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...

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Main Authors: Yingxue Wang, Zachary Roth, Eva Pastalkova
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2016-09-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/20697
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spelling doaj-1981fed0a8024ae79e6bb93b62d7076e2021-05-05T00:36:30ZengeLife Sciences Publications LtdeLife2050-084X2016-09-01510.7554/eLife.20697Synchronized excitability in a network enables generation of internal neuronal sequencesYingxue Wang0Zachary Roth1Eva Pastalkova2https://orcid.org/0000-0001-5518-9590Janelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, United StatesJanelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, United States; Department of Mathematics, University of Nebraska-Lincoln, Lincoln, United StatesJanelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, United StatesHippocampal 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.https://elifesciences.org/articles/20697hippocampusmemorysharp wavessequenceselectrophysiologymedial septum
collection DOAJ
language English
format Article
sources DOAJ
author Yingxue Wang
Zachary Roth
Eva Pastalkova
spellingShingle Yingxue Wang
Zachary Roth
Eva Pastalkova
Synchronized excitability in a network enables generation of internal neuronal sequences
eLife
hippocampus
memory
sharp waves
sequences
electrophysiology
medial septum
author_facet Yingxue Wang
Zachary Roth
Eva Pastalkova
author_sort Yingxue Wang
title 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_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_sort synchronized excitability in a network enables generation of internal neuronal sequences
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2016-09-01
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.
topic hippocampus
memory
sharp waves
sequences
electrophysiology
medial septum
url https://elifesciences.org/articles/20697
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AT zacharyroth synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences
AT evapastalkova synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences
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