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The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans

Context-related extinction learning and renewal in humans is mediated by hippocampal and prefrontal regions. Renewal is defined as the reoccurrence of an extinguished response if the contexts present during extinction learning and recall differ. Animal studies implicate hippocampal γ-aminobutyric ac...

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Autores principales: Lissek, Silke, Golisch, Anne, Glaubitz, Benjamin, Tegenthoff, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707232/
https://www.ncbi.nlm.nih.gov/pubmed/27928709
http://dx.doi.org/10.1007/s11682-016-9662-y
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author Lissek, Silke
Golisch, Anne
Glaubitz, Benjamin
Tegenthoff, Martin
author_facet Lissek, Silke
Golisch, Anne
Glaubitz, Benjamin
Tegenthoff, Martin
author_sort Lissek, Silke
collection PubMed
description Context-related extinction learning and renewal in humans is mediated by hippocampal and prefrontal regions. Renewal is defined as the reoccurrence of an extinguished response if the contexts present during extinction learning and recall differ. Animal studies implicate hippocampal γ-aminobutyric acid (GABA) A receptors in extinction and renewal. However, human studies on GABAergic mechanisms in extinction learning are lacking. In this fMRI study, we therefore investigated the role of the GABAergic system in context-related extinction learning and renewal. Participants treated with the GABA A agonist lorazepam prior to extinction learning were impaired in encoding changed associations during extinction learning, regardless of context, and in retrieving extinction associations during recall. In contrast, retrieval of associations learned during acquisition was largely unaffected, which led to reduced genuine renewal, since acquisition associations were retrieved context-independently. These deficits, which were presumably due to weak encoding of extinction associations, were related to altered BOLD activation in regions relevant for context processing and retrieval, as well as response selection: reduced activation in bilateral PFC and hippocampus during extinction learning and recall, and increased ventromedial/orbitofrontal cortex activation during recall. Our findings indicate that the GABergic system is involved in context-related extinction learning and recall in humans, by modulating hippocampus-based context processing and PFC-based processing of changed associations and subsequent response selection.
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spelling pubmed-57072322017-12-04 The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans Lissek, Silke Golisch, Anne Glaubitz, Benjamin Tegenthoff, Martin Brain Imaging Behav Original Research Context-related extinction learning and renewal in humans is mediated by hippocampal and prefrontal regions. Renewal is defined as the reoccurrence of an extinguished response if the contexts present during extinction learning and recall differ. Animal studies implicate hippocampal γ-aminobutyric acid (GABA) A receptors in extinction and renewal. However, human studies on GABAergic mechanisms in extinction learning are lacking. In this fMRI study, we therefore investigated the role of the GABAergic system in context-related extinction learning and renewal. Participants treated with the GABA A agonist lorazepam prior to extinction learning were impaired in encoding changed associations during extinction learning, regardless of context, and in retrieving extinction associations during recall. In contrast, retrieval of associations learned during acquisition was largely unaffected, which led to reduced genuine renewal, since acquisition associations were retrieved context-independently. These deficits, which were presumably due to weak encoding of extinction associations, were related to altered BOLD activation in regions relevant for context processing and retrieval, as well as response selection: reduced activation in bilateral PFC and hippocampus during extinction learning and recall, and increased ventromedial/orbitofrontal cortex activation during recall. Our findings indicate that the GABergic system is involved in context-related extinction learning and recall in humans, by modulating hippocampus-based context processing and PFC-based processing of changed associations and subsequent response selection. Springer US 2016-12-07 2017 /pmc/articles/PMC5707232/ /pubmed/27928709 http://dx.doi.org/10.1007/s11682-016-9662-y Text en © The Author(s) 2016 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 Research
Lissek, Silke
Golisch, Anne
Glaubitz, Benjamin
Tegenthoff, Martin
The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans
title The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans
title_full The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans
title_fullStr The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans
title_full_unstemmed The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans
title_short The GABAergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans
title_sort gabaergic system in prefrontal cortex and hippocampus modulates context-related extinction learning and renewal in humans
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707232/
https://www.ncbi.nlm.nih.gov/pubmed/27928709
http://dx.doi.org/10.1007/s11682-016-9662-y
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