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State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current

Thalamic neurons fluctuate between two states: a hyperpolarized state associated with burst firing and sleep spindles, and a depolarized state associated with tonic firing and rapid, reliable information transmission between the sensory periphery and cortex. The thalamic reticular nucleus (TRN) play...

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Autores principales: Haas, Julie S., Landisman, Carole E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263475/
https://www.ncbi.nlm.nih.gov/pubmed/22319469
http://dx.doi.org/10.3389/fncel.2011.00031
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author Haas, Julie S.
Landisman, Carole E.
author_facet Haas, Julie S.
Landisman, Carole E.
author_sort Haas, Julie S.
collection PubMed
description Thalamic neurons fluctuate between two states: a hyperpolarized state associated with burst firing and sleep spindles, and a depolarized state associated with tonic firing and rapid, reliable information transmission between the sensory periphery and cortex. The thalamic reticular nucleus (TRN) plays a central role in thalamocortical processing by providing feed-forward and feedback inhibition to thalamic relay cells; TRN cells participate in the generation of sleep spindles, and have been suggested to focus the neural “searchlight” of attention. The mechanisms underlying synchrony in the TRN during different behavioral states are largely unknown. TRN cells are densely interconnected by electrical synapses. Here we show that activation of the persistent sodium current (I(NaP)) by depolarization causes up to fourfold changes in electrical synaptic efficacy between TRN neurons. We further show that amplification of electrical synaptic responses strongly enhances tonic spike synchrony but, surprisingly, does not affect burst coordination. We use a Hodgkin–Huxley model to gain insight into the differences between the effects of burstlets, spikelets, and amplification on burst and spike times.
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spelling pubmed-32634752012-02-08 State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current Haas, Julie S. Landisman, Carole E. Front Cell Neurosci Neuroscience Thalamic neurons fluctuate between two states: a hyperpolarized state associated with burst firing and sleep spindles, and a depolarized state associated with tonic firing and rapid, reliable information transmission between the sensory periphery and cortex. The thalamic reticular nucleus (TRN) plays a central role in thalamocortical processing by providing feed-forward and feedback inhibition to thalamic relay cells; TRN cells participate in the generation of sleep spindles, and have been suggested to focus the neural “searchlight” of attention. The mechanisms underlying synchrony in the TRN during different behavioral states are largely unknown. TRN cells are densely interconnected by electrical synapses. Here we show that activation of the persistent sodium current (I(NaP)) by depolarization causes up to fourfold changes in electrical synaptic efficacy between TRN neurons. We further show that amplification of electrical synaptic responses strongly enhances tonic spike synchrony but, surprisingly, does not affect burst coordination. We use a Hodgkin–Huxley model to gain insight into the differences between the effects of burstlets, spikelets, and amplification on burst and spike times. Frontiers Research Foundation 2012-01-23 /pmc/articles/PMC3263475/ /pubmed/22319469 http://dx.doi.org/10.3389/fncel.2011.00031 Text en Copyright © 2012 Haas and Landisman. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroscience
Haas, Julie S.
Landisman, Carole E.
State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current
title State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current
title_full State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current
title_fullStr State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current
title_full_unstemmed State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current
title_short State-Dependent Modulation of Gap Junction Signaling by the Persistent Sodium Current
title_sort state-dependent modulation of gap junction signaling by the persistent sodium current
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263475/
https://www.ncbi.nlm.nih.gov/pubmed/22319469
http://dx.doi.org/10.3389/fncel.2011.00031
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