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The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse

A population of uncoupled neurons can often be brought close to synchrony by a single strong inhibitory input pulse affecting all neurons equally. This mechanism is thought to underlie some brain rhythms, in particular gamma frequency (30–80 Hz) oscillations in the hippocampus and neocortex. Here we...

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Detalles Bibliográficos
Autores principales: Börgers, Christoph, Krupa, Martin, Gielen, Stan
Formato: Texto
Lenguaje:English
Publicado: Springer US 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880705/
https://www.ncbi.nlm.nih.gov/pubmed/20387110
http://dx.doi.org/10.1007/s10827-010-0233-8
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author Börgers, Christoph
Krupa, Martin
Gielen, Stan
author_facet Börgers, Christoph
Krupa, Martin
Gielen, Stan
author_sort Börgers, Christoph
collection PubMed
description A population of uncoupled neurons can often be brought close to synchrony by a single strong inhibitory input pulse affecting all neurons equally. This mechanism is thought to underlie some brain rhythms, in particular gamma frequency (30–80 Hz) oscillations in the hippocampus and neocortex. Here we show that synchronization by an inhibitory input pulse often fails for populations of classical Hodgkin–Huxley neurons. Our reasoning suggests that in general, synchronization by inhibitory input pulses can fail when the transition of the target neurons from rest to spiking involves a Hopf bifurcation, especially when inhibition is shunting, not hyperpolarizing. Surprisingly, synchronization is more likely to fail when the inhibitory pulse is stronger or longer-lasting. These findings have potential implications for the question which neurons participate in brain rhythms, in particular in gamma oscillations.
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spelling pubmed-28807052010-06-10 The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse Börgers, Christoph Krupa, Martin Gielen, Stan J Comput Neurosci Article A population of uncoupled neurons can often be brought close to synchrony by a single strong inhibitory input pulse affecting all neurons equally. This mechanism is thought to underlie some brain rhythms, in particular gamma frequency (30–80 Hz) oscillations in the hippocampus and neocortex. Here we show that synchronization by an inhibitory input pulse often fails for populations of classical Hodgkin–Huxley neurons. Our reasoning suggests that in general, synchronization by inhibitory input pulses can fail when the transition of the target neurons from rest to spiking involves a Hopf bifurcation, especially when inhibition is shunting, not hyperpolarizing. Surprisingly, synchronization is more likely to fail when the inhibitory pulse is stronger or longer-lasting. These findings have potential implications for the question which neurons participate in brain rhythms, in particular in gamma oscillations. Springer US 2010-04-13 2010 /pmc/articles/PMC2880705/ /pubmed/20387110 http://dx.doi.org/10.1007/s10827-010-0233-8 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Börgers, Christoph
Krupa, Martin
Gielen, Stan
The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse
title The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse
title_full The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse
title_fullStr The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse
title_full_unstemmed The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse
title_short The response of a classical Hodgkin–Huxley neuron to an inhibitory input pulse
title_sort response of a classical hodgkin–huxley neuron to an inhibitory input pulse
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880705/
https://www.ncbi.nlm.nih.gov/pubmed/20387110
http://dx.doi.org/10.1007/s10827-010-0233-8
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