نتایج جستجو برای: cyp2c9

تعداد نتایج: 1925  

2014
Ngome L. Makia Sailesh Surapureddi Katalin Monostory Russell A. Prough Joyce A. Goldstein

Cytochrome P450 (CYP)2C9 and CYP2C19 are important human enzymes that metabolize therapeutic drugs, environmental chemicals, and physiologically important endogenous compounds. Initial studies using primary human hepatocytes showed induction of both the CYP2C9 and CYP2C19 genes by tertbutylhydroquinone (tBHQ). As a pro-oxidant, tBHQ regulates the expression of cytoprotective genes by activation...

2011
Ram Lakhan Ritu Kumari Kavita Singh Jayanti Kalita Usha Kant Misra Balraj Mittal

BACKGROUND & OBJECTIVES Multiple drug resistance in epilepsy is a common problem and one third of epilepsy patients remain non responsive to antiepileptic drug (AED) therapy. In this study we aimed to investigate the relationship between the genetic polymorphism of cytochrome P450 genes, namely CYP2C9 and CYP2C19 with multiple drug resistance in epilepsy patients. METHODS A total of 402 patie...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2014
Mengchun Chen Youting Zhang Peipei Pan Li Wang Yunyun Zhan Hui Jin Mengmin Xia Xianqin Wang Dapeng Dai Jianping Cai Guoxin Hu

Cytochrome P450 (P450) 2C9 is an important member of the P450 enzyme superfamily, with 58 CYP2C9 allelic variants previously reported. Genetic polymorphisms of CYP2C9 significantly influence the efficacy and safety of some drugs, which might cause adverse effects and therapeutic failure. The aim of this study was to assess the catalytic activities of 38 human CYP2C9 alleles, including 24 novel ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2001
S Gerbal-Chaloin J M Pascussi L Pichard-Garcia M Daujat F Waechter J M Fabre N Carrère P Maurel

The expression and inducibility of four CYP2C genes, including CYP2C8, -2C9, -2C18, and -2C19, was investigated in primary cultures of human hepatocytes. By the use of RNase protection assay and specific antibodies, each CYP2C mRNA and protein were quantified unequivocally. The four CYP2C mRNAs were expressed in human livers and cultured primary hepatocytes, but only the CYP2C18 protein was not...

Journal: :American journal of physiology. Heart and circulatory physiology 2003
Meetha Medhora John Daniels Kavita Mundey Beate Fisslthaler Rudi Busse Elizabeth R Jacobs David R Harder

Angiogenesis is one of the most recent physiological functions attributed to products of cytochrome P-450 (CYP450) enymes. To test this at a molecular level in human cells, we used a cloned cDNA for the human endothelial enzyme CYP450 2C9 (CYP2C9) to study growth as well as differentiation of human microvascular endothelial cells from the lung (HMVEC-L). Using adenoviral vectors overexpressing ...

2014
SABARIAH ISMAIL ABAS HJ HUSSIN KIT LAM CHAN

Objective: The aim of this study was to evaluate the inhibitory effect of E. longifolia extract on five human cytochrome P450 isoforms. Methods: The inhibitory effect of E. longifolia standardized extract (TAF-273) on five human cytochrome P450 isoforms, namely CYP1A2, CYP3A4, CYP2C9, CYP2C19 and CYP2D6, was determined using a luminescence method. The effect of eurycomanone on cytochrome P450 i...

Journal: :Annals of clinical and laboratory science 2011
Hee-Won Moon Jaekwang Noh Yeo-Min Yun Hahn Young Kim Ik Jin Yun Junghan Song Jin Q Kim

The therapeutic dose of warfarin is dependent upon intrinsic patient characteristics that are highly variable. We assessed the effects of CYP2C9, VKORC1 1173 C/T polymorphisms, and old age on warfarin dosing and sensitivity by measuring plasma S-/R-warfarin levels in Korean patients. INR and the plasma S-/R-warfarin concentrations were determined in 58 patients who had the VKORC1 1173C/T CYP2C9...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2008
Vikas Kumar Richard C Brundage William S Oetting Ilo E Leppik Timothy S Tracy

The effects of genetic polymorphisms in drug-metabolizing enzymes (e.g., CYP2C9(*)3) on drug clearance have been well characterized but much less is known about whether these polymorphisms alter susceptibility to drug-drug interactions. Previous in vitro work has demonstrated that genotype-dependent inhibition of CYP2C9 mediated flurbiprofen metabolism, suggesting the possibility of genotype-de...

Journal: :Molecular pharmacology 2008
Melissa A Kramer Allan E Rettie Mark J Rieder Erwin T Cabacungan Ronald N Hines

There are a considerable number of reports identifying and characterizing genetic variants within the CYP2C9 coding region. Much less is known about polymorphic promoter sequences that also might contribute to interindividual differences in CYP2C9 expression. To address this problem, approximately 10,000 base pairs of CYP2C9 upstream information were resequenced using 24 DNA samples from the Co...

2015
Behzad Poopak Saghar Rabieipoor Nazila Safari Emadedin Naraghi Fatemeh Sheikhsofla Gelareh Khosravipoor

BACKGROUND Although catalytic properties of different genetic polymorphisms of VKORC1 and CYP2C9 products have been identified, there is limited study available regarding warfarin dose requirement in Iranian patient population. This study investigates the impact of these polymorphisms on 115 patients, referred to Payvand Clinical and Specialty Laboratory for determining the appropriate dose of ...

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