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...
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2016-01-01
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Online Access: | http://journal.frontiersin.org/Journal/10.3389/fnbeh.2015.00369/full |
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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 |
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