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The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices
The general anesthetic propofol has been in clinical use for more than 30 years and has become the agent of choice for rapid intravenous induction. While its hypnotic and anti-convulsant properties are well known, the propensity for propofol to promote seizure activity is less well characterised. El...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690829/ https://www.ncbi.nlm.nih.gov/pubmed/26722636 http://dx.doi.org/10.1186/s40064-015-1623-1 |
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author | Voss, Logan J. Andersson, Liisa Jadelind, Anna |
author_facet | Voss, Logan J. Andersson, Liisa Jadelind, Anna |
author_sort | Voss, Logan J. |
collection | PubMed |
description | The general anesthetic propofol has been in clinical use for more than 30 years and has become the agent of choice for rapid intravenous induction. While its hypnotic and anti-convulsant properties are well known, the propensity for propofol to promote seizure activity is less well characterised. Electroencephalogram-confirmed reports of propofol-induced seizure activity implicate a predisposition in epileptic subjects. The aim of this study was to investigate the seizure-promoting action of propofol in mouse brain slices—with the goal of establishing an in vitro model of propofol pro-convulsant action for future mechanistic studies. Coronal slices were exposed to either normal artificial cerebrospinal fluid (aCSF) or no-magnesium (no-Mg) aCSF—and extracellular field potential recordings made from the hippocampus, entorhinal cortex and neocortex. Propofol (and etomidate for comparison) were delivered at three stepwise concentrations corresponding to clinically relevant levels. The main finding was that propofol induced ictal-like seizures in seven out of ten hippocampal recordings (p = 0.004 compared to controls) following pre-exposure to no-Mg aCSF—but strongly inhibited seizure-like event (SLE) activity in the neocortex. Propofol did not induce seizure activity in slices exposed to normal aCSF. The results support the contention that propofol has the capacity to promote seizure activity, particularly when there is an underlying seizure predisposition. This study establishes an in vitro model for exploring the mechanisms by which propofol promotes subcortical seizure activity. |
format | Online Article Text |
id | pubmed-4690829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-46908292015-12-31 The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices Voss, Logan J. Andersson, Liisa Jadelind, Anna Springerplus Research The general anesthetic propofol has been in clinical use for more than 30 years and has become the agent of choice for rapid intravenous induction. While its hypnotic and anti-convulsant properties are well known, the propensity for propofol to promote seizure activity is less well characterised. Electroencephalogram-confirmed reports of propofol-induced seizure activity implicate a predisposition in epileptic subjects. The aim of this study was to investigate the seizure-promoting action of propofol in mouse brain slices—with the goal of establishing an in vitro model of propofol pro-convulsant action for future mechanistic studies. Coronal slices were exposed to either normal artificial cerebrospinal fluid (aCSF) or no-magnesium (no-Mg) aCSF—and extracellular field potential recordings made from the hippocampus, entorhinal cortex and neocortex. Propofol (and etomidate for comparison) were delivered at three stepwise concentrations corresponding to clinically relevant levels. The main finding was that propofol induced ictal-like seizures in seven out of ten hippocampal recordings (p = 0.004 compared to controls) following pre-exposure to no-Mg aCSF—but strongly inhibited seizure-like event (SLE) activity in the neocortex. Propofol did not induce seizure activity in slices exposed to normal aCSF. The results support the contention that propofol has the capacity to promote seizure activity, particularly when there is an underlying seizure predisposition. This study establishes an in vitro model for exploring the mechanisms by which propofol promotes subcortical seizure activity. Springer International Publishing 2015-12-24 /pmc/articles/PMC4690829/ /pubmed/26722636 http://dx.doi.org/10.1186/s40064-015-1623-1 Text en © Voss et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Voss, Logan J. Andersson, Liisa Jadelind, Anna The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices |
title | The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices |
title_full | The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices |
title_fullStr | The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices |
title_full_unstemmed | The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices |
title_short | The general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices |
title_sort | general anesthetic propofol induces ictal-like seizure activity in hippocampal mouse brain slices |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690829/ https://www.ncbi.nlm.nih.gov/pubmed/26722636 http://dx.doi.org/10.1186/s40064-015-1623-1 |
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