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Quantitative investigation into methods for evaluating neocortical slice viability

BACKGROUND: In cortical and hippocampal brain slice experiments, the viability of processed tissue is usually judged by the amplitude of extracellularly-recorded seizure-like event (SLE) activity. Surprisingly, the suitability of this approach for evaluating slice quality has not been objectively st...

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Autores principales: Voss, Logan J, van Kan, Claudia, Sleigh, James W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228277/
https://www.ncbi.nlm.nih.gov/pubmed/24195598
http://dx.doi.org/10.1186/1471-2202-14-137
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author Voss, Logan J
van Kan, Claudia
Sleigh, James W
author_facet Voss, Logan J
van Kan, Claudia
Sleigh, James W
author_sort Voss, Logan J
collection PubMed
description BACKGROUND: In cortical and hippocampal brain slice experiments, the viability of processed tissue is usually judged by the amplitude of extracellularly-recorded seizure-like event (SLE) activity. Surprisingly, the suitability of this approach for evaluating slice quality has not been objectively studied. Furthermore, a method for gauging the viability of quiescent tissue, in which SLE activity is intentionally suppressed, has not been documented. In this study we undertook to address both of these matters using the zero-magnesium SLE model in neocortical slices. METHODS: Using zero-magnesium SLE activity as the output parameter, we investigated: 1) changes in the pattern (amplitude, frequency and length) of SLE activity as slice health either deteriorated; or was compromised by altering the preparation methodology and; 2) in quiescent tissue, whether the triggering of high frequency field activity following electrode insertion predicted subsequent development of SLE activity — and hence slice viability. RESULTS: SLE amplitude was the single most important variable correlating with slice viability, with a value less than 50 μV indicative of tissue unlikely to be able to sustain population activity for more than 30–60 minutes. In quiescent slices, an increase in high frequency field activity immediately after electrode insertion predicted the development of SLE activity in 100% of cases. Furthermore, the magnitude of the increase in spectral power correlated with the amplitude of succeeding SLE activity (R(2) 40.9%, p < 0.0001). CONCLUSION: In conclusion, the findings confirm that the amplitude of population activity is a suitable field potential parameter for judging brain slice viability — and can be applied independent of the mechanism of tissue activation.
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spelling pubmed-42282772014-11-13 Quantitative investigation into methods for evaluating neocortical slice viability Voss, Logan J van Kan, Claudia Sleigh, James W BMC Neurosci Methodology Article BACKGROUND: In cortical and hippocampal brain slice experiments, the viability of processed tissue is usually judged by the amplitude of extracellularly-recorded seizure-like event (SLE) activity. Surprisingly, the suitability of this approach for evaluating slice quality has not been objectively studied. Furthermore, a method for gauging the viability of quiescent tissue, in which SLE activity is intentionally suppressed, has not been documented. In this study we undertook to address both of these matters using the zero-magnesium SLE model in neocortical slices. METHODS: Using zero-magnesium SLE activity as the output parameter, we investigated: 1) changes in the pattern (amplitude, frequency and length) of SLE activity as slice health either deteriorated; or was compromised by altering the preparation methodology and; 2) in quiescent tissue, whether the triggering of high frequency field activity following electrode insertion predicted subsequent development of SLE activity — and hence slice viability. RESULTS: SLE amplitude was the single most important variable correlating with slice viability, with a value less than 50 μV indicative of tissue unlikely to be able to sustain population activity for more than 30–60 minutes. In quiescent slices, an increase in high frequency field activity immediately after electrode insertion predicted the development of SLE activity in 100% of cases. Furthermore, the magnitude of the increase in spectral power correlated with the amplitude of succeeding SLE activity (R(2) 40.9%, p < 0.0001). CONCLUSION: In conclusion, the findings confirm that the amplitude of population activity is a suitable field potential parameter for judging brain slice viability — and can be applied independent of the mechanism of tissue activation. BioMed Central 2013-11-06 /pmc/articles/PMC4228277/ /pubmed/24195598 http://dx.doi.org/10.1186/1471-2202-14-137 Text en Copyright © 2013 Voss et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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 Methodology Article
Voss, Logan J
van Kan, Claudia
Sleigh, James W
Quantitative investigation into methods for evaluating neocortical slice viability
title Quantitative investigation into methods for evaluating neocortical slice viability
title_full Quantitative investigation into methods for evaluating neocortical slice viability
title_fullStr Quantitative investigation into methods for evaluating neocortical slice viability
title_full_unstemmed Quantitative investigation into methods for evaluating neocortical slice viability
title_short Quantitative investigation into methods for evaluating neocortical slice viability
title_sort quantitative investigation into methods for evaluating neocortical slice viability
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228277/
https://www.ncbi.nlm.nih.gov/pubmed/24195598
http://dx.doi.org/10.1186/1471-2202-14-137
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