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Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples

A prevalent model is that sharp-wave ripples (SWR) arise ‘spontaneously’ in CA3 and propagate recent memory traces outward to the neocortex to facilitate memory consolidation there. Using voltage and extracellular glutamate transient recording over widespread regions of mice dorsal neocortex in rela...

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Autores principales: Karimi Abadchi, J, Nazari-Ahangarkolaee, Mojtaba, Gattas, Sandra, Bermudez-Contreras, Edgar, Luczak, Artur, McNaughton, Bruce L, Mohajerani, Majid H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096182/
https://www.ncbi.nlm.nih.gov/pubmed/32167467
http://dx.doi.org/10.7554/eLife.51972
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author Karimi Abadchi, J
Nazari-Ahangarkolaee, Mojtaba
Gattas, Sandra
Bermudez-Contreras, Edgar
Luczak, Artur
McNaughton, Bruce L
Mohajerani, Majid H
author_facet Karimi Abadchi, J
Nazari-Ahangarkolaee, Mojtaba
Gattas, Sandra
Bermudez-Contreras, Edgar
Luczak, Artur
McNaughton, Bruce L
Mohajerani, Majid H
author_sort Karimi Abadchi, J
collection PubMed
description A prevalent model is that sharp-wave ripples (SWR) arise ‘spontaneously’ in CA3 and propagate recent memory traces outward to the neocortex to facilitate memory consolidation there. Using voltage and extracellular glutamate transient recording over widespread regions of mice dorsal neocortex in relation to CA1 multiunit activity (MUA) and SWR, we find that the largest SWR-related modulation occurs in retrosplenial cortex; however, contrary to the unidirectional hypothesis, neocortical activation exhibited a continuum of activation timings relative to SWRs, varying from leading to lagging. Thus, contrary to the model in which SWRs arise ‘spontaneously’ in the hippocampus, neocortical activation often precedes SWRs and may thus constitute a trigger event in which neocortical information seeds associative reactivation of hippocampal ‘indices’. This timing continuum is consistent with a dynamics in which older, more consolidated memories may in fact initiate the hippocampal-neocortical dialog, whereas reactivation of newer memories may be initiated predominantly in the hippocampus.
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spelling pubmed-70961822020-03-30 Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples Karimi Abadchi, J Nazari-Ahangarkolaee, Mojtaba Gattas, Sandra Bermudez-Contreras, Edgar Luczak, Artur McNaughton, Bruce L Mohajerani, Majid H eLife Neuroscience A prevalent model is that sharp-wave ripples (SWR) arise ‘spontaneously’ in CA3 and propagate recent memory traces outward to the neocortex to facilitate memory consolidation there. Using voltage and extracellular glutamate transient recording over widespread regions of mice dorsal neocortex in relation to CA1 multiunit activity (MUA) and SWR, we find that the largest SWR-related modulation occurs in retrosplenial cortex; however, contrary to the unidirectional hypothesis, neocortical activation exhibited a continuum of activation timings relative to SWRs, varying from leading to lagging. Thus, contrary to the model in which SWRs arise ‘spontaneously’ in the hippocampus, neocortical activation often precedes SWRs and may thus constitute a trigger event in which neocortical information seeds associative reactivation of hippocampal ‘indices’. This timing continuum is consistent with a dynamics in which older, more consolidated memories may in fact initiate the hippocampal-neocortical dialog, whereas reactivation of newer memories may be initiated predominantly in the hippocampus. eLife Sciences Publications, Ltd 2020-03-13 /pmc/articles/PMC7096182/ /pubmed/32167467 http://dx.doi.org/10.7554/eLife.51972 Text en © 2020, Karimi Abadchi et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Karimi Abadchi, J
Nazari-Ahangarkolaee, Mojtaba
Gattas, Sandra
Bermudez-Contreras, Edgar
Luczak, Artur
McNaughton, Bruce L
Mohajerani, Majid H
Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples
title Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples
title_full Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples
title_fullStr Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples
title_full_unstemmed Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples
title_short Spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples
title_sort spatiotemporal patterns of neocortical activity around hippocampal sharp-wave ripples
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096182/
https://www.ncbi.nlm.nih.gov/pubmed/32167467
http://dx.doi.org/10.7554/eLife.51972
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