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Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task

Altered medial prefrontal cortex (mPFC) and amygdala function is associated with anxiety-related disorders. While the mPFC-amygdala pathway has a clear role in fear conditioning, these structures are also involved in active avoidance. Given that avoidance perseveration represents a core symptom of a...

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Autores principales: Jiao, Xilu, Beck, Kevin D., Myers, Catherine E., Servatius, Richard J., Pang, Kevin C. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569748/
https://www.ncbi.nlm.nih.gov/pubmed/26441578
http://dx.doi.org/10.3389/fnbeh.2015.00249
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author Jiao, Xilu
Beck, Kevin D.
Myers, Catherine E.
Servatius, Richard J.
Pang, Kevin C. H.
author_facet Jiao, Xilu
Beck, Kevin D.
Myers, Catherine E.
Servatius, Richard J.
Pang, Kevin C. H.
author_sort Jiao, Xilu
collection PubMed
description Altered medial prefrontal cortex (mPFC) and amygdala function is associated with anxiety-related disorders. While the mPFC-amygdala pathway has a clear role in fear conditioning, these structures are also involved in active avoidance. Given that avoidance perseveration represents a core symptom of anxiety disorders, the neural substrate of avoidance, especially its extinction, requires better understanding. The present study was designed to investigate the activity, particularly, inhibitory neuronal activity in mPFC and amygdala during acquisition and extinction of lever-press avoidance in rats. Neural activity was examined in the mPFC, intercalated cell clusters (ITCs) lateral (LA), basal (BA) and central (CeA) amygdala, at various time points during acquisition and extinction, using induction of the immediate early gene product, c-Fos. Neural activity was greater in the mPFC, LA, BA, and ITC during the extinction phase as compared to the acquisition phase. In contrast, the CeA was the only region that was more activated during acquisition than during extinction. Our results indicate inhibitory neurons are more activated during late phase of acquisition and extinction in the mPFC and LA, suggesting the dynamic involvement of inhibitory circuits in the development and extinction of avoidance response. Together, these data start to identify the key brain regions important in active avoidance behavior, areas that could be associated with avoidance perseveration in anxiety disorders.
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spelling pubmed-45697482015-10-05 Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task Jiao, Xilu Beck, Kevin D. Myers, Catherine E. Servatius, Richard J. Pang, Kevin C. H. Front Behav Neurosci Neuroscience Altered medial prefrontal cortex (mPFC) and amygdala function is associated with anxiety-related disorders. While the mPFC-amygdala pathway has a clear role in fear conditioning, these structures are also involved in active avoidance. Given that avoidance perseveration represents a core symptom of anxiety disorders, the neural substrate of avoidance, especially its extinction, requires better understanding. The present study was designed to investigate the activity, particularly, inhibitory neuronal activity in mPFC and amygdala during acquisition and extinction of lever-press avoidance in rats. Neural activity was examined in the mPFC, intercalated cell clusters (ITCs) lateral (LA), basal (BA) and central (CeA) amygdala, at various time points during acquisition and extinction, using induction of the immediate early gene product, c-Fos. Neural activity was greater in the mPFC, LA, BA, and ITC during the extinction phase as compared to the acquisition phase. In contrast, the CeA was the only region that was more activated during acquisition than during extinction. Our results indicate inhibitory neurons are more activated during late phase of acquisition and extinction in the mPFC and LA, suggesting the dynamic involvement of inhibitory circuits in the development and extinction of avoidance response. Together, these data start to identify the key brain regions important in active avoidance behavior, areas that could be associated with avoidance perseveration in anxiety disorders. Frontiers Media S.A. 2015-09-15 /pmc/articles/PMC4569748/ /pubmed/26441578 http://dx.doi.org/10.3389/fnbeh.2015.00249 Text en Copyright © 2015 Jiao, Beck, Myers, Servatius and Pang. 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 and 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
Jiao, Xilu
Beck, Kevin D.
Myers, Catherine E.
Servatius, Richard J.
Pang, Kevin C. H.
Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task
title Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task
title_full Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task
title_fullStr Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task
title_full_unstemmed Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task
title_short Altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task
title_sort altered activity of the medial prefrontal cortex and amygdala during acquisition and extinction of an active avoidance task
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569748/
https://www.ncbi.nlm.nih.gov/pubmed/26441578
http://dx.doi.org/10.3389/fnbeh.2015.00249
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