Methadone enantiomer plasma levels, CYP2B6, CYP2C19, and CYP2C9 genotypes, and response to treatment

作者: S CRETTOL , J DEGLON , J BESSON , M CROQUETTEKROKKAR , I GOTHUEY

DOI: 10.1016/J.CLPT.2005.08.011

关键词: EndocrinologyPharmacologyChemistryPharmacokineticsMethadone maintenanceMethadoneDoseInternal medicineOpioidCYP2C9Blood plasmaCYP2C19

摘要: Background and Objective Recent in vitro studies have suggested an important role of cytochrome P450 (CYP) 2B6 and CYP2C19 in methadone metabolism. We aimed to …

参考文章(45)
Vishal Lamba, Jatinder Lamba, Kazuto Yasuda, Stephen Strom, Julio Davila, Michael L. Hancock, James D. Fackenthal, Peter K. Rogan, Barbara Ring, Steven A. Wrighton, Erin G. Schuetz, Hepatic CYP2B6 expression: gender and ethnic differences and relationship to CYP2B6 genotype and CAR (constitutive androstane receptor) expression. Journal of Pharmacology and Experimental Therapeutics. ,vol. 307, pp. 906- 922 ,(2003) , 10.1124/JPET.103.054866
J KIRCHHEINER, J BROCKMOLLER, Clinical consequences of cytochrome P450 2C9 polymorphisms. Clinical Pharmacology & Therapeutics. ,vol. 77, pp. 1- 16 ,(2005) , 10.1016/J.CLPT.2004.08.009
David J. Waxman, Georg F. Weber, Charles L. Crespi, Thomas K. H. Chang, Differential Activation of Cyclophosphamide and Ifosphamide by Cytochromes P-450 2B and 3A in Human Liver Microsomes Cancer Research. ,vol. 53, pp. 5629- 5637 ,(1993)
David J. Waxman, Olga Tretyakov, Joel Wright, Partha Roy, Stereoselective Metabolism of Ifosfamide by Human P-450s 3A4 and 2B6. Favorable Metabolic Properties of R-Enantiomer Drug Metabolism and Disposition. ,vol. 27, pp. 1309- 1318 ,(1999)
Messaoud Benmebarek, Corinne Devaud, Marianne Gex‐Fabry, Kerry Powell Golay, Christian Brogli, Pierre Baumann, Bruno Gravier, Chin B Eap, Effects of grapefruit juice on the pharmacokinetics of the enantiomers of methadone. Clinical Pharmacology & Therapeutics. ,vol. 76, pp. 55- 63 ,(2004) , 10.1016/J.CLPT.2004.03.007
Mario E. Alburges, Jerry M. Collins, David E. Moody, Robert J. Parker, John M. Strong, The involvement of cytochrome P450 3A4 in the N-demethylation of L-alpha-acetylmethadol (LAAM), norLAAM, and methadone. Drug Metabolism and Disposition. ,vol. 25, pp. 1347- 1353 ,(1997)
Klaus-Peter Kreth, Karl-Artur Kovar, Matthias Schwab, Ulrich M Zanger, Identification of the human cytochromes P450 involved in the oxidative metabolism of "Ecstasy"-related designer drugs. Biochemical Pharmacology. ,vol. 59, pp. 1563- 1571 ,(2000) , 10.1016/S0006-2952(00)00284-7
John G. Gerber, Robert J. Rhodes, Joseph Gal, Stereoselective metabolism of methadone N-demethylation by cytochrome P4502B6 and 2C19. Chirality. ,vol. 16, pp. 36- 44 ,(2004) , 10.1002/CHIR.10303
Robyn M Jacob, Elaine C Johnstone, Matt J Neville, Robert T Walton, Identification of CYP2B6 sequence variants by use of multiplex PCR with allele-specific genotyping. Clinical Chemistry. ,vol. 50, pp. 1372- 1377 ,(2004) , 10.1373/CLINCHEM.2004.031708
Lisa L. Von Moltke, Karthik Venkatakrishnan, Richard I. Shader, David J. Greenblatt, S. U. X. Duan, Michael H. Court, Leah M. Hesse, CYP2B6 mediates the in vitro hydroxylation of bupropion: potential drug interactions with other antidepressants. Drug Metabolism and Disposition. ,vol. 28, pp. 1176- 1183 ,(2000)