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The usage of a three-compartment model to investigate the metabolic differences between hepatic reductase null and wild-type mice.
- Source :
-
Mathematical medicine and biology : a journal of the IMA [Math Med Biol] 2017 Mar 01; Vol. 34 (1), pp. 1-13. - Publication Year :
- 2017
-
Abstract
- 278: The Cytochrome P450 (CYP) system is involved in 90% of the human body's interactions with xenobiotics and due to this, it has become an area of avid research including the creation of transgenic mice. This paper proposes a three-compartment model which is used to explain the drug metabolism in the Hepatic Reductase Null (HRN) mouse developed by the University of Dundee (Henderson, C. J., Otto, D. M. E., Carrie, D., Magnuson, M. A., McLaren, A. W., Rosewell, I. and Wolf, C. R. (2003) Inactivation of the hepatic cytochrome p450 system by conditional deletion of hepatic cytochrome p450 reductase. J. Biol. Chem. , 13480-13486). The model is compared with a two-compartment model using experimental data from studies using wild-type and HRN mice. This comparison allowed for metabolic differences between the two types of mice to be isolated. The three sets of drug data (Gefitinib, Midazolam and Thalidomide) showed that the transgenic mouse has a decreased rate of metabolism.<br /> (© The authors 2015. Published by Oxford University Press on behalf of the Institute of Mathematics and its Applications. All rights reserved.)
- Subjects :
- Angiogenesis Inhibitors metabolism
Animals
Disease Models, Animal
GABA Modulators metabolism
Gefitinib
Mice
Mice, Transgenic metabolism
Midazolam metabolism
Protein Kinase Inhibitors metabolism
Quinazolines metabolism
Thalidomide metabolism
Cytochrome P-450 Enzyme System metabolism
Liver enzymology
Models, Biological
NADPH-Ferrihemoprotein Reductase metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1477-8602
- Volume :
- 34
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Mathematical medicine and biology : a journal of the IMA
- Publication Type :
- Academic Journal
- Accession number :
- 26443812
- Full Text :
- https://doi.org/10.1093/imammb/dqv029