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Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice
Translational comparison of rodent models of neurological and neuropsychiatric diseases to human electroencephalography (EEG) biomarkers in these conditions will require multisite rodent EEG on the skull surface, rather than local area electrocorticography (ECoG) or multisite local field potential (...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213968/ https://www.ncbi.nlm.nih.gov/pubmed/30416434 http://dx.doi.org/10.3389/fnint.2018.00053 |
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author | Jonak, Carrie R. Lovelace, Jonathan W. Ethell, Iryna M. Razak, Khaleel A. Binder, Devin K. |
author_facet | Jonak, Carrie R. Lovelace, Jonathan W. Ethell, Iryna M. Razak, Khaleel A. Binder, Devin K. |
author_sort | Jonak, Carrie R. |
collection | PubMed |
description | Translational comparison of rodent models of neurological and neuropsychiatric diseases to human electroencephalography (EEG) biomarkers in these conditions will require multisite rodent EEG on the skull surface, rather than local area electrocorticography (ECoG) or multisite local field potential (LFP) recording. We have developed a technique for planar multielectrode array (MEA) implantation on the mouse skull surface, which enables multisite EEG in awake and freely moving mice and reusability of the MEA probes. With this method, we reliably obtain 30-channel low-noise EEG from awake mice. Baseline and stimulus-evoked EEG recordings can be readily obtained and analyzed. For example, we have demonstrated EEG responses to auditory stimuli. Broadband noise elicits reliable 30-channel auditory event-related potentials (ERPs), and chirp stimuli induce phase-locked EEG responses just as in human sound presentation paradigms. This method is unique in achieving chronic implantation of novel MEA technology onto the mouse skull surface for chronic multisite EEG recordings. Furthermore, we demonstrate a reliable method for reusing MEA probes for multiple serial implantations without loss of EEG quality. This skull surface MEA methodology can be used to obtain simultaneous multisite EEG recordings and to test EEG biomarkers in diverse mouse models of human neurological and neuropsychiatric diseases. Reusability of the MEA probes makes it more cost-effective to deploy this system for various studies. |
format | Online Article Text |
id | pubmed-6213968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62139682018-11-09 Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice Jonak, Carrie R. Lovelace, Jonathan W. Ethell, Iryna M. Razak, Khaleel A. Binder, Devin K. Front Integr Neurosci Neuroscience Translational comparison of rodent models of neurological and neuropsychiatric diseases to human electroencephalography (EEG) biomarkers in these conditions will require multisite rodent EEG on the skull surface, rather than local area electrocorticography (ECoG) or multisite local field potential (LFP) recording. We have developed a technique for planar multielectrode array (MEA) implantation on the mouse skull surface, which enables multisite EEG in awake and freely moving mice and reusability of the MEA probes. With this method, we reliably obtain 30-channel low-noise EEG from awake mice. Baseline and stimulus-evoked EEG recordings can be readily obtained and analyzed. For example, we have demonstrated EEG responses to auditory stimuli. Broadband noise elicits reliable 30-channel auditory event-related potentials (ERPs), and chirp stimuli induce phase-locked EEG responses just as in human sound presentation paradigms. This method is unique in achieving chronic implantation of novel MEA technology onto the mouse skull surface for chronic multisite EEG recordings. Furthermore, we demonstrate a reliable method for reusing MEA probes for multiple serial implantations without loss of EEG quality. This skull surface MEA methodology can be used to obtain simultaneous multisite EEG recordings and to test EEG biomarkers in diverse mouse models of human neurological and neuropsychiatric diseases. Reusability of the MEA probes makes it more cost-effective to deploy this system for various studies. Frontiers Media S.A. 2018-10-26 /pmc/articles/PMC6213968/ /pubmed/30416434 http://dx.doi.org/10.3389/fnint.2018.00053 Text en Copyright © 2018 Jonak, Lovelace, Ethell, Razak and Binder. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Jonak, Carrie R. Lovelace, Jonathan W. Ethell, Iryna M. Razak, Khaleel A. Binder, Devin K. Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice |
title | Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice |
title_full | Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice |
title_fullStr | Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice |
title_full_unstemmed | Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice |
title_short | Reusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice |
title_sort | reusable multielectrode array technique for electroencephalography in awake freely moving mice |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6213968/ https://www.ncbi.nlm.nih.gov/pubmed/30416434 http://dx.doi.org/10.3389/fnint.2018.00053 |
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