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Volumn 25, Issue 10, 1997, Pages 1191-1199

In vitro metabolism of simvastatin in humans [SBT]identification of metabolizlng enzymes and effect of the drug on hepatic P450S

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450; DRUG METABOLITE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; ITRACONAZOLE; KETOCONAZOLE; LACTONE; LIVER ENZYME; PRODRUG; SIMVASTATIN;

EID: 0030812885     PISSN: 00909556     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (271)

References (33)
  • 1
    • 0027394378 scopus 로고
    • Clinical pharmacokinetics and practical applications of simvastain
    • V. F. Mauro: Clinical pharmacokinetics and practical applications of simvastain. Clin. Pharmacokinet. 24, 195-202 (1993).
    • (1993) Clin. Pharmacokinet. , vol.24 , pp. 195-202
    • Mauro, V.F.1
  • 5
    • 0025240977 scopus 로고
    • Metabolic disposition studies of simvastatin. a cholesterol-lowering prodrug
    • S. Vickers, C. A. Duncan, I.-W. Chen, A. Rosegay, and D. E. Duggan: Metabolic disposition studies of simvastatin. a cholesterol-lowering prodrug. Drug Metab. Dispos. 18, 138-145 (1990).
    • (1990) Drug Metab. Dispos. , vol.18 , pp. 138-145
    • Vickers, S.1    Duncan, C.A.2    Chen, I.-W.3    Rosegay, A.4    Duggan, D.E.5
  • 6
    • 0025944905 scopus 로고
    • Biotransformation of lovastatin: IV. Identification of cytochrome P450 3A proteins as the major enzymes responsible for the oxidative metabolism of lovastatin in rat and human liver microsomes
    • R. W. Wang, P. H. Kari, A. Y. H. Lu, P. E. Thomas, F. P. Guengerich, and K. P. Vyas: Biotransformation of lovastatin: IV. Identification of cytochrome P450 3A proteins as the major enzymes responsible for the oxidative metabolism of lovastatin in rat and human liver microsomes. Arch. Biochem. Biophys. 290, 355-361 (1991).
    • (1991) Arch. Biochem. Biophys. , vol.290 , pp. 355-361
    • Wang, R.W.1    Kari, P.H.2    Lu, A.Y.H.3    Thomas, P.E.4    Guengerich, F.P.5    Vyas, K.P.6
  • 7
    • 0025992864 scopus 로고
    • Oxidation of toxic and carcinogenic chemicals by human cytochrome P450 enzymes
    • F. P. Guengerich and T. Shimadu: Oxidation of toxic and carcinogenic chemicals by human cytochrome P450 enzymes. Chem. Res. Toxicol. 4, 341-407 (1991).
    • (1991) Chem. Res. Toxicol. , vol.4 , pp. 341-407
    • Guengerich, F.P.1    Shimadu, T.2
  • 8
    • 0029998275 scopus 로고    scopus 로고
    • Comparative studies of drug metabolizing enzymes in dog, monkey and human small intestines and in Caco-2 cells
    • T. Prueksaritanont, L. M. Gorham, J. Hochman, L. Tran, and K. P. Vyas: Comparative studies of drug metabolizing enzymes in dog, monkey and human small intestines and in Caco-2 cells. Drug Metab. Dispos. 24, 634-642 (1996).
    • (1996) Drug Metab. Dispos. , vol.24 , pp. 634-642
    • Prueksaritanont, T.1    Gorham, L.M.2    Hochman, J.3    Tran, L.4    Vyas, K.P.5
  • 9
    • 0028858960 scopus 로고
    • Cytochrome P450 inhibitors: Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
    • D. J. Newton, K. W. Wang, and A. Y. H. Lu: Cytochrome P450 inhibitors: Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab. Dispos. 23, 154-158 (1995).
    • (1995) Drug Metab. Dispos. , vol.23 , pp. 154-158
    • Newton, D.J.1    Wang, K.W.2    Lu, A.Y.H.3
  • 10
    • 0028174881 scopus 로고
    • Evaluation of triacetyloleandromycin. α-naphthoflavone and diethyldithiocarbamate as selective chemical probes for inhibition of human cytochromes P450
    • T. K. H. Chang, F. J. Gonzalez, and D. J. Waxman: Evaluation of triacetyloleandromycin. α-naphthoflavone and diethyldithiocarbamate as selective chemical probes for inhibition of human cytochromes P450. Arch. Biochem. Biophys. 311, 437-442 (1994).
    • (1994) Arch. Biochem. Biophys. , vol.311 , pp. 437-442
    • Chang, T.K.H.1    Gonzalez, F.J.2    Waxman, D.J.3
  • 11
    • 0026744568 scopus 로고
    • Cytochrome P450 2E1. and 2A6: Enzymes as major catalysts for metabolic activation of N-nitrosodialkylamines and tobacco-related nitrosamines in human liver microsomes
    • H. Yumazaki, Y. Inui, C-H. Yun, F. P. Guengerich, and T. Shimada, Cytochrome P450 2E1. and 2A6: enzymes as major catalysts for metabolic activation of N-nitrosodialkylamines and tobacco-related nitrosamines in human liver microsomes. Carcinogenesis 13, 1789-1794 (1992).
    • (1992) Carcinogenesis , vol.13 , pp. 1789-1794
    • Yumazaki, H.1    Inui, Y.2    Yun, C.-H.3    Guengerich, F.P.4    Shimada, T.5
  • 15
    • 0027366623 scopus 로고
    • Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytom 4′-hydroxylation
    • K. Chiba, K. Kobayashi, K. Manabe, M. Tam, T. Kamataki, and T. Ishizaki: Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytom 4′-hydroxylation. J. Pharmacol. Exp. Ther. 266, 52-59 (1993)
    • (1993) J. Pharmacol. Exp. Ther. , vol.266 , pp. 52-59
    • Chiba, K.1    Kobayashi, K.2    Manabe, K.3    Tam, M.4    Kamataki, T.5    Ishizaki, T.6
  • 16
    • 0028793072 scopus 로고
    • ( +)-Bufuralol 1′-hydroxylase activity in human and rhesus monkey intestine and liver
    • T. Prueksaritanont, L. M. Dwyer, and A. E. Cribb: ( +)-Bufuralol 1′-hydroxylase activity in human and rhesus monkey intestine and liver. Biochem. Pharmacol. 50, 1521-1525 (1995).
    • (1995) Biochem. Pharmacol. , vol.50 , pp. 1521-1525
    • Prueksaritanont, T.1    Dwyer, L.M.2    Cribb, A.E.3
  • 17
    • 0024993177 scopus 로고
    • Comparison of plasma profiles ot Iovastatin (mevinolin). simvastatin (epistatin) and pravastatin (eptastatin) in the dog
    • R. J. Stubbs, M. S. Schwartz, R. J. Gerson, T. J. Thornton, and W. F. Bayne: Comparison of plasma profiles ot Iovastatin (mevinolin). simvastatin (epistatin) and pravastatin (eptastatin) in the dog. Drug Invest. 2(Suppl. 2), 18-28 (1990).
    • (1990) Drug Invest. , vol.2 , Issue.SUPPL. 2 , pp. 18-28
    • Stubbs, R.J.1    Schwartz, M.S.2    Gerson, R.J.3    Thornton, T.J.4    Bayne, W.F.5
  • 18
    • 0028361593 scopus 로고
    • Inhibition of human CYP3A catalyzed 1′-hydroxy midazolam formation by ketoconazole. nifedipine. erythromycin, cimetidine, and nizatidine
    • S. A. Wrighton, and B. J. Ring: Inhibition of human CYP3A catalyzed 1′-hydroxy midazolam formation by ketoconazole. nifedipine. erythromycin, cimetidine, and nizatidine. Pharm. Res. 11, 921-924 (1994).
    • (1994) Pharm. Res. , vol.11 , pp. 921-924
    • Wrighton, S.A.1    Ring, B.J.2
  • 19
    • 0343083503 scopus 로고
    • 4-lovaslatin as a new cytochrome P450 3A catalyzed metabolite of lovastatin in rat and human liver microsomes
    • 4-lovaslatin as a new cytochrome P450 3A catalyzed metabolite of lovastatin in rat and human liver microsomes. ISSX Proc: 4, 35 (1993).
    • (1993) ISSX Proc. , vol.4 , pp. 35
    • Vyas, K.P.1    Kari, P.H.2    Pitzenberger, S.M.3    Wang, R.W.4    Lu, A.H.Y.5
  • 20
    • 0029114038 scopus 로고
    • Species differences in the metabolism of a potent HIV-I reverse transcriptase inhibitor L-738,372: In vivo and in vitro studies in rats, dogs, nonkeys. and humans
    • T. Prueksaritanont, S. K. Balani, L. M. Dwyer, J. D. Ellis, L. R. Kauffman. S. L. Varga, S. M. Pitzenberger, and A. D. Theoharides: Species differences in the metabolism of a potent HIV-I reverse transcriptase inhibitor L-738,372: In vivo and in vitro studies in rats, dogs, nonkeys. and humans. Drug Metab. Dispos 23, 688-695 (1995).
    • (1995) Drug Metab. Dispos , vol.23 , pp. 688-695
    • Prueksaritanont, T.1    Balani, S.K.2    Dwyer, L.M.3    Ellis, J.D.4    Kauffman, L.R.5    Varga, S.L.6    Pitzenberger, S.M.7    Theoharides, A.D.8
  • 21
    • 0017335453 scopus 로고
    • Prediction of hepatic extraction from in vitro measurement of intrinsic clearance
    • A. Rane. G. R. Wilkinson. and D. G. Shand: Prediction of hepatic extraction from in vitro measurement of intrinsic clearance. J. Pharmacol. Exp. Ther: 200, 420-424 (1977).
    • (1977) J. Pharmacol. Exp. Ther , vol.200 , pp. 420-424
    • Rane, A.1    Wilkinson, G.R.2    Shand, D.G.3
  • 22
    • 0026750647 scopus 로고
    • The human hepatic cytochromes P450 involved in drug metabolism
    • S. A. Wrighton, and J. C. Stevens: The human hepatic cytochromes P450 involved in drug metabolism. Crit. Rev. Toxicol. 22, 1-21 (1992).
    • (1992) Crit. Rev. Toxicol. , vol.22 , pp. 1-21
    • Wrighton, S.A.1    Stevens, J.C.2
  • 23
    • 0028237729 scopus 로고
    • Interindividual variations in human liver cylochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians
    • T. Shimada, H. Yamazaki, M. Mimura, Y. Inui, and F. P. Guengerich: Interindividual variations in human liver cylochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians. J. Pharmacol. Exp. Ther. 270, 414-423 (1994).
    • (1994) J. Pharmacol. Exp. Ther. , vol.270 , pp. 414-423
    • Shimada, T.1    Yamazaki, H.2    Mimura, M.3    Inui, Y.4    Guengerich, F.P.5
  • 25
    • 0025999285 scopus 로고
    • In vitro forcasting of drugs which may interfere with the biotransformation ot midazolam
    • M.-P. Gascon, and P. Dayer: In vitro forcasting of drugs which may interfere with the biotransformation ot midazolam. Eur. J. Clin, Pharmacol. 41, 573-578 (1991).
    • (1991) Eur. J. Clin, Pharmacol. , vol.41 , pp. 573-578
    • Gascon, M.-P.1    Dayer, P.2
  • 26
    • 0029743080 scopus 로고    scopus 로고
    • Midazolam hydroxylation by human liver microsomes in vitro: Inhibition by fluoxetine, norfluoxetine, and by azole antifungal agents
    • L. L. von Moltke, D. J. Greenblatt, J. Schmider, S. X. Duan, C. H. Wright, J. S. Harmatz, and R. I. Shader: Midazolam hydroxylation by human liver microsomes in vitro: Inhibition by fluoxetine, norfluoxetine, and by azole antifungal agents. J. Clin. Pharmacol. 36, 783-791 (1996).
    • (1996) J. Clin. Pharmacol. , vol.36 , pp. 783-791
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Schmider, J.3    Duan, S.X.4    Wright, C.H.5    Harmatz, J.S.6    Shader, R.I.7
  • 27
    • 0029664974 scopus 로고    scopus 로고
    • The effect of the systemic antimycotics. itraconazole and fluconazole, on the pharmacokinetics and pharmacodynamics of intravenous and oral midazolam
    • K. T. Olkkola, J. Ahonen, and P. J. Neuvonen: The effect of the systemic antimycotics. itraconazole and fluconazole, on the pharmacokinetics and pharmacodynamics of intravenous and oral midazolam. Anesth. Anal. 82. 511-516 (1996).
    • (1996) Anesth. Anal. , vol.82 , pp. 511-516
    • Olkkola, K.T.1    Ahonen, J.2    Neuvonen, P.J.3
  • 28
    • 0028357256 scopus 로고
    • Midazolam should be avoided in patients receiving the systemic antimycotics ketoconazole or itraconazole
    • K. T. Olkkola, J. T. Backman, and P. J. Neuvonen: Midazolam should be avoided in patients receiving the systemic antimycotics ketoconazole or itraconazole. Clin. Pharmacol. Ther. 55, 481-485 (1994).
    • (1994) Clin. Pharmacol. Ther. , vol.55 , pp. 481-485
    • Olkkola, K.T.1    Backman, J.T.2    Neuvonen, P.J.3
  • 29
    • 0026591839 scopus 로고
    • Influence of age and gender on the plasma profiles of 3-hydroxy-3-methylglutaryl-Coenzyme A (HMGCoA) reductase inhibitors activity following multiple doses of lovastatin and simvastatin
    • H. Cheng, J. D. Rogers, A. E. Sweany, M. R. Dobrinska, H. A. Stein, A. C. Tate, R. D. Amin, and H. Quan: Influence of age and gender on the plasma profiles of 3-hydroxy-3-methylglutaryl-Coenzyme A (HMGCoA) reductase inhibitors activity following multiple doses of lovastatin and simvastatin. Pharm. Res. 9, 1629-1633 (1992).
    • (1992) Pharm. Res. , vol.9 , pp. 1629-1633
    • Cheng, H.1    Rogers, J.D.2    Sweany, A.E.3    Dobrinska, M.R.4    Stein, H.A.5    Tate, A.C.6    Amin, R.D.7    Quan, H.8
  • 30
    • 0030004755 scopus 로고    scopus 로고
    • In vitro comparative inhibition profiles of major human drug metabolising cytochrome P450 isozymes (CYP2C9, CYP2D6 and CYP3A4) by HMO-CoA reductase inhibitors
    • C. Transon, T. Leemann, and P. Dayer: In vitro comparative inhibition profiles of major human drug metabolising cytochrome P450 isozymes (CYP2C9, CYP2D6 and CYP3A4) by HMO-CoA reductase inhibitors. Eur. J. Clin. Pharmacol. 50, 209-215 (1996).
    • (1996) Eur. J. Clin. Pharmacol. , vol.50 , pp. 209-215
    • Transon, C.1    Leemann, T.2    Dayer, P.3
  • 31
    • 0008854756 scopus 로고    scopus 로고
    • Inhibition of CYP3A by 3-hydroxy-3-methylglularyl-CoA (HMG-CoA) reductase inhibitors
    • T. Ikeda, M. Ishigami, T. Komai, Y. Yamazoe, and Y. Ohno: Inhibition of CYP3A by 3-hydroxy-3-methylglularyl-CoA (HMG-CoA) reductase inhibitors. ISSX Proc. 10, 386 (1996).
    • (1996) ISSX Proc. , vol.10 , pp. 386
    • Ikeda, T.1    Ishigami, M.2    Komai, T.3    Yamazoe, Y.4    Ohno, Y.5
  • 32
    • 0030039063 scopus 로고    scopus 로고
    • Simvastain-oral anticoagulant interaction
    • E. Grau, M. Perella, and E. Pastor: Simvastain-oral anticoagulant interaction. Lancet 347, 405-406 (1996).
    • (1996) Lancet , vol.347 , pp. 405-406
    • Grau, E.1    Perella, M.2    Pastor, E.3
  • 33
    • 0027267722 scopus 로고
    • Human liver microsomal metabolism of the enantiomers of warfarin and acenocoumarol: P450 isozyme diversity determines the differences in their pharmacokinetics
    • J. J. R. Hermans, and H. H. W. Thijssen: Human liver microsomal metabolism of the enantiomers of warfarin and acenocoumarol: P450 isozyme diversity determines the differences in their pharmacokinetics. Br: J. Pharmacol. 110, 482-490 (1993).
    • (1993) Br: J. Pharmacol. , vol.110 , pp. 482-490
    • Hermans, J.J.R.1    Thijssen, H.H.W.2


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