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Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method

This protocol is a practical guide to the N-methyl-D-glucamine (NMDG) protective recovery method of brain slice preparation. Numerous recent studies have validated the utility of this method for enhancing neuronal preservation and overall brain slice viability. The implementation of this technique b...

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Autores principales: Ting, Jonathan T., Lee, Brian R., Chong, Peter, Soler-Llavina, Gilberto, Cobbs, Charles, Koch, Christof, Zeng, Hongkui, Lein, Ed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931343/
https://www.ncbi.nlm.nih.gov/pubmed/29553547
http://dx.doi.org/10.3791/53825
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author Ting, Jonathan T.
Lee, Brian R.
Chong, Peter
Soler-Llavina, Gilberto
Cobbs, Charles
Koch, Christof
Zeng, Hongkui
Lein, Ed
author_facet Ting, Jonathan T.
Lee, Brian R.
Chong, Peter
Soler-Llavina, Gilberto
Cobbs, Charles
Koch, Christof
Zeng, Hongkui
Lein, Ed
author_sort Ting, Jonathan T.
collection PubMed
description This protocol is a practical guide to the N-methyl-D-glucamine (NMDG) protective recovery method of brain slice preparation. Numerous recent studies have validated the utility of this method for enhancing neuronal preservation and overall brain slice viability. The implementation of this technique by early adopters has facilitated detailed investigations into brain function using diverse experimental applications and spanning a wide range of animal ages, brain regions, and cell types. Steps are outlined for carrying out the protective recovery brain slice technique using an optimized NMDG artificial cerebrospinal fluid (aCSF) media formulation and enhanced procedure to reliably obtain healthy brain slices for patch clamp electrophysiology. With this updated approach, a substantial improvement is observed in the speed and reliability of gigaohm seal formation during targeted patch clamp recording experiments while maintaining excellent neuronal preservation, thereby facilitating challenging experimental applications. Representative results are provided from multi-neuron patch clamp recording experiments to assay synaptic connectivity in neocortical brain slices prepared from young adult transgenic mice and mature adult human neurosurgical specimens. Furthermore, the optimized NMDG protective recovery method of brain slicing is compatible with both juvenile and adult animals, thus resolving a limitation of the original methodology. In summary, a single media formulation and brain slicing procedure can be implemented across various species and ages to achieve excellent viability and tissue preservation.
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spelling pubmed-59313432018-05-16 Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method Ting, Jonathan T. Lee, Brian R. Chong, Peter Soler-Llavina, Gilberto Cobbs, Charles Koch, Christof Zeng, Hongkui Lein, Ed J Vis Exp Neuroscience This protocol is a practical guide to the N-methyl-D-glucamine (NMDG) protective recovery method of brain slice preparation. Numerous recent studies have validated the utility of this method for enhancing neuronal preservation and overall brain slice viability. The implementation of this technique by early adopters has facilitated detailed investigations into brain function using diverse experimental applications and spanning a wide range of animal ages, brain regions, and cell types. Steps are outlined for carrying out the protective recovery brain slice technique using an optimized NMDG artificial cerebrospinal fluid (aCSF) media formulation and enhanced procedure to reliably obtain healthy brain slices for patch clamp electrophysiology. With this updated approach, a substantial improvement is observed in the speed and reliability of gigaohm seal formation during targeted patch clamp recording experiments while maintaining excellent neuronal preservation, thereby facilitating challenging experimental applications. Representative results are provided from multi-neuron patch clamp recording experiments to assay synaptic connectivity in neocortical brain slices prepared from young adult transgenic mice and mature adult human neurosurgical specimens. Furthermore, the optimized NMDG protective recovery method of brain slicing is compatible with both juvenile and adult animals, thus resolving a limitation of the original methodology. In summary, a single media formulation and brain slicing procedure can be implemented across various species and ages to achieve excellent viability and tissue preservation. MyJove Corporation 2018-02-26 /pmc/articles/PMC5931343/ /pubmed/29553547 http://dx.doi.org/10.3791/53825 Text en Copyright © 2018, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Neuroscience
Ting, Jonathan T.
Lee, Brian R.
Chong, Peter
Soler-Llavina, Gilberto
Cobbs, Charles
Koch, Christof
Zeng, Hongkui
Lein, Ed
Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method
title Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method
title_full Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method
title_fullStr Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method
title_full_unstemmed Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method
title_short Preparation of Acute Brain Slices Using an Optimized N-Methyl-D-glucamine Protective Recovery Method
title_sort preparation of acute brain slices using an optimized n-methyl-d-glucamine protective recovery method
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931343/
https://www.ncbi.nlm.nih.gov/pubmed/29553547
http://dx.doi.org/10.3791/53825
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