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New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents
In neuroscience, single-shank penetrating multi-electrode arrays are standard for sequentially sampling several cortical sites with high spatial and temporal resolution, with the disadvantage of neuronal damage. Non-penetrating surface grids used in electrocorticography (ECoG) permit simultaneous re...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830616/ https://www.ncbi.nlm.nih.gov/pubmed/29491453 http://dx.doi.org/10.1038/s41598-018-22051-z |
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author | Konerding, W. S. Froriep, U. P. Kral, A. Baumhoff, P. |
author_facet | Konerding, W. S. Froriep, U. P. Kral, A. Baumhoff, P. |
author_sort | Konerding, W. S. |
collection | PubMed |
description | In neuroscience, single-shank penetrating multi-electrode arrays are standard for sequentially sampling several cortical sites with high spatial and temporal resolution, with the disadvantage of neuronal damage. Non-penetrating surface grids used in electrocorticography (ECoG) permit simultaneous recording of multiple cortical sites, with limited spatial resolution, due to distance to neuronal tissue, large contact size and high impedances. Here we compared new thin-film parylene C ECoG grids, covering the guinea pig primary auditory cortex, with simultaneous recordings from penetrating electrode array (PEAs), inserted through openings in the grid material. ECoG grid local field potentials (LFP) showed higher response thresholds and amplitudes compared to PEAs. They enabled, however, fast and reliable tonotopic mapping of the auditory cortex (place-frequency slope: 0.7 mm/octave), with tuning widths similar to PEAs. The ECoG signal correlated best with supragranular layers, exponentially decreasing with cortical depth. The grids also enabled recording of multi-unit activity (MUA), yielding several advantages over LFP recordings, including sharper frequency tunings. ECoG first spike latency showed highest similarity to superficial PEA contacts and MUA traces maximally correlated with PEA recordings from the granular layer. These results confirm high quality of the ECoG grid recordings and the possibility to collect LFP and MUA simultaneously. |
format | Online Article Text |
id | pubmed-5830616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58306162018-03-05 New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents Konerding, W. S. Froriep, U. P. Kral, A. Baumhoff, P. Sci Rep Article In neuroscience, single-shank penetrating multi-electrode arrays are standard for sequentially sampling several cortical sites with high spatial and temporal resolution, with the disadvantage of neuronal damage. Non-penetrating surface grids used in electrocorticography (ECoG) permit simultaneous recording of multiple cortical sites, with limited spatial resolution, due to distance to neuronal tissue, large contact size and high impedances. Here we compared new thin-film parylene C ECoG grids, covering the guinea pig primary auditory cortex, with simultaneous recordings from penetrating electrode array (PEAs), inserted through openings in the grid material. ECoG grid local field potentials (LFP) showed higher response thresholds and amplitudes compared to PEAs. They enabled, however, fast and reliable tonotopic mapping of the auditory cortex (place-frequency slope: 0.7 mm/octave), with tuning widths similar to PEAs. The ECoG signal correlated best with supragranular layers, exponentially decreasing with cortical depth. The grids also enabled recording of multi-unit activity (MUA), yielding several advantages over LFP recordings, including sharper frequency tunings. ECoG first spike latency showed highest similarity to superficial PEA contacts and MUA traces maximally correlated with PEA recordings from the granular layer. These results confirm high quality of the ECoG grid recordings and the possibility to collect LFP and MUA simultaneously. Nature Publishing Group UK 2018-02-28 /pmc/articles/PMC5830616/ /pubmed/29491453 http://dx.doi.org/10.1038/s41598-018-22051-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Konerding, W. S. Froriep, U. P. Kral, A. Baumhoff, P. New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents |
title | New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents |
title_full | New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents |
title_fullStr | New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents |
title_full_unstemmed | New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents |
title_short | New thin-film surface electrode array enables brain mapping with high spatial acuity in rodents |
title_sort | new thin-film surface electrode array enables brain mapping with high spatial acuity in rodents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830616/ https://www.ncbi.nlm.nih.gov/pubmed/29491453 http://dx.doi.org/10.1038/s41598-018-22051-z |
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