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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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 |
work_keys_str_mv |
AT yingxuewang synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences AT zacharyroth synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences AT evapastalkova synchronizedexcitabilityinanetworkenablesgenerationofinternalneuronalsequences |
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1721476120453316608 |