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Volumn 37, Issue 9, 2009, Pages 1793-1796

Glucuronidation of the antiretroviral drug efavirenz by UGT2B7 and an in vitro investigation of drug-drug interaction with zidovudine

Author keywords

[No Author keywords available]

Indexed keywords

EFAVIRENZ; GLUCURONOSYLTRANSFERASE 1A1; GLUCURONOSYLTRANSFERASE 2B7; ZIDOVUDINE;

EID: 70349108450     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.109.027706     Document Type: Article
Times cited : (137)

References (23)
  • 3
    • 0031894377 scopus 로고    scopus 로고
    • The glucuronidation of opioids, other xenobiotics, and androgens by human UGT2B7Y(268) and UGT2B7H(268)
    • Coffman BL, King CD, Rios GR, and Tephly TR (1998) The glucuronidation of opioids, other xenobiotics, and androgens by human UGT2B7Y(268) and UGT2B7H(268). Drug Metab Dispos 26:73-77. (Pubitemid 28071328)
    • (1998) Drug Metabolism and Disposition , vol.26 , Issue.1 , pp. 73-77
    • Coffman, B.L.1    King, C.D.2    Rios, G.R.3    Tephly, T.R.4
  • 5
    • 1542286160 scopus 로고    scopus 로고
    • A novel functional polymorphism in the uridine diphosphate- Glucuronosyltransferase 2B7 promoter with significant impact on promoter activity
    • DOI 10.1016/j.clpt.2003.10.006, PII S0009923603003333
    • Duguay Y, Báár C, Skorpen F, and Guillemette C (2004) A novel functional polymorphism in the uridine diphosphate-glucuronosyltransferase 2B7 promoter with significant impact on promoter activity. Clin Pharmacol Ther 75:223-233. (Pubitemid 38314872)
    • (2004) Clinical Pharmacology and Therapeutics , vol.75 , Issue.3 , pp. 223-233
    • Duguay, Y.1    Baar, C.2    Skorpen, F.3    Guillemette, C.4
  • 7
    • 0026655104 scopus 로고
    • Glucuronidation of 3′-azido-3′-deoxythymidine in human liver microsomes: Enzyme inhibition by drugs and steroid hormones
    • Herber R, Magdalou J, Haumont M, Bidault R, van Es H, and Siest G (1992) Glucuronidation of 3′-azido-3′-deoxythymidine in human liver microsomes: enzyme inhibition by drugs and steroid hormones. Biochim Biophys Acta 1139:20-24.
    • (1992) Biochim Biophys Acta , vol.1139 , pp. 20-24
    • Herber, R.1    Magdalou, J.2    Haumont, M.3    Bidault, R.4    Van Es, H.5    Siest, G.6
  • 8
    • 0032759235 scopus 로고    scopus 로고
    • Pharmacology of antiretroviral drugs
    • Hoetelmans RM (1999) Pharmacology of antiretroviral drugs. Antivir Ther 4 (Suppl 3):29-41.
    • (1999) Antivir Ther , vol.4 , Issue.SUPPL. 3 , pp. 29-41
    • Hoetelmans, R.M.1
  • 10
    • 0031723235 scopus 로고    scopus 로고
    • Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver
    • Ito K, Iwatsubo T, Kanamitsu S, Ueda K, Suzuki H, and Sugiyama Y (1998) Prediction of pharmacokinetic alterations caused by drug-drug interactions: metabolic interaction in the liver. Pharmacol Rev 50:387-412. (Pubitemid 28477680)
    • (1998) Pharmacological Reviews , vol.50 , Issue.3 , pp. 387-411
    • Ito, K.1    Iwatsubo, T.2    Kanamitsu, S.3    Ueda, K.4    Suzuki, H.5    Sugiyama, Y.6
  • 12
    • 0035875828 scopus 로고    scopus 로고
    • Efavirenz plasma levels can predict treatment failure and central nervous system side effects in HIV-1-infected patients
    • DOI 10.1097/00002030-200101050-00011
    • Marzolini C, Telenti A, Decosterd LA, Greub G, Biollaz J, and Buclin T (2001) Efavirenz plasma levels can predict treatment failure and central nervous system side effects in HIV-1-infected patients. AIDS 15:71-75. (Pubitemid 32055781)
    • (2001) AIDS , vol.15 , Issue.1 , pp. 71-75
    • Marzolini, C.1    Telenti, A.2    Decosterd, L.A.3    Greub, G.4    Biollaz, J.5    Buclin, T.6
  • 13
    • 0032589627 scopus 로고    scopus 로고
    • Identification and characterization of efavirenz metabolites by liquid chromatography/mass spectrometry and high field NMR: Species differences in the metabolism of efavirenz
    • Mutlib AE, Chen H, Nemeth GA, Markwalder JA, Seitz SP, Gan LS, and Christ DD (1999) Identification and characterization of efavirenz metabolites by liquid chromatography/mass spectrometry and high field NMR: species differences in the metabolism of efavirenz. Drug Metab Dispos 27:1319-1333.
    • (1999) Drug Metab Dispos , vol.27 , pp. 1319-1333
    • Mutlib, A.E.1    Chen, H.2    Nemeth, G.A.3    Markwalder, J.A.4    Seitz, S.P.5    Gan, L.S.6    Christ, D.D.7
  • 14
    • 55349116078 scopus 로고    scopus 로고
    • Efavirenz versus nevirapine-based initial treatment of HIV infection: Clinical and virological outcomes in Southern African adults
    • Nachega JB, Hislop M, Dowdy DW, Gallant JE, Chaisson RE, Regensberg L, and Maartens G (2008) Efavirenz versus nevirapine-based initial treatment of HIV infection: clinical and virological outcomes in Southern African adults. AIDS 22:2117-2125.
    • (2008) AIDS , vol.22 , pp. 2117-2125
    • Nachega, J.B.1    Hislop, M.2    Dowdy, D.W.3    Gallant, J.E.4    Chaisson, R.E.5    Regensberg, L.6    Maartens, G.7
  • 15
    • 0025871397 scopus 로고
    • Glucuronidation of 3′-azido-3′-deoxythymidine catalyzed by human liver UDP-glucuronosyltransferase. Significance of nucleoside hydrophobicity and inhibition by xenobiotics
    • Resetar A, Minick D, and Spector T (1991) Glucuronidation of 3′-azido-3′-deoxythymidine catalyzed by human liver UDP-glucuronosyltransferase. Significance of nucleoside hydrophobicity and inhibition by xenobiotics. Biochem Pharmacol 42:559-568.
    • (1991) Biochem Pharmacol , vol.42 , pp. 559-568
    • Resetar, A.1    Minick, D.2    Spector, T.3
  • 17
    • 17644414659 scopus 로고    scopus 로고
    • Influence of 516G>T polymorphisms at the gene encoding the CYP450-2B6 isoenzyme on efavirenz plasma concentrations in HIV-infected subjects
    • DOI 10.1086/429327
    • Rodriguez-Novoa S, Barreiro P, Rendón A, Jiménez-Nacher I, González-Lahoz J, and Soriano V (2005) Influence of 516G>T polymorphisms at the gene encoding the CYP450-2B6 isoenzyme on efavirenz plasma concentrations in HIV-infected subjects. Clin Infect Dis 40:1358-1361. (Pubitemid 40570249)
    • (2005) Clinical Infectious Diseases , vol.40 , Issue.9 , pp. 1358-1361
    • Rodriguez-Novoa, S.1    Barreiro, P.2    Rendon, A.3    Jimenez-Nacher, I.4    Gonzalez-Lahoz, J.5    Soriano, V.6
  • 18
    • 33947398317 scopus 로고    scopus 로고
    • Binding of inhibitory fatty acids is responsible for the enhancement of UDP-glucuronosyltransferase 2B7 activity by albumin: Implications for in vitro-in vivo extrapolation
    • DOI 10.1124/jpet.106.118216
    • Rowland A, Gaganis P, Elliot DJ, Mackenzie PI, Knights KM, and Miners JO (2007) Binding of inhibitory fatty acids is responsible for the enhancement of UDP-glucuronosyltransferase 2B7 activity by albumin: implications for in vitro-in vivo extrapolation. J Pharmacol Exp Ther 321:137-147. (Pubitemid 46456976)
    • (2007) Journal of Pharmacology and Experimental Therapeutics , vol.321 , Issue.1 , pp. 137-147
    • Rowland, A.1    Gaganis, P.2    Elliot, D.J.3    Mackenzie, P.I.4    Knights, K.M.5    Miners, J.O.6
  • 19
    • 0034807892 scopus 로고    scopus 로고
    • Optimizing drug development: Strategies to assess drug metabolism/transporter interaction potential - Toward a consensus
    • DOI 10.1023/A:1010994022294
    • Tucker GT, Houston JB, and Huang SM (2001) Optimizing drug development: strategies to assess drug metabolism/transporter interaction potential-toward a consensus. Pharm Res 18:1071-1080. (Pubitemid 32900389)
    • (2001) Pharmaceutical Research , vol.18 , Issue.8 , pp. 1071-1080
    • Tucker, G.T.1    Houston, J.B.2    Huang, S.-M.3
  • 20
    • 52949103260 scopus 로고    scopus 로고
    • Kinetic modeling of the interactions between 4-methylumbelliferone, 1-naphthol, and zidovudine glucuronidation by UDP-glucuronosyltransferase 2B7 (UGT2B7) provides evidence for multiple substrate binding and effector sites
    • Uchaipichat V, Galetin A, Houston JB, Mackenzie PI, Williams JA, and Miners JO (2008) Kinetic modeling of the interactions between 4-methylumbelliferone, 1-naphthol, and zidovudine glucuronidation by UDP-glucuronosyltransferase 2B7 (UGT2B7) provides evidence for multiple substrate binding and effector sites. Mol Pharmacol 74:1152-1162.
    • (2008) Mol Pharmacol , vol.74 , pp. 1152-1162
    • Uchaipichat, V.1    Galetin, A.2    Houston, J.B.3    Mackenzie, P.I.4    Williams, J.A.5    Miners, J.O.6
  • 21
    • 0141519502 scopus 로고    scopus 로고
    • Novel functional polymorphisms in the UGT1A7 and UGT1A9 glucuronidating enzymes in Caucasian and African-American subjects and their impact on the metabolism of 7-ethyl-10-hydroxycamptothecin and flavopiridol anticancer drugs
    • DOI 10.1124/jpet.103.054072
    • Villeneuve L, Girard H, Fortier LC, Gagné JF, and Guillemette C (2003) Novel functional polymorphisms in the UGT1A7 and UGT1A9 glucuronidating enzymes in Caucasian and African-American subjects and their impact on the metabolism of 7-ethyl-10-hydroxycamptothecin and flavopiridol anticancer drugs. J Pharmacol Exp Ther 307:117-128. (Pubitemid 37151897)
    • (2003) Journal of Pharmacology and Experimental Therapeutics , vol.307 , Issue.1 , pp. 117-128
    • Villeneuve, L.1    Girard, H.2    Fortier, L.-C.3    Gagne, J.-F.4    Guillemette, C.5
  • 22
    • 0038002981 scopus 로고    scopus 로고
    • The cytochrome P450 2B6 (CYP2B6) is the main catalyst of efavirenz primary and secondary metabolism: Implication for HIV/AIDS therapy and utility of efavirenz as a substrate marker of CYP2B6 catalytic activity
    • Ward BA, Gorski JC, Jones DR, Hall SD, Flockhart DA, and Desta Z (2003) The cytochrome P450 2B6 (CYP2B6) is the main catalyst of efavirenz primary and secondary metabolism: implication for HIV/AIDS therapy and utility of efavirenz as a substrate marker of CYP2B6 catalytic activity. J Pharmacol Exp Ther 306:287-300.
    • (2003) J Pharmacol Exp Ther , vol.306 , pp. 287-300
    • Ward, B.A.1    Gorski, J.C.2    Jones, D.R.3    Hall, S.D.4    Flockhart, D.A.5    Desta, Z.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.