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Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype

RATIONALE: Long-term cannabis and cocaine use has been associated with impairments in reversal learning. However, how acute cannabis and cocaine administration affect reversal learning in humans is not known. OBJECTIVE: In this study, we aimed to establish the acute effects of administration of cann...

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Autores principales: Spronk, Desirée B., Van der Schaaf, Marieke E., Cools, Roshan, De Bruijn, Ellen R. A., Franke, Barbara, van Wel, Janelle H. P., Ramaekers, Johannes G., Verkes, Robbert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700084/
https://www.ncbi.nlm.nih.gov/pubmed/26572896
http://dx.doi.org/10.1007/s00213-015-4141-5
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author Spronk, Desirée B.
Van der Schaaf, Marieke E.
Cools, Roshan
De Bruijn, Ellen R. A.
Franke, Barbara
van Wel, Janelle H. P.
Ramaekers, Johannes G.
Verkes, Robbert J.
author_facet Spronk, Desirée B.
Van der Schaaf, Marieke E.
Cools, Roshan
De Bruijn, Ellen R. A.
Franke, Barbara
van Wel, Janelle H. P.
Ramaekers, Johannes G.
Verkes, Robbert J.
author_sort Spronk, Desirée B.
collection PubMed
description RATIONALE: Long-term cannabis and cocaine use has been associated with impairments in reversal learning. However, how acute cannabis and cocaine administration affect reversal learning in humans is not known. OBJECTIVE: In this study, we aimed to establish the acute effects of administration of cannabis and cocaine on valence-dependent reversal learning as a function of DRD2 Taq1A (rs1800497) and COMT Val108/158Met (rs4680) genotype. METHODS: A double-blind placebo-controlled randomized 3-way crossover design was used. Sixty-one regular poly-drug users completed a deterministic reversal learning task under the influence of cocaine, cannabis, and placebo that enabled assessment of both reward- and punishment-based reversal learning. RESULTS: Proportion correct on the reversal learning task was increased by cocaine, but decreased by cannabis. Effects of cocaine depended on the DRD2 genotype, as increases in proportion correct were seen only in the A1 carriers, and not in the A2/A2 homozygotes. COMT genotype did not modulate drug-induced effects on reversal learning. CONCLUSIONS: These data indicate that acute administration of cannabis and cocaine has opposite effects on reversal learning. The effects of cocaine, but not cannabis, depend on interindividual genetic differences in the dopamine D2 receptor gene. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00213-015-4141-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-47000842016-01-11 Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype Spronk, Desirée B. Van der Schaaf, Marieke E. Cools, Roshan De Bruijn, Ellen R. A. Franke, Barbara van Wel, Janelle H. P. Ramaekers, Johannes G. Verkes, Robbert J. Psychopharmacology (Berl) Original Investigation RATIONALE: Long-term cannabis and cocaine use has been associated with impairments in reversal learning. However, how acute cannabis and cocaine administration affect reversal learning in humans is not known. OBJECTIVE: In this study, we aimed to establish the acute effects of administration of cannabis and cocaine on valence-dependent reversal learning as a function of DRD2 Taq1A (rs1800497) and COMT Val108/158Met (rs4680) genotype. METHODS: A double-blind placebo-controlled randomized 3-way crossover design was used. Sixty-one regular poly-drug users completed a deterministic reversal learning task under the influence of cocaine, cannabis, and placebo that enabled assessment of both reward- and punishment-based reversal learning. RESULTS: Proportion correct on the reversal learning task was increased by cocaine, but decreased by cannabis. Effects of cocaine depended on the DRD2 genotype, as increases in proportion correct were seen only in the A1 carriers, and not in the A2/A2 homozygotes. COMT genotype did not modulate drug-induced effects on reversal learning. CONCLUSIONS: These data indicate that acute administration of cannabis and cocaine has opposite effects on reversal learning. The effects of cocaine, but not cannabis, depend on interindividual genetic differences in the dopamine D2 receptor gene. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00213-015-4141-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-11-17 2016 /pmc/articles/PMC4700084/ /pubmed/26572896 http://dx.doi.org/10.1007/s00213-015-4141-5 Text en © The Author(s) 2015 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.
spellingShingle Original Investigation
Spronk, Desirée B.
Van der Schaaf, Marieke E.
Cools, Roshan
De Bruijn, Ellen R. A.
Franke, Barbara
van Wel, Janelle H. P.
Ramaekers, Johannes G.
Verkes, Robbert J.
Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype
title Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype
title_full Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype
title_fullStr Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype
title_full_unstemmed Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype
title_short Acute effects of cocaine and cannabis on reversal learning as a function of COMT and DRD2 genotype
title_sort acute effects of cocaine and cannabis on reversal learning as a function of comt and drd2 genotype
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700084/
https://www.ncbi.nlm.nih.gov/pubmed/26572896
http://dx.doi.org/10.1007/s00213-015-4141-5
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