The acute effects of cannabidiol on the neural correlates of reward anticipation and feedback in healthy volunteers

Author:

Lawn Will1ORCID,Hill James2,Hindocha Chandni123ORCID,Yim Jocelyn2,Yamamori Yumeya245,Jones Gus2,Walker Hannah2,Green Sebastian F2ORCID,Wall Matthew B16,Howes Oliver D7,Curran H Valerie13,Freeman Tom P1289,Bloomfield Michael AP123710ORCID

Affiliation:

1. Clinical Psychopharmacology Unit, University College London, London, UK

2. Translational Psychiatry Research Group, University College London, London, UK

3. NIHR University College London Hospitals Biomedical Research Centre, University College Hospital, London, UK

4. Institute of Cognitive Neuroscience, University College London, London, UK

5. Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK

6. Invicro London, Hammersmith Hospital, London, UK

7. Psychiatric Imaging Group, Imperial College London, London, UK

8. Addiction and Mental Health Group (AIM), University of Bath, Bath, UK

9. National Addiction Centre, Institute of Psychiatry, Psychology and Neuroscience, London, UK

10. The Traumatic Stress Clinic, St Pancras Hospital, London, UK

Abstract

Background: Cannabidiol has potential therapeutic benefits for people with psychiatric disorders characterised by reward function impairment. There is existing evidence that cannabidiol may influence some aspects of reward processing. However, it is unknown whether cannabidiol acutely affects brain function underpinning reward anticipation and feedback. Hypotheses: We predicted that cannabidiol would augment brain activity associated with reward anticipation and feedback. Methods: We administered a single 600 mg oral dose of cannabidiol and matched placebo to 23 healthy participants in a double-blind, placebo-controlled, repeated-measures design. We employed the monetary incentive delay task during functional magnetic resonance imaging to assay the neural correlates of reward anticipation and feedback. We conducted whole brain analyses and region-of-interest analyses in pre-specified reward-related brain regions. Results: The monetary incentive delay task elicited expected brain activity during reward anticipation and feedback, including in the insula, caudate, nucleus accumbens, anterior cingulate and orbitofrontal cortex. However, across the whole brain, we did not find any evidence that cannabidiol altered reward-related brain activity. Moreover, our Bayesian analyses showed that activity in our regions-of-interest was similar following cannabidiol and placebo. Additionally, our behavioural measures of motivation for reward did not show a significant difference between cannabidiol and placebo. Discussion: Cannabidiol did not acutely affect the neural correlates of reward anticipation and feedback in healthy participants. Future research should explore the effects of cannabidiol on different components of reward processing, employ different doses and administration regimens, and test its reward-related effects in people with psychiatric disorders.

Funder

British Medical Association Foundation for Medical Research Margaret Temple Award

UCL Excellence Fellowship

medical research council

national institute for health research biomedical research centre at moorfields eye hospital nhs foundation trust and ucl institute of ophthalmology

society for the study of addiction

Invicro LLC

Publisher

SAGE Publications

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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