메뉴 건너뛰기




Volumn 166, Issue 8, 2012, Pages 2362-2370

The paraoxonase-1 pathway is not a major bioactivation pathway of clopidogrel in vitro

Author keywords

clopidogrel; cytochrome P450; metabolism; paraoxonase 1; polymorphism

Indexed keywords

2 OXO CLOPIDOGREL; ANTIBODY; ARYLDIALKYLPHOSPHATASE 1; CLOPIDOGREL; CYTOCHROME P450 2B6; CYTOCHROME P450 2C19; CYTOCHROME P450 3A; DRUG METABOLITE; EDETIC ACID; ENZYME INHIBITOR; RECOMBINANT ARYLDIALKYLPHOSPHATASE 1; UNCLASSIFIED DRUG;

EID: 84863482802     PISSN: 00071188     EISSN: 14765381     Source Type: Journal    
DOI: 10.1111/j.1476-5381.2012.01946.x     Document Type: Article
Times cited : (20)

References (44)
  • 1
    • 79952355781 scopus 로고    scopus 로고
    • Impact of genetic polymorphisms and drug-drug interactions on clopidogrel and prasugrel response variability
    • Ancrenaz V, Daali Y, Fontana P, Besson M, Samer C, Dayer P, et al,. (2010). Impact of genetic polymorphisms and drug-drug interactions on clopidogrel and prasugrel response variability. Curr Drug Metab 11: 667-677.
    • (2010) Curr Drug Metab , vol.11 , pp. 667-677
    • Ancrenaz, V.1    Daali, Y.2    Fontana, P.3    Besson, M.4    Samer, C.5    Dayer, P.6
  • 2
    • 0028152793 scopus 로고
    • Quantification of human serum paraoxonase by enzyme linked immunoassay: Population differences in protein concentrations
    • Blatter Garin MC, Abbott C, Messmer S, Mackness M, Durrington P, Pometta D, et al,. (1994). Quantification of human serum paraoxonase by enzyme-linked immunoassay: population differences in protein concentrations. Biochem J 304: 549-554. (Pubitemid 24368237)
    • (1994) Biochemical Journal , vol.304 , Issue.2 , pp. 549-554
    • Blatter Garin, M.-C.1    Abbott, C.2    Messmer, S.3    Mackness, M.4    Durrington, P.5    Pometta, D.6    James, R.W.7
  • 4
    • 0038508970 scopus 로고    scopus 로고
    • The metabolism of clopidogrel is catalyzed by human cytochrome P450 3A and is inhibited by atorvastatin
    • DOI 10.1124/dmd.31.1.53
    • Clarke TA, Waskell LA, (2003). The metabolism of clopidogrel is catalyzed by human cytochrome P450 3A and is inhibited by atorvastatin. Drug Metab Dispos 31: 53-59. (Pubitemid 36735258)
    • (2003) Drug Metabolism and Disposition , vol.31 , Issue.1 , pp. 53-59
    • Clarke, T.A.1    Waskell, L.A.2
  • 5
    • 77953753809 scopus 로고    scopus 로고
    • Clinical implications of clopidogrel non-response in cardiovascular patients: A systematic review and meta-analysis
    • Combescure C, Fontana P, Mallouk N, Berdague P, Labruyere C, Barazer I, et al,. (2010). Clinical implications of clopidogrel non-response in cardiovascular patients: a systematic review and meta-analysis. J Thromb Haemost 8: 923-933.
    • (2010) J Thromb Haemost , vol.8 , pp. 923-933
    • Combescure, C.1    Fontana, P.2    Mallouk, N.3    Berdague, P.4    Labruyere, C.5    Barazer, I.6
  • 6
    • 80052497112 scopus 로고    scopus 로고
    • Paraoxonase-1 and clopidogrel efficacy
    • Author reply 1042-1044.
    • Dansette PM, Rosi J, Bertho G, Mansuy D, (2011). Paraoxonase-1 and clopidogrel efficacy. Nat Med 17: 1040-1041. Author reply 1042-1044.
    • (2011) Nat Med , vol.17 , pp. 1040-1041
    • Dansette, P.M.1    Rosi, J.2    Bertho, G.3    Mansuy, D.4
  • 7
    • 34248586394 scopus 로고    scopus 로고
    • Pharmacogenetic interaction between paraoxonase-1 gene promoter polymorphism C-107T and statin
    • DOI 10.1097/FPC.0b013e3280925716, PII 0121301120070600000008
    • Deakin S, Guernier S, James RW, (2007). Pharmacogenetic interaction between paraoxonase-1 gene promoter polymorphism C-107T and statin. Pharmacogenet Genomics 17: 451-457. (Pubitemid 46763390)
    • (2007) Pharmacogenetics and Genomics , vol.17 , Issue.6 , pp. 451-457
    • Deakin, S.1    Guernier, S.2    James, R.W.3
  • 9
    • 0035157254 scopus 로고    scopus 로고
    • A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry
    • Dierks EA, Stams KR, Lim HK, Cornelius G, Zhang H, Ball SE, (2001). A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry. Drug Metab Dispos 29: 23-29. (Pubitemid 32041675)
    • (2001) Drug Metabolism and Disposition , vol.29 , Issue.1 , pp. 23-29
    • Dierks, E.A.1    Stams, K.R.2    Lim, H.-K.3    Cornelius, G.4    Zhang, H.5    Ball, S.E.6
  • 12
    • 34548858712 scopus 로고    scopus 로고
    • Influence of CYP2C19 and CYP3A4 gene polymorphisms on clopidogrel responsiveness in healthy subjects [4]
    • DOI 10.1111/j.1538-7836.2007.02722.x
    • Fontana P, Hulot JS, De Moerloose P, Gaussem P, (2007). Influence of CYP2C19 and CYP3A4 gene polymorphisms on clopidogrel responsiveness in healthy subjects. J Thromb Haemost 5: 2153-2155. (Pubitemid 47450038)
    • (2007) Journal of Thrombosis and Haemostasis , vol.5 , Issue.10 , pp. 2153-2155
    • Fontana, P.1    Hulot, J.-S.2    De Moerloose, P.3    Gaussem, P.4
  • 13
    • 80051584505 scopus 로고    scopus 로고
    • Relationship between paraoxonase-1 activity, its Q192R genetic variant and clopidogrel responsiveness in the ADRIE study
    • Fontana P, James R, Barazer I, Berdague P, Schved JF, Rebsamen M, et al,. (2011). Relationship between paraoxonase-1 activity, its Q192R genetic variant and clopidogrel responsiveness in the ADRIE study. J Thromb Haemost 9: 1664-1666.
    • (2011) J Thromb Haemost , vol.9 , pp. 1664-1666
    • Fontana, P.1    James, R.2    Barazer, I.3    Berdague, P.4    Schved, J.F.5    Rebsamen, M.6
  • 14
    • 65449158776 scopus 로고    scopus 로고
    • Clopidogrel resistance: Pharmacokinetic or pharmacogenetic?
    • Ford NF, (2009). Clopidogrel resistance: pharmacokinetic or pharmacogenetic? J Clin Pharmacol 49: 506-512.
    • (2009) J Clin Pharmacol , vol.49 , pp. 506-512
    • Ford, N.F.1
  • 15
    • 77952309437 scopus 로고    scopus 로고
    • In vitro characterization of sarizotan metabolism: Hepatic clearance, identification and characterization of metabolites, drug-metabolizing enzyme identification, and evaluation of cytochrome p450 inhibition
    • Gallemann D, Wimmer E, Hofer CC, Freisleben A, Fluck M, Ladstetter B, et al,. (2010). In vitro characterization of sarizotan metabolism: hepatic clearance, identification and characterization of metabolites, drug-metabolizing enzyme identification, and evaluation of cytochrome p450 inhibition. Drug Metab Dispos 38: 905-916.
    • (2010) Drug Metab Dispos , vol.38 , pp. 905-916
    • Gallemann, D.1    Wimmer, E.2    Hofer, C.C.3    Freisleben, A.4    Fluck, M.5    Ladstetter, B.6
  • 16
    • 38349065084 scopus 로고    scopus 로고
    • Influence of omeprazole on the antiplatelet action of clopidogrel associated with aspirin: The randomized, double-blind OCLA (Omeprazole CLopidogrel Aspirin) study
    • Gilard M, Arnaud B, Cornily JC, Le Gal G, Lacut K, Le Calvez G, et al,. (2008). Influence of omeprazole on the antiplatelet action of clopidogrel associated with aspirin: the randomized, double-blind OCLA (Omeprazole CLopidogrel Aspirin) study. J Am Coll Cardiol 51: 256-260.
    • (2008) J Am Coll Cardiol , vol.51 , pp. 256-260
    • Gilard, M.1    Arnaud, B.2    Cornily, J.C.3    Le Gal, G.4    Lacut, K.5    Le Calvez, G.6
  • 17
    • 0031214358 scopus 로고    scopus 로고
    • Inhibition of paraoxonase activity in human liver microsomes by exposure to EDTA, metals and mercurials
    • DOI 10.1016/S0009-2797(97)00046-X, PII S000927979700046X
    • Gonzalvo MC, Gil F, Hernandez AF, Villanueva E, Pla A, (1997). Inhibition of paraoxonase activity in human liver microsomes by exposure to EDTA, metals and mercurials. Chem Biol Interact 105: 169-179. (Pubitemid 27353307)
    • (1997) Chemico-Biological Interactions , vol.105 , Issue.3 , pp. 169-179
    • Gonzalvo, M.C.1    Gil, F.2    Hernandez, A.F.3    Villanueva, E.4    Pla, A.5
  • 18
    • 0038649988 scopus 로고    scopus 로고
    • Clopidogrel for coronary stenting: Response variability, drug resistance, and the effect of pretreatment platelet reactivity
    • DOI 10.1161/01.CIR.0000072771.11429.83
    • Gurbel PA, Bliden KP, Hiatt BL, O'Connor CM, (2003). Clopidogrel for coronary stenting: response variability, drug resistance, and the effect of pretreatment platelet reactivity. Circulation 107: 2908-2913. (Pubitemid 36736631)
    • (2003) Circulation , vol.107 , Issue.23 , pp. 2908-2913
    • Gurbel, P.A.1    Bliden, K.P.2    Hiatt, B.L.3    O'Connor, C.M.4
  • 19
    • 68149180722 scopus 로고    scopus 로고
    • Recent developments in clopidogrel pharmacology and their relation to clinical outcomes
    • Gurbel PA, Antonino MJ, Tantry US, (2009). Recent developments in clopidogrel pharmacology and their relation to clinical outcomes. Expert Opin Drug Metab Toxicol 5: 989-1004.
    • (2009) Expert Opin Drug Metab Toxicol , vol.5 , pp. 989-1004
    • Gurbel, P.A.1    Antonino, M.J.2    Tantry, U.S.3
  • 20
    • 61449085761 scopus 로고    scopus 로고
    • Comparison of human cytochrome P450 inhibition by the thienopyridines prasugrel, clopidogrel, and ticlopidine
    • Hagihara K, Nishiya Y, Kurihara A, Kazui M, Farid NA, Ikeda T, (2008). Comparison of human cytochrome P450 inhibition by the thienopyridines prasugrel, clopidogrel, and ticlopidine. Drug Metab Pharmacokinet 23: 412-420.
    • (2008) Drug Metab Pharmacokinet , vol.23 , pp. 412-420
    • Hagihara, K.1    Nishiya, Y.2    Kurihara, A.3    Kazui, M.4    Farid, N.A.5    Ikeda, T.6
  • 21
    • 33749339075 scopus 로고    scopus 로고
    • Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects
    • DOI 10.1182/blood-2006-04-013052
    • Hulot JS, Bura A, Villard E, Azizi M, Remones V, Goyenvalle C, et al,. (2006). Cytochrome P450 2C19 loss-of-function polymorphism is a major determinant of clopidogrel responsiveness in healthy subjects. Blood 108: 2244-2247. (Pubitemid 44497506)
    • (2006) Blood , vol.108 , Issue.7 , pp. 2244-2247
    • Hulot, J.-S.1    Bura, A.2    Villard, E.3    Azizi, M.4    Remones, V.5    Goyenvalle, C.6    Aiach, M.7    Lechat, P.8    Gaussem, P.9
  • 22
    • 82955240702 scopus 로고    scopus 로고
    • CYP2C19 but not PON1 Genetic variants influence clopidogrel pharmacokinetics, pharmacodynamics, and clinical efficacy in post-myocardial infarction patients
    • Hulot JS, Collet JP, Cayla G, Silvain J, Allanic F, Bellemain-Appaix A, et al,. (2011). CYP2C19 but not PON1 Genetic variants influence clopidogrel pharmacokinetics, pharmacodynamics, and clinical efficacy in post-myocardial infarction patients. Circ Cardiovasc Interv 4: 422-428.
    • (2011) Circ Cardiovasc Interv , vol.4 , pp. 422-428
    • Hulot, J.S.1    Collet, J.P.2    Cayla, G.3    Silvain, J.4    Allanic, F.5    Bellemain-Appaix, A.6
  • 23
    • 73449130146 scopus 로고    scopus 로고
    • Proton pump inhibitors and clopidogrel: Putting the interaction in perspective
    • Juurlink DN, (2009). Proton pump inhibitors and clopidogrel: putting the interaction in perspective. Circulation 120: 2310-2312.
    • (2009) Circulation , vol.120 , pp. 2310-2312
    • Juurlink, D.N.1
  • 24
    • 73149119363 scopus 로고    scopus 로고
    • Identification of the human cytochrome P450 enzymes involved in the two oxidative steps in the bioactivation of clopidogrel to its pharmacologically active metabolite
    • Kazui M, Nishiya Y, Ishizuka T, Hagihara K, Farid NA, Okazaki O, et al,. (2010). Identification of the human cytochrome P450 enzymes involved in the two oxidative steps in the bioactivation of clopidogrel to its pharmacologically active metabolite. Drug Metab Dispos 38: 92-99.
    • (2010) Drug Metab Dispos , vol.38 , pp. 92-99
    • Kazui, M.1    Nishiya, Y.2    Ishizuka, T.3    Hagihara, K.4    Farid, N.A.5    Okazaki, O.6
  • 26
    • 34047233676 scopus 로고    scopus 로고
    • New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis
    • DOI 10.1038/sj.bjp.0707173, PII 0707173
    • Korhonen LE, Turpeinen M, Rahnasto M, Wittekindt C, Poso A, Pelkonen O, et al,. (2007). New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis. Br J Pharmacol 150: 932-942. (Pubitemid 46536632)
    • (2007) British Journal of Pharmacology , vol.150 , Issue.7 , pp. 932-942
    • Korhonen, L.E.1    Turpeinen, M.2    Rahnasto, M.3    Wittekindt, C.4    Poso, A.5    Pelkonen, O.6    Raunio, H.7    Juvonen, R.O.8
  • 28
    • 16644401883 scopus 로고    scopus 로고
    • Clinical significance of the atorvastatin-clopidogrel drug-drug interaction
    • Author reply e66-e67.
    • Lau WC, Carville DG, Bates ER, (2004a). Clinical significance of the atorvastatin-clopidogrel drug-drug interaction. Circulation 110: e66-e67. Author reply e66-e67.
    • (2004) Circulation , vol.110
    • Lau, W.C.1    Carville, D.G.2    Bates, E.R.3
  • 32
    • 74049132714 scopus 로고    scopus 로고
    • The P450 oxidoreductase genotype is associated with CYP3A activity in vivo as measured by the midazolam phenotyping test
    • Oneda B, Crettol S, Jaquenoud Sirot E, Bochud M, Ansermot N, Eap CB, (2009). The P450 oxidoreductase genotype is associated with CYP3A activity in vivo as measured by the midazolam phenotyping test. Pharmacogenet Genomics 19: 877-883.
    • (2009) Pharmacogenet Genomics , vol.19 , pp. 877-883
    • Oneda, B.1    Crettol, S.2    Jaquenoud Sirot, E.3    Bochud, M.4    Ansermot, N.5    Eap, C.B.6
  • 33
    • 0032879820 scopus 로고    scopus 로고
    • Ticlopidine and clopidogrel
    • Quinn MJ, Fitzgerald DJ, (1999). Ticlopidine and clopidogrel. Circulation 100: 1667-1672. (Pubitemid 29477278)
    • (1999) Circulation , vol.100 , Issue.15 , pp. 1667-1672
    • Quinn, M.J.1    Fitzgerald, D.J.2
  • 36
    • 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, (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. (Pubitemid 24229655)
    • (1994) Journal of Pharmacology and Experimental Therapeutics , vol.270 , Issue.1 , pp. 414-423
    • Shimada, T.1    Yamazaki, H.2    Mimura, M.3    Inui, Y.4    Guengerich, F.P.5
  • 37
    • 69249219296 scopus 로고    scopus 로고
    • Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy
    • Shuldiner AR, O'Connell JR, Bliden KP, Gandhi A, Ryan K, Horenstein RB, et al,. (2009). Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. JAMA 302: 849-857.
    • (2009) JAMA , vol.302 , pp. 849-857
    • Shuldiner, A.R.1    O'Connell, J.R.2    Bliden, K.P.3    Gandhi, A.4    Ryan, K.5    Horenstein, R.B.6
  • 38
  • 39
    • 79960012663 scopus 로고    scopus 로고
    • No association of paraoxonase-1 Q192R genotypes with platelet response to clopidogrel and risk of stent thrombosis after coronary stenting
    • Sibbing D, Koch W, Massberg S, Byrne RA, Mehilli J, Schulz S, et al,. (2011). No association of paraoxonase-1 Q192R genotypes with platelet response to clopidogrel and risk of stent thrombosis after coronary stenting. Eur Heart J 32: 1605-1613.
    • (2011) Eur Heart J , vol.32 , pp. 1605-1613
    • Sibbing, D.1    Koch, W.2    Massberg, S.3    Byrne, R.A.4    Mehilli, J.5    Schulz, S.6
  • 42
    • 0026026523 scopus 로고
    • Characteristics of the genetically determined allozymic forms of human serum paraoxonase/arylesterase
    • Smolen A, Eckerson HW, Gan KN, Hailat N, La Du BN, (1991). Characteristics of the genetically determined allozymic forms of human serum paraoxonase/arylesterase. Drug Metab Dispos 19: 107-112.
    • (1991) Drug Metab Dispos , vol.19 , pp. 107-112
    • Smolen, A.1    Eckerson, H.W.2    Gan, K.N.3    Hailat, N.4    La Du, B.N.5
  • 43
    • 80052790906 scopus 로고    scopus 로고
    • Paraoxonase-1 Q192R polymorphism and antiplatelet effects of clopidogrel in patients undergoing elective coronary stent placement
    • Trenk D, Hochholzer W, Fromm MF, Zolk O, Valina CM, Stratz C, et al,. (2011). Paraoxonase-1 Q192R polymorphism and antiplatelet effects of clopidogrel in patients undergoing elective coronary stent placement. Circ Cardiovasc Genet 4: 429-436.
    • (2011) Circ Cardiovasc Genet , vol.4 , pp. 429-436
    • Trenk, D.1    Hochholzer, W.2    Fromm, M.F.3    Zolk, O.4    Valina, C.M.5    Stratz, C.6
  • 44
    • 1542331537 scopus 로고    scopus 로고
    • Four paraoxonase gene polymorphisms in 11 212 cases of coronary heart disease and 12 786 controls: Meta-analysis of 43 studies
    • DOI 10.1016/S0140-6736(04)15642-0, PII S0140673604156420
    • Wheeler JG, Keavney BD, Watkins H, Collins R, Danesh J, (2004). Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: meta-analysis of 43 studies. Lancet 363: 689-695. (Pubitemid 38296555)
    • (2004) Lancet , vol.363 , Issue.9410 , pp. 689-695
    • Wheeler, J.G.1    Keavney, B.D.2    Watkins, H.3    Collins, R.4    Danesh, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.