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Volumn 63, Issue 1, 2011, Pages 59-68

HepaRG human hepatic cell line utility as a surrogate for primary human hepatocytes in drug metabolism assessment in vitro

Author keywords

Cytochrome P450; HepaRG; Hepatocyte characterization methods; Intrinsic clearance; P450 enzyme induction; Primary human hepatocytes

Indexed keywords

ALBUMIN; AMIODARONE; BETA NAPHTHOFLAVONE; CARBAMAZEPINE; CLOZAPINE; CYTOCHROME P450 2C19; CYTOCHROME P450 2C9; CYTOCHROME P450 2D6; CYTOCHROME P450 3A4; DEXTROMETHORPHAN; DICLOFENAC; GALACTOSE; GLUCOSE; LACTIC ACID; METHOTREXATE; MEVINOLIN; RIFAMPICIN; SORBITOL; TACRINE; TROGLITAZONE; UREA; VERAPAMIL;

EID: 78650773222     PISSN: 10568719     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vascn.2010.04.013     Document Type: Article
Times cited : (176)

References (42)
  • 3
    • 0021201874 scopus 로고
    • Isolation, culture and characterization of adult human hepatocytes from surgical liver biopsies
    • Ballet F., Bouma M.E., Wang S.R., Amit N., Marais J., Infante R. Isolation, culture and characterization of adult human hepatocytes from surgical liver biopsies. Hepatology 1984, 4:849-854.
    • (1984) Hepatology , vol.4 , pp. 849-854
    • Ballet, F.1    Bouma, M.E.2    Wang, S.R.3    Amit, N.4    Marais, J.5    Infante, R.6
  • 4
    • 0031970304 scopus 로고    scopus 로고
    • Use of heterologously expressed human cytochrome P450 1A2 to predict tacrine-fluvoxamine drug interaction in man
    • Becquemont L., Le Bot M.A., Riche C., Funck-Brentano C., Jaillon P., Beaune P. Use of heterologously expressed human cytochrome P450 1A2 to predict tacrine-fluvoxamine drug interaction in man. Pharmacogenetics 1998, 8:101-108.
    • (1998) Pharmacogenetics , vol.8 , pp. 101-108
    • Becquemont, L.1    Le Bot, M.A.2    Riche, C.3    Funck-Brentano, C.4    Jaillon, P.5    Beaune, P.6
  • 6
    • 0028023851 scopus 로고
    • Contribution of amine oxidases to the metabolism of xenobiotics
    • Benedetti M.S., Dostert P. Contribution of amine oxidases to the metabolism of xenobiotics. Drug Metabolism Reviews 1994, 26:507-535.
    • (1994) Drug Metabolism Reviews , vol.26 , pp. 507-535
    • Benedetti, M.S.1    Dostert, P.2
  • 9
    • 41049105457 scopus 로고    scopus 로고
    • Drug interaction between oral atorvastatin and verapamil in healthy subjects: Effects of atorvastatin on the pharmacokinetics of verapamil and norverapamil
    • Choi D.H., Shin W.G., Choi J.S. Drug interaction between oral atorvastatin and verapamil in healthy subjects: Effects of atorvastatin on the pharmacokinetics of verapamil and norverapamil. European Journal of Clinical Pharmacology 2008, 64:445-449.
    • (2008) European Journal of Clinical Pharmacology , vol.64 , pp. 445-449
    • Choi, D.H.1    Shin, W.G.2    Choi, J.S.3
  • 11
    • 0037272197 scopus 로고    scopus 로고
    • Strategies and molecular probes to investigate the role of cytochrome P450 in drug metabolism: Focus on in vitro studies
    • Donato M.T., Castell J.V. Strategies and molecular probes to investigate the role of cytochrome P450 in drug metabolism: Focus on in vitro studies. Clinical Pharmacokinetics 2003, 42:153-178.
    • (2003) Clinical Pharmacokinetics , vol.42 , pp. 153-178
    • Donato, M.T.1    Castell, J.V.2
  • 14
    • 0031171612 scopus 로고    scopus 로고
    • Time-dependent expression of cytochrome P450 genes in primary cultures of well-differentiated human hepatocytes
    • George J., Goodwin B., Liddle C., Tapner M., Farrel G.C. Time-dependent expression of cytochrome P450 genes in primary cultures of well-differentiated human hepatocytes. Journal of Laboratory and Clinical Medicine 1997, 129:638-648.
    • (1997) Journal of Laboratory and Clinical Medicine , vol.129 , pp. 638-648
    • George, J.1    Goodwin, B.2    Liddle, C.3    Tapner, M.4    Farrel, G.C.5
  • 16
    • 11144326909 scopus 로고    scopus 로고
    • Prediction of in vitro intrinsic clearance from hepatocytes: Comparison of suspensions and monolayer cultures
    • Griffin S.J., Houston J.B. Prediction of in vitro intrinsic clearance from hepatocytes: Comparison of suspensions and monolayer cultures. Drug Metabolism and Disposition 2005, 33:115-120.
    • (2005) Drug Metabolism and Disposition , vol.33 , pp. 115-120
    • Griffin, S.J.1    Houston, J.B.2
  • 18
    • 34247517355 scopus 로고    scopus 로고
    • The human hepatoma HepaRG cells: A highly differentiated model for studies of liver metabolism and toxicity of xenobiotics
    • Guillouzo A., Corlu A., Aninat C., Glaise D., Morel F., Guguen- Guillouzo C. The human hepatoma HepaRG cells: A highly differentiated model for studies of liver metabolism and toxicity of xenobiotics. Chemico-Biological Interactions 2007, 168:66-73.
    • (2007) Chemico-Biological Interactions , vol.168 , pp. 66-73
    • Guillouzo, A.1    Corlu, A.2    Aninat, C.3    Glaise, D.4    Morel, F.5    Guguen- Guillouzo, C.6
  • 19
    • 0027489375 scopus 로고
    • Use of human hepatocyte cultures for drug metabolism studies
    • Guillouzo A., Morel F., Fardel O., Meunier B. Use of human hepatocyte cultures for drug metabolism studies. Toxicology 1993, 82:209-219.
    • (1993) Toxicology , vol.82 , pp. 209-219
    • Guillouzo, A.1    Morel, F.2    Fardel, O.3    Meunier, B.4
  • 20
    • 0034955153 scopus 로고    scopus 로고
    • Studies comparing in vivo: In vitro metabolism of three pharmaceutical compounds in rat, dog, monkey, and human using cryopreserved hepatocytes, microsomes, and collagen gel immobilized hepatocyte cultures
    • Hewitt N.J., Bühring K.U., Dasenbrock J., Haunschild J., Ladstetter B., Utesch D. Studies comparing in vivo: In vitro metabolism of three pharmaceutical compounds in rat, dog, monkey, and human using cryopreserved hepatocytes, microsomes, and collagen gel immobilized hepatocyte cultures. Drug Metabolism and Disposition 2001, 29:1042-1050.
    • (2001) Drug Metabolism and Disposition , vol.29 , pp. 1042-1050
    • Hewitt, N.J.1    Bühring, K.U.2    Dasenbrock, J.3    Haunschild, J.4    Ladstetter, B.5    Utesch, D.6
  • 21
    • 0031921010 scopus 로고    scopus 로고
    • Evaluation of the selectivity of in vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities
    • Hickman D., Wang J.P., Wang Y., Unadkat J.D. Evaluation of the selectivity of in vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities. Drug Metabolism and Disposition 1998, 26:207-215.
    • (1998) Drug Metabolism and Disposition , vol.26 , pp. 207-215
    • Hickman, D.1    Wang, J.P.2    Wang, Y.3    Unadkat, J.D.4
  • 23
  • 27
    • 46449089949 scopus 로고    scopus 로고
    • Evaluation of HepaRG cells as an in vitro model for human drug metabolism studies
    • Kannebratt K.P., Anderson T.B. Evaluation of HepaRG cells as an in vitro model for human drug metabolism studies. Drug Metabolism and Disposition 2008, 36:1444-1452.
    • (2008) Drug Metabolism and Disposition , vol.36 , pp. 1444-1452
    • Kannebratt, K.P.1    Anderson, T.B.2
  • 28
    • 37549004782 scopus 로고    scopus 로고
    • HepaRG cells as an in vitro model for evaluation of cytochrome P450 induction in humans
    • Kannebratt K.P., Andersson T.B. HepaRG cells as an in vitro model for evaluation of cytochrome P450 induction in humans. Drug Metabolism and Disposition 2008, 36:137-145.
    • (2008) Drug Metabolism and Disposition , vol.36 , pp. 137-145
    • Kannebratt, K.P.1    Andersson, T.B.2
  • 29
    • 0024616032 scopus 로고
    • Analysis of plasma protein and lipoprotein synthesis in long-term primary cultures of baboon hepatocytes maintained in serum-free medium
    • Lanford R.E., Carey K.D., Estlack L.E., Smith G.C., Hay R.V. Analysis of plasma protein and lipoprotein synthesis in long-term primary cultures of baboon hepatocytes maintained in serum-free medium. In Vitro Cellular and Developmental Biology 1989, 2:174-182.
    • (1989) In Vitro Cellular and Developmental Biology , vol.2 , pp. 174-182
    • Lanford, R.E.1    Carey, K.D.2    Estlack, L.E.3    Smith, G.C.4    Hay, R.V.5
  • 30
    • 59649100717 scopus 로고    scopus 로고
    • Species-specific toxicity of diclofenac and troglitazone in primary human and rat hepatocytes
    • Lauer B., Tuschl G., Kling M., Mueller S.O. Species-specific toxicity of diclofenac and troglitazone in primary human and rat hepatocytes. Chemico-Biological Interactions 2009, 179:17-24.
    • (2009) Chemico-Biological Interactions , vol.179 , pp. 17-24
    • Lauer, B.1    Tuschl, G.2    Kling, M.3    Mueller, S.O.4
  • 32
    • 33846424676 scopus 로고    scopus 로고
    • Metabolic and non-metabolic factors determining troglitazone hepatotoxicity: A review
    • Masubuchi Y. Metabolic and non-metabolic factors determining troglitazone hepatotoxicity: A review. Drug Metabolism and Pharmacokinetics 2006, 21:347-356.
    • (2006) Drug Metabolism and Pharmacokinetics , vol.21 , pp. 347-356
    • Masubuchi, Y.1
  • 33
    • 0031438749 scopus 로고    scopus 로고
    • Expression of the human aryl hydrocarbon receptor complex in yeast. Activation of transcription by indole compounds
    • Miller C.A. Expression of the human aryl hydrocarbon receptor complex in yeast. Activation of transcription by indole compounds. The Journal of Biological Chemistry 1997, 272:32824-32829.
    • (1997) The Journal of Biological Chemistry , vol.272 , pp. 32824-32829
    • Miller, C.A.1
  • 35
    • 0032733974 scopus 로고    scopus 로고
    • Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
    • Obach R.S. Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes. Drug Metabolism and Disposition 1999, 27:1350-1359.
    • (1999) Drug Metabolism and Disposition , vol.27 , pp. 1350-1359
    • Obach, R.S.1
  • 36
    • 0034925896 scopus 로고    scopus 로고
    • Contributions of five human cytochrome P450 isoforms to the N-demethylation of clozapine in vitro at low and high concentrations
    • Olesen O.V., Linnet K. Contributions of five human cytochrome P450 isoforms to the N-demethylation of clozapine in vitro at low and high concentrations. The Journal of Clinical Pharmacology 2001, 41:823-832.
    • (2001) The Journal of Clinical Pharmacology , vol.41 , pp. 823-832
    • Olesen, O.V.1    Linnet, K.2
  • 37
    • 47949120265 scopus 로고    scopus 로고
    • Pathways of carbamazepine bioactivation in vitro. III. The role of human cytochrome P450 enzymes in the formation of 2, 3-dihydroxycarbamazepine
    • Pearce R.E., Lu W., Wang Y., Uetrecht J.P., Correia M.A., Leeder J.S. Pathways of carbamazepine bioactivation in vitro. III. The role of human cytochrome P450 enzymes in the formation of 2, 3-dihydroxycarbamazepine. Drug Metabolism and Disposition 2008, 36:1637-1649.
    • (2008) Drug Metabolism and Disposition , vol.36 , pp. 1637-1649
    • Pearce, R.E.1    Lu, W.2    Wang, Y.3    Uetrecht, J.P.4    Correia, M.A.5    Leeder, J.S.6
  • 40
    • 0038650658 scopus 로고    scopus 로고
    • Mechanisms of troglitazone hepatotoxicity
    • Smith M.T. Mechanisms of troglitazone hepatotoxicity. Chemical Research in Toxicology 2003, 16:679-687.
    • (2003) Chemical Research in Toxicology , vol.16 , pp. 679-687
    • Smith, M.T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.