نتایج جستجو برای: cyp3a5

تعداد نتایج: 885  

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2012
Eric Chun Yong Chan Lee Sun New Teck Beng Chua Chun Wei Yap Han Kiat Ho Sidney D Nelson

Lapatinib, an oral tyrosine kinase inhibitor used for breast cancer, has been reported to cause idiosyncratic hepatotoxicity. Recently, it has been found that lapatinib forms a metabolite-inhibitor complex (MIC) with CYP3A4 via the formation of an alkylnitroso intermediate. Because CYP3A5 is highly polymorphic compared with CYP3A4 and also oxidizes lapatinib, we investigated the interactions of...

2018
Lucy Chen G V Ramesh Prasad

Tacrolimus is a commonly used immunosuppressant after kidney transplantation. It has a narrow therapeutic range and demonstrates wide interindividual variability in pharmacokinetics, leading to potential underimmunosuppression or toxicity. Genetic polymorphism in CYP3A5 enzyme expression contributes to differences in tacrolimus bioavailability between individuals. Individuals carrying one or mo...

Journal: :Biochemical and biophysical research communications 2010
Eliecer Coto Beatriz Tavira Rafael Marín Francisco Ortega Carlos López-Larrea Marta Ruiz-Ortega Alberto Ortiz Marta Díaz Ana I Corao Belén Alonso Victoria Alvarez

An intronic single nucleotide polymorphism (SNP) in the CYP3A5 gene (CYP3A5*3; SNP rs776746) affects RNA splicing and enzymatic activity. The CYP3A5*3 frequency increased with distance from the equator and natural selection has been proposed to explain the worldwide distribution of this allele. CYP3A activity has been related with the risk for hypertension in pregnancy, a major cause of morbidi...

Journal: :Genetics and molecular research : GMR 2015
L Wang L H Liu W H Tong M X Wang S C Lu

We examined the influence of the cytochrome P450 3A5 (CYP3A5) genes in both donors and recipients on the concentration-dosage ratio (C/D) of tacrolimus in Chinese liver transplant patients. Fifty-one adult liver transplant patients who received tacrolimus were included in this study. The CYP3A5 polymorphism in donors and recipients was determined at the time of transplantation, and tacrolimus-b...

2013
Yoshiyuki Shirasaka Shu-Ying Chang Mary F. Grubb Chi-Chi Peng Kenneth E. Thummel Nina Isoherranen David Rodrigues

The purpose of this study was to determine the impact of CYP3A5 expression on inhibitory potency (Ki or IC50 values) of CYP3A inhibitors, using recombinant CYP3A4 and CYP3A5 (rCYP3A4 and rCYP3A5) and CYP3A5 genotyped human liver microsomes (HLMs). IC50 ratios between rCYP3A4 and rCYP3A5 (rCYP3A5/rCYP3A4) of ketoconazole (KTZ) and itraconazole (ITZ) were 8.5 and 8.8 for midazolam (MDZ), 4.7 and ...

Journal: :Journal of hypertension 2006
Murielle Bochud Chin B Eap Robert C Elston Pascal Bovet Marc Maillard Laurent Schild Conrad Shamlaye Michel Burnier

OBJECTIVE Renal cytochrome P450 3A5 (CYP3A5) activity has been associated with blood pressure and salt sensitivity in humans. We determined whether CYP3A5 polymorphisms are associated with ambulatory blood pressure (ABP) and with glomerular filtration rate (GFR) in African families. METHODS Using a cross-sectional design, 375 individuals from 72 families, each with at least two hypertensive s...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2005
Ying-Hong Wang David R Jones Stephen D Hall

The genetic basis for polymorphic expression of CYP3A5 has been recently identified, but the significance of CYP3A5 expression is unclear. The purpose of this study is to quantify the capability of verapamil, a mechanism-based inhibitor of CYP3A, and its metabolites to inhibit the activities of CYP3A4 and CYP3A5, and to determine whether CYP3A5 expression in human liver microsomes alters the in...

2016

Tacrolimus is a potent immunosuppressant clinically used for the long term treatment of antirejection of transplanted organs in liver and kidney transplant recipients although dose optimization is often poorly managed. So far, no study has been carried out in the South Indian kidney transplant patients. The objective of this study was to evaluate the potential influence of a functional polymorp...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2014
Xiaohai Li Valer Jeso Scott Heyward Gregory S Walker Raman Sharma Glenn C Micalizio Michael D Cameron

Almost half of prescription medications are metabolized by cytochrome P450 3A4 and 3A5. CYP3A4 and 3A5 have significant substrate overlap, and there is currently no way to selectively monitor the activity of these two enzymes, which has led to the erroneous habit of attributing the cumulative activity to CYP3A4. While CYP3A4 expression is ubiquitous, CYP3A5 expression is polymorphic, with large...

ژورنال: :ارمغان دانش 0
مصطفی بختیاری طجر m bakhtiari tajar islamic azad universityدانشگاه ازاد اسلامی خدیجه عنصری kh onsory islamic azad universityدانشگاه ازاد اسلامی پژمان شادپور p shadpoor tehran universityدانشکده پزشکی، دانشگاه تهران، تهران محمد ظفرمند m zafarmand islamic azad universityدانشگاه ازاد اسلامی

مقدمه و هدف: فرضیه مواد کارسینوژن محیطی در ایجاد تومور نمایانگر این است که بسیاری از کارسینوژنها نیاز به فعالیت متابولیکی توسط آنزیمهایی متابولیزه کننده دارند. آنزیم cyp3a باعث تبدیل تعداد بسیار زیادی از زنوبیوتیکها شامل داروها و کارسینوژنها به مواد غیر سمی می گردد که باعث فعال نمودن پروکارسینوژن و غیر فعال نمودن کارسینوژنها در مسیر متابولیکی در هنگام تومورزایی می گردد cyp3a5 مهمترین آنزیم کبدی...

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