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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yingxue, Roth, Zachary, Pastalkova, Eva
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