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Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy

Electrical stimulation is one of the candidates for elongation-driven regeneration of damaged peripheral nerves. Different organs and tissues have an inherent cell structure and size. This leads to variation in the tissue-specific electrical properties of the frequency of interfacial polarization. A...

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Autores principales: Otagiri, Risa, Kawai, Hideki, Takatsuka, Masanobu, Shinyashiki, Naoki, Ito, Akira, Ikeguchi, Ryosuke, Aoyama, Tomoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8171940/
https://www.ncbi.nlm.nih.gov/pubmed/34077459
http://dx.doi.org/10.1371/journal.pone.0252589
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author Otagiri, Risa
Kawai, Hideki
Takatsuka, Masanobu
Shinyashiki, Naoki
Ito, Akira
Ikeguchi, Ryosuke
Aoyama, Tomoki
author_facet Otagiri, Risa
Kawai, Hideki
Takatsuka, Masanobu
Shinyashiki, Naoki
Ito, Akira
Ikeguchi, Ryosuke
Aoyama, Tomoki
author_sort Otagiri, Risa
collection PubMed
description Electrical stimulation is one of the candidates for elongation-driven regeneration of damaged peripheral nerves. Different organs and tissues have an inherent cell structure and size. This leads to variation in the tissue-specific electrical properties of the frequency of interfacial polarization. Although nervous tissues have a membrane potential, the electrical reaction inside these tissues following electrical stimulation from outside remains unexplored. Furthermore, the pathophysiological reaction of an injured nerve is unclear. Here, we investigated the electrical reaction of injured and non-injured rat sciatic nerves via broadband dielectric spectroscopy. Crush injured and non-injured sciatic nerves of six 12-week-old male Lewis rats were used, 6 days after infliction of the injury. Both sides of the nerves (with and without injury) were exposed, and impedance measurements were performed at room temperature (approximately 25°C) at frequencies ranging from 100 mHz to 5.5 MHz and electric potential ranging from 0.100 to 1.00 V. The measured interfacial polarization potentially originated from the polarization by ion transport around nerve membranes at frequencies between 3.2 kHz and 1.6 MHz. The polarization strength of the injured nerves was smaller than that of non-injured nerves. However, the difference in polarization between injured and non-injured nerves might be caused by inflammation and edema. The suitable frequency range of the interfacial polarization can be expected to be critical for electrical stimulation of injured peripheral nerves.
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spelling pubmed-81719402021-06-14 Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy Otagiri, Risa Kawai, Hideki Takatsuka, Masanobu Shinyashiki, Naoki Ito, Akira Ikeguchi, Ryosuke Aoyama, Tomoki PLoS One Research Article Electrical stimulation is one of the candidates for elongation-driven regeneration of damaged peripheral nerves. Different organs and tissues have an inherent cell structure and size. This leads to variation in the tissue-specific electrical properties of the frequency of interfacial polarization. Although nervous tissues have a membrane potential, the electrical reaction inside these tissues following electrical stimulation from outside remains unexplored. Furthermore, the pathophysiological reaction of an injured nerve is unclear. Here, we investigated the electrical reaction of injured and non-injured rat sciatic nerves via broadband dielectric spectroscopy. Crush injured and non-injured sciatic nerves of six 12-week-old male Lewis rats were used, 6 days after infliction of the injury. Both sides of the nerves (with and without injury) were exposed, and impedance measurements were performed at room temperature (approximately 25°C) at frequencies ranging from 100 mHz to 5.5 MHz and electric potential ranging from 0.100 to 1.00 V. The measured interfacial polarization potentially originated from the polarization by ion transport around nerve membranes at frequencies between 3.2 kHz and 1.6 MHz. The polarization strength of the injured nerves was smaller than that of non-injured nerves. However, the difference in polarization between injured and non-injured nerves might be caused by inflammation and edema. The suitable frequency range of the interfacial polarization can be expected to be critical for electrical stimulation of injured peripheral nerves. Public Library of Science 2021-06-02 /pmc/articles/PMC8171940/ /pubmed/34077459 http://dx.doi.org/10.1371/journal.pone.0252589 Text en © 2021 Otagiri et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Otagiri, Risa
Kawai, Hideki
Takatsuka, Masanobu
Shinyashiki, Naoki
Ito, Akira
Ikeguchi, Ryosuke
Aoyama, Tomoki
Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy
title Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy
title_full Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy
title_fullStr Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy
title_full_unstemmed Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy
title_short Interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy
title_sort interfacial polarization of in vivo rat sciatic nerve with crush injury studied via broadband dielectric spectroscopy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8171940/
https://www.ncbi.nlm.nih.gov/pubmed/34077459
http://dx.doi.org/10.1371/journal.pone.0252589
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