Literature DB >> 20654512

Imipramine for Cytochrome P450 Activity Determination: a Multiple-species Metabolic Probe.

S Bull1, P Catalani, M Garle, S Coecke, R Clothier.   

Abstract

Imipramine is metabolized in vitro by rat, mouse or human microsomes to several metabolites including 2-hydroxyimipramine, 2-hydroxydesipramine, desipramine, didesmethylimipramine and imipramine-N-oxide. Heat treatment (which inhibits FMO), verified the role of this group of enzymes in the oxidation of imipramine to imipramine N-oxide. These studies demonstrate that while rats and humans showed similar metabolic profiles, producing several minor metabolites in addition to the 2-hydroxyimipramne and desipramine, differences were seen in the mouse microsomes. In these samples, few minor metabolites were produced. In addition, imipramine N-oxide was the major metabolite in mouse, whereas none was detected in human samples. To conclude, the metabolic profile of imipramine can be used to reveal a number of cytochrome P450 enzymes active in microsomal fractions.

Entities:  

Year:  1999        PMID: 20654512     DOI: 10.1016/s0887-2333(99)00022-3

Source DB:  PubMed          Journal:  Toxicol In Vitro        ISSN: 0887-2333            Impact factor:   3.500


  1 in total

1.  Effect of Water-miscible Organic Solvents on CYP450-mediated Metoprolol and Imipramine Metabolism in Rat Liver Microsomes.

Authors:  T S Shah; S H Kamble; Pranali G Patil; K R Iyer
Journal:  Indian J Pharm Sci       Date:  2015 Jul-Aug       Impact factor: 0.975

  1 in total

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