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Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum

Appetitive conditioning refers to the process of learning cue-reward associations and is mediated by the mesocorticolimbic system. Appetitive conditioned responses are difficult to extinguish, especially for highly salient reward such as food and drugs. We investigate whether aversive counterconditi...

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Autores principales: Kaag, Anne Marije, Schluter, Renée S., Karel, Peter, Homberg, Judith, van den Brink, Wim, Reneman, Liesbeth, van Wingen, Guido A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990538/
https://www.ncbi.nlm.nih.gov/pubmed/27594829
http://dx.doi.org/10.3389/fnhum.2016.00418
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author Kaag, Anne Marije
Schluter, Renée S.
Karel, Peter
Homberg, Judith
van den Brink, Wim
Reneman, Liesbeth
van Wingen, Guido A.
author_facet Kaag, Anne Marije
Schluter, Renée S.
Karel, Peter
Homberg, Judith
van den Brink, Wim
Reneman, Liesbeth
van Wingen, Guido A.
author_sort Kaag, Anne Marije
collection PubMed
description Appetitive conditioning refers to the process of learning cue-reward associations and is mediated by the mesocorticolimbic system. Appetitive conditioned responses are difficult to extinguish, especially for highly salient reward such as food and drugs. We investigate whether aversive counterconditioning can alter reward reinstatement in the ventral striatum in healthy volunteers using functional magnetic resonance imaging (fMRI). In the initial conditioning phase, two different stimuli were reinforced with a monetary reward. In the subsequent counterconditioning phase, one of these stimuli was paired with an aversive shock to the wrist. In the following extinction phase, none of the stimuli were reinforced. In the final reinstatement phase, reward was reinstated by informing the participants that the monetary gain could be doubled. Our fMRI data revealed that reward signaling in the ventral striatum and ventral tegmental area following reinstatement was smaller for the stimulus that was counterconditioned with an electrical shock, compared to the non-counterconditioned stimulus. A functional connectivity analysis showed that aversive counterconditioning strengthened striatal connectivity with the hippocampus and insula. These results suggest that reward signaling in the ventral striatum can be attenuated through aversive counterconditioning, possibly by concurrent retrieval of the aversive association through enhanced connectivity with hippocampus and insula.
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spelling pubmed-49905382016-09-02 Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum Kaag, Anne Marije Schluter, Renée S. Karel, Peter Homberg, Judith van den Brink, Wim Reneman, Liesbeth van Wingen, Guido A. Front Hum Neurosci Neuroscience Appetitive conditioning refers to the process of learning cue-reward associations and is mediated by the mesocorticolimbic system. Appetitive conditioned responses are difficult to extinguish, especially for highly salient reward such as food and drugs. We investigate whether aversive counterconditioning can alter reward reinstatement in the ventral striatum in healthy volunteers using functional magnetic resonance imaging (fMRI). In the initial conditioning phase, two different stimuli were reinforced with a monetary reward. In the subsequent counterconditioning phase, one of these stimuli was paired with an aversive shock to the wrist. In the following extinction phase, none of the stimuli were reinforced. In the final reinstatement phase, reward was reinstated by informing the participants that the monetary gain could be doubled. Our fMRI data revealed that reward signaling in the ventral striatum and ventral tegmental area following reinstatement was smaller for the stimulus that was counterconditioned with an electrical shock, compared to the non-counterconditioned stimulus. A functional connectivity analysis showed that aversive counterconditioning strengthened striatal connectivity with the hippocampus and insula. These results suggest that reward signaling in the ventral striatum can be attenuated through aversive counterconditioning, possibly by concurrent retrieval of the aversive association through enhanced connectivity with hippocampus and insula. Frontiers Media S.A. 2016-08-19 /pmc/articles/PMC4990538/ /pubmed/27594829 http://dx.doi.org/10.3389/fnhum.2016.00418 Text en Copyright © 2016 Kaag, Schluter, Karel, Homberg, van den Brink, Reneman and van Wingen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Kaag, Anne Marije
Schluter, Renée S.
Karel, Peter
Homberg, Judith
van den Brink, Wim
Reneman, Liesbeth
van Wingen, Guido A.
Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum
title Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum
title_full Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum
title_fullStr Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum
title_full_unstemmed Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum
title_short Aversive Counterconditioning Attenuates Reward Signaling in the Ventral Striatum
title_sort aversive counterconditioning attenuates reward signaling in the ventral striatum
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990538/
https://www.ncbi.nlm.nih.gov/pubmed/27594829
http://dx.doi.org/10.3389/fnhum.2016.00418
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