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Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice
Devices that electrically modulate the deep brain have enabled important breakthroughs in the management of neurological and psychiatric disorders. Such devices are typically centimeter-scale, requiring surgical implantation and wired-in powering, which increases the risk of hemorrhage, infection, a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806222/ https://www.ncbi.nlm.nih.gov/pubmed/33523872 http://dx.doi.org/10.1126/sciadv.abc4189 |
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author | Kozielski, K. L. Jahanshahi, A. Gilbert, H. B. Yu, Y. Erin, Ö. Francisco, D. Alosaimi, F. Temel, Y. Sitti, M. |
author_facet | Kozielski, K. L. Jahanshahi, A. Gilbert, H. B. Yu, Y. Erin, Ö. Francisco, D. Alosaimi, F. Temel, Y. Sitti, M. |
author_sort | Kozielski, K. L. |
collection | PubMed |
description | Devices that electrically modulate the deep brain have enabled important breakthroughs in the management of neurological and psychiatric disorders. Such devices are typically centimeter-scale, requiring surgical implantation and wired-in powering, which increases the risk of hemorrhage, infection, and damage during daily activity. Using smaller, remotely powered materials could lead to less invasive neuromodulation. Here, we present injectable, magnetoelectric nanoelectrodes that wirelessly transmit electrical signals to the brain in response to an external magnetic field. This mechanism of modulation requires no genetic modification of neural tissue, allows animals to freely move during stimulation, and uses nonresonant carrier frequencies. Using these nanoelectrodes, we demonstrate neuronal modulation in vitro and in deep brain targets in vivo. We also show that local subthalamic modulation promotes modulation in other regions connected via basal ganglia circuitry, leading to behavioral changes in mice. Magnetoelectric materials present a versatile platform technology for less invasive, deep brain neuromodulation. |
format | Online Article Text |
id | pubmed-7806222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78062222021-01-21 Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice Kozielski, K. L. Jahanshahi, A. Gilbert, H. B. Yu, Y. Erin, Ö. Francisco, D. Alosaimi, F. Temel, Y. Sitti, M. Sci Adv Research Articles Devices that electrically modulate the deep brain have enabled important breakthroughs in the management of neurological and psychiatric disorders. Such devices are typically centimeter-scale, requiring surgical implantation and wired-in powering, which increases the risk of hemorrhage, infection, and damage during daily activity. Using smaller, remotely powered materials could lead to less invasive neuromodulation. Here, we present injectable, magnetoelectric nanoelectrodes that wirelessly transmit electrical signals to the brain in response to an external magnetic field. This mechanism of modulation requires no genetic modification of neural tissue, allows animals to freely move during stimulation, and uses nonresonant carrier frequencies. Using these nanoelectrodes, we demonstrate neuronal modulation in vitro and in deep brain targets in vivo. We also show that local subthalamic modulation promotes modulation in other regions connected via basal ganglia circuitry, leading to behavioral changes in mice. Magnetoelectric materials present a versatile platform technology for less invasive, deep brain neuromodulation. American Association for the Advancement of Science 2021-01-13 /pmc/articles/PMC7806222/ /pubmed/33523872 http://dx.doi.org/10.1126/sciadv.abc4189 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Kozielski, K. L. Jahanshahi, A. Gilbert, H. B. Yu, Y. Erin, Ö. Francisco, D. Alosaimi, F. Temel, Y. Sitti, M. Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice |
title | Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice |
title_full | Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice |
title_fullStr | Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice |
title_full_unstemmed | Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice |
title_short | Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice |
title_sort | nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806222/ https://www.ncbi.nlm.nih.gov/pubmed/33523872 http://dx.doi.org/10.1126/sciadv.abc4189 |
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