Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Voss, Logan J., Harvey, Martyn G., Sleigh, James W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
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
_version_ 1782442126538178560
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
work_keys_str_mv AT vossloganj inhibitionofastrocytemetabolismisnottheprimarymechanismforanaesthetichypnosis
AT harveymartyng inhibitionofastrocytemetabolismisnottheprimarymechanismforanaesthetichypnosis
AT sleighjamesw inhibitionofastrocytemetabolismisnottheprimarymechanismforanaesthetichypnosis