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Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space
Neuronal stimulation causes ∼30% shrinkage of the extracellular space (ECS) between neurons and surrounding astrocytes in grey and white matter under experimental conditions. Despite its possible implications for a proper understanding of basic aspects of potassium clearance and astrocyte function,...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613522/ https://www.ncbi.nlm.nih.gov/pubmed/19165313 http://dx.doi.org/10.1371/journal.pcbi.1000272 |
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author | Østby, Ivar Øyehaug, Leiv Einevoll, Gaute T. Nagelhus, Erlend A. Plahte, Erik Zeuthen, Thomas Lloyd, Catherine M. Ottersen, Ole P. Omholt, Stig W. |
author_facet | Østby, Ivar Øyehaug, Leiv Einevoll, Gaute T. Nagelhus, Erlend A. Plahte, Erik Zeuthen, Thomas Lloyd, Catherine M. Ottersen, Ole P. Omholt, Stig W. |
author_sort | Østby, Ivar |
collection | PubMed |
description | Neuronal stimulation causes ∼30% shrinkage of the extracellular space (ECS) between neurons and surrounding astrocytes in grey and white matter under experimental conditions. Despite its possible implications for a proper understanding of basic aspects of potassium clearance and astrocyte function, the phenomenon remains unexplained. Here we present a dynamic model that accounts for current experimental data related to the shrinkage phenomenon in wild-type as well as in gene knockout individuals. We find that neuronal release of potassium and uptake of sodium during stimulation, astrocyte uptake of potassium, sodium, and chloride in passive channels, action of the Na/K/ATPase pump, and osmotically driven transport of water through the astrocyte membrane together seem sufficient for generating ECS shrinkage as such. However, when taking into account ECS and astrocyte ion concentrations observed in connection with neuronal stimulation, the actions of the Na(+)/K(+)/Cl(−) (NKCC1) and the Na(+)/HCO(3) (−) (NBC) cotransporters appear to be critical determinants for achieving observed quantitative levels of ECS shrinkage. Considering the current state of knowledge, the model framework appears sufficiently detailed and constrained to guide future key experiments and pave the way for more comprehensive astroglia–neuron interaction models for normal as well as pathophysiological situations. |
format | Text |
id | pubmed-2613522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26135222009-01-23 Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space Østby, Ivar Øyehaug, Leiv Einevoll, Gaute T. Nagelhus, Erlend A. Plahte, Erik Zeuthen, Thomas Lloyd, Catherine M. Ottersen, Ole P. Omholt, Stig W. PLoS Comput Biol Research Article Neuronal stimulation causes ∼30% shrinkage of the extracellular space (ECS) between neurons and surrounding astrocytes in grey and white matter under experimental conditions. Despite its possible implications for a proper understanding of basic aspects of potassium clearance and astrocyte function, the phenomenon remains unexplained. Here we present a dynamic model that accounts for current experimental data related to the shrinkage phenomenon in wild-type as well as in gene knockout individuals. We find that neuronal release of potassium and uptake of sodium during stimulation, astrocyte uptake of potassium, sodium, and chloride in passive channels, action of the Na/K/ATPase pump, and osmotically driven transport of water through the astrocyte membrane together seem sufficient for generating ECS shrinkage as such. However, when taking into account ECS and astrocyte ion concentrations observed in connection with neuronal stimulation, the actions of the Na(+)/K(+)/Cl(−) (NKCC1) and the Na(+)/HCO(3) (−) (NBC) cotransporters appear to be critical determinants for achieving observed quantitative levels of ECS shrinkage. Considering the current state of knowledge, the model framework appears sufficiently detailed and constrained to guide future key experiments and pave the way for more comprehensive astroglia–neuron interaction models for normal as well as pathophysiological situations. Public Library of Science 2009-01-23 /pmc/articles/PMC2613522/ /pubmed/19165313 http://dx.doi.org/10.1371/journal.pcbi.1000272 Text en Østby 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 Østby, Ivar Øyehaug, Leiv Einevoll, Gaute T. Nagelhus, Erlend A. Plahte, Erik Zeuthen, Thomas Lloyd, Catherine M. Ottersen, Ole P. Omholt, Stig W. Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space |
title | Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space |
title_full | Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space |
title_fullStr | Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space |
title_full_unstemmed | Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space |
title_short | Astrocytic Mechanisms Explaining Neural-Activity-Induced Shrinkage of Extraneuronal Space |
title_sort | astrocytic mechanisms explaining neural-activity-induced shrinkage of extraneuronal space |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2613522/ https://www.ncbi.nlm.nih.gov/pubmed/19165313 http://dx.doi.org/10.1371/journal.pcbi.1000272 |
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