Characterization of equine cytochrome P450: role of CYP3A in the metabolism of diazepam

Author:

Nakayama S. M. M.1,Ikenaka Y.12,Hayami A.1,Mizukawa H.3,Darwish W. S.14,Watanabe K. P.1,Kawai Y. K.15,Ishizuka M.1

Affiliation:

1. Laboratory of Toxicology; Department of Environmental Veterinary Sciences; Graduate School of Veterinary Medicine; Hokkaido University; Kita-ku Sapporo Japan

2. Water Research Group; Unit for Environmental Sciences and Management; North-West University; Potchefstroom South Africa

3. Department of Environmental Veterinary Sciences; Graduate School of Veterinary Medicine; Hokkaido University; Kita-ku Sapporo Japan

4. Food Control Department; Faculty of Veterinary Medicine; Zagazig University; Zagazig Egypt

5. Diagnostic Center for Animal Health and Food Safety; Obihiro University of Agriculture and Veterinary Medicine; Obihiro Japan

Funder

Ministry of Education, Culture, Sports, Science, and Technology

JSPS Core to Core Program

Bilateral Joint Research Project

Mitsui and Company

Publisher

Wiley

Subject

General Veterinary,Pharmacology

Reference34 articles.

1. Effect of omeprazole and cimetidine on plasma diazepam levels;Andersson;European Journal of Clinical Pharmacology,1990

2. Diazepam metabolism by human liver microsomes is mediated by both S-mephenytoin hydroxylase and CYP3A isoforms;Andersson;British Journal of Clinical Pharmacology,1994

3. In vitro comparison of cytochrome P450-mediated metabolic activities in human, dog, cat, and horse;Chauret;Drug Metabolism and Disposition,1997

4. Substrate selectivity of drug-metabolizing cytochrome P450s predicted from crystal structures and in silico modeling;Dong;Drug Metabolism Reviews,2002

5. MUSCLE: multiple sequence alignment with high accuracy and high throughput;Edgar;Nucleic Acids Research,2004

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