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dc.contributor.authorLawn, W
dc.contributor.authorFreeman, TP
dc.contributor.authorPope, RA
dc.contributor.authorJoye, A
dc.contributor.authorHarvey, L
dc.contributor.authorHindocha, C
dc.contributor.authorMokrysz, C
dc.contributor.authorMoss, A
dc.contributor.authorWall, MB
dc.contributor.authorBloomfield, MA
dc.contributor.authorDas, RK
dc.contributor.authorMorgan, CJ
dc.contributor.authorNutt, DJ
dc.contributor.authorCurran, HV
dc.date.accessioned2016-12-05T15:28:14Z
dc.date.issued2016-10
dc.description.abstractRATIONALE: Anecdotally, both acute and chronic cannabis use have been associated with apathy, amotivation, and other reward processing deficits. To date, empirical support for these effects is limited, and no previous studies have assessed both acute effects of Δ-9-tetrahydrocannabinol (THC) and cannabidiol (CBD), as well as associations with cannabis dependence. OBJECTIVES: The objectives of this study were (1) to examine acute effects of cannabis with CBD (Cann + CBD) and without CBD (Cann-CBD) on effort-related decision-making and (2) to examine associations between cannabis dependence, effort-related decision-making and reward learning. METHODS: In study 1, 17 participants each received three acute vaporized treatments, namely Cann-CBD (8 mg THC), Cann + CBD (8 mg THC + 10 mg CBD) and matched placebo, followed by a 50 % dose top-up 1.5 h later, and completed the Effort Expenditure for Rewards Task (EEfRT). In study 2, 20 cannabis-dependent participants were compared with 20 non-dependent, drug-using control participants on the EEfRT and the Probabilistic Reward Task (PRT) in a non-intoxicated state. RESULTS: Cann-CBD reduced the likelihood of high-effort choices relative to placebo (p = 0.042) and increased sensitivity to expected value compared to both placebo (p = 0.014) and Cann + CBD (p = 0.006). The cannabis-dependent and control groups did not differ on the EEfRT. However, the cannabis-dependent group exhibited a weaker response bias than the control group on the PRT (p = 0.007). CONCLUSIONS: Cannabis acutely induced a transient amotivational state and CBD influenced the effects of THC on expected value. In contrast, cannabis dependence was associated with preserved motivation alongside impaired reward learning, although confounding factors, including depression, cannot be disregarded. This is the first well powered, fully controlled study to objectively demonstrate the acute amotivational effects of THC.en_GB
dc.description.sponsorshipStudy 1 was funded by Drug Science. The cannabis used in study 1 was bought from Bedrocan (Veendam, thew Netherlands). Study 2 was funded by WL’s PhD grant from the BBSRC and University College Londonen_GB
dc.identifier.citationVol. 233, pp. 3537 - 3552en_GB
dc.identifier.doi10.1007/s00213-016-4383-x
dc.identifier.urihttp://hdl.handle.net/10871/24745
dc.language.isoenen_GB
dc.publisherSpringer Verlag (Germany)en_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/27585792en_GB
dc.rights© The Author(s) 2016. This article is published with open access at Springerlink.com Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http:// creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.en_GB
dc.subjectAddictionen_GB
dc.subjectCannabidiolen_GB
dc.subjectCannabinoidsen_GB
dc.subjectCannabisen_GB
dc.subjectEffort-related decision-makingen_GB
dc.subjectMotivationen_GB
dc.subjectReinforcement learningen_GB
dc.subjectRewarden_GB
dc.subjectTHCen_GB
dc.titleAcute and chronic effects of cannabinoids on effort-related decision-making and reward learning: an evaluation of the cannabis 'amotivational' hypothesesen_GB
dc.typeArticleen_GB
dc.date.available2016-12-05T15:28:14Z
dc.identifier.issn0033-3158
exeter.place-of-publicationGermanyen_GB
dc.descriptionThis is the final version of the article. Available from the publisher via the DOI in this record.en_GB
dc.identifier.journalPsychopharmacologyen_GB
dc.identifier.pmcidPMC5021728
dc.identifier.pmid27585792


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