메뉴 건너뛰기




Volumn 78, Issue 12, 2009, Pages 1483-1490

Identification of the major human hepatic and placental enzymes responsible for the biotransformation of glyburide

Author keywords

Enzymes; Glyburide; Glyburide metabolism; Human liver; Human placenta

Indexed keywords

4 METHYLPYRAZOLE; ALPHA NAPHTHOFLAVONE; AROMATASE; CYTOCHROME P450; CYTOCHROME P450 2C19; CYTOCHROME P450 2C8; CYTOCHROME P450 2C9; CYTOCHROME P450 3A4; DRUG METABOLITE; FORMESTANE; GLIBENCLAMIDE; KETOCONAZOLE; LANSOPRAZOLE; QUINIDINE; SULFAPHENAZOLE; TROLEANDOMYCIN;

EID: 70349989948     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcp.2009.08.003     Document Type: Article
Times cited : (61)

References (42)
  • 1
    • 0034687440 scopus 로고    scopus 로고
    • A comparison of glyburide and insulin in women with gestational diabetes mellitus
    • Langer O., Conway D.L., Bercus M.D., Xenakis E.M.-J., and Gonzales O. A comparison of glyburide and insulin in women with gestational diabetes mellitus. N Engl J Med 343 (2000) 1134-1138
    • (2000) N Engl J Med , vol.343 , pp. 1134-1138
    • Langer, O.1    Conway, D.L.2    Bercus, M.D.3    Xenakis, E.M.-J.4    Gonzales, O.5
  • 2
    • 22244442141 scopus 로고    scopus 로고
    • Comparison of glyburide and insulin for the management of gestational diabetes in a large managed care organization
    • Jacobson G.F., Ramos G.A., Ching J.Y., Kirby R.S., Ferrara A., and Field R. Comparison of glyburide and insulin for the management of gestational diabetes in a large managed care organization. Am J Obstet Gynecol 193 (2005) 118-124
    • (2005) Am J Obstet Gynecol , vol.193 , pp. 118-124
    • Jacobson, G.F.1    Ramos, G.A.2    Ching, J.Y.3    Kirby, R.S.4    Ferrara, A.5    Field, R.6
  • 3
    • 67349105306 scopus 로고    scopus 로고
    • Are we optimizing gestational diabetes treatment with glyburide? The pharmacologic basis for better clinical practice
    • Hebert M.F., Ma X., Naraharisetti S.B., Krudys K.M., Umans J., Hankins G.D.V., et al. Are we optimizing gestational diabetes treatment with glyburide? The pharmacologic basis for better clinical practice. Clin Pharmacol Ther 85 (2009) 607-614
    • (2009) Clin Pharmacol Ther , vol.85 , pp. 607-614
    • Hebert, M.F.1    Ma, X.2    Naraharisetti, S.B.3    Krudys, K.M.4    Umans, J.5    Hankins, G.D.V.6
  • 6
    • 33751085933 scopus 로고    scopus 로고
    • Identification of glyburide metabolites formed by hepatic and placental microsomes of humans and baboons
    • Ravindran S., Zharikova O.L., Hill R.A., Nanovskaya T.N., Hankins G.D., and Ahmed M.S. Identification of glyburide metabolites formed by hepatic and placental microsomes of humans and baboons. Biochem Pharmacol 72 (2006) 1730-1737
    • (2006) Biochem Pharmacol , vol.72 , pp. 1730-1737
    • Ravindran, S.1    Zharikova, O.L.2    Hill, R.A.3    Nanovskaya, T.N.4    Hankins, G.D.5    Ahmed, M.S.6
  • 8
    • 0000327981 scopus 로고
    • Resorption, excretion and metabolism after intravenous and oral administration of HB 419-14C in man
    • [in German]
    • Rupp W., Christ O., and Heptner W. Resorption, excretion and metabolism after intravenous and oral administration of HB 419-14C in man. Arzneimittelforschung 19 (1969) 1428-1434 [in German]
    • (1969) Arzneimittelforschung , vol.19 , pp. 1428-1434
    • Rupp, W.1    Christ, O.2    Heptner, W.3
  • 9
    • 0015578693 scopus 로고
    • Metabolism and kinetics of the hypoglycemic agent glipizide in man-comparison with glibenclamide
    • Fuccella L.M., Tamassia V., and Valzelli G. Metabolism and kinetics of the hypoglycemic agent glipizide in man-comparison with glibenclamide. J Clin Pharmacol 13 (1973) 68-75
    • (1973) J Clin Pharmacol , vol.13 , pp. 68-75
    • Fuccella, L.M.1    Tamassia, V.2    Valzelli, G.3
  • 10
    • 0016435231 scopus 로고
    • Comparison of the pharmacokinetics of glipizide and glibenclamide in man
    • Balant L., Fabre J., and Zahnd G.R. Comparison of the pharmacokinetics of glipizide and glibenclamide in man. Eur J Clin Pharmacol 8 (1975) 63-69
    • (1975) Eur J Clin Pharmacol , vol.8 , pp. 63-69
    • Balant, L.1    Fabre, J.2    Zahnd, G.R.3
  • 11
    • 0026064513 scopus 로고
    • Determination of glibenclamide and its two major metabolites in human serum and urine by column liquid chromatography
    • Rydberg T., Wǻhlin-Boll E., and Melander A. Determination of glibenclamide and its two major metabolites in human serum and urine by column liquid chromatography. J Chromatogr 564 (1991) 223-233
    • (1991) J Chromatogr , vol.564 , pp. 223-233
    • Rydberg, T.1    Wǻhlin-Boll, E.2    Melander, A.3
  • 12
    • 0030947756 scopus 로고    scopus 로고
    • Concentration-effect relations of glibenclamide and its active metabolites in man: modelling of pharmacokinetics and pharmacodynamics
    • Rydberg T., Jönsson A., Karisson M.O., and Melander A. Concentration-effect relations of glibenclamide and its active metabolites in man: modelling of pharmacokinetics and pharmacodynamics. Br J Clin Pharmacol 43 (1997) 373-381
    • (1997) Br J Clin Pharmacol , vol.43 , pp. 373-381
    • Rydberg, T.1    Jönsson, A.2    Karisson, M.O.3    Melander, A.4
  • 13
    • 0035666448 scopus 로고    scopus 로고
    • Effects and serum levels of glibenclamide and its active metabolites in patients with type 2 diabetes
    • Jönsson A., Hallengren B., Rydberg T., and Melander A. Effects and serum levels of glibenclamide and its active metabolites in patients with type 2 diabetes. Diabetes Obes Metab 3 (2001) 403-409
    • (2001) Diabetes Obes Metab , vol.3 , pp. 403-409
    • Jönsson, A.1    Hallengren, B.2    Rydberg, T.3    Melander, A.4
  • 14
    • 0032559355 scopus 로고    scopus 로고
    • Application of liquid chromatography-mass spectrometry analyses to the characterization of novel glyburide metabolites formed in vitro
    • Tiller P.R., Land A.P., Jardine I., Murphy D.M., Sozio R., Ayrton A., et al. Application of liquid chromatography-mass spectrometry analyses to the characterization of novel glyburide metabolites formed in vitro. J Chromatogr A 794 (1998) 15-25
    • (1998) J Chromatogr A , vol.794 , pp. 15-25
    • Tiller, P.R.1    Land, A.P.2    Jardine, I.3    Murphy, D.M.4    Sozio, R.5    Ayrton, A.6
  • 15
    • 0036231580 scopus 로고    scopus 로고
    • Impact of CYP2C9 amino acid polymorphisms on glyburide kinetics and on the insulin and glucose response in healthy volunteers
    • Kirchheiner J., Brockmöller J., Meineke I., Bauer S., Rohde W., Meisel C., et al. Impact of CYP2C9 amino acid polymorphisms on glyburide kinetics and on the insulin and glucose response in healthy volunteers. Clin Pharmacol Ther 71 (2002) 286-296
    • (2002) Clin Pharmacol Ther , vol.71 , pp. 286-296
    • Kirchheiner, J.1    Brockmöller, J.2    Meineke, I.3    Bauer, S.4    Rohde, W.5    Meisel, C.6
  • 17
    • 25844461719 scopus 로고    scopus 로고
    • Chow MSS. CYP2C9, but not CYP2C19, polymorphisms affect the pharmacokinetics and pharmacodynamics of glyburide in Chinese subjects
    • Yin O.Q.P., and Tomlinson B. Chow MSS. CYP2C9, but not CYP2C19, polymorphisms affect the pharmacokinetics and pharmacodynamics of glyburide in Chinese subjects. Clin Pharmacol Ther 78 (2005) 370-377
    • (2005) Clin Pharmacol Ther , vol.78 , pp. 370-377
    • Yin, O.Q.P.1    Tomlinson, B.2
  • 18
    • 0036227955 scopus 로고    scopus 로고
    • In vivo and in vitro studies exploring the pharmacokinetic interaction between bosentan, a dual endothelin receptor antagonist, and glyburide
    • Van Giersbergen P.L., Treiber A., Clozel M., Bodin F., and Dingemanse J. In vivo and in vitro studies exploring the pharmacokinetic interaction between bosentan, a dual endothelin receptor antagonist, and glyburide. Clin Pharmacol Ther 71 (2002) 253-262
    • (2002) Clin Pharmacol Ther , vol.71 , pp. 253-262
    • Van Giersbergen, P.L.1    Treiber, A.2    Clozel, M.3    Bodin, F.4    Dingemanse, J.5
  • 19
    • 3142559792 scopus 로고    scopus 로고
    • Identification and relative contributions of human cytochrome P450 isoforms involved in the metabolism of glibenclamide and lansoprazole: evaluation of an approach based on the in vitro substrate disappearance rate
    • Naritomi Y., Terashita S., and Kagayama A. Identification and relative contributions of human cytochrome P450 isoforms involved in the metabolism of glibenclamide and lansoprazole: evaluation of an approach based on the in vitro substrate disappearance rate. Xenobiotica 34 (2004) 415-427
    • (2004) Xenobiotica , vol.34 , pp. 415-427
    • Naritomi, Y.1    Terashita, S.2    Kagayama, A.3
  • 20
    • 0345084436 scopus 로고    scopus 로고
    • The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite
    • Fischer V., Rodríguez-Gascón A., Heitz F., Tynes R., Hauck C., Cohen D., et al. The multidrug resistance modulator valspodar (PSC 833) is metabolized by human cytochrome P450 3A. Implications for drug-drug interactions and pharmacological activity of the main metabolite. Drug Metab Dispos 26 (1998) 802-811
    • (1998) Drug Metab Dispos , vol.26 , pp. 802-811
    • Fischer, V.1    Rodríguez-Gascón, A.2    Heitz, F.3    Tynes, R.4    Hauck, C.5    Cohen, D.6
  • 21
    • 0037401962 scopus 로고    scopus 로고
    • Hydroxyl-substituted sulfonylureas as potent inhibitors of specific [3H] glyburide binding to rat brain synaptosomes
    • Hill R.A., Rudra S., Peng B., Roane D.S., Bounds J.K., Zhang Y., et al. Hydroxyl-substituted sulfonylureas as potent inhibitors of specific [3H] glyburide binding to rat brain synaptosomes. Bioorg Med Chem 11 (2003) 2099-2113
    • (2003) Bioorg Med Chem , vol.11 , pp. 2099-2113
    • Hill, R.A.1    Rudra, S.2    Peng, B.3    Roane, D.S.4    Bounds, J.K.5    Zhang, Y.6
  • 23
    • 0028858960 scopus 로고
    • Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
    • Newton D.J., Wang R.W., and Lu A.Y.H. Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab Dispos 23 (1995) 154-158
    • (1995) Drug Metab Dispos , vol.23 , pp. 154-158
    • Newton, D.J.1    Wang, R.W.2    Lu, A.Y.H.3
  • 24
    • 0030430033 scopus 로고    scopus 로고
    • Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human microsomes
    • Bourrie M., Meunier V., Berger Y., and Fabre G. Cytochrome P450 isoform inhibitors as a tool for the investigation of metabolic reactions catalyzed by human microsomes. J Pharmacol Exp Ther 277 (1996) 321-332
    • (1996) J Pharmacol Exp Ther , vol.277 , pp. 321-332
    • Bourrie, M.1    Meunier, V.2    Berger, Y.3    Fabre, G.4
  • 25
    • 0033105118 scopus 로고    scopus 로고
    • Integrated cytochrome P450 reaction phenotyping. Attempting to bridge the gap between cDNA-expressed cytochromes P450 and native human liver microsomes
    • Rodrigues A.D. Integrated cytochrome P450 reaction phenotyping. Attempting to bridge the gap between cDNA-expressed cytochromes P450 and native human liver microsomes. Biochem Pharmacol 57 (1999) 465-480
    • (1999) Biochem Pharmacol , vol.57 , pp. 465-480
    • Rodrigues, A.D.1
  • 26
    • 0034013033 scopus 로고    scopus 로고
    • Assessment of specificity of eight chemical inhibitors using cDNA-expressed cytochromes P450
    • Sai Y., Dai R., Yang T.J., Krausz K.W., Gonzalez F.J., Gelboin H.V., et al. Assessment of specificity of eight chemical inhibitors using cDNA-expressed cytochromes P450. Xenobiotica 30 (2000) 327-343
    • (2000) Xenobiotica , vol.30 , pp. 327-343
    • Sai, Y.1    Dai, R.2    Yang, T.J.3    Krausz, K.W.4    Gonzalez, F.J.5    Gelboin, H.V.6
  • 27
    • 0034633287 scopus 로고    scopus 로고
    • A high-throughput screen to identify inhibitors of aromatase (CYP19)
    • [it is added for a-napht]
    • Stresser D.M., Turner S.D., McNamara J., Stocker P., Miller V.P., Crespi C.L., et al. A high-throughput screen to identify inhibitors of aromatase (CYP19). Anal Biochem 284 (2000) 427-430 [it is added for a-napht]
    • (2000) Anal Biochem , vol.284 , pp. 427-430
    • Stresser, D.M.1    Turner, S.D.2    McNamara, J.3    Stocker, P.4    Miller, V.P.5    Crespi, C.L.6
  • 28
    • 3242676832 scopus 로고    scopus 로고
    • Comparison of inhibitory effects of the proton pump-inhibiting drugs omeprazole, esomeprazole, lansoprazole, pantoprazole, and rabeprazole on human cytochrome P450 activities
    • Li X.Q., Andersson T.B., Ahlström, and Weidolf L. Comparison of inhibitory effects of the proton pump-inhibiting drugs omeprazole, esomeprazole, lansoprazole, pantoprazole, and rabeprazole on human cytochrome P450 activities. Drug Metab Dispos 32 (2004) 821-827
    • (2004) Drug Metab Dispos , vol.32 , pp. 821-827
    • Li, X.Q.1    Andersson, T.B.2    Ahlström3    Weidolf, L.4
  • 30
    • 0034979614 scopus 로고    scopus 로고
    • Effects of rifampin on the pharmacokinetics and pharmacodynamics of glyburide and glipizide
    • Niemi M., Backman J.T., Neuvonen M., Neuvonen P.J., and Kivistö K.T. Effects of rifampin on the pharmacokinetics and pharmacodynamics of glyburide and glipizide. Clin Pharmacol Ther 69 (2001) 400-406
    • (2001) Clin Pharmacol Ther , vol.69 , pp. 400-406
    • Niemi, M.1    Backman, J.T.2    Neuvonen, M.3    Neuvonen, P.J.4    Kivistö, K.T.5
  • 31
    • 0035201366 scopus 로고    scopus 로고
    • Rifampin is a selective, pleiotropic inducer of drug metabolism genes in human hepatocytes: studies with cDNA and oligonucleotide expression arrays
    • Rae J.M., Johnson M.D., Lippman M.E., and Flockhart D.A. Rifampin is a selective, pleiotropic inducer of drug metabolism genes in human hepatocytes: studies with cDNA and oligonucleotide expression arrays. J Pharmacol Exp Ther 299 (2001) 849-857
    • (2001) J Pharmacol Exp Ther , vol.299 , pp. 849-857
    • Rae, J.M.1    Johnson, M.D.2    Lippman, M.E.3    Flockhart, D.A.4
  • 32
    • 10944231356 scopus 로고    scopus 로고
    • Clinical pharmacology of bosentan, a dual endothelin receptor antagonist
    • Dingemanse J., and van Giersbergen P.L. Clinical pharmacology of bosentan, a dual endothelin receptor antagonist. Clin Pharmacokinet 43 (2004) 1089-1115
    • (2004) Clin Pharmacokinet , vol.43 , pp. 1089-1115
    • Dingemanse, J.1    van Giersbergen, P.L.2
  • 33
    • 0042357521 scopus 로고    scopus 로고
    • Inhibitory effect of glyburide on human cytochrome P450 isoforms in human liver microsomes
    • Kim K.A., and Park J.Y. Inhibitory effect of glyburide on human cytochrome P450 isoforms in human liver microsomes. Drug Metab Dispos 31 (2003) 1090-1092
    • (2003) Drug Metab Dispos , vol.31 , pp. 1090-1092
    • Kim, K.A.1    Park, J.Y.2
  • 34
    • 34547899883 scopus 로고    scopus 로고
    • Reverse transcriptase-PCR quantification of mRNA levels from cytochrome (CYP)1, CYP2 and CYP3 families in 22 different human tissues
    • Bièche I., Narjoz C., Asselah T., Vacher S., Marcellin P., Lidereau R., et al. Reverse transcriptase-PCR quantification of mRNA levels from cytochrome (CYP)1, CYP2 and CYP3 families in 22 different human tissues. Pharmacogenet Genomics 17 9 (2007) 731-742
    • (2007) Pharmacogenet Genomics , vol.17 , Issue.9 , pp. 731-742
    • Bièche, I.1    Narjoz, C.2    Asselah, T.3    Vacher, S.4    Marcellin, P.5    Lidereau, R.6
  • 35
    • 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 F.P. 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 (1994) 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
  • 36
    • 0026542525 scopus 로고
    • Relative expression of cytochrome P450 isoenzymes in human liver and association with the metabolism of drugs and xenobiotics
    • Forrester L.M., Henderson C.J., Glancey M.J., Back D.J., Park B.K., Ball S.E., et al. Relative expression of cytochrome P450 isoenzymes in human liver and association with the metabolism of drugs and xenobiotics. Biochem J 281 (1992) 359-368
    • (1992) Biochem J , vol.281 , pp. 359-368
    • Forrester, L.M.1    Henderson, C.J.2    Glancey, M.J.3    Back, D.J.4    Park, B.K.5    Ball, S.E.6
  • 37
    • 0033828454 scopus 로고    scopus 로고
    • The CYP2C19 enzyme polymorphism
    • Wedlund P.J. The CYP2C19 enzyme polymorphism. Pharmacology 61 (2000) 174-183
    • (2000) Pharmacology , vol.61 , pp. 174-183
    • Wedlund, P.J.1
  • 38
    • 0041922374 scopus 로고    scopus 로고
    • Tissue distribution of mRNA expression of human cytochrome P450 isoforms assessed by high-sensitivity real-time reverse transcription PCR
    • Nishimura M., Yaguti H., Yoshitsugu H., Naito S., and Satoh T. Tissue distribution of mRNA expression of human cytochrome P450 isoforms assessed by high-sensitivity real-time reverse transcription PCR. Yakugaku Zasshi 123 (2003) 369-375
    • (2003) Yakugaku Zasshi , vol.123 , pp. 369-375
    • Nishimura, M.1    Yaguti, H.2    Yoshitsugu, H.3    Naito, S.4    Satoh, T.5
  • 40
    • 3042725709 scopus 로고    scopus 로고
    • Drug transfer and metabolism by the human placenta
    • Syme M.R., Paxton J.W., and Keelan J.A. Drug transfer and metabolism by the human placenta. Clin Pharmacokinet 43 (2004) 487-514
    • (2004) Clin Pharmacokinet , vol.43 , pp. 487-514
    • Syme, M.R.1    Paxton, J.W.2    Keelan, J.A.3
  • 41
    • 0042934006 scopus 로고    scopus 로고
    • Aromatase is the major enzyme metabolizing buprenorphine in human placenta
    • Deshmukh S.V., Nanovskaya T.N., and Ahmed M.S. Aromatase is the major enzyme metabolizing buprenorphine in human placenta. J Pharmacol Exp Ther 306 (2003) 1099-1105
    • (2003) J Pharmacol Exp Ther , vol.306 , pp. 1099-1105
    • Deshmukh, S.V.1    Nanovskaya, T.N.2    Ahmed, M.S.3
  • 42
    • 1042263306 scopus 로고    scopus 로고
    • N-demethylation of levo-alpha-acetylmethadol by human placental aromatase
    • Deshmukh S.V., Nanovskaya T.N., Hankins G.D., and Ahmed M.S. N-demethylation of levo-alpha-acetylmethadol by human placental aromatase. Biochem Pharmacol 67 (2004) 885-892
    • (2004) Biochem Pharmacol , vol.67 , pp. 885-892
    • Deshmukh, S.V.1    Nanovskaya, T.N.2    Hankins, G.D.3    Ahmed, M.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.