نتایج جستجو برای: cyp2c18

تعداد نتایج: 71  

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2008
Susanne Löfgren R Michael Baldwin Masahiro Hiratsuka Annelie Lindqvist Anne Carlberg Sarah C Sim Meint Schülke Michael Snait Anne Edenro Ronny Fransson-Steen Ylva Terelius Magnus Ingelman-Sundberg

CYP2C19 is an important enzyme for human drug metabolism, and it also participates in the metabolism of endogenous substrates, whereas the CYP2C18 enzyme is not expressed in human liver despite high mRNA expression. Mice transgenic for the human CYP2C18 and CYP2C19 genes were generated. Quantitative mRNA analysis showed CYP2C18 and CYP2C19 transcripts in liver, kidneys, and heart to be expresse...

Journal: :Acta Veterinaria Scandinavica 2008
Susanne Löfgren Stina Ekman Ylva Terelius Ronny Fransson-Steen

BACKGROUND This study was performed to characterize a gene-addition transgenic mouse containing a BAC (bacterial artificial chromosome) clone spanning the human CYP2C18&19 genes (tg-CYP2C18&19). METHODS Hemizygous tg-CYP2C18&19, 11 week old mice were compared with wild-type littermates to obtain information regarding clinical status, clinical pathology and anatomical pathology. After one week...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2009
Susanne Löfgren R Michael Baldwin Margareta Carlerös Ylva Terelius Ronny Fransson-Steen Jessica Mwinyi David J Waxman Magnus Ingelman-Sundberg

The hormonal regulation of human CYP2C18 and CYP2C19, which are expressed in a male-specific manner in liver and kidney in a mouse transgenic model, was examined. The influence of prepubertal castration in male mice and testosterone treatment of female mice was investigated, as was the effect of continuous administration of growth hormone (GH) to transgenic males. Prepubertal castration of tran...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2000
H R Winter Y Wang J D Unadkat

Using selective cytochrome P450 (CYP) inhibitors and clinical concentrations (4 microM) of dapsone (DDS), we found a major contribution of CYP2C9 and little or no contribution (< or = 10%) of CYP3A4 and CYP2E1 to dapsone N-hydroxylation (DDS-NHY) in human liver microsomes. Sulfaphenazole (2.16 microM) and tolbutamide (500 microM), selective inhibitors of CYP2C9 (or 2C8/9), inhibited DDS-NHY by ...

Background: Genetic polymorphisms of cytochrome p450 in humans are the main cause of differences in the metabolism. The allele and genotype frequencies of CYP2C19 and CYP2C9 have been studied in some Iranian populations. The aim of present study was to examine the frequencies of CYP2C18m1, and CYP2C18m2, alleles in the Mazandarani ethnic group among Iranian Population. Materials and Methods: I...

Journal: :research in molecular medicine 0
adeleh rafati 1department of nanobiotechnology, faculty of new sciences and technologies, university of isfahan, isfahan, iran pooria gill 2research centre for immunogenetics, faculty of medicine, mazandaran university of medical sciences, sari, iran mehdi shabani 3molecular and cell biology research centre, faculty of medicine, mazandaran university of medical sciences, sari, iran; maryam peyrovei 3molecular and cell biology research centre, faculty of medicine, mazandaran university of medical sciences, sari, iran; seyed mohammad bagher hashemi-soteh 2research centre for immunogenetics, faculty of medicine, mazandaran university of medical sciences, sari, iran mohammad-reza shiran 4psychiatry and behavioral sciences research centre, faculty of medicine, mazandaran university of medical sciences, sari, iran

background: genetic polymorphisms of cytochrome p450 in humans are the main cause of differences in the metabolism. the allele and genotype frequencies of cyp2c19 and cyp2c9 have been studied in some iranian populations. the aim of present study was to examine the frequencies of cyp2c18m1, and cyp2c18m2, alleles in the mazandarani ethnic group among iranian population. materials and methods: in...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2000
T Schulz-Utermoehl R J Mountfield K Madsen P N Jørgensen K T Hansen

A conformationally targeted anti-peptide antibody was produced by immunizing a rabbit with a cyclized peptide corresponding to a loop region of human CYP2C19 (residues 250-261). In an enzyme-linked immunosorbent assay, the antibody bound strongly to recombinant CYP2C19 and poorly to recombinant CYP2C8, CYP2C9, and CYP2C18. In immunoblotting studies, the antibody bound strongly to recombinant CY...

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: :Nucleic acids research 1999
Peter G. Zaphiropoulos

Reverse transcription-PCR analysis in human epidermis, using primers from CYP2C18 and CYP2C19, revealed products containing combinations between canonically defined exons of these two genes. The major RNA species identified contained 2C18 exon 8 spliced with 2C19 exon 2. However, the terminal exons 1 and 9 were never detected in any of these composite molecules. When similar experiments were pe...

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