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Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex
Trace fear conditioning is characterized by a stimulus-free trace interval (TI) between the conditioned stimulus (CS) and the unconditioned stimulus (US), which requires an array of brain structures to support the formation and storage of associative memory. The entorhinal cortex (EC) has been propo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Brain and Neural Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017844/ https://www.ncbi.nlm.nih.gov/pubmed/36919333 http://dx.doi.org/10.5607/en22042 |
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author | Kong, Mi-Seon Kim, Namsoo Jo, Kyeong Im Kim, Sung-Phil Choi, June-Seek |
author_facet | Kong, Mi-Seon Kim, Namsoo Jo, Kyeong Im Kim, Sung-Phil Choi, June-Seek |
author_sort | Kong, Mi-Seon |
collection | PubMed |
description | Trace fear conditioning is characterized by a stimulus-free trace interval (TI) between the conditioned stimulus (CS) and the unconditioned stimulus (US), which requires an array of brain structures to support the formation and storage of associative memory. The entorhinal cortex (EC) has been proposed to provide essential neural code for resolving temporal discontinuity in conjunction with the hippocampus. However, how the CS and TI are encoded at the neuronal level in the EC is not clear. In Exp. 1, we tested the effect of bilateral pre-training electrolytic lesions of EC on trace vs. delay fear conditioning using rats as subjects. We found that the lesions impaired the acquisition of trace but not delay fear conditioning confirming that EC is a critical brain area for trace fear memory formation. In Exp. 2, single-unit activities from EC were recorded during the pre-training baseline and post-training retention sessions following trace or delay conditioning. The recording results showed that a significant proportion of the EC neurons modulated their firing during TI after the trace conditioning, but not after the delay fear conditioning. Further analysis revealed that the majority of modulated units decreased the firing rate during the TI or the CS. Taken together, these results suggest that EC critically contributes to trace fear conditioning by modulating neuronal activity during the TI to facilitate the association between the CS and US across a temporal gap. |
format | Online Article Text |
id | pubmed-10017844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Korean Society for Brain and Neural Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-100178442023-03-17 Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex Kong, Mi-Seon Kim, Namsoo Jo, Kyeong Im Kim, Sung-Phil Choi, June-Seek Exp Neurobiol Original Article Trace fear conditioning is characterized by a stimulus-free trace interval (TI) between the conditioned stimulus (CS) and the unconditioned stimulus (US), which requires an array of brain structures to support the formation and storage of associative memory. The entorhinal cortex (EC) has been proposed to provide essential neural code for resolving temporal discontinuity in conjunction with the hippocampus. However, how the CS and TI are encoded at the neuronal level in the EC is not clear. In Exp. 1, we tested the effect of bilateral pre-training electrolytic lesions of EC on trace vs. delay fear conditioning using rats as subjects. We found that the lesions impaired the acquisition of trace but not delay fear conditioning confirming that EC is a critical brain area for trace fear memory formation. In Exp. 2, single-unit activities from EC were recorded during the pre-training baseline and post-training retention sessions following trace or delay conditioning. The recording results showed that a significant proportion of the EC neurons modulated their firing during TI after the trace conditioning, but not after the delay fear conditioning. Further analysis revealed that the majority of modulated units decreased the firing rate during the TI or the CS. Taken together, these results suggest that EC critically contributes to trace fear conditioning by modulating neuronal activity during the TI to facilitate the association between the CS and US across a temporal gap. The Korean Society for Brain and Neural Sciences 2023-02-28 2023-02-28 /pmc/articles/PMC10017844/ /pubmed/36919333 http://dx.doi.org/10.5607/en22042 Text en Copyright © Experimental Neurobiology 2023 https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kong, Mi-Seon Kim, Namsoo Jo, Kyeong Im Kim, Sung-Phil Choi, June-Seek Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex |
title | Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex |
title_full | Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex |
title_fullStr | Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex |
title_full_unstemmed | Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex |
title_short | Differential Encoding of Trace and Delay Fear Memory in the Entorhinal Cortex |
title_sort | differential encoding of trace and delay fear memory in the entorhinal cortex |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017844/ https://www.ncbi.nlm.nih.gov/pubmed/36919333 http://dx.doi.org/10.5607/en22042 |
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