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Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model

Using an electrophysiological compartmental model of a Purkinje cell we quantified the contribution of individual active dendritic currents to processing of synaptic activity from granule cells. We used mutual information as a measure to quantify the information from the total excitatory input curre...

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Autores principales: Coop, Allan D., Cornelis, Hugo, Santamaria, Fidel
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856590/
https://www.ncbi.nlm.nih.gov/pubmed/20407613
http://dx.doi.org/10.3389/fncom.2010.00006
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author Coop, Allan D.
Cornelis, Hugo
Santamaria, Fidel
author_facet Coop, Allan D.
Cornelis, Hugo
Santamaria, Fidel
author_sort Coop, Allan D.
collection PubMed
description Using an electrophysiological compartmental model of a Purkinje cell we quantified the contribution of individual active dendritic currents to processing of synaptic activity from granule cells. We used mutual information as a measure to quantify the information from the total excitatory input current (I(Glu)) encoded in each dendritic current. In this context, each active current was considered an information channel. Our analyses showed that most of the information was encoded by the calcium (I(CaP)) and calcium activated potassium (I(Kc)) currents. Mutual information between I(Glu) and I(CaP) and I(Kc) was sensitive to different levels of excitatory and inhibitory synaptic activity that, at the same time, resulted in the same firing rate at the soma. Since dendritic excitability could be a mechanism to regulate information processing in neurons we quantified the changes in mutual information between I(Glu) and all Purkinje cell currents as a function of the density of dendritic Ca (g(CaP)) and Kca (g(Kc)) conductances. We extended our analysis to determine the window of temporal integration of I(Glu) by I(CaP) and I(Kc) as a function of channel density and synaptic activity. The window of information integration has a stronger dependence on increasing values of g(Kc) than on g(CaP), but at high levels of synaptic stimulation information integration is reduced to a few milliseconds. Overall, our results show that different dendritic conductances differentially encode synaptic activity and that dendritic excitability and the level of synaptic activity regulate the flow of information in dendrites.
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spelling pubmed-28565902010-04-20 Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model Coop, Allan D. Cornelis, Hugo Santamaria, Fidel Front Comput Neurosci Neuroscience Using an electrophysiological compartmental model of a Purkinje cell we quantified the contribution of individual active dendritic currents to processing of synaptic activity from granule cells. We used mutual information as a measure to quantify the information from the total excitatory input current (I(Glu)) encoded in each dendritic current. In this context, each active current was considered an information channel. Our analyses showed that most of the information was encoded by the calcium (I(CaP)) and calcium activated potassium (I(Kc)) currents. Mutual information between I(Glu) and I(CaP) and I(Kc) was sensitive to different levels of excitatory and inhibitory synaptic activity that, at the same time, resulted in the same firing rate at the soma. Since dendritic excitability could be a mechanism to regulate information processing in neurons we quantified the changes in mutual information between I(Glu) and all Purkinje cell currents as a function of the density of dendritic Ca (g(CaP)) and Kca (g(Kc)) conductances. We extended our analysis to determine the window of temporal integration of I(Glu) by I(CaP) and I(Kc) as a function of channel density and synaptic activity. The window of information integration has a stronger dependence on increasing values of g(Kc) than on g(CaP), but at high levels of synaptic stimulation information integration is reduced to a few milliseconds. Overall, our results show that different dendritic conductances differentially encode synaptic activity and that dendritic excitability and the level of synaptic activity regulate the flow of information in dendrites. Frontiers Research Foundation 2010-03-30 /pmc/articles/PMC2856590/ /pubmed/20407613 http://dx.doi.org/10.3389/fncom.2010.00006 Text en Copyright © 2010 Coop, Cornelis and Santamaria. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Coop, Allan D.
Cornelis, Hugo
Santamaria, Fidel
Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model
title Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model
title_full Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model
title_fullStr Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model
title_full_unstemmed Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model
title_short Dendritic Excitability Modulates Dendritic Information Processing in a Purkinje Cell Model
title_sort dendritic excitability modulates dendritic information processing in a purkinje cell model
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856590/
https://www.ncbi.nlm.nih.gov/pubmed/20407613
http://dx.doi.org/10.3389/fncom.2010.00006
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