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Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells

In realistic neuronal modeling, once the ionic channel complement has been defined, the maximum ionic conductance (G(i-max)) values need to be tuned in order to match the firing pattern revealed by electrophysiological recordings. Recently, selection/mutation genetic algorithms have been proposed to...

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Autores principales: Masoli, Stefano, Rizza, Martina F., Sgritta, Martina, Van Geit, Werner, Schürmann, Felix, D'Angelo, Egidio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350144/
https://www.ncbi.nlm.nih.gov/pubmed/28360841
http://dx.doi.org/10.3389/fncel.2017.00071
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author Masoli, Stefano
Rizza, Martina F.
Sgritta, Martina
Van Geit, Werner
Schürmann, Felix
D'Angelo, Egidio
author_facet Masoli, Stefano
Rizza, Martina F.
Sgritta, Martina
Van Geit, Werner
Schürmann, Felix
D'Angelo, Egidio
author_sort Masoli, Stefano
collection PubMed
description In realistic neuronal modeling, once the ionic channel complement has been defined, the maximum ionic conductance (G(i-max)) values need to be tuned in order to match the firing pattern revealed by electrophysiological recordings. Recently, selection/mutation genetic algorithms have been proposed to efficiently and automatically tune these parameters. Nonetheless, since similar firing patterns can be achieved through different combinations of G(i-max) values, it is not clear how well these algorithms approximate the corresponding properties of real cells. Here we have evaluated the issue by exploiting a unique opportunity offered by the cerebellar granule cell (GrC), which is electrotonically compact and has therefore allowed the direct experimental measurement of ionic currents. Previous models were constructed using empirical tuning of G(i-max) values to match the original data set. Here, by using repetitive discharge patterns as a template, the optimization procedure yielded models that closely approximated the experimental G(i-max) values. These models, in addition to repetitive firing, captured additional features, including inward rectification, near-threshold oscillations, and resonance, which were not used as features. Thus, parameter optimization using genetic algorithms provided an efficient modeling strategy for reconstructing the biophysical properties of neurons and for the subsequent reconstruction of large-scale neuronal network models.
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spelling pubmed-53501442017-03-30 Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells Masoli, Stefano Rizza, Martina F. Sgritta, Martina Van Geit, Werner Schürmann, Felix D'Angelo, Egidio Front Cell Neurosci Neuroscience In realistic neuronal modeling, once the ionic channel complement has been defined, the maximum ionic conductance (G(i-max)) values need to be tuned in order to match the firing pattern revealed by electrophysiological recordings. Recently, selection/mutation genetic algorithms have been proposed to efficiently and automatically tune these parameters. Nonetheless, since similar firing patterns can be achieved through different combinations of G(i-max) values, it is not clear how well these algorithms approximate the corresponding properties of real cells. Here we have evaluated the issue by exploiting a unique opportunity offered by the cerebellar granule cell (GrC), which is electrotonically compact and has therefore allowed the direct experimental measurement of ionic currents. Previous models were constructed using empirical tuning of G(i-max) values to match the original data set. Here, by using repetitive discharge patterns as a template, the optimization procedure yielded models that closely approximated the experimental G(i-max) values. These models, in addition to repetitive firing, captured additional features, including inward rectification, near-threshold oscillations, and resonance, which were not used as features. Thus, parameter optimization using genetic algorithms provided an efficient modeling strategy for reconstructing the biophysical properties of neurons and for the subsequent reconstruction of large-scale neuronal network models. Frontiers Media S.A. 2017-03-15 /pmc/articles/PMC5350144/ /pubmed/28360841 http://dx.doi.org/10.3389/fncel.2017.00071 Text en Copyright © 2017 Masoli, Rizza, Sgritta, Van Geit, Schürmann and D'Angelo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Masoli, Stefano
Rizza, Martina F.
Sgritta, Martina
Van Geit, Werner
Schürmann, Felix
D'Angelo, Egidio
Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells
title Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells
title_full Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells
title_fullStr Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells
title_full_unstemmed Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells
title_short Single Neuron Optimization as a Basis for Accurate Biophysical Modeling: The Case of Cerebellar Granule Cells
title_sort single neuron optimization as a basis for accurate biophysical modeling: the case of cerebellar granule cells
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350144/
https://www.ncbi.nlm.nih.gov/pubmed/28360841
http://dx.doi.org/10.3389/fncel.2017.00071
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