Cargando…
Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex
Within multiscale brain dynamics, the structure–function relationship between cellular changes at a lower scale and coordinated oscillations at a higher scale is not well understood. This relationship may be particularly relevant for understanding functional impairments after a mild traumatic brain...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461262/ https://www.ncbi.nlm.nih.gov/pubmed/28638364 http://dx.doi.org/10.3389/fneur.2017.00236 |
_version_ | 1783242301751951360 |
---|---|
author | Boothe, David L. Yu, Alfred B. Kudela, Pawel Anderson, William S. Vettel, Jean M. Franaszczuk, Piotr J. |
author_facet | Boothe, David L. Yu, Alfred B. Kudela, Pawel Anderson, William S. Vettel, Jean M. Franaszczuk, Piotr J. |
author_sort | Boothe, David L. |
collection | PubMed |
description | Within multiscale brain dynamics, the structure–function relationship between cellular changes at a lower scale and coordinated oscillations at a higher scale is not well understood. This relationship may be particularly relevant for understanding functional impairments after a mild traumatic brain injury (mTBI) when current neuroimaging methods do not reveal morphological changes to the brain common in moderate to severe TBI such as diffuse axonal injury or gray matter lesions. Here, we created a physiology-based model of cerebral cortex using a publicly released modeling framework (GEneral NEural SImulation System) to explore the possibility that performance deficits characteristic of blast-induced mTBI may reflect dysfunctional, local network activity influenced by microscale neuronal damage at the cellular level. We operationalized microscale damage to neurons as the formation of pores on the neuronal membrane based on research using blast paradigms, and in our model, pores were simulated by a change in membrane conductance. We then tracked changes in simulated electrical activity. Our model contained 585 simulated neurons, comprised of 14 types of cortical and thalamic neurons each with its own compartmental morphology and electrophysiological properties. Comparing the functional activity of neurons before and after simulated damage, we found that simulated pores in the membrane reduced both action potential generation and local field potential (LFP) power in the 1–40 Hz range of the power spectrum. Furthermore, the location of damage modulated the strength of these effects: pore formation on simulated axons reduced LFP power more strongly than did pore formation on the soma and the dendrites. These results indicate that even small amounts of cellular damage can negatively impact functional activity of larger scale oscillations, and our findings suggest that multiscale modeling provides a promising avenue to elucidate these relationships. |
format | Online Article Text |
id | pubmed-5461262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54612622017-06-21 Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex Boothe, David L. Yu, Alfred B. Kudela, Pawel Anderson, William S. Vettel, Jean M. Franaszczuk, Piotr J. Front Neurol Neuroscience Within multiscale brain dynamics, the structure–function relationship between cellular changes at a lower scale and coordinated oscillations at a higher scale is not well understood. This relationship may be particularly relevant for understanding functional impairments after a mild traumatic brain injury (mTBI) when current neuroimaging methods do not reveal morphological changes to the brain common in moderate to severe TBI such as diffuse axonal injury or gray matter lesions. Here, we created a physiology-based model of cerebral cortex using a publicly released modeling framework (GEneral NEural SImulation System) to explore the possibility that performance deficits characteristic of blast-induced mTBI may reflect dysfunctional, local network activity influenced by microscale neuronal damage at the cellular level. We operationalized microscale damage to neurons as the formation of pores on the neuronal membrane based on research using blast paradigms, and in our model, pores were simulated by a change in membrane conductance. We then tracked changes in simulated electrical activity. Our model contained 585 simulated neurons, comprised of 14 types of cortical and thalamic neurons each with its own compartmental morphology and electrophysiological properties. Comparing the functional activity of neurons before and after simulated damage, we found that simulated pores in the membrane reduced both action potential generation and local field potential (LFP) power in the 1–40 Hz range of the power spectrum. Furthermore, the location of damage modulated the strength of these effects: pore formation on simulated axons reduced LFP power more strongly than did pore formation on the soma and the dendrites. These results indicate that even small amounts of cellular damage can negatively impact functional activity of larger scale oscillations, and our findings suggest that multiscale modeling provides a promising avenue to elucidate these relationships. Frontiers Media S.A. 2017-06-07 /pmc/articles/PMC5461262/ /pubmed/28638364 http://dx.doi.org/10.3389/fneur.2017.00236 Text en Copyright © 2017 Boothe, Yu, Kudela, Anderson, Vettel and Franaszczuk. 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) or licensor 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 Boothe, David L. Yu, Alfred B. Kudela, Pawel Anderson, William S. Vettel, Jean M. Franaszczuk, Piotr J. Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex |
title | Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex |
title_full | Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex |
title_fullStr | Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex |
title_full_unstemmed | Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex |
title_short | Impact of Neuronal Membrane Damage on the Local Field Potential in a Large-Scale Simulation of Cerebral Cortex |
title_sort | impact of neuronal membrane damage on the local field potential in a large-scale simulation of cerebral cortex |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461262/ https://www.ncbi.nlm.nih.gov/pubmed/28638364 http://dx.doi.org/10.3389/fneur.2017.00236 |
work_keys_str_mv | AT boothedavidl impactofneuronalmembranedamageonthelocalfieldpotentialinalargescalesimulationofcerebralcortex AT yualfredb impactofneuronalmembranedamageonthelocalfieldpotentialinalargescalesimulationofcerebralcortex AT kudelapawel impactofneuronalmembranedamageonthelocalfieldpotentialinalargescalesimulationofcerebralcortex AT andersonwilliams impactofneuronalmembranedamageonthelocalfieldpotentialinalargescalesimulationofcerebralcortex AT vetteljeanm impactofneuronalmembranedamageonthelocalfieldpotentialinalargescalesimulationofcerebralcortex AT franaszczukpiotrj impactofneuronalmembranedamageonthelocalfieldpotentialinalargescalesimulationofcerebralcortex |