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Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents
Implantable deep brain stimulation (DBS) systems are utilized for clinical treatment of diseases such as Parkinson’s disease and chronic pain. However, long-term efficacy of DBS is limited, and chronic neuroplastic changes and associated therapeutic mechanisms are not well understood. Fundamental an...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433476/ https://www.ncbi.nlm.nih.gov/pubmed/34567774 http://dx.doi.org/10.1038/s41378-021-00294-7 |
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author | Burton, Alex Won, Sang Min Sohrabi, Arian Kolahi Stuart, Tucker Amirhossein, Amir Kim, Jong Uk Park, Yoonseok Gabros, Andrew Rogers, John A. Vitale, Flavia Richardson, Andrew G. Gutruf, Philipp |
author_facet | Burton, Alex Won, Sang Min Sohrabi, Arian Kolahi Stuart, Tucker Amirhossein, Amir Kim, Jong Uk Park, Yoonseok Gabros, Andrew Rogers, John A. Vitale, Flavia Richardson, Andrew G. Gutruf, Philipp |
author_sort | Burton, Alex |
collection | PubMed |
description | Implantable deep brain stimulation (DBS) systems are utilized for clinical treatment of diseases such as Parkinson’s disease and chronic pain. However, long-term efficacy of DBS is limited, and chronic neuroplastic changes and associated therapeutic mechanisms are not well understood. Fundamental and mechanistic investigation, typically accomplished in small animal models, is difficult because of the need for chronic stimulators that currently require either frequent handling of test subjects to charge battery-powered systems or specialized setups to manage tethers that restrict experimental paradigms and compromise insight. To overcome these challenges, we demonstrate a fully implantable, wireless, battery-free platform that allows for chronic DBS in rodents with the capability to control stimulation parameters digitally in real time. The devices are able to provide stimulation over a wide range of frequencies with biphasic pulses and constant voltage control via low-impedance, surface-engineered platinum electrodes. The devices utilize off-the-shelf components and feature the ability to customize electrodes to enable broad utility and rapid dissemination. Efficacy of the system is demonstrated with a readout of stimulation-evoked neural activity in vivo and chronic stimulation of the medial forebrain bundle in freely moving rats to evoke characteristic head motion for over 36 days. |
format | Online Article Text |
id | pubmed-8433476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84334762021-09-24 Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents Burton, Alex Won, Sang Min Sohrabi, Arian Kolahi Stuart, Tucker Amirhossein, Amir Kim, Jong Uk Park, Yoonseok Gabros, Andrew Rogers, John A. Vitale, Flavia Richardson, Andrew G. Gutruf, Philipp Microsyst Nanoeng Article Implantable deep brain stimulation (DBS) systems are utilized for clinical treatment of diseases such as Parkinson’s disease and chronic pain. However, long-term efficacy of DBS is limited, and chronic neuroplastic changes and associated therapeutic mechanisms are not well understood. Fundamental and mechanistic investigation, typically accomplished in small animal models, is difficult because of the need for chronic stimulators that currently require either frequent handling of test subjects to charge battery-powered systems or specialized setups to manage tethers that restrict experimental paradigms and compromise insight. To overcome these challenges, we demonstrate a fully implantable, wireless, battery-free platform that allows for chronic DBS in rodents with the capability to control stimulation parameters digitally in real time. The devices are able to provide stimulation over a wide range of frequencies with biphasic pulses and constant voltage control via low-impedance, surface-engineered platinum electrodes. The devices utilize off-the-shelf components and feature the ability to customize electrodes to enable broad utility and rapid dissemination. Efficacy of the system is demonstrated with a readout of stimulation-evoked neural activity in vivo and chronic stimulation of the medial forebrain bundle in freely moving rats to evoke characteristic head motion for over 36 days. Nature Publishing Group UK 2021-08-13 /pmc/articles/PMC8433476/ /pubmed/34567774 http://dx.doi.org/10.1038/s41378-021-00294-7 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Burton, Alex Won, Sang Min Sohrabi, Arian Kolahi Stuart, Tucker Amirhossein, Amir Kim, Jong Uk Park, Yoonseok Gabros, Andrew Rogers, John A. Vitale, Flavia Richardson, Andrew G. Gutruf, Philipp Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
title | Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
title_full | Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
title_fullStr | Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
title_full_unstemmed | Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
title_short | Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
title_sort | wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433476/ https://www.ncbi.nlm.nih.gov/pubmed/34567774 http://dx.doi.org/10.1038/s41378-021-00294-7 |
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