Anandamide metabolism by human liver and kidney microsomal cytochrome p450 enzymes to form hydroxyeicosatetraenoic and epoxyeicosatrienoic acid ethanolamides

• Published in: The Journal of pharmacology and experimental therapeutics Vol. 321; no. 2; p. 590
• Main Authors: Snider, Natasha T, Kornilov, Andrei M, Kent, Ute M, Hollenberg, Paul F
• Format: Journal Article
• Language: English
• Published: United States 01-05-2007
• Subjects: 8,11,14-Eicosatrienoic Acid - analogs & derivatives; 8,11,14-Eicosatrienoic Acid - metabolism; Arachidonic Acids - metabolism; Cytochrome P-450 CYP3A; Cytochrome P-450 Enzyme System - physiology; Endocannabinoids; Epoxy Compounds - metabolism; Humans; Hydrogen-Ion Concentration; Hydroxyeicosatetraenoic Acids - metabolism; Kidney - metabolism; Kinetics; Microsomes, Liver - metabolism; Polyunsaturated Alkamides - metabolism; Spectrometry, Mass, Electrospray Ionization
• ISSN: 0022-3565
• DOI: 10.1124/jpet.107.119321

The endocannabinoid anandamide is an arachidonic acid derivative that is found in most tissues where it acts as an important signaling mediator in neurological, immune, cardiovascular, and other functions. Cytochromes P450 (P450s) are known to oxidize arachidonic acid to the physiologically active molecules hydroxyeicosatetraenoic acids (HETEs) and epoxyeicosatrienoic acids (EETs), which play important roles in blood pressure regulation and inflammation. To determine whether anandamide can also be oxidized by P450s, its metabolism by human liver and kidney microsomes was investigated. The kidney microsomes metabolized anandamide to a single mono-oxygenated product, which was identified as 20-HETE-ethanolamide (EA). Human liver microsomal incubations with anandamide also produced 20-HETE-EA in addition to 5,6-, 8,9-, 11-12, and 14,15-EET-EA. The EET-EAs produced by the liver microsomal P450s were converted to their corresponding dihydroxy derivatives by microsomal epoxide hydrolase. P450 4F2 was identified as the isoform that is most probably responsible for the formation of 20-HETE-EA in both human kidney and human liver, with an apparent Km of 0.7 microM. The apparent Km values of the human liver microsomes for the formation of the EET-EAs were between 4 and 5 microM, and P450 3A4 was identified as the primary P450 in the liver responsible for epoxidation of anandamide. The in vivo formation and biological relevance of the P450-derived HETE and EET ethanolamides remains to be determined.