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Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats

BACKGROUND: Xenon (Xe) is a noble gas that has been used for the last several decades as an anesthetic during surgery. Its antagonistic effect on glutamate subtype of NMDA (N-methyl-d-aspartate) receptors resulted in evaluation of this gas for treatment of CNS pathologies, including psychoemotional...

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Autores principales: Dobrovolsky, A. P., Gedzun, V. R., Bogin, V. I., Ma, D., Ichim, T. E., Sukhanova, Iu. A., Malyshev, A. V., Dubynin, V. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891980/
https://www.ncbi.nlm.nih.gov/pubmed/31796043
http://dx.doi.org/10.1186/s12967-019-02161-6
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author Dobrovolsky, A. P.
Gedzun, V. R.
Bogin, V. I.
Ma, D.
Ichim, T. E.
Sukhanova, Iu. A.
Malyshev, A. V.
Dubynin, V. A.
author_facet Dobrovolsky, A. P.
Gedzun, V. R.
Bogin, V. I.
Ma, D.
Ichim, T. E.
Sukhanova, Iu. A.
Malyshev, A. V.
Dubynin, V. A.
author_sort Dobrovolsky, A. P.
collection PubMed
description BACKGROUND: Xenon (Xe) is a noble gas that has been used for the last several decades as an anesthetic during surgery. Its antagonistic effect on glutamate subtype of NMDA (N-methyl-d-aspartate) receptors resulted in evaluation of this gas for treatment of CNS pathologies, including psychoemotional disorders. The aim of this study was to assess the behavioral effects of acute inhalation of subanesthetic concentrations of Xe and to study the outcomes of Xe exposure in valproic acid (VPA)-induced rodent model of autism. METHODS: We have conducted two series of experiments with a battery of behavioral tests aimed to evaluate locomotion, anxiety- and depression-like behavior, and social behavior in healthy, VPA-treated and Xe-exposed young rats. RESULTS: We have shown that in healthy animals Xe exposure resulted in acute and delayed decrease of exploratory motivation, partial decrease in risk-taking and depressive-like behavior as well as improved sensorimotor integration during the negative geotaxis test. Acute inhalations of Xe in VPA-exposed animals led to improvement in social behavior, decrease in exploratory motivation, and normalization of behavior in forced-swim test. CONCLUSION: Behavioral modulatory effects of Xe are probably related to its generalized action on excitatory/inhibitory balance within the CNS. Our data suggest that subanesthetic short-term exposures to Xe have beneficial effect on several behavioral modalities and deserves further investigation.
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spelling pubmed-68919802019-12-11 Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats Dobrovolsky, A. P. Gedzun, V. R. Bogin, V. I. Ma, D. Ichim, T. E. Sukhanova, Iu. A. Malyshev, A. V. Dubynin, V. A. J Transl Med Research BACKGROUND: Xenon (Xe) is a noble gas that has been used for the last several decades as an anesthetic during surgery. Its antagonistic effect on glutamate subtype of NMDA (N-methyl-d-aspartate) receptors resulted in evaluation of this gas for treatment of CNS pathologies, including psychoemotional disorders. The aim of this study was to assess the behavioral effects of acute inhalation of subanesthetic concentrations of Xe and to study the outcomes of Xe exposure in valproic acid (VPA)-induced rodent model of autism. METHODS: We have conducted two series of experiments with a battery of behavioral tests aimed to evaluate locomotion, anxiety- and depression-like behavior, and social behavior in healthy, VPA-treated and Xe-exposed young rats. RESULTS: We have shown that in healthy animals Xe exposure resulted in acute and delayed decrease of exploratory motivation, partial decrease in risk-taking and depressive-like behavior as well as improved sensorimotor integration during the negative geotaxis test. Acute inhalations of Xe in VPA-exposed animals led to improvement in social behavior, decrease in exploratory motivation, and normalization of behavior in forced-swim test. CONCLUSION: Behavioral modulatory effects of Xe are probably related to its generalized action on excitatory/inhibitory balance within the CNS. Our data suggest that subanesthetic short-term exposures to Xe have beneficial effect on several behavioral modalities and deserves further investigation. BioMed Central 2019-12-03 /pmc/articles/PMC6891980/ /pubmed/31796043 http://dx.doi.org/10.1186/s12967-019-02161-6 Text en © The Author(s) 2019 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dobrovolsky, A. P.
Gedzun, V. R.
Bogin, V. I.
Ma, D.
Ichim, T. E.
Sukhanova, Iu. A.
Malyshev, A. V.
Dubynin, V. A.
Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats
title Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats
title_full Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats
title_fullStr Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats
title_full_unstemmed Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats
title_short Beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats
title_sort beneficial effects of xenon inhalation on behavioral changes in a valproic acid-induced model of autism in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891980/
https://www.ncbi.nlm.nih.gov/pubmed/31796043
http://dx.doi.org/10.1186/s12967-019-02161-6
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