistry , vol.278 , pp. 39706-39710
    • Loo, T.W.1    Bartlett, M.C.2    Clarke, D.M.3
  • 20
    • 0034818922 scopus 로고    scopus 로고
    • Drug transport by reconstituted P-glycoprotein in proteoliposomes. Effect of substrates and modulators, and dependence on bilayer phase state
    • Lu P., Liu R., Sharom F.J. Drug transport by reconstituted P-glycoprotein in proteoliposomes. Effect of substrates and modulators, and dependence on bilayer phase state. European Journal of Biochemistry 2001, 268:1687-1697.
    • (2001) European Journal of Biochemistry , vol.268 , pp. 1687-1697
    • Lu, P.1    Liu, R.2    Sharom, F.J.3
  • 21
    • 27144451192 scopus 로고    scopus 로고
    • Interaction of LDS-751 and rhodamine 123 with P-glycoprotein: evidence for simultaneous binding of both drugs
    • Lugo M.R., Sharom F.J. Interaction of LDS-751 and rhodamine 123 with P-glycoprotein: evidence for simultaneous binding of both drugs. Biochemistry 2005, 44:14020-14029.
    • (2005) Biochemistry , vol.44 , pp. 14020-14029
    • Lugo, M.R.1    Sharom, F.J.2
  • 23
    • 79951973326 scopus 로고    scopus 로고
    • Molecular dissection of dual pseudosymmetric solute translocation pathways in human P-glycoprotein
    • Parveen Z., Stockner T., Bentele C., Pferschy S., Kraupp M., Freissmuth M., et al. Molecular dissection of dual pseudosymmetric solute translocation pathways in human P-glycoprotein. Molecular Pharmacology 2011, 79:443-452.
    • (2011) Molecular Pharmacology , vol.79 , pp. 443-452
    • Parveen, Z.1    Stockner, T.2    Bentele, C.3    Pferschy, S.4    Kraupp, M.5    Freissmuth, M.6
  • 26
    • 78951479924 scopus 로고    scopus 로고
    • Rifampin's acute inhibitory and chronic inductive drug interactions: experimental and model-based approaches to drug-drug interaction trial design
    • Reitman M.L., Chu X., Cai X., Yabut J., Venkatasubramanian R., Zajic S., et al. Rifampin's acute inhibitory and chronic inductive drug interactions: experimental and model-based approaches to drug-drug interaction trial design. Clinical Pharmacology and Therapeutics 2011, 89:234-242.
    • (2011) Clinical Pharmacology and Therapeutics , vol.89 , pp. 234-242
    • Reitman, M.L.1    Chu, X.2    Cai, X.3    Yabut, J.4    Venkatasubramanian, R.5    Zajic, S.6
  • 27
    • 0030757153 scopus 로고    scopus 로고
    • Interaction of P-glycoprotein with defined phospholipid bilayers: a differential scanning calorimetric study
    • Romsicki Y., Sharom F.J. Interaction of P-glycoprotein with defined phospholipid bilayers: a differential scanning calorimetric study. Biochemistry 1997, 36:9807-9815.
    • (1997) Biochemistry , vol.36 , pp. 9807-9815
    • Romsicki, Y.1    Sharom, F.J.2
  • 28
    • 0035849506 scopus 로고    scopus 로고
    • Phospholipid flippase activity of the reconstituted P-glycoprotein multidrug transporter
    • Romsicki Y., Sharom F.J. Phospholipid flippase activity of the reconstituted P-glycoprotein multidrug transporter. Biochemistry 2001, 40:6937-6947.
    • (2001) Biochemistry , vol.40 , pp. 6937-6947
    • Romsicki, Y.1    Sharom, F.J.2
  • 30
    • 0030782511 scopus 로고    scopus 로고
    • Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities
    • Shapiro A.B., Ling V. Positively cooperative sites for drug transport by P-glycoprotein with distinct drug specificities. European Journal of Biochemistry 1997, 250:130-137.
    • (1997) European Journal of Biochemistry , vol.250 , pp. 130-137
    • Shapiro, A.B.1    Ling, V.2
  • 31
    • 0031455482 scopus 로고    scopus 로고
    • The P-glycoprotein efflux pump: how does it transport drugs?
    • Sharom F.J. The P-glycoprotein efflux pump: how does it transport drugs?. Journal of Membrane Biology 1997, 160:161-175.
    • (1997) Journal of Membrane Biology , vol.160 , pp. 161-175
    • Sharom, F.J.1
  • 32
    • 40949121607 scopus 로고    scopus 로고
    • ABC multidrug transporters: structure, function and role in chemoresistance
    • Sharom F.J. ABC multidrug transporters: structure, function and role in chemoresistance. Pharmacogenomics 2008, 9:105-127.
    • (2008) Pharmacogenomics , vol.9 , pp. 105-127
    • Sharom, F.J.1
  • 35
    • 0030769833 scopus 로고    scopus 로고
    • Pharmacological characterization of LY335979: a potent cyclopropyldibenzosuberane modulator of P-glycoprotein
    • Starling J.J., Shepard R.L., Cao J., Law K.L., Norman B.H., Kroin J.S., et al. Pharmacological characterization of LY335979: a potent cyclopropyldibenzosuberane modulator of P-glycoprotein. Advances in Enzyme Regulation 1997, 37:335-347.
    • (1997) Advances in Enzyme Regulation , vol.37 , pp. 335-347
    • Starling, J.J.1    Shepard, R.L.2    Cao, J.3    Law, K.L.4    Norman, B.H.5    Kroin, J.S.6
  • 36
    • 33846448814 scopus 로고    scopus 로고
    • U.S.Department of Health and Human Services Food and Drug Administration (FDA), [Electronic version], Available from:
    • U.S.Department of Health and Human Services Food and Drug Administration (FDA) Guidance for industry: Drug interaction studies - study design, data analysis, and implications for dosing and labelling 2006, [Electronic version], Available from:. http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm072101.pdf.
    • (2006) Guidance for industry: Drug interaction studies - study design, data analysis, and implications for dosing and labelling
  • 37
    • 31044448805 scopus 로고    scopus 로고
    • Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: f2 values
    • Weiss J., Haefeli W.E. Evaluation of inhibitory potencies for compounds inhibiting P-glycoprotein but without maximum effects: f2 values. Drug Metabolism and Disposition: The Biological Fate of Chemicals 2006, 34:203-207.
    • (2006) Drug Metabolism and Disposition: The Biological Fate of Chemicals , vol.34 , pp. 203-207
    • Weiss, J.1    Haefeli, W.E.2
  • 38
    • 79958829984 scopus 로고    scopus 로고
    • Substrate- and species-dependent inhibition of P-glycoprotein-mediated transport: implications for predicting in vivo drug interactions
    • Zolnerciks J.K., Booth-Genthe C.L., Gupta A., Harris J., Unadkat J.D. Substrate- and species-dependent inhibition of P-glycoprotein-mediated transport: implications for predicting in vivo drug interactions. Journal of Pharmaceutical Sciences 2011, 100:3055-3061.
    • (2011) Journal of Pharmaceutical Sciences , vol.100 , pp. 3055-3061
    • Zolnerciks, J.K.1    Booth-Genthe, C.L.2    Gupta, A.3    Harris, J.4    Unadkat, J.D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.