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The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal

Renewal describes the recovery of an extinguished response if recall is tested in a context different from the extinction context. Behavioral studies demonstrated that attention to relevant context strengthens renewal. Neurotransmitters mediating attention and learning such as the dopaminergic (DA)...

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Autores principales: Lissek, Silke, Glaubitz, Benjamin, Wolf, Oliver T., Tegenthoff, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558976/
https://www.ncbi.nlm.nih.gov/pubmed/26388752
http://dx.doi.org/10.3389/fnbeh.2015.00238
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author Lissek, Silke
Glaubitz, Benjamin
Wolf, Oliver T.
Tegenthoff, Martin
author_facet Lissek, Silke
Glaubitz, Benjamin
Wolf, Oliver T.
Tegenthoff, Martin
author_sort Lissek, Silke
collection PubMed
description Renewal describes the recovery of an extinguished response if recall is tested in a context different from the extinction context. Behavioral studies demonstrated that attention to relevant context strengthens renewal. Neurotransmitters mediating attention and learning such as the dopaminergic (DA) system presumably modulate extinction learning and renewal. However, the role of DA for non-fear-based extinction learning and renewal in humans has not yet been investigated. This fMRI study investigated effects of DA-antagonism upon context-related extinction in a predictive learning task in which extinction occurred either in a novel (ABA) or an unchanged (AAA) context. The tiapride-treated group (TIA) showed significantly impaired ABA extinction learning and a significant within-group difference between ABA and AAA extinction, compared to placebo (PLAC). Groups did not differ in their level of ABA renewal. In ABA extinction, TIA showed reduced activation in dlPFC and OFC, hippocampus, and temporal regions. Across groups, activation in PFC and hippocampus correlated negatively with ABA extinction errors. Results suggest that in context-related extinction learning DA in PFC and hippocampus is involved in readjusting the cue-outcome relationship in the presence of a novel context. However, relating context to the appropriate association during recall does not appear to rely exclusively on DA signaling.
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spelling pubmed-45589762015-09-18 The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal Lissek, Silke Glaubitz, Benjamin Wolf, Oliver T. Tegenthoff, Martin Front Behav Neurosci Neuroscience Renewal describes the recovery of an extinguished response if recall is tested in a context different from the extinction context. Behavioral studies demonstrated that attention to relevant context strengthens renewal. Neurotransmitters mediating attention and learning such as the dopaminergic (DA) system presumably modulate extinction learning and renewal. However, the role of DA for non-fear-based extinction learning and renewal in humans has not yet been investigated. This fMRI study investigated effects of DA-antagonism upon context-related extinction in a predictive learning task in which extinction occurred either in a novel (ABA) or an unchanged (AAA) context. The tiapride-treated group (TIA) showed significantly impaired ABA extinction learning and a significant within-group difference between ABA and AAA extinction, compared to placebo (PLAC). Groups did not differ in their level of ABA renewal. In ABA extinction, TIA showed reduced activation in dlPFC and OFC, hippocampus, and temporal regions. Across groups, activation in PFC and hippocampus correlated negatively with ABA extinction errors. Results suggest that in context-related extinction learning DA in PFC and hippocampus is involved in readjusting the cue-outcome relationship in the presence of a novel context. However, relating context to the appropriate association during recall does not appear to rely exclusively on DA signaling. Frontiers Media S.A. 2015-09-03 /pmc/articles/PMC4558976/ /pubmed/26388752 http://dx.doi.org/10.3389/fnbeh.2015.00238 Text en Copyright © 2015 Lissek, Glaubitz, Wolf and Tegenthoff. 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
Lissek, Silke
Glaubitz, Benjamin
Wolf, Oliver T.
Tegenthoff, Martin
The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal
title The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal
title_full The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal
title_fullStr The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal
title_full_unstemmed The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal
title_short The DA antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal
title_sort da antagonist tiapride impairs context-related extinction learning in a novel context without affecting renewal
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558976/
https://www.ncbi.nlm.nih.gov/pubmed/26388752
http://dx.doi.org/10.3389/fnbeh.2015.00238
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