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Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models

Leaky integrate-and-fire (LIF) network models are commonly used to study how the spiking dynamics of neural networks changes with stimuli, tasks or dynamic network states. However, neurophysiological studies in vivo often rather measure the mass activity of neuronal microcircuits with the local fiel...

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Autores principales: Mazzoni, Alberto, Lindén, Henrik, Cuntz, Hermann, Lansner, Anders, Panzeri, Stefano, Einevoll, Gaute T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682791/
https://www.ncbi.nlm.nih.gov/pubmed/26657024
http://dx.doi.org/10.1371/journal.pcbi.1004584
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author Mazzoni, Alberto
Lindén, Henrik
Cuntz, Hermann
Lansner, Anders
Panzeri, Stefano
Einevoll, Gaute T.
author_facet Mazzoni, Alberto
Lindén, Henrik
Cuntz, Hermann
Lansner, Anders
Panzeri, Stefano
Einevoll, Gaute T.
author_sort Mazzoni, Alberto
collection PubMed
description Leaky integrate-and-fire (LIF) network models are commonly used to study how the spiking dynamics of neural networks changes with stimuli, tasks or dynamic network states. However, neurophysiological studies in vivo often rather measure the mass activity of neuronal microcircuits with the local field potential (LFP). Given that LFPs are generated by spatially separated currents across the neuronal membrane, they cannot be computed directly from quantities defined in models of point-like LIF neurons. Here, we explore the best approximation for predicting the LFP based on standard output from point-neuron LIF networks. To search for this best “LFP proxy”, we compared LFP predictions from candidate proxies based on LIF network output (e.g, firing rates, membrane potentials, synaptic currents) with “ground-truth” LFP obtained when the LIF network synaptic input currents were injected into an analogous three-dimensional (3D) network model of multi-compartmental neurons with realistic morphology, spatial distributions of somata and synapses. We found that a specific fixed linear combination of the LIF synaptic currents provided an accurate LFP proxy, accounting for most of the variance of the LFP time course observed in the 3D network for all recording locations. This proxy performed well over a broad set of conditions, including substantial variations of the neuronal morphologies. Our results provide a simple formula for estimating the time course of the LFP from LIF network simulations in cases where a single pyramidal population dominates the LFP generation, and thereby facilitate quantitative comparison between computational models and experimental LFP recordings in vivo.
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spelling pubmed-46827912015-12-31 Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models Mazzoni, Alberto Lindén, Henrik Cuntz, Hermann Lansner, Anders Panzeri, Stefano Einevoll, Gaute T. PLoS Comput Biol Research Article Leaky integrate-and-fire (LIF) network models are commonly used to study how the spiking dynamics of neural networks changes with stimuli, tasks or dynamic network states. However, neurophysiological studies in vivo often rather measure the mass activity of neuronal microcircuits with the local field potential (LFP). Given that LFPs are generated by spatially separated currents across the neuronal membrane, they cannot be computed directly from quantities defined in models of point-like LIF neurons. Here, we explore the best approximation for predicting the LFP based on standard output from point-neuron LIF networks. To search for this best “LFP proxy”, we compared LFP predictions from candidate proxies based on LIF network output (e.g, firing rates, membrane potentials, synaptic currents) with “ground-truth” LFP obtained when the LIF network synaptic input currents were injected into an analogous three-dimensional (3D) network model of multi-compartmental neurons with realistic morphology, spatial distributions of somata and synapses. We found that a specific fixed linear combination of the LIF synaptic currents provided an accurate LFP proxy, accounting for most of the variance of the LFP time course observed in the 3D network for all recording locations. This proxy performed well over a broad set of conditions, including substantial variations of the neuronal morphologies. Our results provide a simple formula for estimating the time course of the LFP from LIF network simulations in cases where a single pyramidal population dominates the LFP generation, and thereby facilitate quantitative comparison between computational models and experimental LFP recordings in vivo. Public Library of Science 2015-12-14 /pmc/articles/PMC4682791/ /pubmed/26657024 http://dx.doi.org/10.1371/journal.pcbi.1004584 Text en © 2015 Mazzoni 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mazzoni, Alberto
Lindén, Henrik
Cuntz, Hermann
Lansner, Anders
Panzeri, Stefano
Einevoll, Gaute T.
Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
title Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
title_full Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
title_fullStr Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
title_full_unstemmed Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
title_short Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
title_sort computing the local field potential (lfp) from integrate-and-fire network models
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682791/
https://www.ncbi.nlm.nih.gov/pubmed/26657024
http://dx.doi.org/10.1371/journal.pcbi.1004584
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