Cargando…
Biophysically grounded mean-field models of neural populations under electrical stimulation
Electrical stimulation of neural systems is a key tool for understanding neural dynamics and ultimately for developing clinical treatments. Many applications of electrical stimulation affect large populations of neurons. However, computational models of large networks of spiking neurons are inherent...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200022/ https://www.ncbi.nlm.nih.gov/pubmed/32324734 http://dx.doi.org/10.1371/journal.pcbi.1007822 |
_version_ | 1783529258550820864 |
---|---|
author | Cakan, Caglar Obermayer, Klaus |
author_facet | Cakan, Caglar Obermayer, Klaus |
author_sort | Cakan, Caglar |
collection | PubMed |
description | Electrical stimulation of neural systems is a key tool for understanding neural dynamics and ultimately for developing clinical treatments. Many applications of electrical stimulation affect large populations of neurons. However, computational models of large networks of spiking neurons are inherently hard to simulate and analyze. We evaluate a reduced mean-field model of excitatory and inhibitory adaptive exponential integrate-and-fire (AdEx) neurons which can be used to efficiently study the effects of electrical stimulation on large neural populations. The rich dynamical properties of this basic cortical model are described in detail and validated using large network simulations. Bifurcation diagrams reflecting the network’s state reveal asynchronous up- and down-states, bistable regimes, and oscillatory regions corresponding to fast excitation-inhibition and slow excitation-adaptation feedback loops. The biophysical parameters of the AdEx neuron can be coupled to an electric field with realistic field strengths which then can be propagated up to the population description. We show how on the edge of bifurcation, direct electrical inputs cause network state transitions, such as turning on and off oscillations of the population rate. Oscillatory input can frequency-entrain and phase-lock endogenous oscillations. Relatively weak electric field strengths on the order of 1 V/m are able to produce these effects, indicating that field effects are strongly amplified in the network. The effects of time-varying external stimulation are well-predicted by the mean-field model, further underpinning the utility of low-dimensional neural mass models. |
format | Online Article Text |
id | pubmed-7200022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72000222020-05-12 Biophysically grounded mean-field models of neural populations under electrical stimulation Cakan, Caglar Obermayer, Klaus PLoS Comput Biol Research Article Electrical stimulation of neural systems is a key tool for understanding neural dynamics and ultimately for developing clinical treatments. Many applications of electrical stimulation affect large populations of neurons. However, computational models of large networks of spiking neurons are inherently hard to simulate and analyze. We evaluate a reduced mean-field model of excitatory and inhibitory adaptive exponential integrate-and-fire (AdEx) neurons which can be used to efficiently study the effects of electrical stimulation on large neural populations. The rich dynamical properties of this basic cortical model are described in detail and validated using large network simulations. Bifurcation diagrams reflecting the network’s state reveal asynchronous up- and down-states, bistable regimes, and oscillatory regions corresponding to fast excitation-inhibition and slow excitation-adaptation feedback loops. The biophysical parameters of the AdEx neuron can be coupled to an electric field with realistic field strengths which then can be propagated up to the population description. We show how on the edge of bifurcation, direct electrical inputs cause network state transitions, such as turning on and off oscillations of the population rate. Oscillatory input can frequency-entrain and phase-lock endogenous oscillations. Relatively weak electric field strengths on the order of 1 V/m are able to produce these effects, indicating that field effects are strongly amplified in the network. The effects of time-varying external stimulation are well-predicted by the mean-field model, further underpinning the utility of low-dimensional neural mass models. Public Library of Science 2020-04-23 /pmc/articles/PMC7200022/ /pubmed/32324734 http://dx.doi.org/10.1371/journal.pcbi.1007822 Text en © 2020 Cakan, Obermayer 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 Cakan, Caglar Obermayer, Klaus Biophysically grounded mean-field models of neural populations under electrical stimulation |
title | Biophysically grounded mean-field models of neural populations under electrical stimulation |
title_full | Biophysically grounded mean-field models of neural populations under electrical stimulation |
title_fullStr | Biophysically grounded mean-field models of neural populations under electrical stimulation |
title_full_unstemmed | Biophysically grounded mean-field models of neural populations under electrical stimulation |
title_short | Biophysically grounded mean-field models of neural populations under electrical stimulation |
title_sort | biophysically grounded mean-field models of neural populations under electrical stimulation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200022/ https://www.ncbi.nlm.nih.gov/pubmed/32324734 http://dx.doi.org/10.1371/journal.pcbi.1007822 |
work_keys_str_mv | AT cakancaglar biophysicallygroundedmeanfieldmodelsofneuralpopulationsunderelectricalstimulation AT obermayerklaus biophysicallygroundedmeanfieldmodelsofneuralpopulationsunderelectricalstimulation |