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Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation
Sharp-wave ripples (SWRs) are spontaneous neuronal population events that occur in the hippocampus during sleep and quiet restfulness, and are thought to play a critical role in the consolidation of episodic memory. SWRs occur at a rate of 30–200 events per minute. Their overall abundance may, howev...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862867/ https://www.ncbi.nlm.nih.gov/pubmed/29599704 http://dx.doi.org/10.3389/fnins.2018.00164 |
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author | Jiang, Huiyi Liu, Shicheng Geng, Xinling Caccavano, Adam Conant, Katherine Vicini, Stefano Wu, Jianyoung |
author_facet | Jiang, Huiyi Liu, Shicheng Geng, Xinling Caccavano, Adam Conant, Katherine Vicini, Stefano Wu, Jianyoung |
author_sort | Jiang, Huiyi |
collection | PubMed |
description | Sharp-wave ripples (SWRs) are spontaneous neuronal population events that occur in the hippocampus during sleep and quiet restfulness, and are thought to play a critical role in the consolidation of episodic memory. SWRs occur at a rate of 30–200 events per minute. Their overall abundance may, however, be reduced with aging and neurodegenerative disease. Here we report that the abundance of SWR within murine hippocampal slices can be increased by paced administration of a weak electrical stimulus, especially when the spontaneously occurring rate is low or compromised. Resultant SWRs have large variations in amplitude and ripple patterns, which are morphologically indistinguishable from those of spontaneous SWRs, despite identical stimulus parameters which presumably activate the same CA3 neurons surrounding the electrode. The stimulus intensity for reliably pacing SWRs is weaker than that required for inducing detectable evoked field potentials in CA1. Moreover, repetitive ~1 Hz stimuli with low intensity can reliably evoke thousands of SWRs without detectable LTD or “habituation.” Our results suggest that weak stimuli may facilitate the spontaneous emergence of SWRs without significantly altering their characteristics. Pacing SWRs with weak electric stimuli could potentially be useful for restoring their abundance in the damaged hippocampus. |
format | Online Article Text |
id | pubmed-5862867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58628672018-03-29 Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation Jiang, Huiyi Liu, Shicheng Geng, Xinling Caccavano, Adam Conant, Katherine Vicini, Stefano Wu, Jianyoung Front Neurosci Neuroscience Sharp-wave ripples (SWRs) are spontaneous neuronal population events that occur in the hippocampus during sleep and quiet restfulness, and are thought to play a critical role in the consolidation of episodic memory. SWRs occur at a rate of 30–200 events per minute. Their overall abundance may, however, be reduced with aging and neurodegenerative disease. Here we report that the abundance of SWR within murine hippocampal slices can be increased by paced administration of a weak electrical stimulus, especially when the spontaneously occurring rate is low or compromised. Resultant SWRs have large variations in amplitude and ripple patterns, which are morphologically indistinguishable from those of spontaneous SWRs, despite identical stimulus parameters which presumably activate the same CA3 neurons surrounding the electrode. The stimulus intensity for reliably pacing SWRs is weaker than that required for inducing detectable evoked field potentials in CA1. Moreover, repetitive ~1 Hz stimuli with low intensity can reliably evoke thousands of SWRs without detectable LTD or “habituation.” Our results suggest that weak stimuli may facilitate the spontaneous emergence of SWRs without significantly altering their characteristics. Pacing SWRs with weak electric stimuli could potentially be useful for restoring their abundance in the damaged hippocampus. Frontiers Media S.A. 2018-03-15 /pmc/articles/PMC5862867/ /pubmed/29599704 http://dx.doi.org/10.3389/fnins.2018.00164 Text en Copyright © 2018 Jiang, Liu, Geng, Caccavano, Conant, Vicini and Wu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Jiang, Huiyi Liu, Shicheng Geng, Xinling Caccavano, Adam Conant, Katherine Vicini, Stefano Wu, Jianyoung Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation |
title | Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation |
title_full | Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation |
title_fullStr | Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation |
title_full_unstemmed | Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation |
title_short | Pacing Hippocampal Sharp-Wave Ripples With Weak Electric Stimulation |
title_sort | pacing hippocampal sharp-wave ripples with weak electric stimulation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862867/ https://www.ncbi.nlm.nih.gov/pubmed/29599704 http://dx.doi.org/10.3389/fnins.2018.00164 |
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