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Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue

Hypoxic-ischaemic brain injury is a major cause of morbidity and mortality internationally. Using an in vitro isolated cortex model, this study investigated the optimal cerebrospinal fluid oxygenation parameters for rescuing metabolically challenged cortical tissue. In particular, we asked whether m...

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Autores principales: Voss, Logan J., Whittle, Nicola, Lamber, Oliver, Envall, Gustav, Sleigh, Jamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670121/
https://www.ncbi.nlm.nih.gov/pubmed/33235940
http://dx.doi.org/10.1016/j.ibror.2020.10.007
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author Voss, Logan J.
Whittle, Nicola
Lamber, Oliver
Envall, Gustav
Sleigh, Jamie
author_facet Voss, Logan J.
Whittle, Nicola
Lamber, Oliver
Envall, Gustav
Sleigh, Jamie
author_sort Voss, Logan J.
collection PubMed
description Hypoxic-ischaemic brain injury is a major cause of morbidity and mortality internationally. Using an in vitro isolated cortex model, this study investigated the optimal cerebrospinal fluid oxygenation parameters for rescuing metabolically challenged cortical tissue. In particular, we asked whether maximizing oxygen content with oxygen nanobubbles could support improved tissue recovery. Mouse cortical slices were metabolically starved, followed by recovery in artificial cerebrospinal fluid (aCSF) containing different levels of dissolved oxygen ranging from mean(SD) 2(0.5) to 39(1.0) mg/L; with and without oxygen nanobubbles. Tissue recovery was assessed by quantifying and comparing the amplitude, length, high frequency content and event frequency of seizure-like events generated in no-magnesium aCSF at the beginning and end of the protocol. In general, there was improved recovery with increasing oxygen content up to 25–34 mg/L. The outcome of slices recovered in nanobubbled aCSF was no different to conventionally oxygenated slices with similar dissolved oxygen content. Dissolved oxygen content above 34 mg/L afforded no additional benefit. In conclusion, aCSF dissolved oxygen content of approximately 30 mg/L is optimal for cortical tissue recovery from metabolic starvation, which is easily achievable using conventional oxygenation methods. Oxygen in the form of nanobubbles does not appear to be readily available for tissue oxidative processes in this model.
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spelling pubmed-76701212020-11-23 Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue Voss, Logan J. Whittle, Nicola Lamber, Oliver Envall, Gustav Sleigh, Jamie IBRO Rep Research Paper Hypoxic-ischaemic brain injury is a major cause of morbidity and mortality internationally. Using an in vitro isolated cortex model, this study investigated the optimal cerebrospinal fluid oxygenation parameters for rescuing metabolically challenged cortical tissue. In particular, we asked whether maximizing oxygen content with oxygen nanobubbles could support improved tissue recovery. Mouse cortical slices were metabolically starved, followed by recovery in artificial cerebrospinal fluid (aCSF) containing different levels of dissolved oxygen ranging from mean(SD) 2(0.5) to 39(1.0) mg/L; with and without oxygen nanobubbles. Tissue recovery was assessed by quantifying and comparing the amplitude, length, high frequency content and event frequency of seizure-like events generated in no-magnesium aCSF at the beginning and end of the protocol. In general, there was improved recovery with increasing oxygen content up to 25–34 mg/L. The outcome of slices recovered in nanobubbled aCSF was no different to conventionally oxygenated slices with similar dissolved oxygen content. Dissolved oxygen content above 34 mg/L afforded no additional benefit. In conclusion, aCSF dissolved oxygen content of approximately 30 mg/L is optimal for cortical tissue recovery from metabolic starvation, which is easily achievable using conventional oxygenation methods. Oxygen in the form of nanobubbles does not appear to be readily available for tissue oxidative processes in this model. Elsevier 2020-11-04 /pmc/articles/PMC7670121/ /pubmed/33235940 http://dx.doi.org/10.1016/j.ibror.2020.10.007 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Voss, Logan J.
Whittle, Nicola
Lamber, Oliver
Envall, Gustav
Sleigh, Jamie
Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue
title Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue
title_full Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue
title_fullStr Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue
title_full_unstemmed Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue
title_short Cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue
title_sort cerebrospinal fluid oxygen optimisation for rescue of metabolically challenged in vitro cortical brain tissue
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670121/
https://www.ncbi.nlm.nih.gov/pubmed/33235940
http://dx.doi.org/10.1016/j.ibror.2020.10.007
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