Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats

Pairing a previously neutral conditioned stimulus (CS; e.g., a tone) to an aversive unconditioned stimulus (US; e.g., a footshock) leads to associative learning such that the tone alone comes to elicit a conditioned response (e.g., freezing). We have previously shown that an extinction session that...

Full description

Bibliographic Details
Main Authors: Hongjoo Joanne Lee, Rebecca P Haberman, Rheall eRoquet, Marie H Monfils
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-01-01
Series:Frontiers in Behavioral Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnbeh.2015.00369/full
id doaj-b17c8b0ec9224c55ac5299be2cdefe41
record_format Article
spelling doaj-b17c8b0ec9224c55ac5299be2cdefe412020-11-24T23:11:29ZengFrontiers Media S.A.Frontiers in Behavioral Neuroscience1662-51532016-01-01910.3389/fnbeh.2015.00369172218Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in ratsHongjoo Joanne Lee0Rebecca P Haberman1Rheall eRoquet2Marie H Monfils3University of Texas at AustinJohns Hopkins UniversityUniversity of Texas at AustinUniversity of Texas at AustinPairing a previously neutral conditioned stimulus (CS; e.g., a tone) to an aversive unconditioned stimulus (US; e.g., a footshock) leads to associative learning such that the tone alone comes to elicit a conditioned response (e.g., freezing). We have previously shown that an extinction session that occurs within the reconsolidation window (termed retrieval+extinction) attenuates fear responding and prevents the return of fear in Pavlovian fear conditioning (Monfils et al., 2009). To date, the mechanisms that explain the different behavioral outcomes between standard extinction and retrieval+extinction remain poorly understood. Here we sought to examine the differential temporal engagement of specific neural systems by these 2 approaches using Arc catFISH (cellular compartment analysis of temporal activity using fluorescence in situ hybridization). Our results demonstrate that extinction and retrieval+extinction lead to differential patterns of expression, suggesting that they engage different networks. These findings provide insight into the neural mechanisms that allow extinction during reconsolidation to prevent the return of fear in rats.http://journal.frontiersin.org/Journal/10.3389/fnbeh.2015.00369/fullFear conditioningextinctionreconsolidationRetrieval+extinctionArc catFISH
collection DOAJ
language English
format Article
sources DOAJ
author Hongjoo Joanne Lee
Rebecca P Haberman
Rheall eRoquet
Marie H Monfils
spellingShingle Hongjoo Joanne Lee
Rebecca P Haberman
Rheall eRoquet
Marie H Monfils
Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats
Frontiers in Behavioral Neuroscience
Fear conditioning
extinction
reconsolidation
Retrieval+extinction
Arc catFISH
author_facet Hongjoo Joanne Lee
Rebecca P Haberman
Rheall eRoquet
Marie H Monfils
author_sort Hongjoo Joanne Lee
title Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats
title_short Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats
title_full Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats
title_fullStr Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats
title_full_unstemmed Extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats
title_sort extinction and retrieval+extinction of conditioned fear differentially activate medial prefrontal cortex and amygdala in rats
publisher Frontiers Media S.A.
series Frontiers in Behavioral Neuroscience
issn 1662-5153
publishDate 2016-01-01
description Pairing a previously neutral conditioned stimulus (CS; e.g., a tone) to an aversive unconditioned stimulus (US; e.g., a footshock) leads to associative learning such that the tone alone comes to elicit a conditioned response (e.g., freezing). We have previously shown that an extinction session that occurs within the reconsolidation window (termed retrieval+extinction) attenuates fear responding and prevents the return of fear in Pavlovian fear conditioning (Monfils et al., 2009). To date, the mechanisms that explain the different behavioral outcomes between standard extinction and retrieval+extinction remain poorly understood. Here we sought to examine the differential temporal engagement of specific neural systems by these 2 approaches using Arc catFISH (cellular compartment analysis of temporal activity using fluorescence in situ hybridization). Our results demonstrate that extinction and retrieval+extinction lead to differential patterns of expression, suggesting that they engage different networks. These findings provide insight into the neural mechanisms that allow extinction during reconsolidation to prevent the return of fear in rats.
topic Fear conditioning
extinction
reconsolidation
Retrieval+extinction
Arc catFISH
url http://journal.frontiersin.org/Journal/10.3389/fnbeh.2015.00369/full
work_keys_str_mv AT hongjoojoannelee extinctionandretrievalextinctionofconditionedfeardifferentiallyactivatemedialprefrontalcortexandamygdalainrats
AT rebeccaphaberman extinctionandretrievalextinctionofconditionedfeardifferentiallyactivatemedialprefrontalcortexandamygdalainrats
AT rhealleroquet extinctionandretrievalextinctionofconditionedfeardifferentiallyactivatemedialprefrontalcortexandamygdalainrats
AT mariehmonfils extinctionandretrievalextinctionofconditionedfeardifferentiallyactivatemedialprefrontalcortexandamygdalainrats
_version_ 1725604195107602432