Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.

Fear conditioning is relevant for elucidating the pathophysiology of anxiety, but may also be useful in the context of chronic pain syndromes which often overlap with anxiety. Thus far, no fear conditioning studies have employed aversive visceral stimuli from the lower gastrointestinal tract. Theref...

Full description

Bibliographic Details
Main Authors: Joswin Kattoor, Elke R Gizewski, Vassilios Kotsis, Sven Benson, Carolin Gramsch, Nina Theysohn, Stefan Maderwald, Michael Forsting, Manfred Schedlowski, Sigrid Elsenbruch
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3582635?pdf=render
id doaj-a5fd91a23a8a426a9c684911a9da55b7
record_format Article
spelling doaj-a5fd91a23a8a426a9c684911a9da55b72020-11-25T01:13:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5114910.1371/journal.pone.0051149Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.Joswin KattoorElke R GizewskiVassilios KotsisSven BensonCarolin GramschNina TheysohnStefan MaderwaldMichael ForstingManfred SchedlowskiSigrid ElsenbruchFear conditioning is relevant for elucidating the pathophysiology of anxiety, but may also be useful in the context of chronic pain syndromes which often overlap with anxiety. Thus far, no fear conditioning studies have employed aversive visceral stimuli from the lower gastrointestinal tract. Therefore, we implemented a fear conditioning paradigm to analyze the conditioned response to rectal pain stimuli using fMRI during associative learning, extinction and reinstatement. In N = 21 healthy humans, visual conditioned stimuli (CS(+)) were paired with painful rectal distensions as unconditioned stimuli (US), while different visual stimuli (CS(-)) were presented without US. During extinction, all CSs were presented without US, whereas during reinstatement, a single, unpaired US was presented. In region-of-interest analyses, conditioned anticipatory neural activation was assessed along with perceived CS-US contingency and CS unpleasantness. Fear conditioning resulted in significant contingency awareness and valence change, i.e., learned unpleasantness of a previously neutral stimulus. This was paralleled by anticipatory activation of the anterior cingulate cortex, the somatosensory cortex and precuneus (all during early acquisition) and the amygdala (late acquisition) in response to the CS(+). During extinction, anticipatory activation of the dorsolateral prefrontal cortex to the CS(-) was observed. In the reinstatement phase, a tendency for parahippocampal activation was found. Fear conditioning with rectal pain stimuli is feasible and leads to learned unpleasantness of previously neutral stimuli. Within the brain, conditioned anticipatory activations are seen in core areas of the central fear network including the amygdala and the anterior cingulate cortex. During extinction, conditioned responses quickly disappear, and learning of new predictive cue properties is paralleled by prefrontal activation. A tendency for parahippocampal activation during reinstatement could indicate a reactivation of the old memory trace. Together, these findings contribute to our understanding of aversive visceral learning and memory processes relevant to the pathophysiology of chronic abdominal pain.http://europepmc.org/articles/PMC3582635?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Joswin Kattoor
Elke R Gizewski
Vassilios Kotsis
Sven Benson
Carolin Gramsch
Nina Theysohn
Stefan Maderwald
Michael Forsting
Manfred Schedlowski
Sigrid Elsenbruch
spellingShingle Joswin Kattoor
Elke R Gizewski
Vassilios Kotsis
Sven Benson
Carolin Gramsch
Nina Theysohn
Stefan Maderwald
Michael Forsting
Manfred Schedlowski
Sigrid Elsenbruch
Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.
PLoS ONE
author_facet Joswin Kattoor
Elke R Gizewski
Vassilios Kotsis
Sven Benson
Carolin Gramsch
Nina Theysohn
Stefan Maderwald
Michael Forsting
Manfred Schedlowski
Sigrid Elsenbruch
author_sort Joswin Kattoor
title Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.
title_short Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.
title_full Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.
title_fullStr Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.
title_full_unstemmed Fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.
title_sort fear conditioning in an abdominal pain model: neural responses during associative learning and extinction in healthy subjects.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Fear conditioning is relevant for elucidating the pathophysiology of anxiety, but may also be useful in the context of chronic pain syndromes which often overlap with anxiety. Thus far, no fear conditioning studies have employed aversive visceral stimuli from the lower gastrointestinal tract. Therefore, we implemented a fear conditioning paradigm to analyze the conditioned response to rectal pain stimuli using fMRI during associative learning, extinction and reinstatement. In N = 21 healthy humans, visual conditioned stimuli (CS(+)) were paired with painful rectal distensions as unconditioned stimuli (US), while different visual stimuli (CS(-)) were presented without US. During extinction, all CSs were presented without US, whereas during reinstatement, a single, unpaired US was presented. In region-of-interest analyses, conditioned anticipatory neural activation was assessed along with perceived CS-US contingency and CS unpleasantness. Fear conditioning resulted in significant contingency awareness and valence change, i.e., learned unpleasantness of a previously neutral stimulus. This was paralleled by anticipatory activation of the anterior cingulate cortex, the somatosensory cortex and precuneus (all during early acquisition) and the amygdala (late acquisition) in response to the CS(+). During extinction, anticipatory activation of the dorsolateral prefrontal cortex to the CS(-) was observed. In the reinstatement phase, a tendency for parahippocampal activation was found. Fear conditioning with rectal pain stimuli is feasible and leads to learned unpleasantness of previously neutral stimuli. Within the brain, conditioned anticipatory activations are seen in core areas of the central fear network including the amygdala and the anterior cingulate cortex. During extinction, conditioned responses quickly disappear, and learning of new predictive cue properties is paralleled by prefrontal activation. A tendency for parahippocampal activation during reinstatement could indicate a reactivation of the old memory trace. Together, these findings contribute to our understanding of aversive visceral learning and memory processes relevant to the pathophysiology of chronic abdominal pain.
url http://europepmc.org/articles/PMC3582635?pdf=render
work_keys_str_mv AT joswinkattoor fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT elkergizewski fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT vassilioskotsis fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT svenbenson fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT carolingramsch fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT ninatheysohn fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT stefanmaderwald fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT michaelforsting fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT manfredschedlowski fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
AT sigridelsenbruch fearconditioninginanabdominalpainmodelneuralresponsesduringassociativelearningandextinctioninhealthysubjects
_version_ 1725161357651738624