메뉴 건너뛰기




Volumn 38, Issue 2, 1998, Pages 106-111

Protease inhibitors as inhibitors of human cytochromes P450: High risk associated with ritonavir

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA NAPHTHOFLAVONE; ANTIVIRUS AGENT; CHLORZOXAZONE; CYTOCHROME P450; CYTOCHROME P450 INHIBITOR; DESIPRAMINE; DEXTROMETHORPHAN; DIETHYLDITHIOCARBAMIC ACID; FLUOXETINE; INDINAVIR; KETOCONAZOLE; MEPHENYTOIN; NELFINAVIR; PHENACETIN; PROTEINASE INHIBITOR; QUINIDINE; RITONAVIR; SAQUINAVIR; SULFAPHENAZOLE; TOLBUTAMIDE; TRIAZOLAM;

EID: 0031931102     PISSN: 00912700     EISSN: None     Source Type: Journal    
DOI: 10.1002/j.1552-4604.1998.tb04398.x     Document Type: Article
Times cited : (249)

References (31)
  • 1
    • 0031024623 scopus 로고    scopus 로고
    • HIV-1 protease inhibitors: A review for clinicians
    • Deeks SG, Smith M, Holodniy M, Kahn JO: HIV-1 protease inhibitors: a review for clinicians. JAMA 1997;277:145-153.
    • (1997) JAMA , vol.277 , pp. 145-153
    • Deeks, S.G.1    Smith, M.2    Holodniy, M.3    Kahn, J.O.4
  • 3
    • 0030993833 scopus 로고    scopus 로고
    • Human immunodeficiency virus type 1 protease inhibitors
    • McDonald CK, Kuritzkes DR: Human immunodeficiency virus type 1 protease inhibitors. Arch Intern Med 1997;157:951-959.
    • (1997) Arch Intern Med , vol.157 , pp. 951-959
    • McDonald, C.K.1    Kuritzkes, D.R.2
  • 4
    • 0029803481 scopus 로고    scopus 로고
    • Risks and synergies from drug interactions
    • Sahai J: Risks and synergies from drug interactions. AIDS 1996;10(suppl 1):S21-S25.
    • (1996) AIDS , vol.10 , Issue.1 SUPPL.
    • Sahai, J.1
  • 5
    • 0030895312 scopus 로고    scopus 로고
    • Protease inhibitors in patients with HIV disease: Clinically important pharmacokinetic considerations
    • Barry M, Gibbons S, Back D, Mulcahy F: Protease inhibitors in patients with HIV disease: clinically important pharmacokinetic considerations. Clin Pharmacokinet 1997;32:194-209.
    • (1997) Clin Pharmacokinet , vol.32 , pp. 194-209
    • Barry, M.1    Gibbons, S.2    Back, D.3    Mulcahy, F.4
  • 7
    • 0029853923 scopus 로고    scopus 로고
    • Phenacetin O-deethylation by human liver microsomes in vitro: Inhibition by chemical probes, SSRI antidepressants, nefazodone, and venlafaxine
    • von Moltke LL, Greenblatt DJ, Duan SX, Schmider J, Kudchadker L, Fogelman SM, et al: Phenacetin O-deethylation by human liver microsomes in vitro: inhibition by chemical probes, SSRI antidepressants, nefazodone, and venlafaxine. Psychopharmacol 1996;128:398-407.
    • (1996) Psychopharmacol , vol.128 , pp. 398-407
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Duan, S.X.3    Schmider, J.4    Kudchadker, L.5    Fogelman, S.M.6
  • 8
    • 0030706197 scopus 로고    scopus 로고
    • Inhibition of CYP2C9 by selective serotonin reuptake inhibitors in vitro: Studies of phenytoin para-hydroxylation
    • Schmider J, Greenblatt DJ, von Moltke LL, Karsov D, Shader RI: Inhibition of CYP2C9 by selective serotonin reuptake inhibitors in vitro: studies of phenytoin para-hydroxylation. Br J Clin Pharmacol 1997;44:495-498.
    • (1997) Br J Clin Pharmacol , vol.44 , pp. 495-498
    • Schmider, J.1    Greenblatt, D.J.2    Von Moltke, L.L.3    Karsov, D.4    Shader, R.I.5
  • 9
    • 0030041594 scopus 로고    scopus 로고
    • Characterization of six in vitro reactions mediated by human cytochrome P450: Application to the testing of cytochrome P450-directed antibodies
    • Schmider J, Greenblatt DJ, von Moltke LL, Harmatz JS, Duan SX, Karsov D, Shader RI: Characterization of six in vitro reactions mediated by human cytochrome P450: application to the testing of cytochrome P450-directed antibodies. Pharmacology 1996; 52:125-134.
    • (1996) Pharmacology , vol.52 , pp. 125-134
    • Schmider, J.1    Greenblatt, D.J.2    Von Moltke, L.L.3    Harmatz, J.S.4    Duan, S.X.5    Karsov, D.6    Shader, R.I.7
  • 10
    • 0030889604 scopus 로고    scopus 로고
    • Metabolism of dextromethorphan in vitro: Involvement of cytochromes P450 2D6, 3A3/4, with a possible role of 2E1
    • Schmider J, Greenblatt DJ, Fogelman SM, von Moltke LL, Shader RI: Metabolism of dextromethorphan in vitro: involvement of cytochromes P450 2D6, 3A3/4, with a possible role of 2E1. Biopharmaceut Drug Dispos 1997;18:227-240.
    • (1997) Biopharmaceut Drug Dispos , vol.18 , pp. 227-240
    • Schmider, J.1    Greenblatt, D.J.2    Fogelman, S.M.3    Von Moltke, L.L.4    Shader, R.I.5
  • 11
    • 0028194864 scopus 로고
    • Inhibition of desipramine hydroxylation in vitro by serotonin-reuptake-inhibitor antidepressants, and by quinidine and ketoconazole: A model system to predict drug interactions in vivo
    • von Moltke LL, Greenblatt DJ, Cotreau-Bibbo MM, Duan SX, Harmatz JS, Shader RI: Inhibition of desipramine hydroxylation in vitro by serotonin-reuptake-inhibitor antidepressants, and by quinidine and ketoconazole: a model system to predict drug interactions in vivo. J Pharmacol Exp Ther 1994;268:1278-1283.
    • (1994) J Pharmacol Exp Ther , vol.268 , pp. 1278-1283
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Cotreau-Bibbo, M.M.3    Duan, S.X.4    Harmatz, J.S.5    Shader, R.I.6
  • 12
    • 0028898816 scopus 로고
    • Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: Comparison with other selective serotonin reuptake inhibitor antidepressants
    • von Moltke LL, Greenblatt DJ, Court MH, Duan SX, Harmatz JS, Shader RI: Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: comparison with other selective serotonin reuptake inhibitor antidepressants. J Clin Psychopharmacol 1995;15:125-131.
    • (1995) J Clin Psychopharmacol , vol.15 , pp. 125-131
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Court, M.H.3    Duan, S.X.4    Harmatz, J.S.5    Shader, R.I.6
  • 13
    • 0030894106 scopus 로고    scopus 로고
    • Biotransformation of chlorzoxazone by hepatic microsomes from humans and ten other mammalian species
    • Court MH, von Moltke LL, Shader RI, Greenblatt DJ: Biotransformation of chlorzoxazone by hepatic microsomes from humans and ten other mammalian species. Biopharmaceut Drug Dispos 1997;18:213-226.
    • (1997) Biopharmaceut Drug Dispos , vol.18 , pp. 213-226
    • Court, M.H.1    Von Moltke, L.L.2    Shader, R.I.3    Greenblatt, D.J.4
  • 14
    • 0030077245 scopus 로고    scopus 로고
    • Triazolam biotransformation by human liver microsomes in vitro: Effects of metabolic inhibitors, and clinical confirmation of a predicted interaction with ketoconazole
    • von Moltke LL, Greenblatt DJ, Harmatz JS, Duan SX, Harrel LM, Cotreau-Bibbo MM, et al: Triazolam biotransformation by human liver microsomes in vitro: effects of metabolic inhibitors, and clinical confirmation of a predicted interaction with ketoconazole. J Pharmacol Exp Ther 1996;276:370-379.
    • (1996) J Pharmacol Exp Ther , vol.276 , pp. 370-379
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Harmatz, J.S.3    Duan, S.X.4    Harrel, L.M.5    Cotreau-Bibbo, M.M.6
  • 16
    • 0028858960 scopus 로고
    • Cytochrome P450 inhibitors: Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
    • Newton DJ, Wang RW, Lu AYH: Cytochrome P450 inhibitors: evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab Dispos 1995; 23:154-158.
    • (1995) Drug Metab Dispos , vol.23 , pp. 154-158
    • Newton, D.J.1    Wang, R.W.2    Lu, A.Y.H.3
  • 17
    • 0030022629 scopus 로고    scopus 로고
    • An overview of current cytochrome P450 technology for assessing the safety and efficacy of new materials
    • Parkinson A: An overview of current cytochrome P450 technology for assessing the safety and efficacy of new materials. Toxicol Pathol 1996;24:45-57.
    • (1996) Toxicol Pathol , vol.24 , pp. 45-57
    • Parkinson, A.1
  • 19
    • 0030935086 scopus 로고    scopus 로고
    • Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions
    • Bertz RJ, Granneman GR: Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin Pharmacokinet 1997;32:210-258.
    • (1997) Clin Pharmacokinet , vol.32 , pp. 210-258
    • Bertz, R.J.1    Granneman, G.R.2
  • 21
    • 0030852009 scopus 로고    scopus 로고
    • Differential inhibition of cytochrome P450 isoforms by the protease inhibitors, ritonavir, saquinavir and indinavir
    • Eagling VA, Back DJ, Barry MG: Differential inhibition of cytochrome P450 isoforms by the protease inhibitors, ritonavir, saquinavir and indinavir. Br J Clin Pharmacol 1997;44:190-194.
    • (1997) Br J Clin Pharmacol , vol.44 , pp. 190-194
    • Eagling, V.A.1    Back, D.J.2    Barry, M.G.3
  • 22
    • 0030430035 scopus 로고    scopus 로고
    • Cytochrome P450-mediated metabolism of the HIV-1 protease inhibitor ritonavir (ABT-538) in human liver microsomes
    • Kumar GN, Rodrigues AD, Buko AM, Denissen JF: Cytochrome P450-mediated metabolism of the HIV-1 protease inhibitor ritonavir (ABT-538) in human liver microsomes. J Pharmacol Exp Ther 1996;277:423-431.
    • (1996) J Pharmacol Exp Ther , vol.277 , pp. 423-431
    • Kumar, G.N.1    Rodrigues, A.D.2    Buko, A.M.3    Denissen, J.F.4
  • 23
    • 0029872126 scopus 로고    scopus 로고
    • Role of cytochrome P450 3A4 in human metabolism of MK-639, a potent human immunodeficiency virus protease inhibitor
    • Chiba M, Hensleigh M, Nishime JA, Balani SK, Lin JH: Role of cytochrome P450 3A4 in human metabolism of MK-639, a potent human immunodeficiency virus protease inhibitor. Drug Metab Dispos 1996;24:307-314.
    • (1996) Drug Metab Dispos , vol.24 , pp. 307-314
    • Chiba, M.1    Hensleigh, M.2    Nishime, J.A.3    Balani, S.K.4    Lin, J.H.5
  • 24
    • 0030908131 scopus 로고    scopus 로고
    • Hepatic and intestinal metabolism of indinavir, an HIV protease inhibitor, in rat and human microsomes
    • Chiba M, Hensleigh M, Lin JH: Hepatic and intestinal metabolism of indinavir, an HIV protease inhibitor, in rat and human microsomes. Biochem Pharmacol 1997;53:1187-1195.
    • (1997) Biochem Pharmacol , vol.53 , pp. 1187-1195
    • Chiba, M.1    Hensleigh, M.2    Lin, J.H.3
  • 25
    • 0029125984 scopus 로고
    • Metabolism of drugs by cytochrome P450 3A isoforms: Implications for drug interactions in psychopharmacology
    • von Moltke LL, Greenblatt DJ, Schmider J, Harmatz JS, Shader RI: Metabolism of drugs by cytochrome P450 3A isoforms: implications for drug interactions in psychopharmacology. Clin Pharmacokinet 1995;29(suppl 1):33-43.
    • (1995) Clin Pharmacokinet , vol.29 , Issue.1 SUPPL. , pp. 33-43
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Schmider, J.3    Harmatz, J.S.4    Shader, R.I.5
  • 26
    • 0028237729 scopus 로고
    • Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians
    • Shimada T, Yamazaki H, Mimura M, Inui Y, Guengerich FP: Interindividual variations in human liver cytochrome 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 1994;270:414-423.
    • (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
  • 27
    • 0026464616 scopus 로고
    • Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes
    • Kolars JC, Schmiedlin-Ren P, Schuetz JD, Fang C, Watkins PB: Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes. J Clin Invest 1992;90:1871-1878.
    • (1992) J Clin Invest , vol.90 , pp. 1871-1878
    • Kolars, J.C.1    Schmiedlin-Ren, P.2    Schuetz, J.D.3    Fang, C.4    Watkins, P.B.5
  • 28
    • 0030036673 scopus 로고    scopus 로고
    • Relationship of in vitro data on drug metabolism to in vivo pharmacokinetics and drug interactions: Implications for diazepam disposition in humans
    • Schmider J, Greenblatt DJ, von Moltke LL, Shader RI: Relationship of in vitro data on drug metabolism to in vivo pharmacokinetics and drug interactions: implications for diazepam disposition in humans. J Clin Psychopharmacol 1996;16:267-272.
    • (1996) J Clin Psychopharmacol , vol.16 , pp. 267-272
    • Schmider, J.1    Greenblatt, D.J.2    Von Moltke, L.L.3    Shader, R.I.4
  • 29
    • 0031024382 scopus 로고    scopus 로고
    • Selective biotransformation of the human immunodeficiency virus protease inhibitor saquinavir by human small-intestinal cytochrome P4503A4
    • Fitzsimmons ME, Collins JM: Selective biotransformation of the human immunodeficiency virus protease inhibitor saquinavir by human small-intestinal cytochrome P4503A4. Drug Metab Dispos 1997;25:256-266.
    • (1997) Drug Metab Dispos , vol.25 , pp. 256-266
    • Fitzsimmons, M.E.1    Collins, J.M.2
  • 30
    • 0031035968 scopus 로고    scopus 로고
    • Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir
    • Kempf DJ, Marsh KC, Kumar G, Rodrigues AD, Denissen JF, McDonald E, et al: Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir. Antimicrob Agents Chemother 1997;41:654-660.
    • (1997) Antimicrob Agents Chemother , vol.41 , pp. 654-660
    • Kempf, D.J.1    Marsh, K.C.2    Kumar, G.3    Rodrigues, A.D.4    Denissen, J.F.5    McDonald, E.6
  • 31
    • 0031054507 scopus 로고    scopus 로고
    • Saquinavir pharmacokinetics alone and in combination with ritonavir in HIV-infected patients
    • Merry C, Barry MG, Mulcahy F, Ryan M, Heavey J, Tjia JF, et al: Saquinavir pharmacokinetics alone and in combination with ritonavir in HIV-infected patients. AIDS 1997;11:F29-F33.
    • (1997) AIDS , vol.11
    • Merry, C.1    Barry, M.G.2    Mulcahy, F.3    Ryan, M.4    Heavey, J.5    Tjia, J.F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.