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State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices
Synchronized activity plays an important role in sensory coding and memory and is a hallmark of functional network connectivity. However, the effect of sensory activation on synchronization and cortical functional connectivity is largely unknown. In this study, we investigated the effect of whisker...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489558/ https://www.ncbi.nlm.nih.gov/pubmed/34616281 http://dx.doi.org/10.3389/fnsys.2021.713397 |
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author | Khateb, Mohamed Schiller, Jackie Schiller, Yitzhak |
author_facet | Khateb, Mohamed Schiller, Jackie Schiller, Yitzhak |
author_sort | Khateb, Mohamed |
collection | PubMed |
description | Synchronized activity plays an important role in sensory coding and memory and is a hallmark of functional network connectivity. However, the effect of sensory activation on synchronization and cortical functional connectivity is largely unknown. In this study, we investigated the effect of whisker activation on synchronization and functional connectivity of the primary (wS1) and secondary (wS2) whisker somatosensory cortices at the single-cell level. The results showed that during the spontaneous pre-stimulus state, neurons tended to be functionally connected with nearby neurons which shared similar tuning characteristics. Whisker activation using either ramp-and-hold stimulation or artificial whisking against sandpaper has significantly reduced the average overall pairwise synchronization and functional connectivity within the wS1 barrel and wS2 cortices. Whisker stimulation disconnected approximately a third of neuronal pairs that were functionally connected during the unstimulated state. Nearby neurons with congruent tuning properties were more likely to remain functionally connected during whisker activation. The findings of this study indicated that cortical somatosensory networks are organized in non-random small world networks composed of neurons sharing relatively similar tuning properties. Sensory whisker activation intensifies these properties and further subdivides the cortical network into smaller more functionally uniform subnetworks, which possibly serve to increase the computational capacity of the network. |
format | Online Article Text |
id | pubmed-8489558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84895582021-10-05 State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices Khateb, Mohamed Schiller, Jackie Schiller, Yitzhak Front Syst Neurosci Neuroscience Synchronized activity plays an important role in sensory coding and memory and is a hallmark of functional network connectivity. However, the effect of sensory activation on synchronization and cortical functional connectivity is largely unknown. In this study, we investigated the effect of whisker activation on synchronization and functional connectivity of the primary (wS1) and secondary (wS2) whisker somatosensory cortices at the single-cell level. The results showed that during the spontaneous pre-stimulus state, neurons tended to be functionally connected with nearby neurons which shared similar tuning characteristics. Whisker activation using either ramp-and-hold stimulation or artificial whisking against sandpaper has significantly reduced the average overall pairwise synchronization and functional connectivity within the wS1 barrel and wS2 cortices. Whisker stimulation disconnected approximately a third of neuronal pairs that were functionally connected during the unstimulated state. Nearby neurons with congruent tuning properties were more likely to remain functionally connected during whisker activation. The findings of this study indicated that cortical somatosensory networks are organized in non-random small world networks composed of neurons sharing relatively similar tuning properties. Sensory whisker activation intensifies these properties and further subdivides the cortical network into smaller more functionally uniform subnetworks, which possibly serve to increase the computational capacity of the network. Frontiers Media S.A. 2021-09-20 /pmc/articles/PMC8489558/ /pubmed/34616281 http://dx.doi.org/10.3389/fnsys.2021.713397 Text en Copyright © 2021 Khateb, Schiller and Schiller. 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 | Neuroscience Khateb, Mohamed Schiller, Jackie Schiller, Yitzhak State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices |
title | State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices |
title_full | State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices |
title_fullStr | State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices |
title_full_unstemmed | State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices |
title_short | State-Dependent Synchrony and Functional Connectivity in the Primary and Secondary Whisker Somatosensory Cortices |
title_sort | state-dependent synchrony and functional connectivity in the primary and secondary whisker somatosensory cortices |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489558/ https://www.ncbi.nlm.nih.gov/pubmed/34616281 http://dx.doi.org/10.3389/fnsys.2021.713397 |
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