메뉴 건너뛰기




Volumn 70, Issue 6, 2010, Pages 870-880

Repaglinide-gemfibrozil drug interaction: Inhibition of repaglinide glucuronidation as a potential additional contributing mechanism

Author keywords

Drug interaction; Gemfibrozil; Repaglinide; UGT1A1

Indexed keywords

DRUG METABOLITE; GEMFIBROZIL; GEMFIBROZIL GLUCURONIDE; GLUCURONIDE; GLUCURONOSYLTRANSFERASE 1A1; REPAGLINIDE; UNCLASSIFIED DRUG;

EID: 78349291596     PISSN: 03065251     EISSN: 13652125     Source Type: Journal    
DOI: 10.1111/j.1365-2125.2010.03772.x     Document Type: Article
Times cited : (35)

References (31)
  • 2
    • 29244482237 scopus 로고    scopus 로고
    • Effect of genetic polymorphisms in cytochrome P450 (CYP) 2C9 and CYP2C8 on the pharmacokinetics of oral antidiabetic drugs: clinical relevance
    • Kirchheiner J, Roots I, Goldammer M, Rosenkranz B, Brockmoller J. Effect of genetic polymorphisms in cytochrome P450 (CYP) 2C9 and CYP2C8 on the pharmacokinetics of oral antidiabetic drugs: clinical relevance. Clin Pharmacokinet 2005; 44: 1209-25.
    • (2005) Clin Pharmacokinet , vol.44 , pp. 1209-1225
    • Kirchheiner, J.1    Roots, I.2    Goldammer, M.3    Rosenkranz, B.4    Brockmoller, J.5
  • 4
    • 39149108768 scopus 로고    scopus 로고
    • Different effects of SLCO1B1 polymorphism on the pharmacokinetics and pharmacodynamics of repaglinide and nateglinide
    • Kalliokoski A, Neuvonen M, Neuvonen PJ, Niemi M. Different effects of SLCO1B1 polymorphism on the pharmacokinetics and pharmacodynamics of repaglinide and nateglinide. J Clin Pharmacol 2008; 48: 311-21.
    • (2008) J Clin Pharmacol , vol.48 , pp. 311-321
    • Kalliokoski, A.1    Neuvonen, M.2    Neuvonen, P.J.3    Niemi, M.4
  • 6
    • 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
    • Shitara Y, Hirano M, Sato H, Sugiyama Y. 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 2004; 311: 228-36.
    • (2004) J Pharmacol Exp Ther , vol.311 , pp. 228-236
    • Shitara, Y.1    Hirano, M.2    Sato, H.3    Sugiyama, Y.4
  • 7
    • 29944446317 scopus 로고    scopus 로고
    • Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: implications for drug-drug interactions
    • Ogilvie BW, Zhang D, Li W, Rodrigues AD, Gipson AE, Holsapple J, Toren P, Parkinson A. Glucuronidation converts gemfibrozil to a potent, metabolism-dependent inhibitor of CYP2C8: implications for drug-drug interactions. Drug Metab Dispos 2006; 34: 191-7.
    • (2006) Drug Metab Dispos , vol.34 , pp. 191-197
    • Ogilvie, B.W.1    Zhang, D.2    Li, W.3    Rodrigues, A.D.4    Gipson, A.E.5    Holsapple, J.6    Toren, P.7    Parkinson, A.8
  • 8
    • 0042318871 scopus 로고    scopus 로고
    • CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide
    • Bidstrup TB, Bjornsdottir I, Sidelmann UG, Thomsen MS, Hansen KT. CYP2C8 and CYP3A4 are the principal enzymes involved in the human in vitro biotransformation of the insulin secretagogue repaglinide. Br J Clin Pharmacol 2003; 56: 305-14.
    • (2003) Br J Clin Pharmacol , vol.56 , pp. 305-314
    • Bidstrup, T.B.1    Bjornsdottir, I.2    Sidelmann, U.G.3    Thomsen, M.S.4    Hansen, K.T.5
  • 9
  • 10
    • 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
    • Niemi M, Backman JT, Neuvonen M, Neuvonen PJ. Effects of gemfibrozil, itraconazole, and their combination on the pharmacokinetics and pharmacodynamics of repaglinide: potentially hazardous interaction between gemfibrozil and repaglinide. Diabetologia 2003; 46: 347-51.
    • (2003) Diabetologia , vol.46 , pp. 347-351
    • Niemi, M.1    Backman, J.T.2    Neuvonen, M.3    Neuvonen, P.J.4
  • 11
    • 49949093994 scopus 로고    scopus 로고
    • The effect of gemfibrozil on repaglinide pharmacokinetics persists for at least 12 h after the dose: evidence for mechanism-based inhibition of CYP2C8 in vivo
    • Tornio A, Niemi M, Neuvonen M, Laitila J, Kalliokoski A, Neuvonen PJ, Backman JT. The effect of gemfibrozil on repaglinide pharmacokinetics persists for at least 12 h after the dose: evidence for mechanism-based inhibition of CYP2C8 in vivo. Clin Pharmacol Ther 2008; 84: 403-11.
    • (2008) Clin Pharmacol Ther , vol.84 , pp. 403-411
    • Tornio, A.1    Niemi, M.2    Neuvonen, M.3    Laitila, J.4    Kalliokoski, A.5    Neuvonen, P.J.6    Backman, J.T.7
  • 13
    • 0037566974 scopus 로고    scopus 로고
    • Influence of drugs interacting with CYP3A4 on the pharmacokinetics, pharmacodynamics, and safety of the prandial glucose regulator repaglinide
    • Hatorp V, Hansen KT, Thomsen MS. Influence of drugs interacting with CYP3A4 on the pharmacokinetics, pharmacodynamics, and safety of the prandial glucose regulator repaglinide. J Clin Pharmacol 2003; 43: 649-60.
    • (2003) J Clin Pharmacol , vol.43 , pp. 649-660
    • Hatorp, V.1    Hansen, K.T.2    Thomsen, M.S.3
  • 17
    • 7744241812 scopus 로고    scopus 로고
    • Inhibition of human organic anion transporting polypeptide OATP 1B1 as a mechanism of drug-induced hyperbilirubinemia
    • Campbell SD, De Morais SM, Xu JJ. Inhibition of human organic anion transporting polypeptide OATP 1B1 as a mechanism of drug-induced hyperbilirubinemia. Chem Biol Interact 2004; 150: 179-87.
    • (2004) Chem Biol Interact , vol.150 , pp. 179-187
    • Campbell, S.D.1    De Morais, S.M.2    Xu, J.J.3
  • 19
    • 42049097101 scopus 로고    scopus 로고
    • Multiple inhibition mechanisms and prediction of drug-drug interactions: status of metabolism and transporter models as exemplified by gemfibrozil-drug interactions
    • Hinton LK, Galetin A, Houston JB. Multiple inhibition mechanisms and prediction of drug-drug interactions: status of metabolism and transporter models as exemplified by gemfibrozil-drug interactions. Pharm Res 2008; 25: 1063-74.
    • (2008) Pharm Res , vol.25 , pp. 1063-1074
    • Hinton, L.K.1    Galetin, A.2    Houston, J.B.3
  • 20
    • 33644548936 scopus 로고    scopus 로고
    • Telithromycin, but not montelukast, increases the plasma concentrations and effects of the cytochrome P450 3A4 and 2C8 substrate repaglinide
    • Kajosaari LI, Niemi M, Backman JT, Neuvonen PJ. Telithromycin, but not montelukast, increases the plasma concentrations and effects of the cytochrome P450 3A4 and 2C8 substrate repaglinide. Clin Pharmacol Ther 2006; 79: 231-42.
    • (2006) Clin Pharmacol Ther , vol.79 , pp. 231-242
    • Kajosaari, L.I.1    Niemi, M.2    Backman, J.T.3    Neuvonen, P.J.4
  • 21
    • 78349271975 scopus 로고    scopus 로고
    • Center for Drug Evaluation and Research F. Guidance for Industry Drug Interaction Studies- Study Design, Data Analysis, and Implications for Dosing and Labeling: draft guidance. In..
    • Center for Drug Evaluation and Research F. Guidance for Industry Drug Interaction Studies- Study Design, Data Analysis, and Implications for Dosing and Labeling: draft guidance. In. 2006.
    • (2006)
  • 22
    • 0036075924 scopus 로고    scopus 로고
    • Clinical pharmacokinetics and pharmacodynamics of repaglinide
    • Hatorp V. Clinical pharmacokinetics and pharmacodynamics of repaglinide. Clin Pharmacokinet 2002; 41: 471-83.
    • (2002) Clin Pharmacokinet , vol.41 , pp. 471-483
    • Hatorp, V.1
  • 23
    • 78349267877 scopus 로고    scopus 로고
    • Nova Nordisk. Prandin (repaglinide) Tablets (0.5, 1, and 2 mg) Prescribing Information..
    • Nova Nordisk. Prandin (repaglinide) Tablets (0.5, 1, and 2 mg) Prescribing Information. 2006.
    • (2006)
  • 25
    • 34247137295 scopus 로고    scopus 로고
    • Carboxyl-glucuronidation of mitiglinide by human UDP-glucuronosyltransferases
    • Yu L, Lu S, Lin Y, Zeng S. Carboxyl-glucuronidation of mitiglinide by human UDP-glucuronosyltransferases. Biochem Pharmacol 2007; 73: 1842-51.
    • (2007) Biochem Pharmacol , vol.73 , pp. 1842-1851
    • Yu, L.1    Lu, S.2    Lin, Y.3    Zeng, S.4
  • 27
    • 71049130780 scopus 로고    scopus 로고
    • CYP2C8 activity recovers within 96 hours after gemfibrozil dosing: estimation of CYP2C8 half-life using repaglinide as an in vivo probe
    • Backman JT, Honkalammi J, Neuvonen M, Kurkinen KJ, Tornio A, Niemi M, Neuvonen PJ. CYP2C8 activity recovers within 96 hours after gemfibrozil dosing: estimation of CYP2C8 half-life using repaglinide as an in vivo probe. Drug Metab Dispos 2009; 37: 2359-66.
    • (2009) Drug Metab Dispos , vol.37 , pp. 2359-2366
    • Backman, J.T.1    Honkalammi, J.2    Neuvonen, M.3    Kurkinen, K.J.4    Tornio, A.5    Niemi, M.6    Neuvonen, P.J.7
  • 29
    • 34147141506 scopus 로고    scopus 로고
    • Tissue-specific mRNA expression profiles of human phase I metabolizing enzymes except for cytochrome P450 and phase II metabolizing enzymes
    • Nishimura M, Naito S. Tissue-specific mRNA expression profiles of human phase I metabolizing enzymes except for cytochrome P450 and phase II metabolizing enzymes. Drug Metab Pharmacokinet 2006; 21: 357-74.
    • (2006) Drug Metab Pharmacokinet , vol.21 , pp. 357-374
    • Nishimura, M.1    Naito, S.2
  • 30
    • 53749107781 scopus 로고    scopus 로고
    • Absolute quantification of human uridine-diphosphate glucuronosyl transferase (UGT) enzyme isoforms 1A1 and 1A6 by tandem LC-MS
    • Fallon JK, Harbourt DE, Maleki SH, Kessler FK, Ritter JK, Smith PC. Absolute quantification of human uridine-diphosphate glucuronosyl transferase (UGT) enzyme isoforms 1A1 and 1A6 by tandem LC-MS. Drug Metab Lett 2008; 2: 210-22.
    • (2008) Drug Metab Lett , vol.2 , pp. 210-222
    • Fallon, J.K.1    Harbourt, D.E.2    Maleki, S.H.3    Kessler, F.K.4    Ritter, J.K.5    Smith, P.C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.