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A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia
OBJECTIVE: Birth asphyxia (BA) is often associated with seizures that may exacerbate the ensuing hypoxic–ischemic encephalopathy. In rodent models of BA, exposure to hypoxia is used to evoke seizures, that commence already during the insult. This is in stark contrast to clinical BA, in which seizure...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246723/ https://www.ncbi.nlm.nih.gov/pubmed/33338272 http://dx.doi.org/10.1111/epi.16790 |
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author | Ala‐Kurikka, Tommi Pospelov, Alexey Summanen, Milla Alafuzoff, Aleksander Kurki, Samu Voipio, Juha Kaila, Kai |
author_facet | Ala‐Kurikka, Tommi Pospelov, Alexey Summanen, Milla Alafuzoff, Aleksander Kurki, Samu Voipio, Juha Kaila, Kai |
author_sort | Ala‐Kurikka, Tommi |
collection | PubMed |
description | OBJECTIVE: Birth asphyxia (BA) is often associated with seizures that may exacerbate the ensuing hypoxic–ischemic encephalopathy. In rodent models of BA, exposure to hypoxia is used to evoke seizures, that commence already during the insult. This is in stark contrast to clinical BA, in which seizures are typically seen upon recovery. Here, we introduce a term‐equivalent rat model of BA, in which seizures are triggered after exposure to asphyxia. METHODS: Postnatal day 11–12 male rat pups were exposed to steady asphyxia (15 min; air containing 5% O(2) + 20% CO(2)) or to intermittent asphyxia (30 min; three 5 + 5‐min cycles of 9% and 5% O(2) at 20% CO(2)). Cortical activity and electrographic seizures were recorded in freely behaving animals. Simultaneous electrode measurements of intracortical pH, Po(2), and local field potentials (LFPs) were made under urethane anesthesia. RESULTS: Both protocols decreased blood pH to <7.0 and brain pH from 7.3 to 6.7 and led to a fall in base excess by 20 mmol·L(–1). Electrographic seizures with convulsions spanning the entire Racine scale were triggered after intermittent but not steady asphyxia. In the presence of 20% CO(2), brain Po(2) was only transiently affected by 9% ambient O(2) but fell below detection level during the steps to 5% O(2), and LFP activity was nearly abolished. Post‐asphyxia seizures were strongly suppressed when brain pH recovery was slowed down by 5% CO(2). SIGNIFICANCE: The rate of brain pH recovery has a strong influence on post‐asphyxia seizure propensity. The recurring hypoxic episodes during intermittent asphyxia promote neuronal excitability, which leads to seizures only after the suppressing effect of the hypercapnic acidosis is relieved. The present rodent model of BA is to our best knowledge the first one in which, consistent with clinical BA, behavioral and electrographic seizures are triggered after and not during the BA‐mimicking insult. |
format | Online Article Text |
id | pubmed-8246723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82467232021-07-02 A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia Ala‐Kurikka, Tommi Pospelov, Alexey Summanen, Milla Alafuzoff, Aleksander Kurki, Samu Voipio, Juha Kaila, Kai Epilepsia Full‐length Original Research OBJECTIVE: Birth asphyxia (BA) is often associated with seizures that may exacerbate the ensuing hypoxic–ischemic encephalopathy. In rodent models of BA, exposure to hypoxia is used to evoke seizures, that commence already during the insult. This is in stark contrast to clinical BA, in which seizures are typically seen upon recovery. Here, we introduce a term‐equivalent rat model of BA, in which seizures are triggered after exposure to asphyxia. METHODS: Postnatal day 11–12 male rat pups were exposed to steady asphyxia (15 min; air containing 5% O(2) + 20% CO(2)) or to intermittent asphyxia (30 min; three 5 + 5‐min cycles of 9% and 5% O(2) at 20% CO(2)). Cortical activity and electrographic seizures were recorded in freely behaving animals. Simultaneous electrode measurements of intracortical pH, Po(2), and local field potentials (LFPs) were made under urethane anesthesia. RESULTS: Both protocols decreased blood pH to <7.0 and brain pH from 7.3 to 6.7 and led to a fall in base excess by 20 mmol·L(–1). Electrographic seizures with convulsions spanning the entire Racine scale were triggered after intermittent but not steady asphyxia. In the presence of 20% CO(2), brain Po(2) was only transiently affected by 9% ambient O(2) but fell below detection level during the steps to 5% O(2), and LFP activity was nearly abolished. Post‐asphyxia seizures were strongly suppressed when brain pH recovery was slowed down by 5% CO(2). SIGNIFICANCE: The rate of brain pH recovery has a strong influence on post‐asphyxia seizure propensity. The recurring hypoxic episodes during intermittent asphyxia promote neuronal excitability, which leads to seizures only after the suppressing effect of the hypercapnic acidosis is relieved. The present rodent model of BA is to our best knowledge the first one in which, consistent with clinical BA, behavioral and electrographic seizures are triggered after and not during the BA‐mimicking insult. John Wiley and Sons Inc. 2020-12-18 2021-04 /pmc/articles/PMC8246723/ /pubmed/33338272 http://dx.doi.org/10.1111/epi.16790 Text en © 2020 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full‐length Original Research Ala‐Kurikka, Tommi Pospelov, Alexey Summanen, Milla Alafuzoff, Aleksander Kurki, Samu Voipio, Juha Kaila, Kai A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia |
title | A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia |
title_full | A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia |
title_fullStr | A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia |
title_full_unstemmed | A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia |
title_short | A physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia |
title_sort | physiologically validated rat model of term birth asphyxia with seizure generation after, not during, brain hypoxia |
topic | Full‐length Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246723/ https://www.ncbi.nlm.nih.gov/pubmed/33338272 http://dx.doi.org/10.1111/epi.16790 |
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