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Active Dendrites Enhance Neuronal Dynamic Range

Since the first experimental evidences of active conductances in dendrites, most neurons have been shown to exhibit dendritic excitability through the expression of a variety of voltage-gated ion channels. However, despite experimental and theoretical efforts undertaken in the past decades, the role...

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Detalles Bibliográficos
Autores principales: Gollo, Leonardo L., Kinouchi, Osame, Copelli, Mauro
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690843/
https://www.ncbi.nlm.nih.gov/pubmed/19521531
http://dx.doi.org/10.1371/journal.pcbi.1000402
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author Gollo, Leonardo L.
Kinouchi, Osame
Copelli, Mauro
author_facet Gollo, Leonardo L.
Kinouchi, Osame
Copelli, Mauro
author_sort Gollo, Leonardo L.
collection PubMed
description Since the first experimental evidences of active conductances in dendrites, most neurons have been shown to exhibit dendritic excitability through the expression of a variety of voltage-gated ion channels. However, despite experimental and theoretical efforts undertaken in the past decades, the role of this excitability for some kind of dendritic computation has remained elusive. Here we show that, owing to very general properties of excitable media, the average output of a model of an active dendritic tree is a highly non-linear function of its afferent rate, attaining extremely large dynamic ranges (above 50 dB). Moreover, the model yields double-sigmoid response functions as experimentally observed in retinal ganglion cells. We claim that enhancement of dynamic range is the primary functional role of active dendritic conductances. We predict that neurons with larger dendritic trees should have larger dynamic range and that blocking of active conductances should lead to a decrease in dynamic range.
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spelling pubmed-26908432009-06-12 Active Dendrites Enhance Neuronal Dynamic Range Gollo, Leonardo L. Kinouchi, Osame Copelli, Mauro PLoS Comput Biol Research Article Since the first experimental evidences of active conductances in dendrites, most neurons have been shown to exhibit dendritic excitability through the expression of a variety of voltage-gated ion channels. However, despite experimental and theoretical efforts undertaken in the past decades, the role of this excitability for some kind of dendritic computation has remained elusive. Here we show that, owing to very general properties of excitable media, the average output of a model of an active dendritic tree is a highly non-linear function of its afferent rate, attaining extremely large dynamic ranges (above 50 dB). Moreover, the model yields double-sigmoid response functions as experimentally observed in retinal ganglion cells. We claim that enhancement of dynamic range is the primary functional role of active dendritic conductances. We predict that neurons with larger dendritic trees should have larger dynamic range and that blocking of active conductances should lead to a decrease in dynamic range. Public Library of Science 2009-06-12 /pmc/articles/PMC2690843/ /pubmed/19521531 http://dx.doi.org/10.1371/journal.pcbi.1000402 Text en Gollo et al. 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
Gollo, Leonardo L.
Kinouchi, Osame
Copelli, Mauro
Active Dendrites Enhance Neuronal Dynamic Range
title Active Dendrites Enhance Neuronal Dynamic Range
title_full Active Dendrites Enhance Neuronal Dynamic Range
title_fullStr Active Dendrites Enhance Neuronal Dynamic Range
title_full_unstemmed Active Dendrites Enhance Neuronal Dynamic Range
title_short Active Dendrites Enhance Neuronal Dynamic Range
title_sort active dendrites enhance neuronal dynamic range
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690843/
https://www.ncbi.nlm.nih.gov/pubmed/19521531
http://dx.doi.org/10.1371/journal.pcbi.1000402
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