Cargando…
Synchronized excitability in a network enables generation of internal neuronal sequences
Hippocampal place field sequences are supported by sensory cues and network internal mechanisms. In contrast, sharp-wave (SPW) sequences, theta sequences, and episode field sequences are internally generated. The relationship of these sequences to memory is unclear. SPW sequences have been shown to...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089858/ https://www.ncbi.nlm.nih.gov/pubmed/27677848 http://dx.doi.org/10.7554/eLife.20697 |
_version_ | 1782464306684624896 |
---|---|
author | Wang, Yingxue Roth, Zachary Pastalkova, Eva |
author_facet | Wang, Yingxue Roth, Zachary Pastalkova, Eva |
author_sort | Wang, Yingxue |
collection | PubMed |
description | Hippocampal place field sequences are supported by sensory cues and network internal mechanisms. In contrast, sharp-wave (SPW) sequences, theta sequences, and episode field sequences are internally generated. The relationship of these sequences to memory is unclear. SPW sequences have been shown to support learning and have been assumed to also support episodic memory. Conversely, we demonstrate these SPW sequences were present in trained rats even after episodic memory was impaired and after other internal sequences – episode field and theta sequences – were eliminated. SPW sequences did not support memory despite continuing to ‘replay’ all task-related sequences – place- field and episode field sequences. Sequence replay occurred selectively during synchronous increases of population excitability -- SPWs. Similarly, theta sequences depended on the presence of repeated synchronized waves of excitability – theta oscillations. Thus, we suggest that either intermittent or rhythmic synchronized changes of excitability trigger sequential firing of neurons, which in turn supports learning and/or memory. DOI: http://dx.doi.org/10.7554/eLife.20697.001 |
format | Online Article Text |
id | pubmed-5089858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50898582016-11-03 Synchronized excitability in a network enables generation of internal neuronal sequences Wang, Yingxue Roth, Zachary Pastalkova, Eva eLife Neuroscience Hippocampal place field sequences are supported by sensory cues and network internal mechanisms. In contrast, sharp-wave (SPW) sequences, theta sequences, and episode field sequences are internally generated. The relationship of these sequences to memory is unclear. SPW sequences have been shown to support learning and have been assumed to also support episodic memory. Conversely, we demonstrate these SPW sequences were present in trained rats even after episodic memory was impaired and after other internal sequences – episode field and theta sequences – were eliminated. SPW sequences did not support memory despite continuing to ‘replay’ all task-related sequences – place- field and episode field sequences. Sequence replay occurred selectively during synchronous increases of population excitability -- SPWs. Similarly, theta sequences depended on the presence of repeated synchronized waves of excitability – theta oscillations. Thus, we suggest that either intermittent or rhythmic synchronized changes of excitability trigger sequential firing of neurons, which in turn supports learning and/or memory. DOI: http://dx.doi.org/10.7554/eLife.20697.001 eLife Sciences Publications, Ltd 2016-09-28 /pmc/articles/PMC5089858/ /pubmed/27677848 http://dx.doi.org/10.7554/eLife.20697 Text en © 2016, Wang et al 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 Wang, Yingxue Roth, Zachary Pastalkova, Eva Synchronized excitability in a network enables generation of internal neuronal sequences |
title | Synchronized excitability in a network enables generation of internal neuronal sequences |
title_full | Synchronized excitability in a network enables generation of internal neuronal sequences |
title_fullStr | Synchronized excitability in a network enables generation of internal neuronal sequences |
title_full_unstemmed | Synchronized excitability in a network enables generation of internal neuronal sequences |
title_short | Synchronized excitability in a network enables generation of internal neuronal sequences |
title_sort | synchronized excitability in a network enables generation of internal neuronal sequences |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089858/ https://www.ncbi.nlm.nih.gov/pubmed/27677848 http://dx.doi.org/10.7554/eLife.20697 |
work_keys_str_mv | AT wangyingxue synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences AT rothzachary synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences AT pastalkovaeva synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences |