메뉴 건너뛰기




Volumn 32, Issue 3, 2004, Pages 295-304

Impact of incubation conditions on bufuralol human clearance predictions: Enzyme lability and nonspecific binding

Author keywords

[No Author keywords available]

Indexed keywords

BUFURALOL; CYTOCHROME P450; CYTOCHROME P450 2D6; DIMETHYLANILINE MONOOXYGENASE; ENZYME; REACTIVE OXYGEN METABOLITE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE;

EID: 1342323556     PISSN: 00909556     EISSN: None     Source Type: Journal    
DOI: 10.1124/dmd.32.3.295     Document Type: Article
Times cited : (29)

References (34)
  • 1
    • 0037407697 scopus 로고    scopus 로고
    • Development and validation of a 96-well equilibrium dialysis apparatus for measuring plasma protein binding
    • Banker MJ, Clark TH, and Williams JA (2002) Development and validation of a 96-well equilibrium dialysis apparatus for measuring plasma protein binding. J Pharm Sci 92:967-974.
    • (2002) J Pharm Sci , vol.92 , pp. 967-974
    • Banker, M.J.1    Clark, T.H.2    Williams, J.A.3
  • 2
    • 0000234213 scopus 로고    scopus 로고
    • In vitro metabolism: FMO and related oxygenations
    • (Woolf TF ed), Marcel Dekker, Inc., New York
    • Cashman JR (1999) In vitro metabolism: FMO and related oxygenations, in Handbook of Drug Metabolism (Woolf TF ed) pp 478-479, Marcel Dekker, Inc., New York.
    • (1999) Handbook of Drug Metabolism , pp. 478-479
    • Cashman, J.R.1
  • 3
    • 0032428779 scopus 로고    scopus 로고
    • In vitro assessment of human cytochrome P450
    • Clarke SE (1998) In vitro assessment of human cytochrome P450. Xenobiotica 28:1167-1202.
    • (1998) Xenobiotica , vol.28 , pp. 1167-1202
    • Clarke, S.E.1
  • 4
    • 0021848782 scopus 로고
    • Effect of oxidative polymorphism (debrisoquine/sparteine type) on hepatic first-pass metabolism of bufuralol
    • Dayer P, Balant L, Kupfer A, Striberni R, and Leemann T (1985) Effect of oxidative polymorphism (debrisoquine/sparteine type) on hepatic first-pass metabolism of bufuralol. Eur J Clin Pharmacol 28:317-320.
    • (1985) Eur J Clin Pharmacol , vol.28 , pp. 317-320
    • Dayer, P.1    Balant, L.2    Kupfer, A.3    Striberni, R.4    Leemann, T.5
  • 5
    • 0021719455 scopus 로고
    • Characterization of a common genetic defect of cytochrome P-450 function (debrisoquinesparteine type polymorphism)-increased Michaelis constant (Km) and loss of stereoselectivity of bufuralol 1′-hydroxylase in poor metabolizers
    • Dayer P, Gasser R, Gut J, Kronbach T, Robertz G, Eichelbaum M, and Meyer UA (1984) Characterization of a common genetic defect of cytochrome P-450 function (debrisoquinesparteine type polymorphism)-increased Michaelis constant (Km) and loss of stereoselectivity of bufuralol 1′-hydroxylase in poor metabolizers. Biochem Biophys Res Commun 125:374-380.
    • (1984) Biochem Biophys Res Commun , vol.125 , pp. 374-380
    • Dayer, P.1    Gasser, R.2    Gut, J.3    Kronbach, T.4    Robertz, G.5    Eichelbaum, M.6    Meyer, U.A.7
  • 6
    • 0023514460 scopus 로고
    • Enzymatic basis of the debrisoquine/sparteine-type genetic polymorphism of drug oxidation-characterization of bufuralol 1′-hydroxylation in liver microsomes of in vivo phenotyped carriers of the genetic deficiency
    • Dayer P, Kronbach, Eichelbaum M and Meyer UA (1987) Enzymatic basis of the debrisoquine/sparteine-type genetic polymorphism of drug oxidation-characterization of bufuralol 1′-hydroxylation in liver microsomes of in vivo phenotyped carriers of the genetic deficiency. Biochem Pharmacol 36:4145-4152.
    • (1987) Biochem Pharmacol , vol.36 , pp. 4145-4152
    • Dayer, P.1    Kronbach2    Eichelbaum, M.3    Meyer, U.A.4
  • 7
    • 0035367218 scopus 로고    scopus 로고
    • Human NADPH-P450 oxidoreductase modulates the level of cytochrome P450 CYP2D6 holoprotein via haem oxygenase-dependent and -independent pathways
    • Ding S, Yao D, Deeni YY, Burchell B, Wolf CR, and Friedberg T (2001) Human NADPH-P450 oxidoreductase modulates the level of cytochrome P450 CYP2D6 holoprotein via haem oxygenase-dependent and -independent pathways. Biochem J 356:613-619.
    • (2001) Biochem J , vol.356 , pp. 613-619
    • Ding, S.1    Yao, D.2    Deeni, Y.Y.3    Burchell, B.4    Wolf, C.R.5    Friedberg, T.6
  • 8
    • 0033570101 scopus 로고    scopus 로고
    • NADPH-dependent microsomal electron transfer increases degradation of CYP2E1 by the proteasome complex: Role of reactive oxygen species
    • Goasduff T and Cederbaum AI (1999) NADPH-dependent microsomal electron transfer increases degradation of CYP2E1 by the proteasome complex: role of reactive oxygen species. Arch Biochem Biophys 370:258-270.
    • (1999) Arch Biochem Biophys , vol.370 , pp. 258-270
    • Goasduff, T.1    Cederbaum, A.I.2
  • 9
    • 0013922473 scopus 로고
    • Time course differences in the metabolism of drugs by hepatic microsomes from rats, rabbits and mice
    • Gram TE and Fouts JR (1966) Time course differences in the metabolism of drugs by hepatic microsomes from rats, rabbits and mice. J Pharmacol Exp Ther 152:363-371.
    • (1966) J Pharmacol Exp Ther , vol.152 , pp. 363-371
    • Gram, T.E.1    Fouts, J.R.2
  • 10
    • 0036707625 scopus 로고    scopus 로고
    • Catalytic specificity of CYP2D isoforms in rat and human
    • Hiroi T, Chow T, Imaoka S, and Funae Y (2002) Catalytic specificity of CYP2D isoforms in rat and human. Drug Metab Dispos 30:970-976.
    • (2002) Drug Metab Dispos , vol.30 , pp. 970-976
    • Hiroi, T.1    Chow, T.2    Imaoka, S.3    Funae, Y.4
  • 11
    • 0344333422 scopus 로고    scopus 로고
    • Prediction of hepatic clearance from microsomes, hepatocytes and liver slices
    • Houston JB and Carlile DJ (1997) Prediction of hepatic clearance from microsomes, hepatocytes and liver slices. Drug Met Rev 29:981-922.
    • (1997) Drug Met Rev , vol.29 , pp. 981-922
    • Houston, J.B.1    Carlile, D.J.2
  • 12
    • 0034827302 scopus 로고    scopus 로고
    • Influence of microsomal concentration on apparent intrinsic clearance: Implications for scaling in vitro data
    • Kalvass JC, Tess DA, Giragossian C, Linhares MC, and Maurer TS (2001) Influence of microsomal concentration on apparent intrinsic clearance: implications for scaling in vitro data. Drug Metab Dispos 29:1332-1336.
    • (2001) Drug Metab Dispos , vol.29 , pp. 1332-1336
    • Kalvass, J.C.1    Tess, D.A.2    Giragossian, C.3    Linhares, M.C.4    Maurer, T.S.5
  • 13
    • 0023258883 scopus 로고
    • High-performance liquid chromatographic assays for bufuralol 1′-hydroxylase, debrisoquine 4-hydroxylase and dextromethorphan O-demethylase in microsomes and purified cytochrome P-450 isozymes of human liver
    • Kronbach T, Mathys D, Gut J, Catin T, and Meyer UA (1987) High-performance liquid chromatographic assays for bufuralol 1′-hydroxylase, debrisoquine 4-hydroxylase and dextromethorphan O-demethylase in microsomes and purified cytochrome P-450 isozymes of human liver. Anal Biochem 162:24-32.
    • (1987) Anal Biochem , vol.162 , pp. 24-32
    • Kronbach, T.1    Mathys, D.2    Gut, J.3    Catin, T.4    Meyer, U.A.5
  • 14
    • 0032815783 scopus 로고    scopus 로고
    • Comparison of CYP2D6 content and metoprolol oxidation between microsomes isolated from human livers and small intestines
    • Madani S, Paine MF, Lewis L, Thummel KE, and Shen DD (1999) Comparison of CYP2D6 content and metoprolol oxidation between microsomes isolated from human livers and small intestines. Pharm Res (NY) 16:1199-1205.
    • (1999) Pharm Res (NY) , vol.16 , pp. 1199-1205
    • Madani, S.1    Paine, M.F.2    Lewis, L.3    Thummel, K.E.4    Shen, D.D.5
  • 15
    • 0032841888 scopus 로고    scopus 로고
    • The role of CYP2C19 in the metabolism of (+/-) bufuralol, the prototypic substrate of CYP2D6
    • Mankowski DC (1999) The role of CYP2C19 in the metabolism of (+/-) bufuralol, the prototypic substrate of CYP2D6. Drug Metab Dispos 27:1024-1028.
    • (1999) Drug Metab Dispos , vol.27 , pp. 1024-1028
    • Mankowski, D.C.1
  • 16
    • 0036233696 scopus 로고    scopus 로고
    • Characterization of cytochrome P450 2D6.1 (CYP2D6.1), CYP2D6.2, and CYP2D6.17 activities toward model CYP2D6 substrates dextromethorphan, bufuralol, and debrisoquine
    • Marcucci KA, Pearce RE, Crespi C, Steimel DT, Leeder JS, and Gaedigk A (2002) Characterization of cytochrome P450 2D6.1 (CYP2D6.1), CYP2D6.2, and CYP2D6.17 activities toward model CYP2D6 substrates dextromethorphan, bufuralol, and debrisoquine. Drug Metab Dispos 30:595-601.
    • (2002) Drug Metab Dispos , vol.30 , pp. 595-601
    • Marcucci, K.A.1    Pearce, R.E.2    Crespi, C.3    Steimel, D.T.4    Leeder, J.S.5    Gaedigk, A.6
  • 17
    • 0037403747 scopus 로고    scopus 로고
    • Impact of nonspecific binding to microsomes and phospholipid on the inhibition of cytochrome P4502D6: Implications for relating in vitro inhibition data to in vivo drug interactions
    • Margolis JM and Obach RS (2003) Impact of nonspecific binding to microsomes and phospholipid on the inhibition of cytochrome P4502D6: implications for relating in vitro inhibition data to in vivo drug interactions. Drug Metab Dispos 31:606-611.
    • (2003) Drug Metab Dispos , vol.31 , pp. 606-611
    • Margolis, J.M.1    Obach, R.S.2
  • 18
    • 0033790094 scopus 로고    scopus 로고
    • Automated definition of the enzymology of drug oxidation by the major human drug metabolizing cytochrome P450s
    • McGinnity DF, Parker AJ, Soars M, and Riley RJ (2000) Automated definition of the enzymology of drug oxidation by the major human drug metabolizing cytochrome P450s. Drug Met Dispos 28:1327-1344.
    • (2000) Drug Met Dispos , vol.28 , pp. 1327-1344
    • McGinnity, D.F.1    Parker, A.J.2    Soars, M.3    Riley, R.J.4
  • 19
    • 0034956777 scopus 로고    scopus 로고
    • Predicting drug pharmacokinetics in humans from in vitro metabolism studies
    • McGinnity DF and Riley RJ (2001) Predicting drug pharmacokinetics in humans from in vitro metabolism studies. Biochem Soc Trans 29(Pt 2):135-139.
    • (2001) Biochem Soc Trans , vol.29 , Issue.PART 2 , pp. 135-139
    • McGinnity, D.F.1    Riley, R.J.2
  • 20
    • 0034010664 scopus 로고    scopus 로고
    • Nonspecific binding of drugs to human liver microsomes
    • McLure JA, Miners JO, and Birkett DJ (2000) Nonspecific binding of drugs to human liver microsomes. Br J Clin Pharmacol 49:453-461.
    • (2000) Br J Clin Pharmacol , vol.49 , pp. 453-461
    • McLure, J.A.1    Miners, J.O.2    Birkett, D.J.3
  • 21
    • 0028199110 scopus 로고
    • Differential roles of cytochromes P450 2D1, 2C11 and 1A1/2 in the hydroxylation of bufuralol by rat liver microsomes
    • Mimura M, Yamazaki H, Sugahara C, Hiroi T, Funae Y, and Shimada T (1994) Differential roles of cytochromes P450 2D1, 2C11 and 1A1/2 in the hydroxylation of bufuralol by rat liver microsomes. Biochem Pharmacol 47:1957-1963.
    • (1994) Biochem Pharmacol , vol.47 , pp. 1957-1963
    • Mimura, M.1    Yamazaki, H.2    Sugahara, C.3    Hiroi, T.4    Funae, Y.5    Shimada, T.6
  • 22
    • 0021254743 scopus 로고
    • Bufuralol metabolism in human liver: A sensitive probe for the debrisoquine-type polymorphism of drug oxidation
    • Minder EI, Meier PJ, Müller HK, Minder C, and Meyer UA (1983) Bufuralol metabolism in human liver: a sensitive probe for the debrisoquine-type polymorphism of drug oxidation. Eur J Clin Investig 14:184-189.
    • (1983) Eur J Clin Investig , vol.14 , pp. 184-189
    • Minder, E.I.1    Meier, P.J.2    Müller, H.K.3    Minder, C.4    Meyer, U.A.5
  • 24
    • 0034835463 scopus 로고    scopus 로고
    • Prediction of human hepatic clearance from in vivo animal experiments and in vitro metabolic studies with liver microsomes from animals and humans
    • Naritomi Y, Terashita S, Kimura S, Suzuki A, Kagayama A, and Sugiyama Y (2001) Prediction of human hepatic clearance from in vivo animal experiments and in vitro metabolic studies with liver microsomes from animals and humans. Drug Metab Dispos 29:1316-1324.
    • (2001) Drug Metab Dispos , vol.29 , pp. 1316-1324
    • Naritomi, Y.1    Terashita, S.2    Kimura, S.3    Suzuki, A.4    Kagayama, A.5    Sugiyama, Y.6
  • 25
    • 0031466149 scopus 로고    scopus 로고
    • Nonspecific binding to microsomes: Impact of scale-up on in vitro intrinsic clearance to hepatic clearance as assessed through examination of warfarin, imipramine and propranolol
    • Obach RS (1997) Nonspecific binding to microsomes: impact of scale-up on in vitro intrinsic clearance to hepatic clearance as assessed through examination of warfarin, imipramine and propranolol. Drug Metab Dispos 25:1359-1369.
    • (1997) Drug Metab Dispos , vol.25 , pp. 1359-1369
    • Obach, R.S.1
  • 26
    • 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 RS (1999) 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 Metab Dispos 27:1350-1359.
    • (1999) Drug Metab Dispos , vol.27 , pp. 1350-1359
    • Obach, R.S.1
  • 28
    • 0028793072 scopus 로고
    • (+)-bufuralol l′-hydroxylation activity in human and rhesus monkey intestine and liver
    • Prueksaritanont T, Dwyer LM, and Cribb AE (1995) (+)-Bufuralol l′-hydroxylation activity in human and rhesus monkey intestine and liver. Biochem Pharmacol 50:1521-1525.
    • (1995) Biochem Pharmacol , vol.50 , pp. 1521-1525
    • Prueksaritanont, T.1    Dwyer, L.M.2    Cribb, A.E.3
  • 29
    • 0031456698 scopus 로고    scopus 로고
    • Preclinical drug metabolism in the age of high-throughput screening: An industrial perspective
    • Rodrigues AD (1997) Preclinical drug metabolism in the age of high-throughput screening: an industrial perspective. Pharm Res (NY) 14:1504-1510.
    • (1997) Pharm Res (NY) , vol.14 , pp. 1504-1510
    • Rodrigues, A.D.1
  • 30
    • 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, and Guengerich FP (1994) 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 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
  • 31
    • 0026750647 scopus 로고
    • The human hepatic cytochromes P450 involved in drug metabolism
    • Wrighton SA and Stevens JC (1992) The human hepatic cytochromes P450 involved in drug metabolism. Crit Rev Toxicol 22:1-21.
    • (1992) Crit Rev Toxicol , vol.22 , pp. 1-21
    • Wrighton, S.A.1    Stevens, J.C.2
  • 34
    • 0036897469 scopus 로고    scopus 로고
    • Expression, purification, biochemical characterization, and comparative function of human cytochrome P450 2D6.1, 2D6.2, 2D6.10 and 2D6.17 allelic isoforms
    • Yu A, Kneller BM, Rettie AE, and Haining RL (2002) Expression, purification, biochemical characterization, and comparative function of human cytochrome P450 2D6.1, 2D6.2, 2D6.10 and 2D6.17 allelic isoforms. J Pharmacol Exp Ther 303:1291-1300.
    • (2002) J Pharmacol Exp Ther , vol.303 , pp. 1291-1300
    • Yu, A.1    Kneller, B.M.2    Rettie, A.E.3    Haining, R.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.