In vitro metabolism of fenofibric acid by carbonyl reducing enzymes.
Article Details
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Malatkova P, Kanavi M, Nobilis M, Wsol V
In vitro metabolism of fenofibric acid by carbonyl reducing enzymes.
Chem Biol Interact. 2016 Oct 25;258:153-8. doi: 10.1016/j.cbi.2016.09.001. Epub 2016 Sep 4.
- PubMed ID
- 27599626 [ View in PubMed]
- Abstract
Fenofibric acid is a hypolipidemic drug that is used as an active ingredient per se or is administered in the form of fenofibrate that releases fenofibric acid after absorption. The metabolism of fenofibric acid is mediated primarily by glucuronidation. However, the other part of fenofibric acid is excreted as reduced fenofibric acid. Enzymes responsible for the formation of reduced fenofibric acid as well as their subcellular localization have remained unknown until now. We have found that the predominant site of fenofibric acid reduction is the human liver cytosol, whereas liver microsomes reduced fenofibric acid to a lower extent and exhibited a lower affinity for this drug (Km > 1000 muM). Of nine carbonyl-reducing enzymes (CREs) tested, CBR1 exhibited the greatest activity for fenofibric acid reduction (CLint = 85.975 mul/mg protein/min). CBR1 predominantly formed (-)-enantiomers of reduced fenofibric acid similar to liver cytosol and in accordance with the in vivo data. AKR1C1, AKR1C2, AKR1C3 and AKR1B1 were also identified as reductases of fenofibric acid but are expected to play only a minor role in fenofibric acid metabolism.
DrugBank Data that Cites this Article
- Drugs
- Drug Enzymes
Drug Enzyme Kind Organism Pharmacological Action Actions Fenofibrate Aldo-keto reductase family 1 member C1 Protein Humans UnknownSubstrateDetails Fenofibrate Aldo-keto reductase family 1 member C2 Protein Humans UnknownSubstrateDetails Fenofibrate Aldo-keto reductase family 1 member C3 Protein Humans UnknownSubstrateDetails Fenofibrate Aldose reductase Protein Humans UnknownSubstrateDetails Fenofibrate Carbonyl reductase [NADPH] 1 Protein Humans UnknownSubstrateDetails - Drug Reactions
Reaction Details
