| Literature DB >> 27245906 |
Shalley N Kudalkar1,2, Philip J Kingsley1,2,3, Lawrence J Marnett4,5,6,7.
Abstract
The endocannabinoids, 2-arachidonoylglycerol (2-AG) and arachidonylethanolamide (AEA), are endogenous ligands for the cannabinoid receptors (CB1 and CB2) and are implicated in a wide array of physiological processes. These neutral arachidonic acid (AA) derivatives have been identified as efficient substrates for the second isoform of the cyclooxygenase enzyme (COX-2). A diverse family of prostaglandin glycerol esters (PG-Gs) and prostaglandin ethanolamides (PG-EAs) is generated by the action of COX-2 (and downstream prostaglandin synthases) on 2-AG and AEA. As the biological importance of the endocannabinoid system becomes more apparent, there is a tremendous need for robust, sensitive, and efficient analytical methodology for the endocannabinoids and their metabolites. In this chapter, we describe methodology suitable for carrying out oxygenation of endocannabinoids by COX-2, and analysis of products of endocannabinoid oxygenation by COX-2 and of endocannabinoids themselves from in vitro and cell assays.Entities:
Keywords: Cell assay; Cyclooxygenase-2; Endocannabinoids; In vitro assay; LC-MS/MS; PG-EAs; PG-Gs
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Year: 2016 PMID: 27245906 PMCID: PMC5289390 DOI: 10.1007/978-1-4939-3539-0_21
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745