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Serotonin, Amygdala and Fear: Assembling the Puzzle

The fear circuitry orchestrates defense mechanisms in response to environmental threats. This circuitry is evolutionarily crucial for survival, but its dysregulation is thought to play a major role in the pathophysiology of psychiatric conditions in humans. The amygdala is a key player in the proces...

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Autores principales: Bocchio, Marco, McHugh, Stephen B., Bannerman, David M., Sharp, Trevor, Capogna, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820447/
https://www.ncbi.nlm.nih.gov/pubmed/27092057
http://dx.doi.org/10.3389/fncir.2016.00024
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author Bocchio, Marco
McHugh, Stephen B.
Bannerman, David M.
Sharp, Trevor
Capogna, Marco
author_facet Bocchio, Marco
McHugh, Stephen B.
Bannerman, David M.
Sharp, Trevor
Capogna, Marco
author_sort Bocchio, Marco
collection PubMed
description The fear circuitry orchestrates defense mechanisms in response to environmental threats. This circuitry is evolutionarily crucial for survival, but its dysregulation is thought to play a major role in the pathophysiology of psychiatric conditions in humans. The amygdala is a key player in the processing of fear. This brain area is prominently modulated by the neurotransmitter serotonin (5-hydroxytryptamine, 5-HT). The 5-HT input to the amygdala has drawn particular interest because genetic and pharmacological alterations of the 5-HT transporter (5-HTT) affect amygdala activation in response to emotional stimuli. Nonetheless, the impact of 5-HT on fear processing remains poorly understood.The aim of this review is to elucidate the physiological role of 5-HT in fear learning via its action on the neuronal circuits of the amygdala. Since 5-HT release increases in the basolateral amygdala (BLA) during both fear memory acquisition and expression, we examine whether and how 5-HT neurons encode aversive stimuli and aversive cues. Next, we describe pharmacological and genetic alterations of 5-HT neurotransmission that, in both rodents and humans, lead to altered fear learning. To explore the mechanisms through which 5-HT could modulate conditioned fear, we focus on the rodent BLA. We propose that a circuit-based approach taking into account the localization of specific 5-HT receptors on neurochemically-defined neurons in the BLA may be essential to decipher the role of 5-HT in emotional behavior. In keeping with a 5-HT control of fear learning, we review electrophysiological data suggesting that 5-HT regulates synaptic plasticity, spike synchrony and theta oscillations in the BLA via actions on different subcellular compartments of principal neurons and distinct GABAergic interneuron populations. Finally, we discuss how recently developed optogenetic tools combined with electrophysiological recordings and behavior could progress the knowledge of the mechanisms underlying 5-HT modulation of fear learning via action on amygdala circuits. Such advancement could pave the way for a deeper understanding of 5-HT in emotional behavior in both health and disease.
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spelling pubmed-48204472016-04-18 Serotonin, Amygdala and Fear: Assembling the Puzzle Bocchio, Marco McHugh, Stephen B. Bannerman, David M. Sharp, Trevor Capogna, Marco Front Neural Circuits Neuroscience The fear circuitry orchestrates defense mechanisms in response to environmental threats. This circuitry is evolutionarily crucial for survival, but its dysregulation is thought to play a major role in the pathophysiology of psychiatric conditions in humans. The amygdala is a key player in the processing of fear. This brain area is prominently modulated by the neurotransmitter serotonin (5-hydroxytryptamine, 5-HT). The 5-HT input to the amygdala has drawn particular interest because genetic and pharmacological alterations of the 5-HT transporter (5-HTT) affect amygdala activation in response to emotional stimuli. Nonetheless, the impact of 5-HT on fear processing remains poorly understood.The aim of this review is to elucidate the physiological role of 5-HT in fear learning via its action on the neuronal circuits of the amygdala. Since 5-HT release increases in the basolateral amygdala (BLA) during both fear memory acquisition and expression, we examine whether and how 5-HT neurons encode aversive stimuli and aversive cues. Next, we describe pharmacological and genetic alterations of 5-HT neurotransmission that, in both rodents and humans, lead to altered fear learning. To explore the mechanisms through which 5-HT could modulate conditioned fear, we focus on the rodent BLA. We propose that a circuit-based approach taking into account the localization of specific 5-HT receptors on neurochemically-defined neurons in the BLA may be essential to decipher the role of 5-HT in emotional behavior. In keeping with a 5-HT control of fear learning, we review electrophysiological data suggesting that 5-HT regulates synaptic plasticity, spike synchrony and theta oscillations in the BLA via actions on different subcellular compartments of principal neurons and distinct GABAergic interneuron populations. Finally, we discuss how recently developed optogenetic tools combined with electrophysiological recordings and behavior could progress the knowledge of the mechanisms underlying 5-HT modulation of fear learning via action on amygdala circuits. Such advancement could pave the way for a deeper understanding of 5-HT in emotional behavior in both health and disease. Frontiers Media S.A. 2016-04-05 /pmc/articles/PMC4820447/ /pubmed/27092057 http://dx.doi.org/10.3389/fncir.2016.00024 Text en Copyright © 2016 Bocchio, McHugh, Bannerman, Sharp and Capogna. 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
Bocchio, Marco
McHugh, Stephen B.
Bannerman, David M.
Sharp, Trevor
Capogna, Marco
Serotonin, Amygdala and Fear: Assembling the Puzzle
title Serotonin, Amygdala and Fear: Assembling the Puzzle
title_full Serotonin, Amygdala and Fear: Assembling the Puzzle
title_fullStr Serotonin, Amygdala and Fear: Assembling the Puzzle
title_full_unstemmed Serotonin, Amygdala and Fear: Assembling the Puzzle
title_short Serotonin, Amygdala and Fear: Assembling the Puzzle
title_sort serotonin, amygdala and fear: assembling the puzzle
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820447/
https://www.ncbi.nlm.nih.gov/pubmed/27092057
http://dx.doi.org/10.3389/fncir.2016.00024
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