Circulating Endocannabinoids and N-Acylethanolamines in Individuals with Cannabis Use Disorder—Preliminary Findings

Author:

Boachie Nadia12,Gaudette Erin12,Bazinet Richard P.3,Lin Lin34,Tyndale Rachel F.567ORCID,Mansouri Esmaeil12ORCID,Huestis Marilyn A.8ORCID,Tong Junchao15ORCID,Le Foll Bernard125679101112ORCID,Kish Stephen J.12567,George Tony P.125679ORCID,Boileau Isabelle125679

Affiliation:

1. Brain Health Imaging Centre, Centre for Addiction and Mental Health, Toronto, ON N6B 1Y6, Canada

2. Institute of Medical Science, University of Toronto, Toronto, ON M5S 1A1, Canada

3. Department of Nutritional Sciences, University of Toronto, Toronto, ON M5S 1A1, Canada

4. Department of Anatomy and Neurobiology, Faculty of Medicine, University of California, Irvine, CA 92697, USA

5. Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON N6B 1Y6, Canada

6. Department of Psychiatry, University of Toronto, Toronto, ON M5S 1A1, Canada

7. Department of Pharmacology and Toxicology, University of Toronto, Toronto, ON M5S 1A1, Canada

8. Institute of Emerging Health Professions, Thomas Jefferson University, Severna Park, Philadelphia, PA 19144, USA

9. Addictions Division and Institute of Mental Health Policy and Research, Centre for Addiction and Mental Health, Toronto, ON N6B 1Y6, Canada

10. Translational Addiction Research Laboratory, Centre for Addiction and Mental Health, Toronto, ON N6B 1Y6, Canada

11. Departments of Family and Community Medicine, University of Toronto, Toronto, ON M5S 1A1, Canada

12. Waypoint Research Institute, Waypoint Centre for Mental Health Care, Penetanguishene, ON L9M 1G3, Canada

Abstract

Background: Endocannabinoids and related N-acylethanolamines (NAEs) are bioactive lipids with important physiological functions and putative roles in mental health and addictions. Although chronic cannabis use is associated with endocannabinoid system changes, the status of circulating endocannabinoids and related NAEs in people with cannabis use disorder (CUD) is uncertain. Methods: Eleven individuals with CUD and 54 healthy non-cannabis using control participants (HC) provided plasma for measurement by high-performance liquid chromatography–mass spectrometry of endocannabinoids (2-arachidonoylglycerol (2-AG) and N-arachidonoylethanolamine (AEA)) and related NAE fatty acids (N-docosahexaenoylethanolamine (DHEA) and N-oleoylethanolamine (OEA)). Participants were genotyped for the functional gene variant of FAAH (rs324420, C385A) which may affect concentrations of AEA as well as other NAEs (OEA, DHEA). Results: In overnight abstinent CUD, AEA, OEA and DHEA concentrations were significantly higher (31–40%; p < 0.05) and concentrations of the endocannabinoid 2-AG were marginally elevated (55%, p = 0.13) relative to HC. There were no significant correlations between endocannabinoids/NAE concentrations and cannabis analytes, self-reported cannabis use frequency or withdrawal symptoms. DHEA concentration was inversely related with marijuana craving (r = −0.86; p = 0.001). Genotype had no significant effect on plasma endocannabinoids/NAE concentrations. Conclusions: Our preliminary findings, requiring replication, might suggest that activity of the endocannabinoid system is elevated in chronic cannabis users. It is unclear whether this elevation is a compensatory response or a predating state. Studies examining endocannabinoids and NAEs during prolonged abstinence as well as the potential role of DHEA in craving are warranted.

Funder

the National Institute of Health and the National Institute of Drug Abuse

Publisher

MDPI AG

Subject

General Neuroscience

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