Non-endocannabinoid N-Acylethanolamines and Monoacylglycerols: Old Molecules New Targets

Harald S. Hansen, Karen Kleberg, Helle Adser Hassing

    2 Citations (Scopus)

    Abstract

    N-Acylethanolamine (NAE) and 2-monoacylglycerol (2-MAG) containing arachidonic acid are being called endocannabinoids since they can activate cannabinoid receptors. The same molecules containing stearic acid, palmitic acid, oleic acid, or linoleic acid cannot activate cannabinoid receptors, and are thus called non-endocannabinoid NAEs and 2-MAGs. However, these molecules do also have biological activities, e.g., via activation of the transcription factor PPARα, which mediate anti-inflammatory, antinociceptive, and anorectic effects. Furthermore, activation of the G-protein coupled receptor GPR119 in the small intestine could mediate release of the incretin hormone GLP-1. The present chapter describes the formation and degradation of these lipid molecules, as well as their pharmacology and their related drug targets.

    Original languageDanish
    Title of host publicationThe Endocannabinoidome : The World of Endocannabinoids and Related Mediators
    EditorsVincenzo Di Marzo, Jenny Wang
    Number of pages13
    VolumeElsevier
    Place of PublicationAmsterdam
    Publication date2015
    Pages1-13
    Chapter1
    ISBN (Print)978-0-12-420126-2
    Publication statusPublished - 2015

    Keywords

    • Faculty of Health and Medical Sciences

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