Cargando…

Noradrenergic Modulation of Fear Conditioning and Extinction

The locus coeruleus norepinephrine (LC-NE) system plays a broad role in learning and memory. Here we begin with an overview of the LC-NE system. We then consider how both direct and indirect manipulations of the LC-NE system affect cued and contextual aversive learning and memory. We propose that NE...

Descripción completa

Detalles Bibliográficos
Autores principales: Giustino, Thomas F., Maren, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859179/
https://www.ncbi.nlm.nih.gov/pubmed/29593511
http://dx.doi.org/10.3389/fnbeh.2018.00043
_version_ 1783307768339365888
author Giustino, Thomas F.
Maren, Stephen
author_facet Giustino, Thomas F.
Maren, Stephen
author_sort Giustino, Thomas F.
collection PubMed
description The locus coeruleus norepinephrine (LC-NE) system plays a broad role in learning and memory. Here we begin with an overview of the LC-NE system. We then consider how both direct and indirect manipulations of the LC-NE system affect cued and contextual aversive learning and memory. We propose that NE dynamically modulates Pavlovian conditioning and extinction, either promoting or impairing learning aversive processes under different levels of behavioral arousal. We suggest that under high levels of stress (e.g., during/soon after fear conditioning) the locus coeruleus (LC) promotes cued fear learning by enhancing amygdala function while simultaneously blunting prefrontal function. Under low levels of arousal, the LC promotes PFC function to promote downstream inhibition of the amygdala and foster the extinction of cued fear. Thus, LC-NE action on the medial prefrontal cortex (mPFC) might be described by an inverted-U function such that it can either enhance or hinder learning depending on arousal states. In addition, LC-NE seems to be particularly important for the acquisition, consolidation and extinction of contextual fear memories. This may be due to dense adrenoceptor expression in the hippocampus (HPC) which encodes contextual information, and the ability of NE to regulate long-term potentiation (LTP). Moreover, recent work reveals that the diversity of LC-NE functions in aversive learning and memory are mediated by functionally heterogeneous populations of LC neurons that are defined by their projection targets. Hence, LC-NE function in learning and memory is determined by projection-specific neuromodulation that accompanies various states of behavioral arousal.
format Online
Article
Text
id pubmed-5859179
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-58591792018-03-28 Noradrenergic Modulation of Fear Conditioning and Extinction Giustino, Thomas F. Maren, Stephen Front Behav Neurosci Neuroscience The locus coeruleus norepinephrine (LC-NE) system plays a broad role in learning and memory. Here we begin with an overview of the LC-NE system. We then consider how both direct and indirect manipulations of the LC-NE system affect cued and contextual aversive learning and memory. We propose that NE dynamically modulates Pavlovian conditioning and extinction, either promoting or impairing learning aversive processes under different levels of behavioral arousal. We suggest that under high levels of stress (e.g., during/soon after fear conditioning) the locus coeruleus (LC) promotes cued fear learning by enhancing amygdala function while simultaneously blunting prefrontal function. Under low levels of arousal, the LC promotes PFC function to promote downstream inhibition of the amygdala and foster the extinction of cued fear. Thus, LC-NE action on the medial prefrontal cortex (mPFC) might be described by an inverted-U function such that it can either enhance or hinder learning depending on arousal states. In addition, LC-NE seems to be particularly important for the acquisition, consolidation and extinction of contextual fear memories. This may be due to dense adrenoceptor expression in the hippocampus (HPC) which encodes contextual information, and the ability of NE to regulate long-term potentiation (LTP). Moreover, recent work reveals that the diversity of LC-NE functions in aversive learning and memory are mediated by functionally heterogeneous populations of LC neurons that are defined by their projection targets. Hence, LC-NE function in learning and memory is determined by projection-specific neuromodulation that accompanies various states of behavioral arousal. Frontiers Media S.A. 2018-03-13 /pmc/articles/PMC5859179/ /pubmed/29593511 http://dx.doi.org/10.3389/fnbeh.2018.00043 Text en Copyright © 2018 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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner 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
Noradrenergic Modulation of Fear Conditioning and Extinction
title Noradrenergic Modulation of Fear Conditioning and Extinction
title_full Noradrenergic Modulation of Fear Conditioning and Extinction
title_fullStr Noradrenergic Modulation of Fear Conditioning and Extinction
title_full_unstemmed Noradrenergic Modulation of Fear Conditioning and Extinction
title_short Noradrenergic Modulation of Fear Conditioning and Extinction
title_sort noradrenergic modulation of fear conditioning and extinction
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859179/
https://www.ncbi.nlm.nih.gov/pubmed/29593511
http://dx.doi.org/10.3389/fnbeh.2018.00043
work_keys_str_mv AT giustinothomasf noradrenergicmodulationoffearconditioningandextinction
AT marenstephen noradrenergicmodulationoffearconditioningandextinction