Enhancement of fear memory by retrieval through reconsolidation
Memory retrieval is considered to have roles in memory enhancement. Recently, memory reconsolidation was suggested to reinforce or integrate new information into reactivated memory. Here, we show that reactivated inhibitory avoidance (IA) memory is enhanced through reconsolidation under conditions i...
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doaj-766718191c4f4716a7c906a3f02677b52021-05-04T23:12:42ZengeLife Sciences Publications LtdeLife2050-084X2014-06-01310.7554/eLife.02736Enhancement of fear memory by retrieval through reconsolidationHotaka Fukushima0Yue Zhang1Georgia Archbold2Rie Ishikawa3Karim Nader4Satoshi Kida5Department of Biosciences, Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan; Core Research for Evolutionary Science and Technology (CREST), Japan Science and Technology Agency, Saitama, JapanDepartment of Biosciences, Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan; Core Research for Evolutionary Science and Technology (CREST), Japan Science and Technology Agency, Saitama, JapanDepartment of Psychology, McGill University, Montreal, CanadaDepartment of Biosciences, Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, JapanDepartment of Psychology, McGill University, Montreal, CanadaDepartment of Biosciences, Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo, Japan; Core Research for Evolutionary Science and Technology (CREST), Japan Science and Technology Agency, Saitama, JapanMemory retrieval is considered to have roles in memory enhancement. Recently, memory reconsolidation was suggested to reinforce or integrate new information into reactivated memory. Here, we show that reactivated inhibitory avoidance (IA) memory is enhanced through reconsolidation under conditions in which memory extinction is not induced. This memory enhancement is mediated by neurons in the amygdala, hippocampus, and medial prefrontal cortex (mPFC) through the simultaneous activation of calcineurin-induced proteasome-dependent protein degradation and cAMP responsive element binding protein-mediated gene expression. Interestingly, the amygdala is required for memory reconsolidation and enhancement, whereas the hippocampus and mPFC are required for only memory enhancement. Furthermore, memory enhancement triggered by retrieval utilizes distinct mechanisms to strengthen IA memory by additional learning that depends only on the amygdala. Our findings indicate that reconsolidation functions to strengthen the original memory and show the dynamic nature of reactivated memory through protein degradation and gene expression in multiple brain regions.https://elifesciences.org/articles/02736reconsolidationfear memoryenhancementcAMP responsive element binding proteinproteasome-dependent protein degradationamygdala |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hotaka Fukushima Yue Zhang Georgia Archbold Rie Ishikawa Karim Nader Satoshi Kida |
spellingShingle |
Hotaka Fukushima Yue Zhang Georgia Archbold Rie Ishikawa Karim Nader Satoshi Kida Enhancement of fear memory by retrieval through reconsolidation eLife reconsolidation fear memory enhancement cAMP responsive element binding protein proteasome-dependent protein degradation amygdala |
author_facet |
Hotaka Fukushima Yue Zhang Georgia Archbold Rie Ishikawa Karim Nader Satoshi Kida |
author_sort |
Hotaka Fukushima |
title |
Enhancement of fear memory by retrieval through reconsolidation |
title_short |
Enhancement of fear memory by retrieval through reconsolidation |
title_full |
Enhancement of fear memory by retrieval through reconsolidation |
title_fullStr |
Enhancement of fear memory by retrieval through reconsolidation |
title_full_unstemmed |
Enhancement of fear memory by retrieval through reconsolidation |
title_sort |
enhancement of fear memory by retrieval through reconsolidation |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2014-06-01 |
description |
Memory retrieval is considered to have roles in memory enhancement. Recently, memory reconsolidation was suggested to reinforce or integrate new information into reactivated memory. Here, we show that reactivated inhibitory avoidance (IA) memory is enhanced through reconsolidation under conditions in which memory extinction is not induced. This memory enhancement is mediated by neurons in the amygdala, hippocampus, and medial prefrontal cortex (mPFC) through the simultaneous activation of calcineurin-induced proteasome-dependent protein degradation and cAMP responsive element binding protein-mediated gene expression. Interestingly, the amygdala is required for memory reconsolidation and enhancement, whereas the hippocampus and mPFC are required for only memory enhancement. Furthermore, memory enhancement triggered by retrieval utilizes distinct mechanisms to strengthen IA memory by additional learning that depends only on the amygdala. Our findings indicate that reconsolidation functions to strengthen the original memory and show the dynamic nature of reactivated memory through protein degradation and gene expression in multiple brain regions. |
topic |
reconsolidation fear memory enhancement cAMP responsive element binding protein proteasome-dependent protein degradation amygdala |
url |
https://elifesciences.org/articles/02736 |
work_keys_str_mv |
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