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Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells
The Golgi cells have been recently shown to beat regularly in vitro (Forti et al., 2006. J. Physiol. 574, 711–729). Four main currents were shown to be involved, namely a persistent sodium current (I (Na-p)), an h current (I (h)), an SK-type calcium-dependent potassium current (I (K-AHP)), and a slo...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525930/ https://www.ncbi.nlm.nih.gov/pubmed/18946520 http://dx.doi.org/10.3389/neuro.03.002.2007 |
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author | Solinas, Sergio Forti, Lia Cesana, Elisabetta Mapelli, Jonathan De Schutter, Erik D'Angelo, Egidio |
author_facet | Solinas, Sergio Forti, Lia Cesana, Elisabetta Mapelli, Jonathan De Schutter, Erik D'Angelo, Egidio |
author_sort | Solinas, Sergio |
collection | PubMed |
description | The Golgi cells have been recently shown to beat regularly in vitro (Forti et al., 2006. J. Physiol. 574, 711–729). Four main currents were shown to be involved, namely a persistent sodium current (I (Na-p)), an h current (I (h)), an SK-type calcium-dependent potassium current (I (K-AHP)), and a slow M-like potassium current (I (K-slow)). These ionic currents could take part, together with others, also to different aspects of neuronal excitability like responses to depolarizing and hyperpolarizing current injection. However, the ionic mechanisms and their interactions remained largely hypothetical. In this work, we have investigated the mechanisms of Golgi cell excitability by developing a computational model. The model predicts that pacemaking is sustained by subthreshold oscillations tightly coupled to spikes. I (Na-p) and I (K-slow) emerged as the critical determinants of oscillations. I (h) also played a role by setting the oscillatory mechanism into the appropriate membrane potential range. I (K-AHP), though taking part to the oscillation, appeared primarily involved in regulating the ISI following spikes. The combination with other currents, in particular a resurgent sodium current (I (Na-r)) and an A-current (I (K-A)), allowed a precise regulation of response frequency and delay. These results provide a coherent reconstruction of the ionic mechanisms determining Golgi cell intrinsic electroresponsiveness and suggests important implications for cerebellar signal processing, which will be fully developed in a companion paper (Solinas et al., 2008. Front. Neurosci. 2:4). |
format | Text |
id | pubmed-2525930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-25259302008-10-22 Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells Solinas, Sergio Forti, Lia Cesana, Elisabetta Mapelli, Jonathan De Schutter, Erik D'Angelo, Egidio Front Cell Neurosci Neuroscience The Golgi cells have been recently shown to beat regularly in vitro (Forti et al., 2006. J. Physiol. 574, 711–729). Four main currents were shown to be involved, namely a persistent sodium current (I (Na-p)), an h current (I (h)), an SK-type calcium-dependent potassium current (I (K-AHP)), and a slow M-like potassium current (I (K-slow)). These ionic currents could take part, together with others, also to different aspects of neuronal excitability like responses to depolarizing and hyperpolarizing current injection. However, the ionic mechanisms and their interactions remained largely hypothetical. In this work, we have investigated the mechanisms of Golgi cell excitability by developing a computational model. The model predicts that pacemaking is sustained by subthreshold oscillations tightly coupled to spikes. I (Na-p) and I (K-slow) emerged as the critical determinants of oscillations. I (h) also played a role by setting the oscillatory mechanism into the appropriate membrane potential range. I (K-AHP), though taking part to the oscillation, appeared primarily involved in regulating the ISI following spikes. The combination with other currents, in particular a resurgent sodium current (I (Na-r)) and an A-current (I (K-A)), allowed a precise regulation of response frequency and delay. These results provide a coherent reconstruction of the ionic mechanisms determining Golgi cell intrinsic electroresponsiveness and suggests important implications for cerebellar signal processing, which will be fully developed in a companion paper (Solinas et al., 2008. Front. Neurosci. 2:4). Frontiers Research Foundation 2007-12-30 /pmc/articles/PMC2525930/ /pubmed/18946520 http://dx.doi.org/10.3389/neuro.03.002.2007 Text en Copyright © 2007 Solinas, Forti, Cesana, Mapelli, De Schutter and D'Angelo. 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 Solinas, Sergio Forti, Lia Cesana, Elisabetta Mapelli, Jonathan De Schutter, Erik D'Angelo, Egidio Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells |
title | Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells |
title_full | Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells |
title_fullStr | Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells |
title_full_unstemmed | Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells |
title_short | Computational Reconstruction of Pacemaking and Intrinsic Electroresponsiveness in Cerebellar Golgi Cells |
title_sort | computational reconstruction of pacemaking and intrinsic electroresponsiveness in cerebellar golgi cells |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2525930/ https://www.ncbi.nlm.nih.gov/pubmed/18946520 http://dx.doi.org/10.3389/neuro.03.002.2007 |
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