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Volumn 78, Issue 4, 2005, Pages 388-399

Cyclosporine markedly raises the plasma concentrations of repaglinide

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOSPORIN; CYCLOSPORIN A; CYTOCHROME P450 2C8; CYTOCHROME P450 3A4; CYTOCHROME P450 3A5; DRUG METABOLITE; GLYCOPROTEIN P; ORGANIC ANION TRANSPORTER; PLACEBO; REPAGLINIDE;

EID: 25844438751     PISSN: 00099236     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clpt.2005.07.005     Document Type: Article
Times cited : (188)

References (42)
  • 1
    • 0029114542 scopus 로고
    • Effects of the hypoglycaemic drugs repaglinide and glibenclamide on ATP-sensitive potassium-channels and cytosolic calcium levels in beta TC3 cells and rat pancreatic beta cells
    • J. Gromada, S. Dissing, H. Kofod, J. Frøkjaer-Jensen Effects of the hypoglycaemic drugs repaglinide and glibenclamide on ATP-sensitive potassium-channels and cytosolic calcium levels in beta TC3 cells and rat pancreatic beta cells Diabetologia 38 1995 1025 1032
    • (1995) Diabetologia , vol.38 , pp. 1025-1032
    • Gromada, J.1    Dissing, S.2    Kofod, H.3    Frøkjaer-Jensen, J.4
  • 2
    • 0036075924 scopus 로고    scopus 로고
    • Clinical pharmacokinetics and pharmacodynamics of repaglinide
    • V. Hatorp Clinical pharmacokinetics and pharmacodynamics of repaglinide Clin Pharmacokinet 41 2002 471 483
    • (2002) Clin Pharmacokinet , vol.41 , pp. 471-483
    • Hatorp, V.1
  • 3
    • 0031593457 scopus 로고    scopus 로고
    • Bioavailability of repaglinide, a novel antidiabetic agent, administered orally in tablet or solution form or intravenously in healthy male volunteers
    • V. Hatorp, S. Oliver, C.A. Su Bioavailability of repaglinide, a novel antidiabetic agent, administered orally in tablet or solution form or intravenously in healthy male volunteers Int J Clin Pharmacol Ther 36 1998 636 641
    • (1998) Int J Clin Pharmacol Ther , vol.36 , pp. 636-641
    • Hatorp, V.1    Oliver, S.2    Su, C.A.3
  • 4
    • 25844448609 scopus 로고    scopus 로고
    • Metabolism of repaglinide by CYP2C8 and CYP3A4 in vitro: Effect of fibrates and rifampicin
    • L.I. Kajosaari, J. Laitila, P.J. Neuvonen, J.T. Backman Metabolism of repaglinide by CYP2C8 and CYP3A4 in vitro effect of fibrates and rifampicin Basic Clin Pharmacol Toxicol 97 2005 249 256
    • (2005) Basic Clin Pharmacol Toxicol , vol.97 , pp. 249-256
    • Kajosaari, L.I.1    Laitila, J.2    Neuvonen, P.J.3    Backman, J.T.4
  • 5
    • 0042318871 scopus 로고    scopus 로고
    • CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide
    • T.B. Bidstrup, I. Bjørnsdottir, U.G. Sidelmann, M.S. Thomsen, K.T. Hansen CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide Br J Clin Pharmacol 56 2003 305 314
    • (2003) Br J Clin Pharmacol , vol.56 , pp. 305-314
    • Bidstrup, T.B.1    Bjørnsdottir, I.2    Sidelmann, U.G.3    Thomsen, M.S.4    Hansen, K.T.5
  • 7
    • 20444466590 scopus 로고    scopus 로고
    • Polymorphic organic anion transporting polypeptide 1B1 (OATP1B1) is a major determinant of repaglinide pharmacokinetics
    • M. Niemi, J.T. Backman, L.I. Kajosaari, J.B. Leathart, M. Neuvonen, A.K. Daly Polymorphic organic anion transporting polypeptide 1B1 (OATP1B1) is a major determinant of repaglinide pharmacokinetics Clin Pharmacol Ther 77 2005 468 478
    • (2005) Clin Pharmacol Ther , vol.77 , pp. 468-478
    • Niemi, M.1    Backman, J.T.2    Kajosaari, L.I.3    Leathart, J.B.4    Neuvonen, M.5    Daly, A.K.6
  • 8
    • 0037566974 scopus 로고    scopus 로고
    • Influence of drugs interacting with CYP3A4 on the pharmacokinetics, pharmacodynamics, and safety of the prandial glucose regulator repaglinide
    • V. Hatorp, K.T. Hansen, M.S. Thomsen Influence of drugs interacting with CYP3A4 on the pharmacokinetics, pharmacodynamics, and safety of the prandial glucose regulator repaglinide J Clin Pharmacol 43 2003 649 660
    • (2003) J Clin Pharmacol , vol.43 , pp. 649-660
    • Hatorp, V.1    Hansen, K.T.2    Thomsen, M.S.3
  • 9
    • 0037627707 scopus 로고    scopus 로고
    • Effects of gemfibrozil, itraconazole, and their combination on the pharmacokinetics and pharmacodynamics of repaglinide: Potentially hazardous interaction between gemfibrozil and repaglinide
    • M. Niemi, J.T. Backman, M. Neuvonen, P.J. Neuvonen Effects of gemfibrozil, itraconazole, and their combination on the pharmacokinetics and pharmacodynamics of repaglinide potentially hazardous interaction between gemfibrozil and repaglinide Diabetologia 46 2003 347 351
    • (2003) Diabetologia , vol.46 , pp. 347-351
    • Niemi, M.1    Backman, J.T.2    Neuvonen, M.3    Neuvonen, P.J.4
  • 10
    • 1942487810 scopus 로고    scopus 로고
    • The CYP2C8 inhibitor trimethoprim increases the plasma concentrations of repaglinide in healthy subjects
    • M. Niemi, L.I. Kajosaari, M. Neuvonen, J.T. Backman, P.J. Neuvonen The CYP2C8 inhibitor trimethoprim increases the plasma concentrations of repaglinide in healthy subjects Br J Clin Pharmacol 57 2004 441 447
    • (2004) Br J Clin Pharmacol , vol.57 , pp. 441-447
    • Niemi, M.1    Kajosaari, L.I.2    Neuvonen, M.3    Backman, J.T.4    Neuvonen, P.J.5
  • 11
    • 0034912196 scopus 로고    scopus 로고
    • The cytochrome P4503A4 inhibitor clarithromycin increases the plasma concentrations and effects of repaglinide
    • M. Niemi, P.J. Neuvonen, K.T. Kivistö The cytochrome P4503A4 inhibitor clarithromycin increases the plasma concentrations and effects of repaglinide Clin Pharmacol Ther 70 2001 58 65
    • (2001) Clin Pharmacol Ther , vol.70 , pp. 58-65
    • Niemi, M.1    Neuvonen, P.J.2    Kivistö, K.T.3
  • 13
    • 0036892714 scopus 로고    scopus 로고
    • Gemfibrozil inhibits CYP2C8-mediated cerivastatin metabolism in human liver microsomes
    • J.S. Wang, M. Neuvonen, X. Wen, J.T. Backman, P.J. Neuvonen Gemfibrozil inhibits CYP2C8-mediated cerivastatin metabolism in human liver microsomes Drug Metab Dispos 30 2002 1352 1356
    • (2002) Drug Metab Dispos , vol.30 , pp. 1352-1356
    • Wang, J.S.1    Neuvonen, M.2    Wen, X.3    Backman, J.T.4    Neuvonen, P.J.5
  • 14
    • 4644301418 scopus 로고    scopus 로고
    • Gemfibrozil and its glucuronide inhibit the organic anion transporting polypeptide 2 (OATP2/OATP1B1:SLC21A6)-mediated hepatic uptake and CYP2C8-mediated metabolism of cerivastatin: Analysis of the mechanism of the clinically relevant drug-drug interaction between cerivastatin and gemfibrozil
    • Y. Shitara, M. Hirano, H. Sato, Y. Sugiyama Gemfibrozil and its glucuronide inhibit the organic anion transporting polypeptide 2 (OATP2/OATP1B1:SLC21A6)-mediated hepatic uptake and CYP2C8-mediated metabolism of cerivastatin analysis of the mechanism of the clinically relevant drug-drug interaction between cerivastatin and gemfibrozil J Pharmacol Exp Ther 311 2004 228 236
    • (2004) J Pharmacol Exp Ther , vol.311 , pp. 228-236
    • Shitara, Y.1    Hirano, M.2    Sato, H.3    Sugiyama, Y.4
  • 15
    • 0035238531 scopus 로고    scopus 로고
    • Cyclosporin: An updated review of the pharmacokinetic properties, clinical efficacy and tolerability of a microemulsion-based formulation (neoral)1 in organ transplantation
    • C.J. Dunn, A.J. Wagstaff, C.M. Perry, G.L. Plosker, K.L. Goa Cyclosporin an updated review of the pharmacokinetic properties, clinical efficacy and tolerability of a microemulsion-based formulation (neoral)1 in organ transplantation Drugs 61 2001 1957 2016
    • (2001) Drugs , vol.61 , pp. 1957-2016
    • Dunn, C.J.1    Wagstaff, A.J.2    Perry, C.M.3    Plosker, G.L.4    Goa, K.L.5
  • 16
    • 0037287596 scopus 로고    scopus 로고
    • Interactions between cyclosporin and lipid-lowering drugs: Implications for organ transplant recipients
    • A. Åsberg Interactions between cyclosporin and lipid-lowering drugs implications for organ transplant recipients Drugs 63 2003 367 378
    • (2003) Drugs , vol.63 , pp. 367-378
    • Åsberg, A.1
  • 17
    • 0037310871 scopus 로고    scopus 로고
    • Inhibition of transporter-mediated hepatic uptake as a mechanism for drug-drug interaction between cerivastatin and cyclosporin a
    • Y. Shitara, T. Itoh, H. Sato, A.P. Li, Y. Sugiyama Inhibition of transporter-mediated hepatic uptake as a mechanism for drug-drug interaction between cerivastatin and cyclosporin A J Pharmacol Exp Ther 304 2003 610 616
    • (2003) J Pharmacol Exp Ther , vol.304 , pp. 610-616
    • Shitara, Y.1    Itoh, T.2    Sato, H.3    Li, A.P.4    Sugiyama, Y.5
  • 18
    • 0343416856 scopus 로고    scopus 로고
    • Contributions of hepatic and intestinal metabolism and P-glycoprotein to cyclosporine and tacrolimus oral drug delivery
    • M.F. Hebert Contributions of hepatic and intestinal metabolism and P-glycoprotein to cyclosporine and tacrolimus oral drug delivery Adv Drug Deliv Rev 27 1997 201 214
    • (1997) Adv Drug Deliv Rev , vol.27 , pp. 201-214
    • Hebert, M.F.1
  • 19
    • 0027949844 scopus 로고
    • Inhibition of rhodamine 123 secretion by cyclosporin a as a model of P-glycoprotein mediated transport in liver
    • V. Stapf, T. Thalhammer, R. Huber-Huber, F. Felberbauer, L. Gajdzik, J. Graf Inhibition of rhodamine 123 secretion by cyclosporin A as a model of P-glycoprotein mediated transport in liver Anticancer Res 14 1994 581 585
    • (1994) Anticancer Res , vol.14 , pp. 581-585
    • Stapf, V.1    Thalhammer, T.2    Huber-Huber, R.3    Felberbauer, F.4    Gajdzik, L.5    Graf, J.6
  • 20
    • 0242606429 scopus 로고    scopus 로고
    • Determination of the pharmacokinetics of cerivastatin when administered in combination with sirolimus and cyclosporin a in patients with kidney transplant, and review of the relevant literature
    • L. Renders, D. Czock, H. Schocklmann, U. Kunzendorf Determination of the pharmacokinetics of cerivastatin when administered in combination with sirolimus and cyclosporin A in patients with kidney transplant, and review of the relevant literature Int J Clin Pharmacol Ther 41 2003 499 503
    • (2003) Int J Clin Pharmacol Ther , vol.41 , pp. 499-503
    • Renders, L.1    Czock, D.2    Schocklmann, H.3    Kunzendorf, U.4
  • 21
    • 3542992126 scopus 로고    scopus 로고
    • Rosuvastatin pharmacokinetics in heart transplant recipients administered an antirejection regimen including cyclosporine
    • S.G. Simonson, A. Raza, P.D. Martin, P.D. Mitchell, J.A. Jarcho, C.D. Brown Rosuvastatin pharmacokinetics in heart transplant recipients administered an antirejection regimen including cyclosporine Clin Pharmacol Ther 76 2004 167 177
    • (2004) Clin Pharmacol Ther , vol.76 , pp. 167-177
    • Simonson, S.G.1    Raza, A.2    Martin, P.D.3    Mitchell, P.D.4    Jarcho, J.A.5    Brown, C.D.6
  • 23
    • 1642523136 scopus 로고    scopus 로고
    • Pharmacokinetics and pharmacodynamics of pravastatin in pediatric and adolescent cardiac transplant recipients on a regimen of triple immunosuppression
    • M. Hedman, P.J. Neuvonen, M. Neuvonen, C. Holmberg, M. Antikainen Pharmacokinetics and pharmacodynamics of pravastatin in pediatric and adolescent cardiac transplant recipients on a regimen of triple immunosuppression Clin Pharmacol Ther 75 2004 101 109
    • (2004) Clin Pharmacol Ther , vol.75 , pp. 101-109
    • Hedman, M.1    Neuvonen, P.J.2    Neuvonen, M.3    Holmberg, C.4    Antikainen, M.5
  • 24
    • 0027988647 scopus 로고
    • Clinical efficacy and pharmacokinetics of HMG-CoA reductase inhibitors in heart transplant patients treated with cyclosporin a
    • M.B. Regazzi, I. Iacona, C. Campana, A. Gavazzi, M. Vigano, G. Perani Clinical efficacy and pharmacokinetics of HMG-CoA reductase inhibitors in heart transplant patients treated with cyclosporin A Transplant Proc 26 1994 2644 2645
    • (1994) Transplant Proc , vol.26 , pp. 2644-2645
    • Regazzi, M.B.1    Iacona, I.2    Campana, C.3    Gavazzi, A.4    Vigano, M.5    Perani, G.6
  • 28
    • 0028357256 scopus 로고
    • Midazolam should be avoided in patients receiving the systemic antimycotics ketoconazole or itraconazole
    • K.T. Olkkola, J.T. Backman, P.J. Neuvonen Midazolam should be avoided in patients receiving the systemic antimycotics ketoconazole or itraconazole Clin Pharmacol Ther 55 1994 481 485
    • (1994) Clin Pharmacol Ther , vol.55 , pp. 481-485
    • Olkkola, K.T.1    Backman, J.T.2    Neuvonen, P.J.3
  • 31
    • 0025103799 scopus 로고
    • Competitive interaction of cyclosporins with the Vinca alkaloid-binding site of P-glycoprotein in multidrug-resistant cells
    • I. Tamai, A.R. Safa Competitive interaction of cyclosporins with the Vinca alkaloid-binding site of P-glycoprotein in multidrug-resistant cells J Biol Chem 265 1990 16509 16513
    • (1990) J Biol Chem , vol.265 , pp. 16509-16513
    • Tamai, I.1    Safa, A.R.2
  • 32
    • 0032753749 scopus 로고    scopus 로고
    • Effect of multidrug resistance-reversing agents on transporting activity of human canalicular multispecific organic anion transporter
    • Z.S. Chen, T. Kawabe, M. Ono, S. Aoki, T. Sumizawa, T. Furukawa Effect of multidrug resistance-reversing agents on transporting activity of human canalicular multispecific organic anion transporter Mol Pharmacol 56 1999 1219 1228
    • (1999) Mol Pharmacol , vol.56 , pp. 1219-1228
    • Chen, Z.S.1    Kawabe, T.2    Ono, M.3    Aoki, S.4    Sumizawa, T.5    Furukawa, T.6
  • 33
    • 0027377733 scopus 로고
    • Plasma concentration profiles of simvastatin 3-hydroxy-3-methyl-glutaryl- coenzyme a reductase inhibitory activity in kidney transplant recipients with and without ciclosporin
    • M. Arnadottir, L.O. Eriksson, H. Thysell, J.D. Karkas Plasma concentration profiles of simvastatin 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase inhibitory activity in kidney transplant recipients with and without ciclosporin Nephron 65 1993 410 413
    • (1993) Nephron , vol.65 , pp. 410-413
    • Arnadottir, M.1    Eriksson, L.O.2    Thysell, H.3    Karkas, J.D.4
  • 34
    • 0030463459 scopus 로고    scopus 로고
    • Evaluation of fluvastatin in the treatment of hypercholesterolemia in renal transplant recipients taking cyclosporine
    • R. Goldberg, D. Roth Evaluation of fluvastatin in the treatment of hypercholesterolemia in renal transplant recipients taking cyclosporine Transplantation 62 1996 1559 1564
    • (1996) Transplantation , vol.62 , pp. 1559-1564
    • Goldberg, R.1    Roth, D.2
  • 36
    • 0037534010 scopus 로고    scopus 로고
    • Gemfibrozil increases plasma pravastatin concentrations and reduces pravastatin renal clearance
    • C. Kyrklund, J.T. Backman, M. Neuvonen, P.J. Neuvonen Gemfibrozil increases plasma pravastatin concentrations and reduces pravastatin renal clearance Clin Pharmacol Ther 73 2003 538 544
    • (2003) Clin Pharmacol Ther , vol.73 , pp. 538-544
    • Kyrklund, C.1    Backman, J.T.2    Neuvonen, M.3    Neuvonen, P.J.4
  • 37
    • 0035337643 scopus 로고    scopus 로고
    • Plasma concentrations of active lovastatin acid are markedly increased by gemfibrozil but not by bezafibrate
    • C. Kyrklund, J.T. Backman, K.T. Kivistö, M. Neuvonen, J. Laitila, P.J. Neuvonen Plasma concentrations of active lovastatin acid are markedly increased by gemfibrozil but not by bezafibrate Clin Pharmacol Ther 69 2001 340 345
    • (2001) Clin Pharmacol Ther , vol.69 , pp. 340-345
    • Kyrklund, C.1    Backman, J.T.2    Kivistö, K.T.3    Neuvonen, M.4    Laitila, J.5    Neuvonen, P.J.6
  • 39
    • 0033601257 scopus 로고    scopus 로고
    • A novel human hepatic organic anion transporting polypeptide (OATP2). Identification of a liver-specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl-CoA reductase inhibitor transporters
    • B. Hsiang, Y. Zhu, Z. Wang, Y. Wu, V. Sasseville, W.P. Yang A novel human hepatic organic anion transporting polypeptide (OATP2). Identification of a liver-specific human organic anion transporting polypeptide and identification of rat and human hydroxymethylglutaryl-CoA reductase inhibitor transporters J Biol Chem 274 1999 37161 37168
    • (1999) J Biol Chem , vol.274 , pp. 37161-37168
    • Hsiang, B.1    Zhu, Y.2    Wang, Z.3    Wu, Y.4    Sasseville, V.5    Yang, W.P.6
  • 40
    • 0035012075 scopus 로고    scopus 로고
    • Human liver-specific organic anion transporter, LST-1, mediates uptake of pravastatin by human hepatocytes
    • D. Nakai, R. Nakagomi, Y. Furuta, T. Tokui, T. Abe, T. Ikeda Human liver-specific organic anion transporter, LST-1, mediates uptake of pravastatin by human hepatocytes J Pharmacol Exp Ther 297 2001 861 867
    • (2001) J Pharmacol Exp Ther , vol.297 , pp. 861-867
    • Nakai, D.1    Nakagomi, R.2    Furuta, Y.3    Tokui, T.4    Abe, T.5    Ikeda, T.6
  • 41
    • 0037229225 scopus 로고    scopus 로고
    • Cytochrome P450 drug interactions within the HMG-CoA reductase inhibitor class: Are they clinically relevant?
    • J. Martin, H. Krum Cytochrome P450 drug interactions within the HMG-CoA reductase inhibitor class are they clinically relevant? Drug Saf 26 2003 13 21
    • (2003) Drug Saf , vol.26 , pp. 13-21
    • Martin, J.1    Krum, H.2
  • 42
    • 4544343104 scopus 로고    scopus 로고
    • Characterisation of cerivastatin as a P-glycoprotein substrate: Studies in P-glycoprotein-expressing cell monolayers and mdr1a/b knock-out mice
    • K.T. Kivistö, J. Zukunft, U. Hofmann, M. Niemi, S. Rekersbrink, S. Schneider Characterisation of cerivastatin as a P-glycoprotein substrate studies in P-glycoprotein-expressing cell monolayers and mdr1a/b knock-out mice Naunyn Schmiedebergs Arch Pharmacol 370 2004 124 130
    • (2004) Naunyn Schmiedebergs Arch Pharmacol , vol.370 , pp. 124-130
    • Kivistö, K.T.1    Zukunft, J.2    Hofmann, U.3    Niemi, M.4    Rekersbrink, S.5    Schneider, S.6


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