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High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics
We have recently shown that the cognitive impairments in a mouse model of high-frequency head impact (HFHI) are caused by chronic changes to synaptic physiology. To better understand these synaptic changes occurring after repeat head impact, we used Thy1-GcCAMP6f mice to study intracellular and inte...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8806157/ https://www.ncbi.nlm.nih.gov/pubmed/35115908 http://dx.doi.org/10.3389/fncel.2021.763423 |
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author | Chapman, Daniel P. Sloley, Stephanie S. Caccavano, Adam P. Vicini, Stefano Burns, Mark P. |
author_facet | Chapman, Daniel P. Sloley, Stephanie S. Caccavano, Adam P. Vicini, Stefano Burns, Mark P. |
author_sort | Chapman, Daniel P. |
collection | PubMed |
description | We have recently shown that the cognitive impairments in a mouse model of high-frequency head impact (HFHI) are caused by chronic changes to synaptic physiology. To better understand these synaptic changes occurring after repeat head impact, we used Thy1-GcCAMP6f mice to study intracellular and intercellular calcium dynamics and neuronal ensembles in HFHI mice. We performed simultaneous calcium imaging and local field potential (LFP) recordings of the CA1 field during an early-LTP paradigm in acute hippocampal slice preparations 24 h post-impact. As previously reported, HFHI causes a decrease in early-LTP in the absence of any shift in the input-output curve. Calcium analytics revealed that HFHI hippocampal slices have similar numbers of active ROIs, however, the number of calcium transients per ROI was significantly increased in HFHI slices. Ensembles consist of coordinated activity between groups of active ROIs. We exposed the CA1 ensemble to Schaffer-collateral stimulation in an abbreviated LTP paradigm and observed novel coordinated patterns of post stimulus calcium ensemble activity. HFHI ensembles displayed qualitatively similar patterns of post-stimulus ensemble activity to shams but showed significant changes in quantitative ensemble inactivation and reactivation. Previous in vivo and in vitro reports have shown that ensemble activity frequently occurs through a similar set of ROIs firing in a repeating fashion. HFHI slices showed a decrease in such coordinated firing patterns during post stimulus ensemble activity. The present study shows that HFHI alters synaptic activity and disrupts neuronal organization of the ensemble, providing further evidence of physiological synaptic adaptation occurring in the brain after a high frequency of non-pathological head impacts. |
format | Online Article Text |
id | pubmed-8806157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88061572022-02-02 High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics Chapman, Daniel P. Sloley, Stephanie S. Caccavano, Adam P. Vicini, Stefano Burns, Mark P. Front Cell Neurosci Cellular Neuroscience We have recently shown that the cognitive impairments in a mouse model of high-frequency head impact (HFHI) are caused by chronic changes to synaptic physiology. To better understand these synaptic changes occurring after repeat head impact, we used Thy1-GcCAMP6f mice to study intracellular and intercellular calcium dynamics and neuronal ensembles in HFHI mice. We performed simultaneous calcium imaging and local field potential (LFP) recordings of the CA1 field during an early-LTP paradigm in acute hippocampal slice preparations 24 h post-impact. As previously reported, HFHI causes a decrease in early-LTP in the absence of any shift in the input-output curve. Calcium analytics revealed that HFHI hippocampal slices have similar numbers of active ROIs, however, the number of calcium transients per ROI was significantly increased in HFHI slices. Ensembles consist of coordinated activity between groups of active ROIs. We exposed the CA1 ensemble to Schaffer-collateral stimulation in an abbreviated LTP paradigm and observed novel coordinated patterns of post stimulus calcium ensemble activity. HFHI ensembles displayed qualitatively similar patterns of post-stimulus ensemble activity to shams but showed significant changes in quantitative ensemble inactivation and reactivation. Previous in vivo and in vitro reports have shown that ensemble activity frequently occurs through a similar set of ROIs firing in a repeating fashion. HFHI slices showed a decrease in such coordinated firing patterns during post stimulus ensemble activity. The present study shows that HFHI alters synaptic activity and disrupts neuronal organization of the ensemble, providing further evidence of physiological synaptic adaptation occurring in the brain after a high frequency of non-pathological head impacts. Frontiers Media S.A. 2022-01-18 /pmc/articles/PMC8806157/ /pubmed/35115908 http://dx.doi.org/10.3389/fncel.2021.763423 Text en Copyright © 2022 Chapman, Sloley, Caccavano, Vicini and Burns. https://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(s) 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 | Cellular Neuroscience Chapman, Daniel P. Sloley, Stephanie S. Caccavano, Adam P. Vicini, Stefano Burns, Mark P. High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics |
title | High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics |
title_full | High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics |
title_fullStr | High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics |
title_full_unstemmed | High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics |
title_short | High-Frequency Head Impact Disrupts Hippocampal Neural Ensemble Dynamics |
title_sort | high-frequency head impact disrupts hippocampal neural ensemble dynamics |
topic | Cellular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8806157/ https://www.ncbi.nlm.nih.gov/pubmed/35115908 http://dx.doi.org/10.3389/fncel.2021.763423 |
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