An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.

In most neuronal models, ion concentrations are assumed to be constant, and effects of concentration variations on ionic reversal potentials, or of ionic diffusion on electrical potentials are not accounted for. Here, we present the electrodiffusive Pinsky-Rinzel (edPR) model, which we believe is th...

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Main Authors: Marte J Sætra, Gaute T Einevoll, Geir Halnes
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-04-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1007661
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spelling doaj-b21fa6bbf6064f4e9c04ae71415cea042021-04-21T15:15:21ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582020-04-01164e100766110.1371/journal.pcbi.1007661An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.Marte J SætraGaute T EinevollGeir HalnesIn most neuronal models, ion concentrations are assumed to be constant, and effects of concentration variations on ionic reversal potentials, or of ionic diffusion on electrical potentials are not accounted for. Here, we present the electrodiffusive Pinsky-Rinzel (edPR) model, which we believe is the first multicompartmental neuron model that accounts for electrodiffusive ion concentration dynamics in a way that ensures a biophysically consistent relationship between ion concentrations, electrical charge, and electrical potentials in both the intra- and extracellular space. The edPR model is an expanded version of the two-compartment Pinsky-Rinzel (PR) model of a hippocampal CA3 neuron. Unlike the PR model, the edPR model includes homeostatic mechanisms and ion-specific leakage currents, and keeps track of all ion concentrations (Na+, K+, Ca2+, and Cl-), electrical potentials, and electrical conductivities in the intra- and extracellular space. The edPR model reproduces the membrane potential dynamics of the PR model for moderate firing activity. For higher activity levels, or when homeostatic mechanisms are impaired, the homeostatic mechanisms fail in maintaining ion concentrations close to baseline, and the edPR model diverges from the PR model as it accounts for effects of concentration changes on neuronal firing. We envision that the edPR model will be useful for the field in three main ways. Firstly, as it relaxes commonly made modeling assumptions, the edPR model can be used to test the validity of these assumptions under various firing conditions, as we show here for a few selected cases. Secondly, the edPR model should supplement the PR model when simulating scenarios where ion concentrations are expected to vary over time. Thirdly, being applicable to conditions with failed homeostasis, the edPR model opens up for simulating a range of pathological conditions, such as spreading depression or epilepsy.https://doi.org/10.1371/journal.pcbi.1007661
collection DOAJ
language English
format Article
sources DOAJ
author Marte J Sætra
Gaute T Einevoll
Geir Halnes
spellingShingle Marte J Sætra
Gaute T Einevoll
Geir Halnes
An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.
PLoS Computational Biology
author_facet Marte J Sætra
Gaute T Einevoll
Geir Halnes
author_sort Marte J Sætra
title An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.
title_short An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.
title_full An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.
title_fullStr An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.
title_full_unstemmed An electrodiffusive, ion conserving Pinsky-Rinzel model with homeostatic mechanisms.
title_sort electrodiffusive, ion conserving pinsky-rinzel model with homeostatic mechanisms.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2020-04-01
description In most neuronal models, ion concentrations are assumed to be constant, and effects of concentration variations on ionic reversal potentials, or of ionic diffusion on electrical potentials are not accounted for. Here, we present the electrodiffusive Pinsky-Rinzel (edPR) model, which we believe is the first multicompartmental neuron model that accounts for electrodiffusive ion concentration dynamics in a way that ensures a biophysically consistent relationship between ion concentrations, electrical charge, and electrical potentials in both the intra- and extracellular space. The edPR model is an expanded version of the two-compartment Pinsky-Rinzel (PR) model of a hippocampal CA3 neuron. Unlike the PR model, the edPR model includes homeostatic mechanisms and ion-specific leakage currents, and keeps track of all ion concentrations (Na+, K+, Ca2+, and Cl-), electrical potentials, and electrical conductivities in the intra- and extracellular space. The edPR model reproduces the membrane potential dynamics of the PR model for moderate firing activity. For higher activity levels, or when homeostatic mechanisms are impaired, the homeostatic mechanisms fail in maintaining ion concentrations close to baseline, and the edPR model diverges from the PR model as it accounts for effects of concentration changes on neuronal firing. We envision that the edPR model will be useful for the field in three main ways. Firstly, as it relaxes commonly made modeling assumptions, the edPR model can be used to test the validity of these assumptions under various firing conditions, as we show here for a few selected cases. Secondly, the edPR model should supplement the PR model when simulating scenarios where ion concentrations are expected to vary over time. Thirdly, being applicable to conditions with failed homeostasis, the edPR model opens up for simulating a range of pathological conditions, such as spreading depression or epilepsy.
url https://doi.org/10.1371/journal.pcbi.1007661
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