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Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium
Rapid increases in cell volume reduce the size of the extracellular space (ECS) and are associated with elevated brain tissue excitability. We recently demonstrated that astrocytes, but not neurons, rapidly swell in elevated extracellular potassium ((∧)[K(+)](o)) up to 26 mM. However, effects of acu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352931/ https://www.ncbi.nlm.nih.gov/pubmed/35936495 http://dx.doi.org/10.3389/fncel.2022.930384 |
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author | Walch, Erin Bilas, Alexander Bebawy, Valine Lam, Angelina Murphy, Thomas R. Sriram, Sandhya Fiacco, Todd A. |
author_facet | Walch, Erin Bilas, Alexander Bebawy, Valine Lam, Angelina Murphy, Thomas R. Sriram, Sandhya Fiacco, Todd A. |
author_sort | Walch, Erin |
collection | PubMed |
description | Rapid increases in cell volume reduce the size of the extracellular space (ECS) and are associated with elevated brain tissue excitability. We recently demonstrated that astrocytes, but not neurons, rapidly swell in elevated extracellular potassium ((∧)[K(+)](o)) up to 26 mM. However, effects of acute astrocyte volume fluctuations on neuronal excitability in (∧)[K(+)](o) have been difficult to evaluate due to direct effects on neuronal membrane potential and generation of action potentials. Here we set out to isolate volume-specific effects occurring in (∧)[K(+)](o) on CA1 pyramidal neurons in acute hippocampal slices by manipulating cell volume while recording neuronal glutamate currents in 10.5 mM [K(+)](o) + tetrodotoxin (TTX) to prevent neuronal firing. Elevating [K(+)](o) to 10.5 mM induced astrocyte swelling and produced significant increases in neuronal excitability in the form of mixed α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)/N-methyl-D-aspartate (NMDA) receptor mEPSCs and NMDA receptor-dependent slow inward currents (SICs). Application of hyperosmolar artificial cerebrospinal fluid (ACSF) by addition of mannitol in the continued presence of 10.5 mM K(+) forced shrinking of astrocytes and to a lesser extent neurons, which resisted swelling in (∧)[K(+)](o). Cell shrinking and dilation of the ECS significantly dampened neuronal excitability in 10.5 mM K(+). Subsequent removal of mannitol amplified effects on neuronal excitability and nearly doubled the volume increase in astrocytes, presumably due to continued glial uptake of K(+) while mannitol was present. Slower, larger amplitude events mainly driven by NMDA receptors were abolished by mannitol-induced expansion of the ECS. Collectively, our findings suggest that cell volume regulation of the ECS in elevated [K(+)](o) is driven predominantly by astrocytes, and that cell volume effects on neuronal excitability can be effectively isolated in elevated [K(+)](o) conditions. |
format | Online Article Text |
id | pubmed-9352931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93529312022-08-06 Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium Walch, Erin Bilas, Alexander Bebawy, Valine Lam, Angelina Murphy, Thomas R. Sriram, Sandhya Fiacco, Todd A. Front Cell Neurosci Neuroscience Rapid increases in cell volume reduce the size of the extracellular space (ECS) and are associated with elevated brain tissue excitability. We recently demonstrated that astrocytes, but not neurons, rapidly swell in elevated extracellular potassium ((∧)[K(+)](o)) up to 26 mM. However, effects of acute astrocyte volume fluctuations on neuronal excitability in (∧)[K(+)](o) have been difficult to evaluate due to direct effects on neuronal membrane potential and generation of action potentials. Here we set out to isolate volume-specific effects occurring in (∧)[K(+)](o) on CA1 pyramidal neurons in acute hippocampal slices by manipulating cell volume while recording neuronal glutamate currents in 10.5 mM [K(+)](o) + tetrodotoxin (TTX) to prevent neuronal firing. Elevating [K(+)](o) to 10.5 mM induced astrocyte swelling and produced significant increases in neuronal excitability in the form of mixed α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)/N-methyl-D-aspartate (NMDA) receptor mEPSCs and NMDA receptor-dependent slow inward currents (SICs). Application of hyperosmolar artificial cerebrospinal fluid (ACSF) by addition of mannitol in the continued presence of 10.5 mM K(+) forced shrinking of astrocytes and to a lesser extent neurons, which resisted swelling in (∧)[K(+)](o). Cell shrinking and dilation of the ECS significantly dampened neuronal excitability in 10.5 mM K(+). Subsequent removal of mannitol amplified effects on neuronal excitability and nearly doubled the volume increase in astrocytes, presumably due to continued glial uptake of K(+) while mannitol was present. Slower, larger amplitude events mainly driven by NMDA receptors were abolished by mannitol-induced expansion of the ECS. Collectively, our findings suggest that cell volume regulation of the ECS in elevated [K(+)](o) is driven predominantly by astrocytes, and that cell volume effects on neuronal excitability can be effectively isolated in elevated [K(+)](o) conditions. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9352931/ /pubmed/35936495 http://dx.doi.org/10.3389/fncel.2022.930384 Text en Copyright © 2022 Walch, Bilas, Bebawy, Lam, Murphy, Sriram and Fiacco. https://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 Walch, Erin Bilas, Alexander Bebawy, Valine Lam, Angelina Murphy, Thomas R. Sriram, Sandhya Fiacco, Todd A. Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium |
title | Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium |
title_full | Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium |
title_fullStr | Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium |
title_full_unstemmed | Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium |
title_short | Contributions of Astrocyte and Neuronal Volume to CA1 Neuron Excitability Changes in Elevated Extracellular Potassium |
title_sort | contributions of astrocyte and neuronal volume to ca1 neuron excitability changes in elevated extracellular potassium |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352931/ https://www.ncbi.nlm.nih.gov/pubmed/35936495 http://dx.doi.org/10.3389/fncel.2022.930384 |
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