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Volumn 35, Issue 11, 2007, Pages 2119-2126

Use of isolated hepatocyte preparations for cytochrome P450 inhibition studies: Comparison with microsomes for Ki determination

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450; CYTOCHROME P450 2C; CYTOCHROME P450 2D; CYTOCHROME P450 3A; CYTOCHROME P450 INHIBITOR; DEXTROMETHORPHAN; FLUCONAZOLE; FLUOXETINE; FLUVOXAMINE; KETOCONAZOLE; MICONAZOLE; MIDAZOLAM; PHENYTOIN; QUININE; TOLBUTAMIDE;

EID: 35548948469     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.107.017095     Document Type: Article
Times cited : (49)

References (40)
  • 1
    • 0029027857 scopus 로고
    • Prediction of in vivo disposition from in vitro systems: Clearance of phenytoin and tolbutamide using rat hepatic microsomal and hepatocyte data
    • Ashforth EIL, Carlile DJ, Chenery R, and Houston JB (1995) Prediction of in vivo disposition from in vitro systems: clearance of phenytoin and tolbutamide using rat hepatic microsomal and hepatocyte data. J Pharmacol Exp Ther 274:761-766.
    • (1995) J Pharmacol Exp Ther , vol.274 , pp. 761-766
    • Ashforth, E.I.L.1    Carlile, D.J.2    Chenery, R.3    Houston, J.B.4
  • 2
    • 14044251501 scopus 로고    scopus 로고
    • The binding of drugs to hepatocytes and its relationship to physicochemical properties
    • Austin RP, Barton P, Mohmed S, and Riley RJ (2005) The binding of drugs to hepatocytes and its relationship to physicochemical properties. Drug Metab Dispos 33:419-425.
    • (2005) Drug Metab Dispos , vol.33 , pp. 419-425
    • Austin, R.P.1    Barton, P.2    Mohmed, S.3    Riley, R.J.4
  • 3
    • 0014645531 scopus 로고
    • High-yield preparation of isolated rat liver parenchymal cells. A biochemical and fine structural study
    • Berry MN and Friend DS (1969) High-yield preparation of isolated rat liver parenchymal cells. A biochemical and fine structural study. J Cell Biol 43:506-520.
    • (1969) J Cell Biol , vol.43 , pp. 506-520
    • Berry, M.N.1    Friend, D.S.2
  • 4
    • 33748946044 scopus 로고    scopus 로고
    • Prediction of in vivo drug-drug interactions from in vitro data: Factors affecting prototypic drug-drug interactions involving CYP2C9, CYP2D6 and CYP3A4
    • Brown HS, Galetin A, Hallifax D, and Houston JB (2006) Prediction of in vivo drug-drug interactions from in vitro data: factors affecting prototypic drug-drug interactions involving CYP2C9, CYP2D6 and CYP3A4. Clin Pharmacokinet 45:1035-1050.
    • (2006) Clin Pharmacokinet , vol.45 , pp. 1035-1050
    • Brown, H.S.1    Galetin, A.2    Hallifax, D.3    Houston, J.B.4
  • 5
    • 33846405266 scopus 로고    scopus 로고
    • Evaluation of cryopreserved human hepatocytes as an alternative in vitro system to microsomes for the prediction of metabolic clearance
    • Brown HS, Griffin M, and Houston JB (2007) Evaluation of cryopreserved human hepatocytes as an alternative in vitro system to microsomes for the prediction of metabolic clearance. Drug Metab Dispos 35:293-301.
    • (2007) Drug Metab Dispos , vol.35 , pp. 293-301
    • Brown, H.S.1    Griffin, M.2    Houston, J.B.3
  • 6
    • 27444445468 scopus 로고    scopus 로고
    • Prediction of in vivo drug-drug interactions from in vitro data: Impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant
    • Brown HS, Ito K, Galetin A, and Houston JB (2005) Prediction of in vivo drug-drug interactions from in vitro data: impact of incorporating parallel pathways of drug elimination and inhibitor absorption rate constant. Br J Clin Pharmacol 60:508-518.
    • (2005) Br J Clin Pharmacol , vol.60 , pp. 508-518
    • Brown, H.S.1    Ito, K.2    Galetin, A.3    Houston, J.B.4
  • 8
    • 0031895693 scopus 로고    scopus 로고
    • In vivo clearance of ethoxycoumarin and its prediction from in vitro systems. Use of drug depletion and metabolite formation methods in hepatic microsomes and isolated hepatocytes
    • Carlile DJ, Stevens AJ, Ashforth EI, Waghela D, and Houston JB (1998) In vivo clearance of ethoxycoumarin and its prediction from in vitro systems. Use of drug depletion and metabolite formation methods in hepatic microsomes and isolated hepatocytes. Drug Metab Dispos 26:216-221.
    • (1998) Drug Metab Dispos , vol.26 , pp. 216-221
    • Carlile, D.J.1    Stevens, A.J.2    Ashforth, E.I.3    Waghela, D.4    Houston, J.B.5
  • 9
    • 34249335038 scopus 로고    scopus 로고
    • Cytochrome P450 probe substrate metabolism kinetics in Sprague Dawley rats
    • Chovan JP, Ring SC, Yu E, and Baldino JP (2007) Cytochrome P450 probe substrate metabolism kinetics in Sprague Dawley rats. Xenobiotica 37:459-473.
    • (2007) Xenobiotica , vol.37 , pp. 459-473
    • Chovan, J.P.1    Ring, S.C.2    Yu, E.3    Baldino, J.P.4
  • 10
    • 0037307139 scopus 로고    scopus 로고
    • Mechanisms of cellular distribution of psychotropic drugs. Significance for drug action and interactions
    • Daniel WA (2003) Mechanisms of cellular distribution of psychotropic drugs. Significance for drug action and interactions. Prog Neuropsychopharmacol Biol Psychiatry 27:65-73.
    • (2003) Prog Neuropsychopharmacol Biol Psychiatry , vol.27 , pp. 65-73
    • Daniel, W.A.1
  • 11
    • 0141782243 scopus 로고    scopus 로고
    • Demethylation of radiolabelled dextromethorphan in rat microsomes and intact hepatocytes: Kinetics and sensitivity to cytochrome P450 2D6 inhibitors
    • Di Marco A, Yao D, and Laufer R (2003) Demethylation of radiolabelled dextromethorphan in rat microsomes and intact hepatocytes: kinetics and sensitivity to cytochrome P450 2D6 inhibitors. Eur J Biochem 270:3768-3777.
    • (2003) Eur J Biochem , vol.270 , pp. 3768-3777
    • Di Marco, A.1    Yao, D.2    Laufer, R.3
  • 12
    • 27544506707 scopus 로고    scopus 로고
    • Altered AZT glucuronidation kinetics in liver microsomes as an explanation for underprediction of in vivo clearance: Comparison to hepatocytes and effect of incubation environment
    • Engtrakul JJ, Foti RS, Strelevitz TJ, and Fisher MB (2005) Altered AZT glucuronidation kinetics in liver microsomes as an explanation for underprediction of in vivo clearance: comparison to hepatocytes and effect of incubation environment. Drug Metab Dispos 33:1621-1627.
    • (2005) Drug Metab Dispos , vol.33 , pp. 1621-1627
    • Engtrakul, J.J.1    Foti, R.S.2    Strelevitz, T.J.3    Fisher, M.B.4
  • 13
    • 0029790347 scopus 로고    scopus 로고
    • Inhibition and kinetics of cytochrome P4503A activity in microsomes from rat, human, and cDNA expressed human cytochrome P450
    • Ghosal A, Satoh H, Thomas PE, Bush E, and Moore D (1996) Inhibition and kinetics of cytochrome P4503A activity in microsomes from rat, human, and cDNA expressed human cytochrome P450. Drug Metab Dispos 24:940-947.
    • (1996) Drug Metab Dispos , vol.24 , pp. 940-947
    • Ghosal, A.1    Satoh, H.2    Thomas, P.E.3    Bush, E.4    Moore, D.5
  • 14
    • 2042504362 scopus 로고    scopus 로고
    • Comparison of fresh and cryopreserved rat hepatocyte suspensions for the prediction of in vitro intrinsic clearance
    • Griffin SJ and Houston JB (2004) Comparison of fresh and cryopreserved rat hepatocyte suspensions for the prediction of in vitro intrinsic clearance. Drug Metab Dispos 32:552-558.
    • (2004) Drug Metab Dispos , vol.32 , pp. 552-558
    • Griffin, S.J.1    Houston, J.B.2
  • 15
    • 33751100417 scopus 로고    scopus 로고
    • Uptake and intracellular binding of lipophilic amine drugs by isolated rat hepatocytes and implications for the prediction of in vivo metabolic clearance
    • Hallifax D and Houston JB (2006) Uptake and intracellular binding of lipophilic amine drugs by isolated rat hepatocytes and implications for the prediction of in vivo metabolic clearance. Drug Metab Dispos 35:1829-1836.
    • (2006) Drug Metab Dispos , vol.35 , pp. 1829-1836
    • Hallifax, D.1    Houston, J.B.2
  • 16
    • 34547163963 scopus 로고    scopus 로고
    • Saturable uptake of lipophilic amine drugs into isolated hepatocytes: Mechanisms and consequences for quantitative clearance prediction
    • Hallifax D and Houston JB (2007) Saturable uptake of lipophilic amine drugs into isolated hepatocytes: mechanisms and consequences for quantitative clearance prediction. Drug Metab Dispos 35:1325-1332.
    • (2007) Drug Metab Dispos , vol.35 , pp. 1325-1332
    • Hallifax, D.1    Houston, J.B.2
  • 17
    • 28144442034 scopus 로고    scopus 로고
    • Prediction of metabolic clearance using cryopreserved human hepatocytes: Kinetic characteristics for five benzodiazepines
    • Hallifax D, Rawden HC, Hakooz N, and Houston JB (2005) Prediction of metabolic clearance using cryopreserved human hepatocytes: kinetic characteristics for five benzodiazepines. Drug Metab Dispos 33:1852-1858.
    • (2005) Drug Metab Dispos , vol.33 , pp. 1852-1858
    • Hallifax, D.1    Rawden, H.C.2    Hakooz, N.3    Houston, J.B.4
  • 18
    • 0028903015 scopus 로고
    • In vivo disposition of caffeine predicted from hepatic microsomal and hepatocyte data
    • Hayes KA, Brennan B, Chenery R, and Houston JB (1995) In vivo disposition of caffeine predicted from hepatic microsomal and hepatocyte data. Drug Metab Dispos 23:349-353.
    • (1995) Drug Metab Dispos , vol.23 , pp. 349-353
    • Hayes, K.A.1    Brennan, B.2    Chenery, R.3    Houston, J.B.4
  • 20
    • 1942455361 scopus 로고    scopus 로고
    • 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 57:473-86. Erratum 58:565-568.
    • 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 57:473-86. Erratum 58:565-568.
  • 22
    • 0031777718 scopus 로고    scopus 로고
    • Quantitative prediction of in vivo drug clearance and drug interactions from in vitro data on metabolism, together with binding and transport
    • Ito K, Iwatsubo T, Kanamitsu S, Nakajima Y, and Sugiyama Y (1998a) Quantitative prediction of in vivo drug clearance and drug interactions from in vitro data on metabolism, together with binding and transport. Annu Rev Pharmacol Toxicol 38:461-499.
    • (1998) Annu Rev Pharmacol Toxicol , vol.38 , pp. 461-499
    • Ito, K.1    Iwatsubo, T.2    Kanamitsu, S.3    Nakajima, Y.4    Sugiyama, Y.5
  • 23
    • 0031723235 scopus 로고    scopus 로고
    • Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver
    • Ito K, Iwatsubo T, Kanamitsu S, Ueda K, Suzuki H, and Sugiyama Y (1998b) Prediction of pharmacokinetic alterations caused by drug-drug interactions: metabolic interaction in the liver. Pharmacol Rev 50:387-411.
    • (1998) Pharmacol Rev , vol.50 , pp. 387-411
    • Ito, K.1    Iwatsubo, T.2    Kanamitsu, S.3    Ueda, K.4    Suzuki, H.5    Sugiyama, Y.6
  • 24
    • 2042447770 scopus 로고    scopus 로고
    • Quantitative prediction of the in vivo inhibition of diazepam metabolism by omeprazole using rat liver microsomes and hepatocytes
    • Jones HM, Hallifax D, and Houston JB (2004) Quantitative prediction of the in vivo inhibition of diazepam metabolism by omeprazole using rat liver microsomes and hepatocytes. Drug Metab Dispos 32:572-580.
    • (2004) Drug Metab Dispos , vol.32 , pp. 572-580
    • Jones, H.M.1    Hallifax, D.2    Houston, J.B.3
  • 25
    • 0038312064 scopus 로고    scopus 로고
    • Selectivities of human cytochrome P450 inhibitors towards rat P450 isoforms: Study with cDNA-expressed systems of the rat
    • Kobayashi K, Urashima K, Shimada N, and Chiba K (2003) Selectivities of human cytochrome P450 inhibitors towards rat P450 isoforms: study with cDNA-expressed systems of the rat. Drug Metab Dispos 31:833-836.
    • (2003) Drug Metab Dispos , vol.31 , pp. 833-836
    • Kobayashi, K.1    Urashima, K.2    Shimada, N.3    Chiba, K.4
  • 26
    • 0033063815 scopus 로고    scopus 로고
    • Contribution of organic anion transporting polypeptides to uptake of its possible substrates into rat hepatocytes
    • Kouzuki H, Suzuki H, Ito K, Ohashi R, and Sugiyama Y (1999) Contribution of organic anion transporting polypeptides to uptake of its possible substrates into rat hepatocytes. J Pharmacol Exp Ther 288:627-634.
    • (1999) J Pharmacol Exp Ther , vol.288 , pp. 627-634
    • Kouzuki, H.1    Suzuki, H.2    Ito, K.3    Ohashi, R.4    Sugiyama, Y.5
  • 27
    • 0036893242 scopus 로고    scopus 로고
    • Development of a novel in vitro method to predict hepatic clearance using fresh, cryopreserved and sandwich-cultured hepatocytes
    • Lau YY, Sapidou E, Cui X, White RE, and Cheng KC (2002) Development of a novel in vitro method to predict hepatic clearance using fresh, cryopreserved and sandwich-cultured hepatocytes. Drug Metab Dispos 30:1446-1454.
    • (2002) Drug Metab Dispos , vol.30 , pp. 1446-1454
    • Lau, Y.Y.1    Sapidou, E.2    Cui, X.3    White, R.E.4    Cheng, K.C.5
  • 30
    • 34047131190 scopus 로고    scopus 로고
    • Comparison of inhibition potentials of drugs against zidovudine glucuronidation in rat hepatocytes and liver microsomes
    • Mano Y, Usui T and Kamimura H (2007) Comparison of inhibition potentials of drugs against zidovudine glucuronidation in rat hepatocytes and liver microsomes. Drug Metab Dispos 35:602-606.
    • (2007) Drug Metab Dispos , vol.35 , pp. 602-606
    • Mano, Y.1    Usui, T.2    Kamimura, H.3
  • 32
    • 0036320379 scopus 로고    scopus 로고
    • Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: An application of serum incubation method
    • Shibata Y, Takahashi H, Chiba M, and Ishii Y (2002) Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: an application of serum incubation method. Drug Metab Dispos 30:892-896.
    • (2002) Drug Metab Dispos , vol.30 , pp. 892-896
    • Shibata, Y.1    Takahashi, H.2    Chiba, M.3    Ishii, Y.4
  • 33
    • 0036194124 scopus 로고    scopus 로고
    • In vitro analysis of human drug glucuronidation and prediction of in vivo metabolic clearance
    • Soars MG, Burchell B, and Riley RJ (2002) In vitro analysis of human drug glucuronidation and prediction of in vivo metabolic clearance. J Pharmacol Exp Ther 301:382-390.
    • (2002) J Pharmacol Exp Ther , vol.301 , pp. 382-390
    • Soars, M.G.1    Burchell, B.2    Riley, R.J.3
  • 34
    • 0026569805 scopus 로고
    • Cytochromes P450 in rats: Structures, functions, properties and relevant human forms
    • Soucek P and Gut I (1992) Cytochromes P450 in rats: structures, functions, properties and relevant human forms. Xenobiotica 22:83-103.
    • (1992) Xenobiotica , vol.22 , pp. 83-103
    • Soucek, P.1    Gut, I.2
  • 35
    • 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, and Shader RI (1994) 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 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
  • 36
    • 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, and Shader RI (1995) Inhibition of Alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: comparison with other selective serotonin reuptake inhibitor antidepressants. J Clin Psychopharmacol 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
  • 37
    • 0032968065 scopus 로고    scopus 로고
    • Sigmoidal kinetics of CYP3A substrates: An approach for scaling dextromethorphan metabolism in hepatic microsomes and isolated hepatocytes to predict in vivo clearance in rat
    • Witherow LE and Houston JB (1999) Sigmoidal kinetics of CYP3A substrates: An approach for scaling dextromethorphan metabolism in hepatic microsomes and isolated hepatocytes to predict in vivo clearance in rat. J Pharmacol Exp Ther 290:58-65.
    • (1999) J Pharmacol Exp Ther , vol.290 , pp. 58-65
    • Witherow, L.E.1    Houston, J.B.2
  • 38
    • 0029807153 scopus 로고    scopus 로고
    • Metabolite kinetics of ondansetron in rat. Comparison of hepatic microsomes, isolated hepatocytes and liver slices, with in vivo disposition
    • Worboys PD, Brennan B, Bradbury A, and Houston JB (1996) Metabolite kinetics of ondansetron in rat. Comparison of hepatic microsomes, isolated hepatocytes and liver slices, with in vivo disposition. Xenobiotica 26:897-907.
    • (1996) Xenobiotica , vol.26 , pp. 897-907
    • Worboys, P.D.1    Brennan, B.2    Bradbury, A.3    Houston, J.B.4
  • 39
    • 17644380257 scopus 로고    scopus 로고
    • Predicting drug disposition via application of BCS: Transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system
    • Wu CY and Benet LZ (2005) Predicting drug disposition via application of BCS: transport/absorption/elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharmacol Res 22:11-23.
    • (2005) Pharmacol Res , vol.22 , pp. 11-23
    • Wu, C.Y.1    Benet, L.Z.2
  • 40
    • 0032941364 scopus 로고    scopus 로고
    • Quantitative prediction of metabolic inhibition of midazolam by itraconazole and ketoconazole in rats: Implication of concentrative uptake of inhibitors into liver
    • Yamano K, Yamamoto K, Kotaki H, Sawada Y, and Iga T (1999) Quantitative prediction of metabolic inhibition of midazolam by itraconazole and ketoconazole in rats: implication of concentrative uptake of inhibitors into liver. Drug Metab Dispos 27:395-402.
    • (1999) Drug Metab Dispos , vol.27 , pp. 395-402
    • Yamano, K.1    Yamamoto, K.2    Kotaki, H.3    Sawada, Y.4    Iga, T.5


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