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Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices
Evaluating redox homeostasis involves gauging the levels of reactive oxygen species (ROS) and reactive nitrogen species (RNS) directly in tissues and cells. The brain is especially metabolically active and is particularly vulnerable to excessive ROS and RNS. Here, we describe a methodology to quanti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868599/ https://www.ncbi.nlm.nih.gov/pubmed/33598661 http://dx.doi.org/10.1016/j.xpro.2021.100332 |
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author | Vasavda, Chirag Snyder, Solomon H. Paul, Bindu D. |
author_facet | Vasavda, Chirag Snyder, Solomon H. Paul, Bindu D. |
author_sort | Vasavda, Chirag |
collection | PubMed |
description | Evaluating redox homeostasis involves gauging the levels of reactive oxygen species (ROS) and reactive nitrogen species (RNS) directly in tissues and cells. The brain is especially metabolically active and is particularly vulnerable to excessive ROS and RNS. Here, we describe a methodology to quantitatively measure ROS in ex vivo mouse brain slices at baseline and after neural stimulation. Evaluating ROS in slices provides a more complete picture of neural redox signaling than when measured in isolated neurons or astrocytes. For complete details on the use and execution of this protocol, please refer to Vasavda et al. (2019). |
format | Online Article Text |
id | pubmed-7868599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78685992021-02-16 Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices Vasavda, Chirag Snyder, Solomon H. Paul, Bindu D. STAR Protoc Protocol Evaluating redox homeostasis involves gauging the levels of reactive oxygen species (ROS) and reactive nitrogen species (RNS) directly in tissues and cells. The brain is especially metabolically active and is particularly vulnerable to excessive ROS and RNS. Here, we describe a methodology to quantitatively measure ROS in ex vivo mouse brain slices at baseline and after neural stimulation. Evaluating ROS in slices provides a more complete picture of neural redox signaling than when measured in isolated neurons or astrocytes. For complete details on the use and execution of this protocol, please refer to Vasavda et al. (2019). Elsevier 2021-02-05 /pmc/articles/PMC7868599/ /pubmed/33598661 http://dx.doi.org/10.1016/j.xpro.2021.100332 Text en © 2021 The Author(s) 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 | Protocol Vasavda, Chirag Snyder, Solomon H. Paul, Bindu D. Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices |
title | Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices |
title_full | Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices |
title_fullStr | Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices |
title_full_unstemmed | Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices |
title_short | Quantitative measurement of reactive oxygen species in ex vivo mouse brain slices |
title_sort | quantitative measurement of reactive oxygen species in ex vivo mouse brain slices |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868599/ https://www.ncbi.nlm.nih.gov/pubmed/33598661 http://dx.doi.org/10.1016/j.xpro.2021.100332 |
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