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Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery

Recent studies have shown that ionic direct current (iDC) can modulate the vestibular system in-vivo, with potential benefits over conventional pulsed stimulation. In this study, the effects of iDC stimulation on vestibular nerve fiber firing rate was investigated using loose-patch nerve fiber recor...

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Autores principales: Manca, Marco, Glowatzki, Elisabeth, Roberts, Dale C., Fridman, Gene Y., Aplin, Felix P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908704/
https://www.ncbi.nlm.nih.gov/pubmed/31831760
http://dx.doi.org/10.1038/s41598-019-55045-6
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author Manca, Marco
Glowatzki, Elisabeth
Roberts, Dale C.
Fridman, Gene Y.
Aplin, Felix P.
author_facet Manca, Marco
Glowatzki, Elisabeth
Roberts, Dale C.
Fridman, Gene Y.
Aplin, Felix P.
author_sort Manca, Marco
collection PubMed
description Recent studies have shown that ionic direct current (iDC) can modulate the vestibular system in-vivo, with potential benefits over conventional pulsed stimulation. In this study, the effects of iDC stimulation on vestibular nerve fiber firing rate was investigated using loose-patch nerve fiber recordings in the acutely excised mouse crista ampullaris of the semicircular canals. Cathodic and anodic iDC steps instantaneously reduced and increased afferent spike rate, with the polarity of this effect dependent on the position of the stimulating electrode. A sustained constant anodic or cathodic current resulted in an adaptation to the stimulus and a return to spontaneous spike rate. Post-adaptation spike rate responses to iDC steps were similar to pre-adaptation controls. At high intensities spike rate response sensitivities were modified by the presence of an adaptation step. Benefits previously observed in behavioral responses to iDC steps delivered after sustained current may be due to post-adaptation changes in afferent sensitivity. These results contribute to an understanding of peripheral spike rate relationships for iDC vestibular stimulation and validate an ex-vivo model for future investigation of cellular mechanisms. In conjunction with previous in-vivo studies, these data help to characterize iDC stimulation as a potential therapy to restore vestibular function after bilateral vestibulopathy.
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spelling pubmed-69087042019-12-16 Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery Manca, Marco Glowatzki, Elisabeth Roberts, Dale C. Fridman, Gene Y. Aplin, Felix P. Sci Rep Article Recent studies have shown that ionic direct current (iDC) can modulate the vestibular system in-vivo, with potential benefits over conventional pulsed stimulation. In this study, the effects of iDC stimulation on vestibular nerve fiber firing rate was investigated using loose-patch nerve fiber recordings in the acutely excised mouse crista ampullaris of the semicircular canals. Cathodic and anodic iDC steps instantaneously reduced and increased afferent spike rate, with the polarity of this effect dependent on the position of the stimulating electrode. A sustained constant anodic or cathodic current resulted in an adaptation to the stimulus and a return to spontaneous spike rate. Post-adaptation spike rate responses to iDC steps were similar to pre-adaptation controls. At high intensities spike rate response sensitivities were modified by the presence of an adaptation step. Benefits previously observed in behavioral responses to iDC steps delivered after sustained current may be due to post-adaptation changes in afferent sensitivity. These results contribute to an understanding of peripheral spike rate relationships for iDC vestibular stimulation and validate an ex-vivo model for future investigation of cellular mechanisms. In conjunction with previous in-vivo studies, these data help to characterize iDC stimulation as a potential therapy to restore vestibular function after bilateral vestibulopathy. Nature Publishing Group UK 2019-12-12 /pmc/articles/PMC6908704/ /pubmed/31831760 http://dx.doi.org/10.1038/s41598-019-55045-6 Text en © The Author(s) 2019 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
Manca, Marco
Glowatzki, Elisabeth
Roberts, Dale C.
Fridman, Gene Y.
Aplin, Felix P.
Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery
title Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery
title_full Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery
title_fullStr Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery
title_full_unstemmed Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery
title_short Ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery
title_sort ionic direct current modulation evokes spike-rate adaptation in the vestibular periphery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908704/
https://www.ncbi.nlm.nih.gov/pubmed/31831760
http://dx.doi.org/10.1038/s41598-019-55045-6
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