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Linking the Autotaxin-LPA Axis to Medicinal Cannabis and the Endocannabinoid System

Authors :
Mathias C. Eymery
Ahcène Boumendjel
Andrew A. McCarthy
Jens Hausmann
Source :
International Journal of Molecular Sciences, Vol 25, Iss 6, p 3212 (2024)
Publication Year :
2024
Publisher :
MDPI AG, 2024.

Abstract

Over the past few decades, many current uses for cannabinoids have been described, ranging from controlling epilepsy to neuropathic pain and anxiety treatment. Medicines containing cannabinoids have been approved by both the FDA and the EMA for the control of specific diseases for which there are few alternatives. However, the molecular-level mechanism of action of cannabinoids is still poorly understood. Recently, cannabinoids have been shown to interact with autotaxin (ATX), a secreted lysophospholipase D enzyme responsible for catalyzing lysophosphatidylcholine (LPC) to lysophosphatidic acid (LPA), a pleiotropic growth factor that interacts with LPA receptors. In addition, a high-resolution structure of ATX in complex with THC has recently been published, accompanied by biochemical studies investigating this interaction. Due to their LPA-like structure, endocannabinoids have been shown to interact with ATX in a less potent manner. This finding opens new areas of research regarding cannabinoids and endocannabinoids, as it could establish the effect of these compounds at the molecular level, particularly in relation to inflammation, which cannot be explained by the interaction with CB1 and CB2 receptors alone. Further research is needed to elucidate the mechanism behind the interaction between cannabinoids and endocannabinoids in humans and to fully explore the therapeutic potential of such approaches.

Details

Language :
English
ISSN :
14220067 and 16616596
Volume :
25
Issue :
6
Database :
Directory of Open Access Journals
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.5dc59ebb43944675a89dbaf83d00eb41
Document Type :
article
Full Text :
https://doi.org/10.3390/ijms25063212