The Endocannabinoid System as a Biomarker for Diagnostic and Therapeutic Applications in Depression and Anxiety.

2-Arachidonoylglycerol anandamide membrane transporter cannabinoid receptors depression diacylglycerol lipase fatty acid amide hydrolase monoacylglycerol lipase

Journal

CNS & neurological disorders drug targets
ISSN: 1996-3181
Titre abrégé: CNS Neurol Disord Drug Targets
Pays: United Arab Emirates
ID NLM: 101269155

Informations de publication

Date de publication:
2023
Historique:
received: 17 09 2021
revised: 11 01 2022
accepted: 16 01 2022
pubmed: 7 4 2022
medline: 17 3 2023
entrez: 6 4 2022
Statut: ppublish

Résumé

Depression and anxiety belong to a family of mental disturbances that have increased significantly in recent years. The etiology of both disorders comprises multiple and complex factors, from genetic background to environmental influence. Since depression and anxiety present severe symptoms, they represent a greater clinical burden and greater therapeutic difficulty. Currently, standardized diagnostic procedures for depression and anxiety allow for the addition of further treatments, including psychotherapy and/or pharmacological intervention, with effective outcomes. However, further steps should be considered with regard to consideration of the endocannabinoid system's role in depression and anxiety. This study aimed to review the evidence from animal research and clinical studies on the role of cannabinoid receptors, the major endocannabinoids -anandamide (AEA) and 2-arachidonoylglycerol (2-AG)- and the enzymes related to the synthesis and degradation of these chemicals as putative biomarkers for diagnostic and therapeutic elements of depression and anxiety. This review included the online search, identification, and analysis of articles (basic and clinical trials) published in English in PubMed linked to the role of cannabinoid receptors, AEA, 2- AG, and the enzymes associated with the synthesis and degradation of these endocannabinoids in depression and anxiety. The neurobiological relevance of the endocannabinoid system offers genetic or pharmacological manipulation of this system as a potential strategy for the diagnostic and clinical management of mood disorders, including depression and anxiety. Although the described approach in this review is promising, no solid evidence is yet available, and along with additional experiments using animal models that mimic human depression and anxiety, clinical trials are needed to explore the role of the endocannabinoid system's elements as well as the anandamide membrane transporter, none of which have been adequately studied in depression and anxiety.

Sections du résumé

BACKGROUND
Depression and anxiety belong to a family of mental disturbances that have increased significantly in recent years. The etiology of both disorders comprises multiple and complex factors, from genetic background to environmental influence. Since depression and anxiety present severe symptoms, they represent a greater clinical burden and greater therapeutic difficulty. Currently, standardized diagnostic procedures for depression and anxiety allow for the addition of further treatments, including psychotherapy and/or pharmacological intervention, with effective outcomes. However, further steps should be considered with regard to consideration of the endocannabinoid system's role in depression and anxiety.
OBJECTIVE
This study aimed to review the evidence from animal research and clinical studies on the role of cannabinoid receptors, the major endocannabinoids -anandamide (AEA) and 2-arachidonoylglycerol (2-AG)- and the enzymes related to the synthesis and degradation of these chemicals as putative biomarkers for diagnostic and therapeutic elements of depression and anxiety.
METHODS
This review included the online search, identification, and analysis of articles (basic and clinical trials) published in English in PubMed linked to the role of cannabinoid receptors, AEA, 2- AG, and the enzymes associated with the synthesis and degradation of these endocannabinoids in depression and anxiety.
RESULTS
The neurobiological relevance of the endocannabinoid system offers genetic or pharmacological manipulation of this system as a potential strategy for the diagnostic and clinical management of mood disorders, including depression and anxiety.
CONCLUSION
Although the described approach in this review is promising, no solid evidence is yet available, and along with additional experiments using animal models that mimic human depression and anxiety, clinical trials are needed to explore the role of the endocannabinoid system's elements as well as the anandamide membrane transporter, none of which have been adequately studied in depression and anxiety.

Identifiants

pubmed: 35382720
pii: CNSNDDT-EPUB-122279
doi: 10.2174/1871527321666220405114402
doi:

Substances chimiques

anandamide UR5G69TJKH
Endocannabinoids 0
Receptors, Cannabinoid 0

Types de publication

Review Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

417-430

Subventions

Organisme : Escuela de Medicina, Universidad Anáhuac Mayab
ID : PresInvEMR2019

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Jocelyne Alcaraz-Silva (J)

Laboratorio de Neurociencias Moleculares e Integrativas, Escuela de Medicina División Ciencias de la Salud, Universidad Anáhuac Mayab, Mérida, Yucatán, México.
Intercontinental Neuroscience Research Group, Merida, Mexico.

Daniel Feingold (D)

Department of Psychology, Ariel University, Ariel, Israel.

Gerardo Viana-Torre (G)

Laboratorio de Neurociencias Moleculares e Integrativas, Escuela de Medicina División Ciencias de la Salud, Universidad Anáhuac Mayab, Mérida, Yucatán, México.
Intercontinental Neuroscience Research Group, Merida, Mexico.

Henning Budde (H)

Intercontinental Neuroscience Research Group, Merida, Mexico.
Institute for Systems Medicine, Faculty of Human Sciences, Medical School Hamburg, Hamburg. Germany.

Claudio Imperatori (C)

Intercontinental Neuroscience Research Group, Merida, Mexico.
Cognitive and Clinical Psychology Laboratory, Department of Human Sciences, European University of Rome, Rome, Italy.

Sérgio Machado (S)

Intercontinental Neuroscience Research Group, Merida, Mexico.
Department of Sports Methods and Techniques, Federal University of Santa Maria, Santa Maria, Brazil.
Laboratory of Physical Activity Neuroscience, Neurodiversity Institute Queimados, Río de Janeiro, Brazil.

Eric Murillo-Rodríguez (E)

Laboratorio de Neurociencias Moleculares e Integrativas, Escuela de Medicina División Ciencias de la Salud, Universidad Anáhuac Mayab, Mérida, Yucatán, México.
Intercontinental Neuroscience Research Group, Merida, Mexico.

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Classifications MeSH