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A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish

Along with the increasing popularity of larval zebrafish as an experimental animal in the fields of drug screening, neuroscience, genetics, and developmental biology, the need for tools to deal with multiple larvae has emerged. Microfluidic channels have been employed to handle multiple larvae simul...

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Autores principales: Lee, Yuhyun, Seo, Hee Won, Lee, Kyeong Jae, Jang, Jae-Won, Kim, Sohee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590171/
https://www.ncbi.nlm.nih.gov/pubmed/33086704
http://dx.doi.org/10.3390/s20205903
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author Lee, Yuhyun
Seo, Hee Won
Lee, Kyeong Jae
Jang, Jae-Won
Kim, Sohee
author_facet Lee, Yuhyun
Seo, Hee Won
Lee, Kyeong Jae
Jang, Jae-Won
Kim, Sohee
author_sort Lee, Yuhyun
collection PubMed
description Along with the increasing popularity of larval zebrafish as an experimental animal in the fields of drug screening, neuroscience, genetics, and developmental biology, the need for tools to deal with multiple larvae has emerged. Microfluidic channels have been employed to handle multiple larvae simultaneously, even for sensing electroencephalogram (EEG). In this study, we developed a microfluidic chip capable of uniform and continuous drug infusion across all microfluidic channels during EEG recording. Owing to the modular design of the microfluidic channels, the number of animals under investigation can be easily increased. Using the optimized design of the microfluidic chip, liquids could be exchanged uniformly across all channels without physically affecting the larvae contained in the channels, which assured a stable environment maintained all the time during EEG recording, by eliminating environmental artifacts and leaving only biological effects to be seen. To demonstrate the usefulness of the developed system in drug screening, we continuously measured EEG from four larvae without and with pentylenetetrazole application, up to 60 min. In addition, we recorded EEG from valproic acid (VPA)-treated zebrafish and demonstrated the suppression of seizure by VPA. The developed microfluidic system could contribute to the mass screening of EEG for drug development to treat neurological disorders such as epilepsy in a short time, owing to its handy size, cheap fabrication cost, and the guaranteed uniform drug infusion across all channels with no environmentally induced artifacts.
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spelling pubmed-75901712020-10-29 A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish Lee, Yuhyun Seo, Hee Won Lee, Kyeong Jae Jang, Jae-Won Kim, Sohee Sensors (Basel) Article Along with the increasing popularity of larval zebrafish as an experimental animal in the fields of drug screening, neuroscience, genetics, and developmental biology, the need for tools to deal with multiple larvae has emerged. Microfluidic channels have been employed to handle multiple larvae simultaneously, even for sensing electroencephalogram (EEG). In this study, we developed a microfluidic chip capable of uniform and continuous drug infusion across all microfluidic channels during EEG recording. Owing to the modular design of the microfluidic channels, the number of animals under investigation can be easily increased. Using the optimized design of the microfluidic chip, liquids could be exchanged uniformly across all channels without physically affecting the larvae contained in the channels, which assured a stable environment maintained all the time during EEG recording, by eliminating environmental artifacts and leaving only biological effects to be seen. To demonstrate the usefulness of the developed system in drug screening, we continuously measured EEG from four larvae without and with pentylenetetrazole application, up to 60 min. In addition, we recorded EEG from valproic acid (VPA)-treated zebrafish and demonstrated the suppression of seizure by VPA. The developed microfluidic system could contribute to the mass screening of EEG for drug development to treat neurological disorders such as epilepsy in a short time, owing to its handy size, cheap fabrication cost, and the guaranteed uniform drug infusion across all channels with no environmentally induced artifacts. MDPI 2020-10-19 /pmc/articles/PMC7590171/ /pubmed/33086704 http://dx.doi.org/10.3390/s20205903 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Yuhyun
Seo, Hee Won
Lee, Kyeong Jae
Jang, Jae-Won
Kim, Sohee
A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish
title A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish
title_full A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish
title_fullStr A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish
title_full_unstemmed A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish
title_short A Microfluidic System for Stable and Continuous EEG Monitoring from Multiple Larval Zebrafish
title_sort microfluidic system for stable and continuous eeg monitoring from multiple larval zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590171/
https://www.ncbi.nlm.nih.gov/pubmed/33086704
http://dx.doi.org/10.3390/s20205903
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