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The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons
BACKGROUND: Cochlear implant-based electrical stimulation may be an important reason to induce the residual hearing loss after cochlear implantation. In our previous study, we found that charge-balanced biphasic electrical stimulation inhibited the neurite growth of spiral ganglion neurons (SGNs) an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490630/ https://www.ncbi.nlm.nih.gov/pubmed/32963515 http://dx.doi.org/10.1155/2020/3108490 |
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author | Shen, Na Zhou, Lei Lai, Bin Li, Shufeng |
author_facet | Shen, Na Zhou, Lei Lai, Bin Li, Shufeng |
author_sort | Shen, Na |
collection | PubMed |
description | BACKGROUND: Cochlear implant-based electrical stimulation may be an important reason to induce the residual hearing loss after cochlear implantation. In our previous study, we found that charge-balanced biphasic electrical stimulation inhibited the neurite growth of spiral ganglion neurons (SGNs) and decreased Schwann cell density in vitro. In this study, we want to know whether cochlear implant-based electrical stimulation can induce the change of electrical activity in cultured SGNs. METHODS: Spiral ganglion neuron electrical stimulation in vitro model is established using the devices delivering cochlear implant-based electrical stimulation. After 48 h treatment by 50 μA or 100 μA electrical stimulation, the action potential (AP) and voltage depended calcium current (I(Ca)) of SGNs are recorded using whole-cell electrophysiological method. RESULTS: The results show that the I(Ca) of SGNs is decreased significantly in 50 μA and 100 μA electrical stimulation groups. The reversal potential of I(Ca) is nearly +80 mV in control SGN, but the reversal potential decreases to +50 mV in 50 μA and 100 μA electrical stimulation groups. Interestingly, the AP amplitude, the AP latency, and the AP duration of SGNs have no statistically significant differences in all three groups. CONCLUSION: Our study suggests cochlear implant-based electrical stimulation only significantly inhibit the I(Ca) of cultured SGNs but has no effect on the firing of AP, and the relation of I(Ca) inhibition and SGN damage induced by electrical stimulation and its mechanism needs to be further studied. |
format | Online Article Text |
id | pubmed-7490630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-74906302020-09-21 The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons Shen, Na Zhou, Lei Lai, Bin Li, Shufeng Neural Plast Research Article BACKGROUND: Cochlear implant-based electrical stimulation may be an important reason to induce the residual hearing loss after cochlear implantation. In our previous study, we found that charge-balanced biphasic electrical stimulation inhibited the neurite growth of spiral ganglion neurons (SGNs) and decreased Schwann cell density in vitro. In this study, we want to know whether cochlear implant-based electrical stimulation can induce the change of electrical activity in cultured SGNs. METHODS: Spiral ganglion neuron electrical stimulation in vitro model is established using the devices delivering cochlear implant-based electrical stimulation. After 48 h treatment by 50 μA or 100 μA electrical stimulation, the action potential (AP) and voltage depended calcium current (I(Ca)) of SGNs are recorded using whole-cell electrophysiological method. RESULTS: The results show that the I(Ca) of SGNs is decreased significantly in 50 μA and 100 μA electrical stimulation groups. The reversal potential of I(Ca) is nearly +80 mV in control SGN, but the reversal potential decreases to +50 mV in 50 μA and 100 μA electrical stimulation groups. Interestingly, the AP amplitude, the AP latency, and the AP duration of SGNs have no statistically significant differences in all three groups. CONCLUSION: Our study suggests cochlear implant-based electrical stimulation only significantly inhibit the I(Ca) of cultured SGNs but has no effect on the firing of AP, and the relation of I(Ca) inhibition and SGN damage induced by electrical stimulation and its mechanism needs to be further studied. Hindawi 2020-09-06 /pmc/articles/PMC7490630/ /pubmed/32963515 http://dx.doi.org/10.1155/2020/3108490 Text en Copyright © 2020 Na Shen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Shen, Na Zhou, Lei Lai, Bin Li, Shufeng The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons |
title | The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons |
title_full | The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons |
title_fullStr | The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons |
title_full_unstemmed | The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons |
title_short | The Influence of Cochlear Implant-Based Electric Stimulation on the Electrophysiological Characteristics of Cultured Spiral Ganglion Neurons |
title_sort | influence of cochlear implant-based electric stimulation on the electrophysiological characteristics of cultured spiral ganglion neurons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490630/ https://www.ncbi.nlm.nih.gov/pubmed/32963515 http://dx.doi.org/10.1155/2020/3108490 |
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