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Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors

The nonapeptide, oxytocin (OT), known for its role in social bonding and attachment formation, has demonstrated anxiolytic properties in animal models and human studies. However, its role in the regulation of fear responses appears more complex, brain site-specific, sex-specific, and dependent on a...

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Autores principales: Olivera-Pasilio, Valentina, Dabrowska, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538630/
https://www.ncbi.nlm.nih.gov/pubmed/33071751
http://dx.doi.org/10.3389/fnins.2020.583878
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author Olivera-Pasilio, Valentina
Dabrowska, Joanna
author_facet Olivera-Pasilio, Valentina
Dabrowska, Joanna
author_sort Olivera-Pasilio, Valentina
collection PubMed
description The nonapeptide, oxytocin (OT), known for its role in social bonding and attachment formation, has demonstrated anxiolytic properties in animal models and human studies. However, its role in the regulation of fear responses appears more complex, brain site-specific, sex-specific, and dependent on a prior stress history. Studies have shown that OT neurons in the hypothalamus are activated during cued and contextual fear conditioning and during fear recall, highlighting the recruitment of endogenous oxytocin system in fear learning. OT is released into the extended amygdala, which contains the central nucleus of the amygdala (CeA) and the bed nucleus of the stria terminalis (BNST), both critical for the regulation of fear and anxiety-like behaviors. Behavioral studies report that OT in the CeA reduces contextual fear responses; whereas in the BNST, OT receptor (OTR) neurotransmission facilitates cued fear and reduces fear responses to un-signaled, diffuse threats. These ostensibly contrasting behavioral effects support growing evidence that OT works to promote fear discrimination by reducing contextual fear or fear of diffuse threats, yet strengthening fear responses to imminent and predictable threats. Recent studies from the basolateral nucleus of the amygdala (BLA) support this notion and show that activation of OTR in the BLA facilitates fear discrimination by increasing fear responses to discrete cues. Also, OTR transmission in the CeA has been shown to mediate a switch from passive freezing to active escape behaviors in confrontation with an imminent, yet escapable threat but reduce reactivity to distant threats. Therefore, OT appears to increase the salience of relevant threat-signaling cues yet reduce fear responses to un-signaled, distant, or diffuse threats. Lastly, OTR signaling has been shown to underlie emotional discrimination between conspecifics during time of distress, social transmission of fear, and social buffering of fear. As OT has been shown to enhance salience of both positive and negative social experiences, it can also serve as a warning system against potential threats in social networks. Here, we extend the social salience hypothesis by proposing that OT enhances the salience of relevant environmental cues also in non-social contexts, and as such promotes active defensive behaviors.
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spelling pubmed-75386302020-10-15 Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors Olivera-Pasilio, Valentina Dabrowska, Joanna Front Neurosci Neuroscience The nonapeptide, oxytocin (OT), known for its role in social bonding and attachment formation, has demonstrated anxiolytic properties in animal models and human studies. However, its role in the regulation of fear responses appears more complex, brain site-specific, sex-specific, and dependent on a prior stress history. Studies have shown that OT neurons in the hypothalamus are activated during cued and contextual fear conditioning and during fear recall, highlighting the recruitment of endogenous oxytocin system in fear learning. OT is released into the extended amygdala, which contains the central nucleus of the amygdala (CeA) and the bed nucleus of the stria terminalis (BNST), both critical for the regulation of fear and anxiety-like behaviors. Behavioral studies report that OT in the CeA reduces contextual fear responses; whereas in the BNST, OT receptor (OTR) neurotransmission facilitates cued fear and reduces fear responses to un-signaled, diffuse threats. These ostensibly contrasting behavioral effects support growing evidence that OT works to promote fear discrimination by reducing contextual fear or fear of diffuse threats, yet strengthening fear responses to imminent and predictable threats. Recent studies from the basolateral nucleus of the amygdala (BLA) support this notion and show that activation of OTR in the BLA facilitates fear discrimination by increasing fear responses to discrete cues. Also, OTR transmission in the CeA has been shown to mediate a switch from passive freezing to active escape behaviors in confrontation with an imminent, yet escapable threat but reduce reactivity to distant threats. Therefore, OT appears to increase the salience of relevant threat-signaling cues yet reduce fear responses to un-signaled, distant, or diffuse threats. Lastly, OTR signaling has been shown to underlie emotional discrimination between conspecifics during time of distress, social transmission of fear, and social buffering of fear. As OT has been shown to enhance salience of both positive and negative social experiences, it can also serve as a warning system against potential threats in social networks. Here, we extend the social salience hypothesis by proposing that OT enhances the salience of relevant environmental cues also in non-social contexts, and as such promotes active defensive behaviors. Frontiers Media S.A. 2020-09-23 /pmc/articles/PMC7538630/ /pubmed/33071751 http://dx.doi.org/10.3389/fnins.2020.583878 Text en Copyright © 2020 Olivera-Pasilio and Dabrowska. 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(s) 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
Olivera-Pasilio, Valentina
Dabrowska, Joanna
Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors
title Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors
title_full Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors
title_fullStr Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors
title_full_unstemmed Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors
title_short Oxytocin Promotes Accurate Fear Discrimination and Adaptive Defensive Behaviors
title_sort oxytocin promotes accurate fear discrimination and adaptive defensive behaviors
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538630/
https://www.ncbi.nlm.nih.gov/pubmed/33071751
http://dx.doi.org/10.3389/fnins.2020.583878
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