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Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents
Neuronal membrane potential resonance (MPR) is associated with subthreshold and network oscillations. A number of voltage-gated ionic currents can contribute to the generation or amplification of MPR, but how the interaction of these currents with linear currents contributes to MPR is not well under...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476304/ https://www.ncbi.nlm.nih.gov/pubmed/28582395 http://dx.doi.org/10.1371/journal.pcbi.1005565 |
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author | Fox, David M. Tseng, Hua-an Smolinski, Tomasz G. Rotstein, Horacio G. Nadim, Farzan |
author_facet | Fox, David M. Tseng, Hua-an Smolinski, Tomasz G. Rotstein, Horacio G. Nadim, Farzan |
author_sort | Fox, David M. |
collection | PubMed |
description | Neuronal membrane potential resonance (MPR) is associated with subthreshold and network oscillations. A number of voltage-gated ionic currents can contribute to the generation or amplification of MPR, but how the interaction of these currents with linear currents contributes to MPR is not well understood. We explored this in the pacemaker PD neurons of the crab pyloric network. The PD neuron MPR is sensitive to blockers of H- (I(H)) and calcium-currents (I(Ca)). We used the impedance profile of the biological PD neuron, measured in voltage clamp, to constrain parameter values of a conductance-based model using a genetic algorithm and obtained many optimal parameter combinations. Unlike most cases of MPR, in these optimal models, the values of resonant- (f(res)) and phasonant- (f(ϕ = 0)) frequencies were almost identical. Taking advantage of this fact, we linked the peak phase of ionic currents to their amplitude, in order to provide a mechanistic explanation the dependence of MPR on the I(Ca) gating variable time constants. Additionally, we found that distinct pairwise correlations between I(Ca) parameters contributed to the maintenance of f(res) and resonance power (Q(Z)). Measurements of the PD neuron MPR at more hyperpolarized voltages resulted in a reduction of f(res) but no change in Q(Z). Constraining the optimal models using these data unmasked a positive correlation between the maximal conductances of I(H) and I(Ca). Thus, although I(H) is not necessary for MPR in this neuron type, it contributes indirectly by constraining the parameters of I(Ca). |
format | Online Article Text |
id | pubmed-5476304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54763042017-07-06 Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents Fox, David M. Tseng, Hua-an Smolinski, Tomasz G. Rotstein, Horacio G. Nadim, Farzan PLoS Comput Biol Research Article Neuronal membrane potential resonance (MPR) is associated with subthreshold and network oscillations. A number of voltage-gated ionic currents can contribute to the generation or amplification of MPR, but how the interaction of these currents with linear currents contributes to MPR is not well understood. We explored this in the pacemaker PD neurons of the crab pyloric network. The PD neuron MPR is sensitive to blockers of H- (I(H)) and calcium-currents (I(Ca)). We used the impedance profile of the biological PD neuron, measured in voltage clamp, to constrain parameter values of a conductance-based model using a genetic algorithm and obtained many optimal parameter combinations. Unlike most cases of MPR, in these optimal models, the values of resonant- (f(res)) and phasonant- (f(ϕ = 0)) frequencies were almost identical. Taking advantage of this fact, we linked the peak phase of ionic currents to their amplitude, in order to provide a mechanistic explanation the dependence of MPR on the I(Ca) gating variable time constants. Additionally, we found that distinct pairwise correlations between I(Ca) parameters contributed to the maintenance of f(res) and resonance power (Q(Z)). Measurements of the PD neuron MPR at more hyperpolarized voltages resulted in a reduction of f(res) but no change in Q(Z). Constraining the optimal models using these data unmasked a positive correlation between the maximal conductances of I(H) and I(Ca). Thus, although I(H) is not necessary for MPR in this neuron type, it contributes indirectly by constraining the parameters of I(Ca). Public Library of Science 2017-06-05 /pmc/articles/PMC5476304/ /pubmed/28582395 http://dx.doi.org/10.1371/journal.pcbi.1005565 Text en © 2017 Fox 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Fox, David M. Tseng, Hua-an Smolinski, Tomasz G. Rotstein, Horacio G. Nadim, Farzan Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents |
title | Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents |
title_full | Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents |
title_fullStr | Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents |
title_full_unstemmed | Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents |
title_short | Mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents |
title_sort | mechanisms of generation of membrane potential resonance in a neuron with multiple resonant ionic currents |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476304/ https://www.ncbi.nlm.nih.gov/pubmed/28582395 http://dx.doi.org/10.1371/journal.pcbi.1005565 |
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