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Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis
Astrocytes have been promoted as a possible mechanistic target for anaesthetic hypnosis. The aim of this study was to explore this using the neocortical brain slice preparation. The methods were in two parts. Firstly, multiple general anaesthetic compounds demonstrating varying in vivo hypnotic pote...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940352/ https://www.ncbi.nlm.nih.gov/pubmed/27462489 http://dx.doi.org/10.1186/s40064-016-2734-z |
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author | Voss, Logan J. Harvey, Martyn G. Sleigh, James W. |
author_facet | Voss, Logan J. Harvey, Martyn G. Sleigh, James W. |
author_sort | Voss, Logan J. |
collection | PubMed |
description | Astrocytes have been promoted as a possible mechanistic target for anaesthetic hypnosis. The aim of this study was to explore this using the neocortical brain slice preparation. The methods were in two parts. Firstly, multiple general anaesthetic compounds demonstrating varying in vivo hypnotic potency were analysed for their effect on “zero-magnesium” seizure-like event (SLE) activity in mouse neocortical slices. Subsequently, the effect of astrocyte metabolic inhibition was investigated in neocortical slices, and compared with that of the anaesthetic drugs. The rationale was that, if suppression of astrocytes was both necessary and sufficient to cause hypnosis in vivo, then inhibition of astrocytic metabolism in slices should mimic the anaesthetic effect. In vivo anaesthetic potency correlated strongly with the magnitude of reduction in SLE frequency in neocortical slices (R(2) 37.7 %, p = 0.002). Conversely, SLE frequency and length were significantly enhanced during exposure to both fluoroacetate (23 and 20 % increase, respectively, p < 0.01) and aminoadipate (12 and 38 % increase, respectively, p < 0.01 and p < 0.05). The capacity of an anaesthetic agent to reduce SLE frequency in the neocortical slice is a good indicator of its in vivo hypnotic potency. The results do not support the hypothesis that astrocytic metabolic inhibition is a mechanism of anaesthetic hypnosis. |
format | Online Article Text |
id | pubmed-4940352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49403522016-07-26 Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis Voss, Logan J. Harvey, Martyn G. Sleigh, James W. Springerplus Research Astrocytes have been promoted as a possible mechanistic target for anaesthetic hypnosis. The aim of this study was to explore this using the neocortical brain slice preparation. The methods were in two parts. Firstly, multiple general anaesthetic compounds demonstrating varying in vivo hypnotic potency were analysed for their effect on “zero-magnesium” seizure-like event (SLE) activity in mouse neocortical slices. Subsequently, the effect of astrocyte metabolic inhibition was investigated in neocortical slices, and compared with that of the anaesthetic drugs. The rationale was that, if suppression of astrocytes was both necessary and sufficient to cause hypnosis in vivo, then inhibition of astrocytic metabolism in slices should mimic the anaesthetic effect. In vivo anaesthetic potency correlated strongly with the magnitude of reduction in SLE frequency in neocortical slices (R(2) 37.7 %, p = 0.002). Conversely, SLE frequency and length were significantly enhanced during exposure to both fluoroacetate (23 and 20 % increase, respectively, p < 0.01) and aminoadipate (12 and 38 % increase, respectively, p < 0.01 and p < 0.05). The capacity of an anaesthetic agent to reduce SLE frequency in the neocortical slice is a good indicator of its in vivo hypnotic potency. The results do not support the hypothesis that astrocytic metabolic inhibition is a mechanism of anaesthetic hypnosis. Springer International Publishing 2016-07-11 /pmc/articles/PMC4940352/ /pubmed/27462489 http://dx.doi.org/10.1186/s40064-016-2734-z Text en © The Author(s) 2016 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. Harvey, Martyn G. Sleigh, James W. Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis |
title | Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis |
title_full | Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis |
title_fullStr | Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis |
title_full_unstemmed | Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis |
title_short | Inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis |
title_sort | inhibition of astrocyte metabolism is not the primary mechanism for anaesthetic hypnosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4940352/ https://www.ncbi.nlm.nih.gov/pubmed/27462489 http://dx.doi.org/10.1186/s40064-016-2734-z |
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