Literature DB >> 20629583

The potential of knockout mouse lines in defining the role of flavin-containing monooxygenases in drug metabolism.

Elizabeth A Shephard1, Ian R Phillips.   

Abstract

IMPORTANCE OF THE FIELD: Flavin-containing monooxygenases (FMOs) metabolize a number of therapeutic drugs. However, their role in drug metabolism has been overlooked compared with that of the cytochromes P450 (CYPs). Genetic variants of FMOs are expected to influence drug response and/or contribute to adverse drug reactions. AREAS COVERED IN THE REVIEW: We review tissue-specific expression of FMOs and genetic variation that may influence drug metabolism. We discuss how the use of mouse lines in which Fmo genes have been deleted can demonstrate the role an FMO plays in the metabolism of a drug, particularly if the drug is subject to metabolism by other enzymes, for example, CYPs, or undergoes retro-reduction. We cite seminal papers and review articles to give the reader an appreciation of the FMO field. WHAT THE READER WILL GAIN: Insights into the problems associated with determining the contribution of an FMO to the metabolism of a drug and how an Fmo-knockout mouse line has revealed the role of FMO1 in the metabolism of imipramine in vivo. TAKE HOME MESSAGE: The use of an Fmo-knockout mouse line demonstrates a more important role for FMOs in multi-pathway drug metabolism than has previously been appreciated.

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Year:  2010        PMID: 20629583     DOI: 10.1517/17425255.2010.503705

Source DB:  PubMed          Journal:  Expert Opin Drug Metab Toxicol        ISSN: 1742-5255            Impact factor:   4.481


  5 in total

1.  Ancestral-sequence reconstruction unveils the structural basis of function in mammalian FMOs.

Authors:  Callum R Nicoll; Gautier Bailleul; Filippo Fiorentini; María Laura Mascotti; Marco W Fraaije; Andrea Mattevi
Journal:  Nat Struct Mol Biol       Date:  2019-12-23       Impact factor: 15.369

2.  In vitro evidence for bakuchiol's influence towards drug metabolism through inhibition of UDP-glucuronosyltransferase (UGT) 2B7.

Authors:  Yu Xu; Peizhong Li; Xin Zhang; Junying Wang; Dongsheng Gu; Yao Wang
Journal:  Afr Health Sci       Date:  2014-09       Impact factor: 0.927

Review 3.  Genetic toxicology and toxicokinetics of arecoline and related areca nut compounds: an updated review.

Authors:  Nuno G Oliveira; Daniela L Ramos; Ricardo Jorge Dinis-Oliveira
Journal:  Arch Toxicol       Date:  2020-10-24       Impact factor: 5.153

4.  Tolerance to acetaminophen hepatotoxicity in the mouse model of autoprotection is associated with induction of flavin-containing monooxygenase-3 (FMO3) in hepatocytes.

Authors:  Swetha Rudraiah; Philip R Rohrer; Igor Gurevich; Michael J Goedken; Theodore Rasmussen; Ronald N Hines; José E Manautou
Journal:  Toxicol Sci       Date:  2014-06-27       Impact factor: 4.849

5.  The phenotype of a knockout mouse identifies flavin-containing monooxygenase 5 (FMO5) as a regulator of metabolic ageing.

Authors:  Sandra G Gonzalez Malagon; Anna N Melidoni; Diana Hernandez; Bilal A Omar; Lyndsey Houseman; Sunil Veeravalli; Flora Scott; Dorsa Varshavi; Jeremy Everett; Yugo Tsuchiya; John F Timms; Ian R Phillips; Elizabeth A Shephard
Journal:  Biochem Pharmacol       Date:  2015-06-04       Impact factor: 5.858

  5 in total

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