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Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations

Computational models of gamma oscillations have helped increase our understanding of the mechanisms that shape these 40–80 Hz cortical rhythms. Evidence suggests that interneurons known as basket cells are responsible for the generation of gamma oscillations. However, current models of gamma oscilla...

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Autor principal: Connelly, William M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938565/
https://www.ncbi.nlm.nih.gov/pubmed/24587175
http://dx.doi.org/10.1371/journal.pone.0089995
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author Connelly, William M.
author_facet Connelly, William M.
author_sort Connelly, William M.
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description Computational models of gamma oscillations have helped increase our understanding of the mechanisms that shape these 40–80 Hz cortical rhythms. Evidence suggests that interneurons known as basket cells are responsible for the generation of gamma oscillations. However, current models of gamma oscillations lack the dynamic short term synaptic plasticity seen at basket cell-basket cell synapses as well as the large autaptic synapses basket cells are known to express. Hence, I sought to extend the Wang-Buzsáki model of gamma oscillations to include these features. I found that autapses increased the synchrony of basket cell membrane potentials across the network during neocortical gamma oscillations as well as allowed the network to oscillate over a broader range of depolarizing drive. I also found that including realistic synaptic depression filtered the output of the network. Depression restricted the network to oscillate in the 60–80 Hz range rather than the 40–120 Hz range seen in the standard model. This work shows the importance of including accurate synapses in any future model of gamma oscillations.
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spelling pubmed-39385652014-03-04 Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations Connelly, William M. PLoS One Research Article Computational models of gamma oscillations have helped increase our understanding of the mechanisms that shape these 40–80 Hz cortical rhythms. Evidence suggests that interneurons known as basket cells are responsible for the generation of gamma oscillations. However, current models of gamma oscillations lack the dynamic short term synaptic plasticity seen at basket cell-basket cell synapses as well as the large autaptic synapses basket cells are known to express. Hence, I sought to extend the Wang-Buzsáki model of gamma oscillations to include these features. I found that autapses increased the synchrony of basket cell membrane potentials across the network during neocortical gamma oscillations as well as allowed the network to oscillate over a broader range of depolarizing drive. I also found that including realistic synaptic depression filtered the output of the network. Depression restricted the network to oscillate in the 60–80 Hz range rather than the 40–120 Hz range seen in the standard model. This work shows the importance of including accurate synapses in any future model of gamma oscillations. Public Library of Science 2014-02-28 /pmc/articles/PMC3938565/ /pubmed/24587175 http://dx.doi.org/10.1371/journal.pone.0089995 Text en © 2014 William M http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Connelly, William M.
Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations
title Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations
title_full Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations
title_fullStr Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations
title_full_unstemmed Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations
title_short Autaptic Connections and Synaptic Depression Constrain and Promote Gamma Oscillations
title_sort autaptic connections and synaptic depression constrain and promote gamma oscillations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938565/
https://www.ncbi.nlm.nih.gov/pubmed/24587175
http://dx.doi.org/10.1371/journal.pone.0089995
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