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Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices

Damage to the hippocampus (HPC) typically causes retrograde amnesia for contextual fear conditioning. Repeating the conditioning over several sessions, however, can eliminate the retrograde amnesic effects. This form of reinstatement thus permits modifications to networks that can support context me...

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Detalles Bibliográficos
Autores principales: Shepherd, Elizabeth H., Fournier, Neil M., Sutherland, Robert J., Lehmann, Hugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525424/
https://www.ncbi.nlm.nih.gov/pubmed/34663693
http://dx.doi.org/10.1101/lm.053396.121
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author Shepherd, Elizabeth H.
Fournier, Neil M.
Sutherland, Robert J.
Lehmann, Hugo
author_facet Shepherd, Elizabeth H.
Fournier, Neil M.
Sutherland, Robert J.
Lehmann, Hugo
author_sort Shepherd, Elizabeth H.
collection PubMed
description Damage to the hippocampus (HPC) typically causes retrograde amnesia for contextual fear conditioning. Repeating the conditioning over several sessions, however, can eliminate the retrograde amnesic effects. This form of reinstatement thus permits modifications to networks that can support context memory retrieval in the absence of the HPC. The present study aims to identify cortical regions that support the nonHPC context memory. Specifically, the contribution of the perirhinal cortex (PRH) and the anterior cingulate cortex (ACC) were examined because of their established importance to context memory. The findings show that context memories established through distributed reinstatement survive damage limited only to the HPC, PRH, or ACC. Combined lesions of the HPC and PRH, as well as the HPC and ACC, caused retrograde amnesia, suggesting that network modifications in the PRH and ACC enable context fear memories to become resistant to HPC damage.
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spelling pubmed-85254242022-11-01 Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices Shepherd, Elizabeth H. Fournier, Neil M. Sutherland, Robert J. Lehmann, Hugo Learn Mem Research Damage to the hippocampus (HPC) typically causes retrograde amnesia for contextual fear conditioning. Repeating the conditioning over several sessions, however, can eliminate the retrograde amnesic effects. This form of reinstatement thus permits modifications to networks that can support context memory retrieval in the absence of the HPC. The present study aims to identify cortical regions that support the nonHPC context memory. Specifically, the contribution of the perirhinal cortex (PRH) and the anterior cingulate cortex (ACC) were examined because of their established importance to context memory. The findings show that context memories established through distributed reinstatement survive damage limited only to the HPC, PRH, or ACC. Combined lesions of the HPC and PRH, as well as the HPC and ACC, caused retrograde amnesia, suggesting that network modifications in the PRH and ACC enable context fear memories to become resistant to HPC damage. Cold Spring Harbor Laboratory Press 2021-11 /pmc/articles/PMC8525424/ /pubmed/34663693 http://dx.doi.org/10.1101/lm.053396.121 Text en © 2021 Shepherd et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Shepherd, Elizabeth H.
Fournier, Neil M.
Sutherland, Robert J.
Lehmann, Hugo
Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
title Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
title_full Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
title_fullStr Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
title_full_unstemmed Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
title_short Distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
title_sort distributed learning episodes create a context fear memory outside the hippocampus that depends on perirhinal and anterior cingulate cortices
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8525424/
https://www.ncbi.nlm.nih.gov/pubmed/34663693
http://dx.doi.org/10.1101/lm.053396.121
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