Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents
Abstract 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. Funda...
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doaj-f49af94935ec4a9d89604ed3e9598fe32021-08-15T11:10:08ZengNature Publishing GroupMicrosystems & Nanoengineering2055-74342021-08-017111210.1038/s41378-021-00294-7Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodentsAlex Burton0Sang Min Won1Arian Kolahi Sohrabi2Tucker Stuart3Amir Amirhossein4Jong Uk Kim5Yoonseok Park6Andrew Gabros7John A. Rogers8Flavia Vitale9Andrew G. Richardson10Philipp Gutruf11Department of Biomedical Engineering, University of ArizonaDepartment of Electrical and Computer Engineering, Sungkyunkwan University (SKKU)Department of Neurosurgery, Perelman School of Medicine, University of PennsylvaniaDepartment of Biomedical Engineering, University of ArizonaDepartment of Biomedical Engineering, University of ArizonaQuerrey Simpson Institute for Bioelectronics, Northwestern UniversityQuerrey Simpson Institute for Bioelectronics, Northwestern UniversityDepartment of Neurosurgery, Perelman School of Medicine, University of PennsylvaniaQuerrey Simpson Institute for Bioelectronics, Northwestern UniversityDepartment of Neurology, Bioengineering, Physical Medicine & Rehabilitation, Center for Neuroengineering and Therapeutics, University of PennsylvaniaDepartment of Neurosurgery, Perelman School of Medicine, University of PennsylvaniaDepartment of Biomedical Engineering, University of ArizonaAbstract 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.https://doi.org/10.1038/s41378-021-00294-7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alex Burton Sang Min Won Arian Kolahi Sohrabi Tucker Stuart Amir Amirhossein Jong Uk Kim Yoonseok Park Andrew Gabros John A. Rogers Flavia Vitale Andrew G. Richardson Philipp Gutruf |
spellingShingle |
Alex Burton Sang Min Won Arian Kolahi Sohrabi Tucker Stuart Amir Amirhossein Jong Uk Kim Yoonseok Park Andrew Gabros John A. Rogers Flavia Vitale Andrew G. Richardson Philipp Gutruf Wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents Microsystems & Nanoengineering |
author_facet |
Alex Burton Sang Min Won Arian Kolahi Sohrabi Tucker Stuart Amir Amirhossein Jong Uk Kim Yoonseok Park Andrew Gabros John A. Rogers Flavia Vitale Andrew G. Richardson Philipp Gutruf |
author_sort |
Alex Burton |
title |
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_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_sort |
wireless, battery-free, and fully implantable electrical neurostimulation in freely moving rodents |
publisher |
Nature Publishing Group |
series |
Microsystems & Nanoengineering |
issn |
2055-7434 |
publishDate |
2021-08-01 |
description |
Abstract 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. |
url |
https://doi.org/10.1038/s41378-021-00294-7 |
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