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On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia

Neuronal signals are usually characterized in terms of their discharge rate, a description inadequate to account for the complex temporal organization of spike trains. Complex temporal properties, which are characteristic of neuronal systems, can only be described with the appropriate, complex mathe...

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Autor principal: Andres, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207592/
https://www.ncbi.nlm.nih.gov/pubmed/30405381
http://dx.doi.org/10.3389/fnhum.2018.00429
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author Andres, Daniela
author_facet Andres, Daniela
author_sort Andres, Daniela
collection PubMed
description Neuronal signals are usually characterized in terms of their discharge rate, a description inadequate to account for the complex temporal organization of spike trains. Complex temporal properties, which are characteristic of neuronal systems, can only be described with the appropriate, complex mathematical tools. Here, I apply high order structure functions to the analysis of neuronal signals recorded from parkinsonian patients during functional neurosurgery, recovering multifractal properties. To achieve an accurate model of such multifractality is critical for understanding the basal ganglia, since other non-linear properties, such as entropy, depend on the fractal properties of complex systems. I propose a new approach to the study of neuronal signals: to study spiking activity in terms of the velocity of spikes, defining it as the inverse function of the instantaneous frequency. I introduce a neural field model that includes a non-linear gradient field, representing neuronal excitability, and a diffusive term to consider the physical properties of the electric field. Multifractality is present in the model for a range of diffusion coefficients, and multifractal temporal properties are mirrored into space. The model reproduces the behavior of human basal ganglia neurons and shows that it is like that of turbulent fluids. The results obtained from the model predict that passive electric properties of neuronal activity, including ephaptic coupling, are far more relevant to the human brain than what is usually considered: passive electric properties determine the temporal and spatial organization of neuronal activity in the neural tissue.
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spelling pubmed-62075922018-11-07 On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia Andres, Daniela Front Hum Neurosci Neuroscience Neuronal signals are usually characterized in terms of their discharge rate, a description inadequate to account for the complex temporal organization of spike trains. Complex temporal properties, which are characteristic of neuronal systems, can only be described with the appropriate, complex mathematical tools. Here, I apply high order structure functions to the analysis of neuronal signals recorded from parkinsonian patients during functional neurosurgery, recovering multifractal properties. To achieve an accurate model of such multifractality is critical for understanding the basal ganglia, since other non-linear properties, such as entropy, depend on the fractal properties of complex systems. I propose a new approach to the study of neuronal signals: to study spiking activity in terms of the velocity of spikes, defining it as the inverse function of the instantaneous frequency. I introduce a neural field model that includes a non-linear gradient field, representing neuronal excitability, and a diffusive term to consider the physical properties of the electric field. Multifractality is present in the model for a range of diffusion coefficients, and multifractal temporal properties are mirrored into space. The model reproduces the behavior of human basal ganglia neurons and shows that it is like that of turbulent fluids. The results obtained from the model predict that passive electric properties of neuronal activity, including ephaptic coupling, are far more relevant to the human brain than what is usually considered: passive electric properties determine the temporal and spatial organization of neuronal activity in the neural tissue. Frontiers Media S.A. 2018-10-24 /pmc/articles/PMC6207592/ /pubmed/30405381 http://dx.doi.org/10.3389/fnhum.2018.00429 Text en Copyright © 2018 Andres. 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) and the copyright owner(s) 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
Andres, Daniela
On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia
title On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia
title_full On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia
title_fullStr On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia
title_full_unstemmed On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia
title_short On the Motion of Spikes: Turbulent-Like Neuronal Activity in the Human Basal Ganglia
title_sort on the motion of spikes: turbulent-like neuronal activity in the human basal ganglia
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207592/
https://www.ncbi.nlm.nih.gov/pubmed/30405381
http://dx.doi.org/10.3389/fnhum.2018.00429
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