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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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Formato: | Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2010
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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. |
format | Text |
id | pubmed-2856590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
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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