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Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex

Hippocampal damage results in profound retrograde, but no anterograde amnesia in contextual fear conditioning (CFC). Although the content learned in the latter have been discussed, alternative regions supporting CFC learning were seldom proposed and never empirically addressed. Here, we employed net...

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Autores principales: Coelho, Cesar A. O., Ferreira, Tatiana L., Kramer-Soares, Juliana C., Sato, João R., Oliveira, Maria Gabriela M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097702/
https://www.ncbi.nlm.nih.gov/pubmed/30086129
http://dx.doi.org/10.1371/journal.pcbi.1006207
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author Coelho, Cesar A. O.
Ferreira, Tatiana L.
Kramer-Soares, Juliana C.
Sato, João R.
Oliveira, Maria Gabriela M.
author_facet Coelho, Cesar A. O.
Ferreira, Tatiana L.
Kramer-Soares, Juliana C.
Sato, João R.
Oliveira, Maria Gabriela M.
author_sort Coelho, Cesar A. O.
collection PubMed
description Hippocampal damage results in profound retrograde, but no anterograde amnesia in contextual fear conditioning (CFC). Although the content learned in the latter have been discussed, alternative regions supporting CFC learning were seldom proposed and never empirically addressed. Here, we employed network analysis of pCREB expression quantified from brain slices of rats with dorsal hippocampal lesion (dHPC) after undergoing CFC session. Using inter-regional correlations of pCREB-positive nuclei between brain regions, we modelled functional networks using different thresholds. The dHPC network showed small-world topology, equivalent to SHAM (control) network. However, diverging hubs were identified in each network. In a direct comparison, hubs in both networks showed consistently higher centrality values compared to the other network. Further, the distribution of correlation coefficients was different between the groups, with most significantly stronger correlation coefficients belonging to the SHAM network. These results suggest that dHPC network engaged in CFC learning is partially different, and engage alternative hubs. We next tested if pre-training lesions of dHPC and one of the new dHPC network hubs (perirhinal, Per; or disgranular retrosplenial, RSC, cortices) would impair CFC. Only dHPC-RSC, but not dHPC-Per, impaired CFC. Interestingly, only RSC showed a consistently higher centrality in the dHPC network, suggesting that the increased centrality reflects an increased functional dependence on RSC. Our results provide evidence that, without hippocampus, the RSC, an anatomically central region in the medial temporal lobe memory system might support CFC learning and memory.
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spelling pubmed-60977022018-08-30 Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex Coelho, Cesar A. O. Ferreira, Tatiana L. Kramer-Soares, Juliana C. Sato, João R. Oliveira, Maria Gabriela M. PLoS Comput Biol Research Article Hippocampal damage results in profound retrograde, but no anterograde amnesia in contextual fear conditioning (CFC). Although the content learned in the latter have been discussed, alternative regions supporting CFC learning were seldom proposed and never empirically addressed. Here, we employed network analysis of pCREB expression quantified from brain slices of rats with dorsal hippocampal lesion (dHPC) after undergoing CFC session. Using inter-regional correlations of pCREB-positive nuclei between brain regions, we modelled functional networks using different thresholds. The dHPC network showed small-world topology, equivalent to SHAM (control) network. However, diverging hubs were identified in each network. In a direct comparison, hubs in both networks showed consistently higher centrality values compared to the other network. Further, the distribution of correlation coefficients was different between the groups, with most significantly stronger correlation coefficients belonging to the SHAM network. These results suggest that dHPC network engaged in CFC learning is partially different, and engage alternative hubs. We next tested if pre-training lesions of dHPC and one of the new dHPC network hubs (perirhinal, Per; or disgranular retrosplenial, RSC, cortices) would impair CFC. Only dHPC-RSC, but not dHPC-Per, impaired CFC. Interestingly, only RSC showed a consistently higher centrality in the dHPC network, suggesting that the increased centrality reflects an increased functional dependence on RSC. Our results provide evidence that, without hippocampus, the RSC, an anatomically central region in the medial temporal lobe memory system might support CFC learning and memory. Public Library of Science 2018-08-07 /pmc/articles/PMC6097702/ /pubmed/30086129 http://dx.doi.org/10.1371/journal.pcbi.1006207 Text en © 2018 Coelho et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Coelho, Cesar A. O.
Ferreira, Tatiana L.
Kramer-Soares, Juliana C.
Sato, João R.
Oliveira, Maria Gabriela M.
Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex
title Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex
title_full Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex
title_fullStr Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex
title_full_unstemmed Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex
title_short Network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex
title_sort network supporting contextual fear learning after dorsal hippocampal damage has increased dependence on retrosplenial cortex
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097702/
https://www.ncbi.nlm.nih.gov/pubmed/30086129
http://dx.doi.org/10.1371/journal.pcbi.1006207
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