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Saccharomyces cerevisiae: an alternative source for human microsomal liver enzymes and its use in drug interaction studies
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 998210
Author(s) Eugster, Hans-Pietro; Sengstag, Christian
Author(s) at UniBasel Sengstag, Christian
Year 1993
Title Saccharomyces cerevisiae: an alternative source for human microsomal liver enzymes and its use in drug interaction studies
Journal Toxicology
Volume 82
Number 1-3
Pages / Article-Number 61-73
Mesh terms Anticonvulsants, pharmacology; Benzoflavones, pharmacology; Carbamazepine, pharmacology; Cloning, Molecular; Cytochrome P-450 CYP1A2; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme System, metabolism; DNA, Complementary; Drug Interactions; Epoxide Hydrolases, metabolism; Humans; Ketoconazole, pharmacology; Microsomes, Liver, enzymology; Oxidoreductases, N-Demethylating, metabolism; Saccharomyces cerevisiae, genetics; Valproic Acid, pharmacology
Abstract Heterologous expression of human cDNAs in the yeast Saccharomyces cerevisiae represents an attractive alternative source of human enzymes and allows metabolic studies to be performed without the need of human tissue. Here we report on the functional expression of human microsomal epoxide hydrolase (hmEH) and cytochrome P450 1A1 and 1A2 in yeast. Microsomal fractions of corresponding yeast strains exhibited enzyme specific activities which allowed the characterization of the heterologous enzymes. The use of these microsomes enabled us to study drug interactions on the respective enzymes with pharmacologically relevant drugs such as carbamazepine epoxide, valpromide and ketoconazole.
Publisher Elsevier
ISSN/ISBN 0300-483X
edoc-URL http://edoc.unibas.ch/46827/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/0300-483x(93)90060-6
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/8236282
ISI-Number WOS:A1993MC36300006
Document type (ISI) Journal Article
 
   

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04/06/2024