نتایج جستجو برای: cyp3a5

تعداد نتایج: 885  

Journal: :Molecular pharmacology 2002
Yvonne S Lin Amy L S Dowling Sean D Quigley Federico M Farin Jiong Zhang Jatinder Lamba Erin G Schuetz Kenneth E Thummel

We recently demonstrated that a variant allele of CYP3A5 (CYP3A5*3) confers low CYP3A5 expression as a result of improper mRNA splicing. In this study, we further evaluated the regulation of CYP3A5 in liver and jejunal mucosa from white donors. For all tissues, high levels of CYP3A5 protein were strongly concordant with the presence of a wild-type allele of the CYP3A5 gene (CYP3A5*1). CYP3A5 re...

2017
Yao Lu Hua Zhong Qing Tang Zhijun Huang Ningning Jing Julie Smith Rujia Miao Yapei Li Hong Yuan

The present study evaluated the ability of a Saccharomyces cerevisiae expression system to predict the pharmacokinetic (PK) activity of a calcium channel blocker in patients with distinct cytochrome P450 3A5 (CYP3A5) polymorphisms. The blood pressure lowering activity of amlodipine in 57 hypertensive patients with CYP3A5*1/*1, CYP3A5*1/*3, CYP3A5*4 and CYP3A5*6 polymorphisms was evaluated by th...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2012
Juliane Bolbrinker Stefanie Seeberg Martin Schostak Carsten Kempkensteffen Hans Baelde Emile de Heer Reinhold Kreutz

Interindividual variability in the drug-metabolizing activity of the CYP3A5 enzyme is mainly due to a single nucleotide polymorphism in CYP3A5, leading to low expression in homozygous CYP3A5*3/*3 individuals compared with CYP3A5*1 allele carriers. In the human kidney, expression of CYP3A5 has been implicated in blood pressure regulation and calcineurin inhibitor-associated nephrotoxicity. The e...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2002
Pei-Shan Shih Jin-Ding Huang

The CYP3A subfamily represents the most abundant cytochrome p450 in the human liver and gastrointestinal tract and plays very important role in xenobiotic metabolism. CYP3A5 is expressed in a relatively small population of whites and Orientals. We recruited 42 Chinese volunteers to determine the genotypes of CYP3A5 by polymerase chain reaction-restriction fragment length polymorphism. Genotype ...

Journal: :Anesthesiology 2005
Theresa Mariero Klees Pamela Sheffels Kenneth E Thummel Evan D Kharasch

BACKGROUND There is considerable unexplained interindividual variability in the clearance of alfentanil. Alfentanil undergoes extensive metabolism by cytochrome P4503A4 (CYP3A4). CYP3A5 is structurally similar to CYP3A4 and metabolizes most CYP3A4 substrates but is polymorphically expressed. Livers with the CYP3A5*1 allele contain higher amounts of the native CYP3A5 protein than livers homozygo...

Journal: :The Journal of pharmacology and experimental therapeutics 2008
Jennifer B Dennison Michael A Mohutsky Robert J Barbuch Steven A Wrighton Stephen D Hall

Vincristine is metabolized to one primary metabolite, M1, by cDNA-expressed CYP3A4 and CYP3A5 and by CYP3A enzymes in human liver microsomes. For both systems, CYP3A5 is predicted to mediate approximately 80% of the CYP3A metabolism for individuals with high CYP3A5 expression (at least one CYP3A5(*)1 allele). In the current study, the role of CYP3A5 was quantified in the metabolism of vincristi...

Journal: :Clinical chemistry 2002
Ron H N van Schaik Ilse P van der Heiden John N van den Anker Jan Lindemans

BACKGROUND Enzymes of the cytochrome P450 3A (CYP3A) family are responsible for the metabolism of >50% of currently prescribed drugs. CYP3A5 is expressed in a limited number of individuals. The absence of CYP3A5 expression in approximately 70% of Caucasians was recently correlated to a genetic polymorphism (CYP3A5*3). Because CYP3A5 may represent up to 50% of total CYP3A protein in individuals ...

2014
Guilherme Suarez-Kurtz Daniela D. Vargens Ana Beatriz Santoro Mara H. Hutz Maria Elisabete de Moraes Sérgio D. J. Pena Ândrea Ribeiro-dos-Santos Marco A. Romano-Silva Claudio José Struchiner

The influence of self-reported "race/color", geographical origin and genetic ancestry on the distribution of three functional CYP3A5 polymorphisms, their imputed haplotypes and inferred phenotypes was examined in 909 healthy, adult Brazilians, self-identified as White, Brown or Black ("race/color" categories of the Brazilian census). The cohort was genotyped for CYP3A5*3 (rs776746), CYP3A5*6 (r...

Journal: :Molecular pharmacology 2005
Florent Busi Thierry Cresteil

The total CYP3A5 mRNA level is significantly greater in carriers of the CYP3A5*1 allele than in CYP3A5*3 homozygotes. Most of the CYP3A5*3 mRNA includes an intronic sequence (exon 3B) containing premature termination codons (PTCs) between exons 3 and 4. Two models were used to investigate the degradation of CYP3A5 mRNA: a CYP3A5 minigene consisting of CYP3A5 exons and introns 3 to 6 transfected...

2016
Leïla Belkhir Laure Elens Francis Zech Nadtha Panin Anne Vincent Jean Cyr Yombi Bernard Vandercam Vincent Haufroid

OBJECTIVES To assess the impact of the loss-of-function CYP3A5*3 allele (rs776746, 6986A>G SNP) on darunavir (DRV) plasma concentrations. METHODS 135 HIV-1 infected patients treated with DRV-based therapy were included in the study and plasma samples were obtained immediately before drug intake in order to determine DRV trough concentrations using an ultra performance liquid chromatography me...

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