Cargando…

Isoflurane anesthesia disrupts the cortical metabolome

Identifying similarities and differences in the brain metabolome during different states of consciousness has broad relevance for neuroscience and state-dependent autonomic function. This study focused on the prefrontal cortex (PFC) as a brain region known to modulate states of consciousness. Anesth...

Descripción completa

Detalles Bibliográficos
Autores principales: Baer, Aaron G., Bourdon, Allen K., Price, Joshua M., Campagna, Shawn R., Jacobson, Daniel A., Baghdoyan, Helen A., Lydic, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814899/
https://www.ncbi.nlm.nih.gov/pubmed/33112692
http://dx.doi.org/10.1152/jn.00375.2020
_version_ 1783638135429660672
author Baer, Aaron G.
Bourdon, Allen K.
Price, Joshua M.
Campagna, Shawn R.
Jacobson, Daniel A.
Baghdoyan, Helen A.
Lydic, Ralph
author_facet Baer, Aaron G.
Bourdon, Allen K.
Price, Joshua M.
Campagna, Shawn R.
Jacobson, Daniel A.
Baghdoyan, Helen A.
Lydic, Ralph
author_sort Baer, Aaron G.
collection PubMed
description Identifying similarities and differences in the brain metabolome during different states of consciousness has broad relevance for neuroscience and state-dependent autonomic function. This study focused on the prefrontal cortex (PFC) as a brain region known to modulate states of consciousness. Anesthesia was used as a tool to eliminate wakefulness. Untargeted metabolomic analyses were performed on microdialysis samples obtained from mouse PFC during wakefulness and during isoflurane anesthesia. Analyses detected 2,153 molecules, 91 of which could be identified. Analytes were grouped as detected during both wakefulness and anesthesia (n = 61) and as unique to wakefulness (n = 23) or anesthesia (n = 7). Data were analyzed using univariate and multivariate approaches. Relative to wakefulness, during anesthesia there was a significant (q < 0.0001) fourfold change in 21 metabolites. During anesthesia 11 of these 21 molecules decreased and 10 increased. The Kyoto Encyclopedia of Genes and Genomes database was used to relate behavioral state-specific changes in the metabolome to metabolic pathways. Relative to wakefulness, most of the amino acids and analogs measured were significantly decreased during isoflurane anesthesia. Nucleosides and analogs were significantly increased during anesthesia. Molecules associated with carbohydrate metabolism, maintenance of lipid membranes, and normal cell functions were significantly decreased during anesthesia. Significant state-specific changes were also discovered among molecules comprising lipids and fatty acids, monosaccharides, and organic acids. Considered together, these molecules regulate point-to-point transmission, volume conduction, and cellular metabolism. The results identify a novel ensemble of candidate molecules in PFC as putative modulators of wakefulness and the loss of wakefulness. NEW & NOTEWORTHY The loss of wakefulness caused by a single concentration of isoflurane significantly altered levels of interrelated metabolites in the prefrontal cortex. The results support the interpretation that states of consciousness reflect dynamic interactions among cortical neuronal networks involving a humbling number of molecules that comprise the brain metabolome.
format Online
Article
Text
id pubmed-7814899
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Physiological Society
record_format MEDLINE/PubMed
spelling pubmed-78148992021-01-29 Isoflurane anesthesia disrupts the cortical metabolome Baer, Aaron G. Bourdon, Allen K. Price, Joshua M. Campagna, Shawn R. Jacobson, Daniel A. Baghdoyan, Helen A. Lydic, Ralph J Neurophysiol Research Article Identifying similarities and differences in the brain metabolome during different states of consciousness has broad relevance for neuroscience and state-dependent autonomic function. This study focused on the prefrontal cortex (PFC) as a brain region known to modulate states of consciousness. Anesthesia was used as a tool to eliminate wakefulness. Untargeted metabolomic analyses were performed on microdialysis samples obtained from mouse PFC during wakefulness and during isoflurane anesthesia. Analyses detected 2,153 molecules, 91 of which could be identified. Analytes were grouped as detected during both wakefulness and anesthesia (n = 61) and as unique to wakefulness (n = 23) or anesthesia (n = 7). Data were analyzed using univariate and multivariate approaches. Relative to wakefulness, during anesthesia there was a significant (q < 0.0001) fourfold change in 21 metabolites. During anesthesia 11 of these 21 molecules decreased and 10 increased. The Kyoto Encyclopedia of Genes and Genomes database was used to relate behavioral state-specific changes in the metabolome to metabolic pathways. Relative to wakefulness, most of the amino acids and analogs measured were significantly decreased during isoflurane anesthesia. Nucleosides and analogs were significantly increased during anesthesia. Molecules associated with carbohydrate metabolism, maintenance of lipid membranes, and normal cell functions were significantly decreased during anesthesia. Significant state-specific changes were also discovered among molecules comprising lipids and fatty acids, monosaccharides, and organic acids. Considered together, these molecules regulate point-to-point transmission, volume conduction, and cellular metabolism. The results identify a novel ensemble of candidate molecules in PFC as putative modulators of wakefulness and the loss of wakefulness. NEW & NOTEWORTHY The loss of wakefulness caused by a single concentration of isoflurane significantly altered levels of interrelated metabolites in the prefrontal cortex. The results support the interpretation that states of consciousness reflect dynamic interactions among cortical neuronal networks involving a humbling number of molecules that comprise the brain metabolome. American Physiological Society 2020-12-01 2020-10-28 /pmc/articles/PMC7814899/ /pubmed/33112692 http://dx.doi.org/10.1152/jn.00375.2020 Text en Copyright © 2020 the Authors http://creativecommons.org/licenses/by/4.0 Licensed under Creative Commons Attribution CC-BY 4.0. Published by the American Physiological Society.
spellingShingle Research Article
Baer, Aaron G.
Bourdon, Allen K.
Price, Joshua M.
Campagna, Shawn R.
Jacobson, Daniel A.
Baghdoyan, Helen A.
Lydic, Ralph
Isoflurane anesthesia disrupts the cortical metabolome
title Isoflurane anesthesia disrupts the cortical metabolome
title_full Isoflurane anesthesia disrupts the cortical metabolome
title_fullStr Isoflurane anesthesia disrupts the cortical metabolome
title_full_unstemmed Isoflurane anesthesia disrupts the cortical metabolome
title_short Isoflurane anesthesia disrupts the cortical metabolome
title_sort isoflurane anesthesia disrupts the cortical metabolome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814899/
https://www.ncbi.nlm.nih.gov/pubmed/33112692
http://dx.doi.org/10.1152/jn.00375.2020
work_keys_str_mv AT baeraarong isofluraneanesthesiadisruptsthecorticalmetabolome
AT bourdonallenk isofluraneanesthesiadisruptsthecorticalmetabolome
AT pricejoshuam isofluraneanesthesiadisruptsthecorticalmetabolome
AT campagnashawnr isofluraneanesthesiadisruptsthecorticalmetabolome
AT jacobsondaniela isofluraneanesthesiadisruptsthecorticalmetabolome
AT baghdoyanhelena isofluraneanesthesiadisruptsthecorticalmetabolome
AT lydicralph isofluraneanesthesiadisruptsthecorticalmetabolome