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Pharmacological characterization of cannabidiol as a negative allosteric modulator of the 5-HT2A receptor.

Etienne Billard, Alexandre Torbey, Antonio Inserra, Emily Grant, Antonella Bertazzo, Danilo de Gregorio, Stefano Comai, David Chatenet, Gabriella Gobbi, Terence E Hébert

Cellular signalling March 1, 2025 DOI: 10.1016/j.cellsig.2025.111588 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Laboratory study Peer reviewed
Population HEK 293 cells and rat primary cortical neurons
Interventions Cannabidiol (CBD) lysergic acid diethylamide (LSD) DOI
Topics CBD Serotonin
Keywords Entheogens Psychedelic drugs Neuroscience brain science Neural research Neurology Drug interactions pharmacology Drug effects 5-ht2a Allosteric modulation Biased signalling Cannabidiol CBD Psychedelics hallucinogens CBD Cannabidiol Hemp extract
Citations 10
Key points CBD acts as a negative allosteric modulator of the 5-HT2A receptor, antagonizing LSD-mediated Gq activation without affecting β-arrestin2 recruitment.

Abstract

Promising clinical evidence suggests that psychedelic compounds, like lysergic acid diethylamide (LSD), have therapeutic value for treatment of psychiatric disorders. However, they often produce hallucinations and dissociative states, likely mediated by the serotonin (5-HT) receptor 5-HT2A, raising challenges regarding therapeutic scalability. Given the reported antipsychotic effects of cannabidiol (CBD) and its promiscuous binding at many receptors, we assessed whether CBD could modulate 5-HT2A signalling. Activation of the 5-HT2A intracellular signalling events were assessed using resonance energy transfer- or fluorescence-based biosensors in HEK 293 cells and in rat primary cortical neurons. In 5-HT2A-transfected HEK 293 T cells, CBD antagonized LSD-mediated Gq activation in a saturable way, while leaving β-arrestin2 recruitment unaffected. CBD decreased Gq activation mediated by the 5-HT2A-specific agonist DOI as well as LSD-mediated activity in primary rat neonatal cortical neurons. Using Site Identification by Ligand Competitive Saturation (SILCS) simulations, we also predicted that the putative binding site of CBD overlapped with that of oleamide, a positive allosteric modulator of 5-HT2A, and could displace the binding of orthosteric ligands toward the external binding pocket. Based on these findings, we propose that CBD acts as a negative allosteric modulator of 5-HT2A.

Comparable studies

Other experimental studies on CBD, most cited first.

Study Year Design Participants
Dissociable effects of cannabis with and without cannabidiol on the human brain’s resting-state functional connectivity Healthy volunteers experienced with cannabis but not regular users 2019 Within-subjects experimental design n = 17
Placebo Effects of Edible Cannabis: Reported Intoxication Effects at a 30-Minute Delay Participants 2017 Within-subjects experimental design n = 20
THC, CBD and minor cannabinoid CBDV differently modulate hippocampal neurons firing. Cultured hippocampal neurons 2025 Experimental study
Acute and Extended Anxiolytic Effects of Cannabidiol in Cannabis Flower: A Quasi-Experimental ad libitum Use Study Participants with anxiety symptoms who were not using cannabis or who used cannabis... 2024 Nonequivalent control group quasiexperimental design n = 300
Baseline affective symptomatology moderates acute subjective effects of high potency THC and CBD cannabis concentrates. Cannabis users (48% female; mean age 29.87 years) 2023 Exploratory experimental study with ad libitum naturalistic use n = 54

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