메뉴 건너뛰기




Volumn 40, Issue 4, 2012, Pages 655-661

Cyclosporine A- and tacrolimus-mediated inhibition of CYP3A4 and CYP3A5 in vitro

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOSPORIN A; CYTOCHROME P450 3A4; CYTOCHROME P450 3A5; MIDAZOLAM; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; TACROLIMUS;

EID: 84858412666     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.111.043018     Document Type: Article
Times cited : (73)

References (40)
  • 1
    • 0037287596 scopus 로고    scopus 로고
    • Interactions between cyclosporin and lipid-lowering drugs: Implications for organ transplant recipients
    • Åsberg A (2003) Interactions between cyclosporin and lipid-lowering drugs: implications for organ transplant recipients. Drugs 63:367-378.
    • (2003) Drugs , vol.63 , pp. 367-378
    • Åsberg, A.1
  • 2
    • 0032876066 scopus 로고    scopus 로고
    • Pharmacokinetic interactions between microemulsion formulated cyclosporine A and diltiazem in renal transplant recipients
    • DOI 10.1007/s002280050644
    • Åsberg A, Christensen H, Hartmann A, Carlson E, Molden E, and Berg KJ. (1999) Pharmacokinetic interactions between microemulsion formulated cyclosporine A and diltiazem in renal transplant recipients. Eur J Clin Pharmacol 55:383-387. (Pubitemid 29344082)
    • (1999) European Journal of Clinical Pharmacology , vol.55 , Issue.5 , pp. 383-387
    • Asberg, A.1    Christensen, H.2    Hartmann, A.3    Carlson, E.4    Molden, E.5    Berg, K.J.6
  • 3
    • 77955994141 scopus 로고    scopus 로고
    • Cyclosporine A, but not tacrolimus, shows relevant inhibition of organic anion-transporting protein 1B1-mediated transport of atorvastatin
    • Amundsen R, Christensen H, Zabihyan B, and Asberg A (2010) Cyclosporine A, but not tacrolimus, shows relevant inhibition of organic anion-transporting protein 1B1-mediated transport of atorvastatin. Drug Metab Dispos 38:1499-1504.
    • (2010) Drug Metab Dispos , vol.38 , pp. 1499-1504
    • Amundsen, R.1    Christensen, H.2    Zabihyan, B.3    Asberg, A.4
  • 4
    • 18844410849 scopus 로고    scopus 로고
    • Predicting inhibitory drug-drug interactions and evaluating drug interaction reports using inhibition constants
    • DOI 10.1345/aph.1E508
    • Bachmann KA and Lewis JD (2005) Predicting inhibitory drug-drug interactions and evaluating drug interaction reports using inhibition constants. Ann Pharmacother 39:1064-1072. (Pubitemid 40695974)
    • (2005) Annals of Pharmacotherapy , vol.39 , Issue.6 , pp. 1064-1072
    • Bachmann, K.A.1    Lewis, J.D.2
  • 5
    • 0030042485 scopus 로고    scopus 로고
    • Clinically significant drug interactions with cyclosporin. An update
    • Campana C, Regazzi MB, Buggia I, and Molinaro M (1996) Clinically significant drug interactions with cyclosporin. An update. Clin Pharmacokinet 30:141-179.
    • (1996) Clin Pharmacokinet , vol.30 , pp. 141-179
    • Campana, C.1    Regazzi, M.B.2    Buggia, I.3    Molinaro, M.4
  • 6
    • 69949133447 scopus 로고    scopus 로고
    • Different enzyme kinetics of midazolam in recombinant CYP3A4 microsomes from human and insect sources
    • Christensen H, Mathiesen L, Postvoll LW, Winther B, and Molden E (2009) Different enzyme kinetics of midazolam in recombinant CYP3A4 microsomes from human and insect sources. Drug Metab Pharmacokinet 24:261-268.
    • (2009) Drug Metab Pharmacokinet , vol.24 , pp. 261-268
    • Christensen, H.1    Mathiesen, L.2    Postvoll, L.W.3    Winther, B.4    Molden, E.5
  • 8
    • 80052023463 scopus 로고    scopus 로고
    • In vivo CYP3A activity is significantly lower in cyclosporine-treated as compared with tacrolimus-treated renal allograft recipients
    • de Jonge H, de Loor H, Verbeke K, Vanrenterghem Y, and Kuypers DR (2011) In vivo CYP3A activity is significantly lower in cyclosporine-treated as compared with tacrolimus-treated renal allograft recipients. Clin Pharmacol Ther 90:414-422.
    • (2011) Clin Pharmacol Ther , vol.90 , pp. 414-422
    • De Jonge, H.1    De Loor, H.2    Verbeke, K.3    Vanrenterghem, Y.4    Kuypers, D.R.5
  • 9
    • 42449085455 scopus 로고    scopus 로고
    • Cinacalcet's effect on the pharmacokinetics of tacrolimus, cyclosporine and mycophenolate in renal transplant recipients
    • DOI 10.1093/ndt/gfm632
    • Falck P, Vethe NT, Asberg A, Midtvedt K, Bergan S, Reubsaet JL, and Holdaas H (2008) Cinacalcet's effect on the pharmacokinetics of tacrolimus, cyclosporine and mycophenolate in renal transplant recipients. Nephrol Dial Transplant 23:1048-1053. (Pubitemid 351767545)
    • (2008) Nephrology Dialysis Transplantation , vol.23 , Issue.3 , pp. 1048-1053
    • Falck, P.1    Vethe, N.T.2    Asberg, A.3    Midtvedt, K.4    Bergan, S.5    Reubsaet, J.L.E.6    Holdaas, H.7
  • 10
    • 29944446485 scopus 로고    scopus 로고
    • Prediction of time-dependent CYP3A4 drug-drug interactions: Impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition
    • DOI 10.1124/dmd.105.006874
    • Galetin A, Burt H, Gibbons L, and Houston JB (2006) Prediction of time-dependent CYP3A4 drug-drug interactions: impact of enzyme degradation, parallel elimination pathways, and intestinal inhibition. Drug Metab Dispos 34:166-175. (Pubitemid 43042658)
    • (2006) Drug Metabolism and Disposition , vol.34 , Issue.1 , pp. 166-175
    • Galetin, A.1    Burt, H.2    Gibbons, L.3    Houston, J.B.4
  • 11
    • 77949281429 scopus 로고    scopus 로고
    • Contribution of intestinal cytochrome P450- mediated metabolism to drug-drug inhibition and induction interactions
    • Galetin A, Gertz M, and Houston JB (2010) Contribution of intestinal cytochrome P450- mediated metabolism to drug-drug inhibition and induction interactions. Drug Metab Pharmacokinet 25:28-47.
    • (2010) Drug Metab Pharmacokinet , vol.25 , pp. 28-47
    • Galetin, A.1    Gertz, M.2    Houston, J.B.3
  • 12
    • 77953737073 scopus 로고    scopus 로고
    • Prediction of human intestinal first-pass metabolism of 25 CYP3A substrates from in vitro clearance and permeability data
    • Gertz M, Harrison A, Houston JB, and Galetin A (2010) Prediction of human intestinal first-pass metabolism of 25 CYP3A substrates from in vitro clearance and permeability data. Drug Metab Dispos 38:1147-1158.
    • (2010) Drug Metab Dispos , vol.38 , pp. 1147-1158
    • Gertz, M.1    Harrison, A.2    Houston, J.B.3    Galetin, A.4
  • 14
    • 67649389519 scopus 로고    scopus 로고
    • The conduct of in vitro studies to address time-dependent inhibition of drug-metabolizing enzymes: A perspective of the pharmaceutical research and manufacturers of America
    • Grimm SW, Einolf HJ, Hall SD, He K, Lim HK, Ling KH, Lu C, Nomeir AA, Seibert E, Skordos KW, et al. (2009) The conduct of in vitro studies to address time-dependent inhibition of drug-metabolizing enzymes: a perspective of the pharmaceutical research and manufacturers of America. Drug Metab Dispos 37:1355-1370.
    • (2009) Drug Metab Dispos , vol.37 , pp. 1355-1370
    • Grimm, S.W.1    Einolf, H.J.2    Hall, S.D.3    He, K.4    Lim, H.K.5    Ling, K.H.6    Lu, C.7    Nomeir, A.A.8    Seibert, E.9    Skordos, K.W.10
  • 15
    • 1942455361 scopus 로고    scopus 로고
    • Database analyses for the prediction of in vivo drug-drug interactions from in vitro data
    • Ito K, Brown HS, and Houston JB (2004) Database analyses for the prediction of in vivo drug-drug interactions from in vitro data. Br J Clin Pharmacol 57:473-486.
    • (2004) Br J Clin Pharmacol , vol.57 , pp. 473-486
    • Ito, K.1    Brown, H.S.2    Houston, J.B.3
  • 16
    • 0032911163 scopus 로고    scopus 로고
    • Comparison of cytochrome P-450-dependent metabolism and drug interactions of the 3-hydroxy-3-methylglutaryl-CoA reductase inhibitors lovastatin and pravastatin in the liver
    • Jacobsen W, Kirchner G, Hallensleben K, Mancinelli L, Deters M, Hackbarth I, Benet LZ, Sewing KF, and Christians U (1999) Comparison of cytochrome P-450-dependent metabolism and drug interactions of the 3-hydroxy-3- methylglutaryl-CoA reductase inhibitors lovastatin and pravastatin in the liver. Drug Metab Dispos 27:173-179.
    • (1999) Drug Metab Dispos , vol.27 , pp. 173-179
    • Jacobsen, W.1    Kirchner, G.2    Hallensleben, K.3    Mancinelli, L.4    Deters, M.5    Hackbarth, I.6    Benet, L.Z.7    Sewing, K.F.8    Christians, U.9
  • 18
    • 0033994866 scopus 로고    scopus 로고
    • Quantitative prediction of in vivo drug-Drug interactions from in vitro data based on physiological pharmacokinetics: Use of maximum unbound concentration of inhibitor at the inlet to the liver
    • DOI 10.1023/A:1007509324428
    • Kanamitsu S, Ito K, and Sugiyama Y (2000) Quantitative prediction of in vivo drug-drug interactions from in vitro data based on physiological pharmacokinetics: use of maximum unbound concentration of inhibitor at the inlet to the liver. Pharm Res 17:336-343. (Pubitemid 30225138)
    • (2000) Pharmaceutical Research , vol.17 , Issue.3 , pp. 336-343
    • Kanamitsu, S.-I.1    Ito, K.2    Sugiyama, Y.3
  • 19
    • 46749154596 scopus 로고    scopus 로고
    • The quantitative prediction of CYP-mediated drug interaction by physiologically based pharmacokinetic modeling
    • Kato M, Shitara Y, Sato H, Yoshisue K, Hirano M, Ikeda T, and Sugiyama Y (2008) The quantitative prediction of CYP-mediated drug interaction by physiologically based pharmacokinetic modeling. Pharm Res 25:1891-1901.
    • (2008) Pharm Res , vol.25 , pp. 1891-1901
    • Kato, M.1    Shitara, Y.2    Sato, H.3    Yoshisue, K.4    Hirano, M.5    Ikeda, T.6    Sugiyama, Y.7
  • 20
    • 0036456710 scopus 로고    scopus 로고
    • In vitro effects of tacrolimus on human cytochrome P450
    • DOI 10.1046/j.1472-8206.2002.00114.x
    • Lecointre K, Furlan V, and Taburet AM (2002) In vitro effects of tacrolimus on human cytochrome P450. Fundam Clin Pharmacol 16:455-460. (Pubitemid 35463881)
    • (2002) Fundamental and Clinical Pharmacology , vol.16 , Issue.6 , pp. 455-460
    • Lecointre, K.1    Furlan, V.2    Taburet, A.-M.3
  • 22
    • 0031001611 scopus 로고    scopus 로고
    • Clinically significant drug interactions with new immunosuppressive agents
    • Mignat C (1997) Clinically significant drug interactions with new immunosuppressive agents. Drug Saf 16:267-278.
    • (1997) Drug Saf , vol.16 , pp. 267-278
    • Mignat, C.1
  • 23
    • 33845420011 scopus 로고    scopus 로고
    • Drug interactions with lipid-lowering drugs: Mechanisms and clinical relevance
    • DOI 10.1016/j.clpt.2006.09.003, PII S0009923606003602
    • Neuvonen PJ, Niemi M, and Backman JT (2006) Drug interactions with lipid-lowering drugs: mechanisms and clinical relevance. Clin Pharmacol Ther 80:565-581. (Pubitemid 44908269)
    • (2006) Clinical Pharmacology and Therapeutics , vol.80 , Issue.6 , pp. 565-581
    • Neuvonen, P.J.1    Niemi, M.2    Backman, J.T.3
  • 24
    • 33846180686 scopus 로고    scopus 로고
    • Effect of cyclosporine and tacrolimus on cytochrome P450 activities in human liver microsomes
    • DOI 10.1248/yakushi.127.209
    • Niwa T, Yamamoto S, Saito M, Shiraga T, and Takagi A (2007) Effect of cyclosporine and tacrolimus on cytochrome P450 activities in human liver microsomes. Yakugaku Zasshi 127:209-216. (Pubitemid 46089919)
    • (2007) Yakugaku Zasshi , vol.127 , Issue.1 , pp. 209-216
    • Niwa, T.1    Yamamoto, S.2    Saito, M.3    Shiraga, T.4    Takagi, A.5
  • 26
    • 33846449874 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions
    • DOI 10.1124/dmd.106.012633
    • Obach RS, Walsky RL, and Venkatakrishnan K (2007) Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions. Drug Metab Dispos 35:246-255. (Pubitemid 46148737)
    • (2007) Drug Metabolism and Disposition , vol.35 , Issue.2 , pp. 246-255
    • Obach, R.S.1    Walsky, R.L.2    Venkatakrishnan, K.3
  • 29
    • 33847406197 scopus 로고    scopus 로고
    • Metabolism of sirolimus in the presence or absence of cyclosporine by genotyped human liver microsomes and recombinant cytochromes P450 3A4 and 3A5
    • Picard N, Djebli N, Sauvage FL, and Marquet P (2007) Metabolism of sirolimus in the presence or absence of cyclosporine by genotyped human liver microsomes and recombinant cytochromes P450 3A4 and 3A5. Drug Metab Dispos 35:350-355.
    • (2007) Drug Metab Dispos , vol.35 , pp. 350-355
    • Picard, N.1    Djebli, N.2    Sauvage, F.L.3    Marquet, P.4
  • 30
    • 34548283499 scopus 로고    scopus 로고
    • In vitro approaches to investigate mechanism-based inactivation of CYP enzymes
    • DOI 10.1517/17425255.3.3.321
    • Polasek TM and Miners JO (2007) In vitro approaches to investigate mechanism-based inactivation of CYP enzymes. Expert Opin Drug Metab Toxicol 3:321-329. (Pubitemid 47316027)
    • (2007) Expert Opinion on Drug Metabolism and Toxicology , vol.3 , Issue.3 , pp. 321-329
    • Polasek, T.M.1    Miners, J.O.2
  • 31
    • 77951916870 scopus 로고    scopus 로고
    • In vitro-in vivo extrapolation of zolpidem as a perpetrator of metabolic interactions involving CYP3A
    • Polasek TM, Sadagopal JS, Elliot DJ, and Miners JO (2010) In vitro-in vivo extrapolation of zolpidem as a perpetrator of metabolic interactions involving CYP3A. Eur J Clin Pharmacol 66:275-283.
    • (2010) Eur J Clin Pharmacol , vol.66 , pp. 275-283
    • Polasek, T.M.1    Sadagopal, J.S.2    Elliot, D.J.3    Miners, J.O.4
  • 32
    • 13244287685 scopus 로고    scopus 로고
    • 'In silico' simulations to assess the 'in vivo' consequences of 'in vitro' metabolic drug-drug interactions
    • DOI 10.1016/j.ddtec.2004.10.002, PII S174067490400037X
    • Rostami-Hodjegan A and Tucker G (2004) 'In silico' simulations to assess the 'in vivo'consequences of 'in vitro' metabolic drug- drug interactions. Drug Discov Today Technol 1:441-448. (Pubitemid 40186348)
    • (2004) Drug Discovery Today: Technologies , vol.1 , Issue.4 , pp. 441-448
    • Rostami-Hodjegan, A.1    Tucker, G.2
  • 33
    • 41049093550 scopus 로고    scopus 로고
    • Oxidative metabolism of tacrolimus and its metabolite by human cytochrome P450 3A subfamily
    • Shiraga T (1999) Oxidative metabolism of tacrolimus and its metabolite by human cytochrome P450 3A subfamily. Drug Metab Pharmacokinet 14:277-285.
    • (1999) Drug Metab Pharmacokinet , vol.14 , pp. 277-285
    • Shiraga, T.1
  • 35
    • 2442690439 scopus 로고    scopus 로고
    • Validated assays for human cytochrome P450 activities
    • DOI 10.1124/dmd.32.6.647
    • Walsky RL and Obach RS (2004) Validated assays for human cytochrome P450 activities. Drug Metab Dispos 32:647-660. (Pubitemid 38668158)
    • (2004) Drug Metabolism and Disposition , vol.32 , Issue.6 , pp. 647-660
    • Walsky, R.L.1    Obach, R.S.2
  • 37
    • 0842282550 scopus 로고    scopus 로고
    • Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites
    • DOI 10.1124/dmd.32.2.259
    • Wang YH, Jones DR, and Hall SD (2004) Prediction of cytochrome P450 3A inhibition by verapamil enantiomers and their metabolites. Drug Metab Dispos 32:259-266. (Pubitemid 38176944)
    • (2004) Drug Metabolism and Disposition , vol.32 , Issue.2 , pp. 259-266
    • Wang, Y.-H.1    Jones, D.R.2    Hall, S.D.3
  • 38
    • 24644441043 scopus 로고    scopus 로고
    • Kinetic values for mechanism-based enzyme inhibition: Assessing the bias introduced by the conventional experimental protocol
    • DOI 10.1016/j.ejps.2005.07.005, PII S0928098705002204
    • Yang J, Jamei M, Yeo KR, Tucker GT, and Rostami-Hodjegan A (2005) Kinetic values for mechanism-based enzyme inhibition: assessing the bias introduced by the conventional experimental protocol. Eur J Pharm Sci 26:334-340. (Pubitemid 41278639)
    • (2005) European Journal of Pharmaceutical Sciences , vol.26 , Issue.3-4 , pp. 334-340
    • Yang, J.1    Jamei, M.2    Yeo, K.R.3    Tucker, G.T.4    Rostami-Hodjegan, A.5
  • 40
    • 36549059303 scopus 로고    scopus 로고
    • Clinically important drug interactions potentially involving mechanism-based inhibition of cytochrome P450 3A4 and the role of therapeutic drug monitoring
    • DOI 10.1097/FTD.0b013e31815c16f5, PII 0000769120071200000002
    • Zhou SF, Xue CC, Yu XQ, Li C, and Wang G (2007) Clinically important drug interactions potentially involving mechanism-based inhibition of cytochrome P450 3A4 and the role of therapeutic drug monitoring. Ther Drug Monit 29:687-710. (Pubitemid 350190847)
    • (2007) Therapeutic Drug Monitoring , vol.29 , Issue.6 , pp. 687-710
    • Zhou, S.-F.1    Xue, C.C.2    Yu, X.-Q.3    Li, C.4    Wang, G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.