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The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear
Once acquired, a fearful memory can persist for a lifetime. Although learned fear can be extinguished, extinction memories are fragile. The resilience of fear memories to extinction may contribute to the maintenance of disorders of fear and anxiety, including post-traumatic stress disorder (PTSD). A...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637424/ https://www.ncbi.nlm.nih.gov/pubmed/26617500 http://dx.doi.org/10.3389/fnbeh.2015.00298 |
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author | Giustino, Thomas F. Maren, Stephen |
author_facet | Giustino, Thomas F. Maren, Stephen |
author_sort | Giustino, Thomas F. |
collection | PubMed |
description | Once acquired, a fearful memory can persist for a lifetime. Although learned fear can be extinguished, extinction memories are fragile. The resilience of fear memories to extinction may contribute to the maintenance of disorders of fear and anxiety, including post-traumatic stress disorder (PTSD). As such, considerable effort has been placed on understanding the neural circuitry underlying the acquisition, expression, and extinction of emotional memories in rodent models as well as in humans. A triad of brain regions, including the prefrontal cortex, hippocampus, and amygdala, form an essential brain circuit involved in fear conditioning and extinction. Within this circuit, the prefrontal cortex is thought to exert top-down control over subcortical structures to regulate appropriate behavioral responses. Importantly, a division of labor has been proposed in which the prelimbic (PL) and infralimbic (IL) subdivisions of the medial prefrontal cortex (mPFC) regulate the expression and suppression of fear in rodents, respectively. Here, we critically review the anatomical and physiological evidence that has led to this proposed dichotomy of function within mPFC. We propose that under some conditions, the PL and IL act in concert, exhibiting similar patterns of neural activity in response to aversive conditioned stimuli and during the expression or inhibition of conditioned fear. This may stem from common synaptic inputs, parallel downstream outputs, or cortico-cortical interactions. Despite this functional covariation, these mPFC subdivisions may still be coding for largely opposing behavioral outcomes, with PL biased towards fear expression and IL towards suppression. |
format | Online Article Text |
id | pubmed-4637424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46374242015-11-27 The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear Giustino, Thomas F. Maren, Stephen Front Behav Neurosci Neuroscience Once acquired, a fearful memory can persist for a lifetime. Although learned fear can be extinguished, extinction memories are fragile. The resilience of fear memories to extinction may contribute to the maintenance of disorders of fear and anxiety, including post-traumatic stress disorder (PTSD). As such, considerable effort has been placed on understanding the neural circuitry underlying the acquisition, expression, and extinction of emotional memories in rodent models as well as in humans. A triad of brain regions, including the prefrontal cortex, hippocampus, and amygdala, form an essential brain circuit involved in fear conditioning and extinction. Within this circuit, the prefrontal cortex is thought to exert top-down control over subcortical structures to regulate appropriate behavioral responses. Importantly, a division of labor has been proposed in which the prelimbic (PL) and infralimbic (IL) subdivisions of the medial prefrontal cortex (mPFC) regulate the expression and suppression of fear in rodents, respectively. Here, we critically review the anatomical and physiological evidence that has led to this proposed dichotomy of function within mPFC. We propose that under some conditions, the PL and IL act in concert, exhibiting similar patterns of neural activity in response to aversive conditioned stimuli and during the expression or inhibition of conditioned fear. This may stem from common synaptic inputs, parallel downstream outputs, or cortico-cortical interactions. Despite this functional covariation, these mPFC subdivisions may still be coding for largely opposing behavioral outcomes, with PL biased towards fear expression and IL towards suppression. Frontiers Media S.A. 2015-11-09 /pmc/articles/PMC4637424/ /pubmed/26617500 http://dx.doi.org/10.3389/fnbeh.2015.00298 Text en Copyright © 2015 Giustino and Maren. 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 Giustino, Thomas F. Maren, Stephen The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear |
title | The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear |
title_full | The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear |
title_fullStr | The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear |
title_full_unstemmed | The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear |
title_short | The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear |
title_sort | role of the medial prefrontal cortex in the conditioning and extinction of fear |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637424/ https://www.ncbi.nlm.nih.gov/pubmed/26617500 http://dx.doi.org/10.3389/fnbeh.2015.00298 |
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