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Argon neuroprotection

Certain noble gases, though inert, exhibit remarkable biological properties. Notably, xenon and argon provide neuroprotection in animal models of central nervous system injury. In the previous issue of Critical Care, Loetscher and colleagues provided further evidence that argon may have therapeutic...

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Detalles Bibliográficos
Autores principales: Sanders, Robert D, Ma, Daqing, Maze, Mervyn
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875517/
https://www.ncbi.nlm.nih.gov/pubmed/20236500
http://dx.doi.org/10.1186/cc8847
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author Sanders, Robert D
Ma, Daqing
Maze, Mervyn
author_facet Sanders, Robert D
Ma, Daqing
Maze, Mervyn
author_sort Sanders, Robert D
collection PubMed
description Certain noble gases, though inert, exhibit remarkable biological properties. Notably, xenon and argon provide neuroprotection in animal models of central nervous system injury. In the previous issue of Critical Care, Loetscher and colleagues provided further evidence that argon may have therapeutic properties for neuronal toxicity by demonstrating protection against both traumatic and oxygen-glucose deprivation injury of organotypic hippocampal cultures in vitro. Their data are of interest as argon is more abundant, and therefore cheaper, than xenon (the latter of which is currently in clinical trials for perinatal hypoxic-ischemic brain injury; TOBYXe; NCT00934700). We eagerly await in vivo data to complement the promising in vitro data hailing argon neuroprotection.
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spelling pubmed-28755172011-02-22 Argon neuroprotection Sanders, Robert D Ma, Daqing Maze, Mervyn Crit Care Commentary Certain noble gases, though inert, exhibit remarkable biological properties. Notably, xenon and argon provide neuroprotection in animal models of central nervous system injury. In the previous issue of Critical Care, Loetscher and colleagues provided further evidence that argon may have therapeutic properties for neuronal toxicity by demonstrating protection against both traumatic and oxygen-glucose deprivation injury of organotypic hippocampal cultures in vitro. Their data are of interest as argon is more abundant, and therefore cheaper, than xenon (the latter of which is currently in clinical trials for perinatal hypoxic-ischemic brain injury; TOBYXe; NCT00934700). We eagerly await in vivo data to complement the promising in vitro data hailing argon neuroprotection. BioMed Central 2010 2010-02-22 /pmc/articles/PMC2875517/ /pubmed/20236500 http://dx.doi.org/10.1186/cc8847 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Commentary
Sanders, Robert D
Ma, Daqing
Maze, Mervyn
Argon neuroprotection
title Argon neuroprotection
title_full Argon neuroprotection
title_fullStr Argon neuroprotection
title_full_unstemmed Argon neuroprotection
title_short Argon neuroprotection
title_sort argon neuroprotection
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875517/
https://www.ncbi.nlm.nih.gov/pubmed/20236500
http://dx.doi.org/10.1186/cc8847
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