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Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro

Cerebral edema is a major, life threatening complication of ischemic brain damage. Previous studies using brain slices have revealed that cellular swelling and a concomitant increase in tissue transparency starts within minutes of the onset of metabolic insult in association with collective anoxic s...

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Autores principales: Juzekaeva, Elvira, Gainutdinov, Azat, Mukhtarov, Marat, Khazipov, Roustem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305551/
https://www.ncbi.nlm.nih.gov/pubmed/30618644
http://dx.doi.org/10.3389/fncel.2018.00502
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author Juzekaeva, Elvira
Gainutdinov, Azat
Mukhtarov, Marat
Khazipov, Roustem
author_facet Juzekaeva, Elvira
Gainutdinov, Azat
Mukhtarov, Marat
Khazipov, Roustem
author_sort Juzekaeva, Elvira
collection PubMed
description Cerebral edema is a major, life threatening complication of ischemic brain damage. Previous studies using brain slices have revealed that cellular swelling and a concomitant increase in tissue transparency starts within minutes of the onset of metabolic insult in association with collective anoxic spreading depolarization (aSD). However, the dynamics of tissue swelling in brain slices under ischemia-like conditions remain elusive. Here, we explored the dynamics of brain tissue swelling induced by oxygen-glucose deprivation (OGD) in submerged rat barrel cortex slices. Video monitoring of the vertical and horizontal position of fluorescent dye-filled neurons and contrast slice surface imaging revealed elevation of the slice surface and a horizontal displacement of the cortical tissue during OGD. The OGD-induced tissue movement was also associated with an expansion of the slice borders. Tissue swelling started several minutes after aSD and continued during reperfusion with normal solution. Thirty minutes after aSD, slice borders had expanded by ~130 μm and the slice surface had moved up to attain a height of ~70 μm above control levels, which corresponded to a volume increase of ~30%. Hyperosmotic sucrose solution partially reduced the OGD-induced slice swelling. Thus, OGD-induced cortical slice tissue swelling in brain slices in vitro recapitulates many features of ischemic cerebral edema in vivo, its onset is tightly linked to aSD and it develops at a relatively slow pace after aSD. We propose that this model of cerebral edema in vitro could be useful for the exploration of the pathophysiological mechanisms underlying ischemic cerebral edema and in the search for an efficient treatment to this devastating condition.
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spelling pubmed-63055512019-01-07 Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro Juzekaeva, Elvira Gainutdinov, Azat Mukhtarov, Marat Khazipov, Roustem Front Cell Neurosci Neuroscience Cerebral edema is a major, life threatening complication of ischemic brain damage. Previous studies using brain slices have revealed that cellular swelling and a concomitant increase in tissue transparency starts within minutes of the onset of metabolic insult in association with collective anoxic spreading depolarization (aSD). However, the dynamics of tissue swelling in brain slices under ischemia-like conditions remain elusive. Here, we explored the dynamics of brain tissue swelling induced by oxygen-glucose deprivation (OGD) in submerged rat barrel cortex slices. Video monitoring of the vertical and horizontal position of fluorescent dye-filled neurons and contrast slice surface imaging revealed elevation of the slice surface and a horizontal displacement of the cortical tissue during OGD. The OGD-induced tissue movement was also associated with an expansion of the slice borders. Tissue swelling started several minutes after aSD and continued during reperfusion with normal solution. Thirty minutes after aSD, slice borders had expanded by ~130 μm and the slice surface had moved up to attain a height of ~70 μm above control levels, which corresponded to a volume increase of ~30%. Hyperosmotic sucrose solution partially reduced the OGD-induced slice swelling. Thus, OGD-induced cortical slice tissue swelling in brain slices in vitro recapitulates many features of ischemic cerebral edema in vivo, its onset is tightly linked to aSD and it develops at a relatively slow pace after aSD. We propose that this model of cerebral edema in vitro could be useful for the exploration of the pathophysiological mechanisms underlying ischemic cerebral edema and in the search for an efficient treatment to this devastating condition. Frontiers Media S.A. 2018-12-18 /pmc/articles/PMC6305551/ /pubmed/30618644 http://dx.doi.org/10.3389/fncel.2018.00502 Text en Copyright © 2018 Juzekaeva, Gainutdinov, Mukhtarov and Khazipov. 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
Juzekaeva, Elvira
Gainutdinov, Azat
Mukhtarov, Marat
Khazipov, Roustem
Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro
title Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro
title_full Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro
title_fullStr Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro
title_full_unstemmed Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro
title_short Dynamics of the Hypoxia—Induced Tissue Edema in the Rat Barrel Cortex in vitro
title_sort dynamics of the hypoxia—induced tissue edema in the rat barrel cortex in vitro
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305551/
https://www.ncbi.nlm.nih.gov/pubmed/30618644
http://dx.doi.org/10.3389/fncel.2018.00502
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