Literature DB >> 8128420

[In vitro metabolism of zidovudine in man].

J F Rajaonarison1, B Lacarelle, A Durand, J Catalin.   

Abstract

The metabolism of zidovudine (AZT) and its modulating factors have been studied in human liver microsomes. In a first step, we demonstrated the involvement of UDP-glucoronosyltransferase (UDPGT) 2 form in AZT glucuronidation. In a second step, in order to predict drug interactions, we screened the effect of 52 drugs, representative of 17 different therapeutic classes, on AZT glucuronidation. We demonstrated that about twenty molecules glucuronidated or not are able to inhibit AZT glucuronidation. Finally, the NADPH-dependent reductive metabolism of AZT which produced a toxic metabolite, 3'-amino-3'-deoxythymidine (AMT) has been studied. Our studies demonstrated that AMT was formed only under anaerobic conditions and that its formation is catalysed by the NADPH-cytochrome P450 reductase.

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Year:  1993        PMID: 8128420

Source DB:  PubMed          Journal:  Therapie        ISSN: 0040-5957            Impact factor:   2.070


  2 in total

1.  Zidovudine azido-reductase in human liver microsomes: activation by ethacrynic acid, dipyridamole, and indomethacin and inhibition by human immunodeficiency virus protease inhibitors.

Authors:  S Fayz; T Inaba
Journal:  Antimicrob Agents Chemother       Date:  1998-07       Impact factor: 5.191

2.  A Single Zidovudine (AZT) Administration Delays Hepatic Cell Proliferation by Altering Oxidative State in the Regenerating Rat Liver.

Authors:  Armando Butanda-Ochoa; Diego Rolando Hernández-Espinosa; Marisela Olguín-Martínez; Lourdes Sánchez-Sevilla; Mario R Rodríguez; Benito Chávez-Rentería; Alberto Aranda-Fraustro; Rolando Hernández-Muñoz
Journal:  Oxid Med Cell Longev       Date:  2017-04-05       Impact factor: 6.543

  2 in total

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