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Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations
The reactivation of experience-based neural activity patterns in the hippocampus is crucial for learning and memory. These reactivation patterns and their associated sharp-wave ripples (SWRs) are highly variable. However, this variability is missed by commonly used spectral methods. Here, we use top...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689241/ https://www.ncbi.nlm.nih.gov/pubmed/37946048 http://dx.doi.org/10.1038/s41593-023-01471-9 |
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author | Sebastian, Enrique R. Quintanilla, Juan P. Sánchez-Aguilera, Alberto Esparza, Julio Cid, Elena de la Prida, Liset M. |
author_facet | Sebastian, Enrique R. Quintanilla, Juan P. Sánchez-Aguilera, Alberto Esparza, Julio Cid, Elena de la Prida, Liset M. |
author_sort | Sebastian, Enrique R. |
collection | PubMed |
description | The reactivation of experience-based neural activity patterns in the hippocampus is crucial for learning and memory. These reactivation patterns and their associated sharp-wave ripples (SWRs) are highly variable. However, this variability is missed by commonly used spectral methods. Here, we use topological and dimensionality reduction techniques to analyze the waveform of ripples recorded at the pyramidal layer of CA1. We show that SWR waveforms distribute along a continuum in a low-dimensional space, which conveys information about the underlying layer-specific synaptic inputs. A decoder trained in this space successfully links individual ripples with their expected sinks and sources, demonstrating how physiological mechanisms shape SWR variability. Furthermore, we found that SWR waveforms segregated differently during wakefulness and sleep before and after a series of cognitive tasks, with striking effects of novelty and learning. Our results thus highlight how the topological analysis of ripple waveforms enables a deeper physiological understanding of SWRs. |
format | Online Article Text |
id | pubmed-10689241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-106892412023-12-02 Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations Sebastian, Enrique R. Quintanilla, Juan P. Sánchez-Aguilera, Alberto Esparza, Julio Cid, Elena de la Prida, Liset M. Nat Neurosci Article The reactivation of experience-based neural activity patterns in the hippocampus is crucial for learning and memory. These reactivation patterns and their associated sharp-wave ripples (SWRs) are highly variable. However, this variability is missed by commonly used spectral methods. Here, we use topological and dimensionality reduction techniques to analyze the waveform of ripples recorded at the pyramidal layer of CA1. We show that SWR waveforms distribute along a continuum in a low-dimensional space, which conveys information about the underlying layer-specific synaptic inputs. A decoder trained in this space successfully links individual ripples with their expected sinks and sources, demonstrating how physiological mechanisms shape SWR variability. Furthermore, we found that SWR waveforms segregated differently during wakefulness and sleep before and after a series of cognitive tasks, with striking effects of novelty and learning. Our results thus highlight how the topological analysis of ripple waveforms enables a deeper physiological understanding of SWRs. Nature Publishing Group US 2023-11-09 2023 /pmc/articles/PMC10689241/ /pubmed/37946048 http://dx.doi.org/10.1038/s41593-023-01471-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sebastian, Enrique R. Quintanilla, Juan P. Sánchez-Aguilera, Alberto Esparza, Julio Cid, Elena de la Prida, Liset M. Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations |
title | Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations |
title_full | Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations |
title_fullStr | Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations |
title_full_unstemmed | Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations |
title_short | Topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations |
title_sort | topological analysis of sharp-wave ripple waveforms reveals input mechanisms behind feature variations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689241/ https://www.ncbi.nlm.nih.gov/pubmed/37946048 http://dx.doi.org/10.1038/s41593-023-01471-9 |
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