نتایج جستجو برای: cyp2b6

تعداد نتایج: 1820  

Journal: :Chirality 2004
John G Gerber Robert J Rhodes Joseph Gal

Methadone is a clinically used opioid agonist that is oxidatively metabolized by cytochrome P450 (CYP) isoforms to a stable metabolite, EDDP. Methadone is a chiral drug administered as the racemic mixture of (R)-(-)- and (S)-(+)-methadone, but (R)-methadone is the active isomer. The cytochrome P450 (CYP) isoform involved in methadone's metabolism is thought to be CYP3A4, but human drug-drug int...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2009
Jagdagsuren Davaalkham Tsunefusa Hayashida Kiyoto Tsuchiya Hiroyuki Gatanaga Dulmaa Nyamkhuu Shinichi Oka

CYP2B6 plays an important role in metabolizing various drugs in common clinical use. Increasing interest in CYP2B6 genetic polymorphism was stimulated by revelations of a specific CYP2B6 genotype significantly affecting the metabolism of efavirenz, an anti-HIV type-1 agent. The present study determined the CYP2B6 haplotype in 100 healthy unrelated Mongolian volunteers by analyzing the genotypes...

2016
Linhao Li Daochuan Li Scott Heyward Hongbing Wang

CYP2B6 plays an increasingly important role in xenobiotic metabolism and detoxification. The constitutive androstane receptor (CAR) and the pregnane X receptor (PXR) have been established as predominant regulators for the inductive expression of CYP2B6 gene in human liver. However, there are dramatic interindividual variabilities in CYP2B6 expression that cannot be fully explained by the CAR/PX...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2011
Ikumi Washio Makiko Maeda Chika Sugiura Ryota Shiga Mitsuhiro Yoshida Shinpei Nonen Yasushi Fujio Junichi Azuma

Smoking induces a wide range of drug-metabolizing enzymes. Among them, CYP2B6 as well as CYP1A2 is well known to be up-regulated in smokers. Although the induction of CYP1A2 is mediated by the aryl hydrocarbon receptor, the molecular mechanisms of CYP2B6 induction by smoking remain to be fully elucidated. In this study, by preparing cigarette smoke extract (CSE), we addressed the possibility th...

2010

Smoking induces a wide range of drug-metabolizing enzymes. Among them, CYP2B6 as well as CYP1A2 is well known to be up-regulated in smokers. Although the induction of CYP1A2 is mediated by the aryl hydrocarbon receptor, the molecular mechanisms of CYP2B6 induction by smoking remain to be fully elucidated. In this study, by preparing cigarette smoke extract (CSE), we addressed the possibility th...

2013
Yibai Li Janet K. Coller Mark R. Hutchinson Kathrin Klein Ulrich M. Zanger Nathan J. Stanley Andrew D. Abell Andrew A. Somogyi

Ketamine is primarily metabolized to norketamine by hepatic CYP2B6 and CYP3A4-mediated N-demethylation. However, the relative contribution from each enzyme remains controversial. The CYP2B6*6 allele is associated with reduced enzyme expression and activity that may lead to interindividual variability in ketamine metabolism. We examined the N-demethylation of individual ketamine enantiomers usin...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2004
Stephanie R Faucette Hongbing Wang Geraldine A Hamilton Summer L Jolley Darryl Gilbert Celeste Lindley Bingfang Yan Masahiko Negishi Edward L LeCluyse

The objectives of this study were to evaluate the ability of 14 compounds, which differentially activate human pregnane X receptor (hPXR), to induce CYP2B6 expression and to compare CYP2B6 and CYP3A4 concentration- and time-dependent induction by select inducers. Three primary human hepatocyte preparations were treated daily for 3 days with three concentrations of all compounds. Additional conc...

Journal: :Clinical chemistry 2004
Koenraad Gijbels Johan De Coster Xavier Bossuyt

could not determine the CYP2B6 genotype of this individual because the PCR-RFLP assays failed to distinguish the two genotypes. An individual classified as CYP2B6*1/*7 or *5/*6 has also been reported by other authors (4). It is necessary to distinguish CYP2B6*1/*7 and *5/*6 because CYP2B6*5, *6, and *7 have been associated with changes in the production and function of CYP2B6, respectively (2, ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2013
Katarina Ilic Roy L Hawke Ranjit K Thirumaran Erin G Schuetz J Heyward Hull Angela D M Kashuba Paul W Stewart Celeste M Lindley Mei-Ling Chen

The effects of sex, ethnicity, and genetic polymorphism on hepatic CYP2B6 (cytochrome P450 2B6) expression and activity were previously demonstrated in vitro. Race/ethnic differences in CYP2B6 genotype and phenotype were observed only in women. To identify important covariates associated with interindividual variation in CYP2B6 activity in vivo, we evaluated these effects in healthy volunteers ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2013
Yibai Li Janet K Coller Mark R Hutchinson Kathrin Klein Ulrich M Zanger Nathan J Stanley Andrew D Abell Andrew A Somogyi

Ketamine is primarily metabolized to norketamine by hepatic CYP2B6 and CYP3A4-mediated N-demethylation. However, the relative contribution from each enzyme remains controversial. The CYP2B6*6 allele is associated with reduced enzyme expression and activity that may lead to interindividual variability in ketamine metabolism. We examined the N-demethylation of individual ketamine enantiomers usin...

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