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Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease

High frequency subthalamic nucleus (STN) deep brain stimulation (DBS) improves the cardinal motor signs of Parkinson’s disease (PD) and attenuates STN alpha/beta band neural synchrony in a voltage-dependent manner. While there is a growing interest in the behavioral effects of lower frequency (60 Hz...

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Autores principales: Blumenfeld, Zack, Velisar, Anca, Miller Koop, Mandy, Hill, Bruce C., Shreve, Lauren A., Quinn, Emma J., Kilbane, Camilla, Yu, Hong, Henderson, Jaimie M., Brontë-Stewart, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373818/
https://www.ncbi.nlm.nih.gov/pubmed/25807463
http://dx.doi.org/10.1371/journal.pone.0121067
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author Blumenfeld, Zack
Velisar, Anca
Miller Koop, Mandy
Hill, Bruce C.
Shreve, Lauren A.
Quinn, Emma J.
Kilbane, Camilla
Yu, Hong
Henderson, Jaimie M.
Brontë-Stewart, Helen
author_facet Blumenfeld, Zack
Velisar, Anca
Miller Koop, Mandy
Hill, Bruce C.
Shreve, Lauren A.
Quinn, Emma J.
Kilbane, Camilla
Yu, Hong
Henderson, Jaimie M.
Brontë-Stewart, Helen
author_sort Blumenfeld, Zack
collection PubMed
description High frequency subthalamic nucleus (STN) deep brain stimulation (DBS) improves the cardinal motor signs of Parkinson’s disease (PD) and attenuates STN alpha/beta band neural synchrony in a voltage-dependent manner. While there is a growing interest in the behavioral effects of lower frequency (60 Hz) DBS, little is known about its effect on STN neural synchrony. Here we demonstrate for the first time that during intra-operative 60 Hz STN DBS, one or more bands of resting state neural synchrony were amplified in the STN in PD. We recorded intra-operative STN resting state local field potentials (LFPs) from twenty-eight STNs in seventeen PD subjects after placement of the DBS lead (model 3389, Medtronic, Inc.) before and during three randomized neurostimulation sets (130 Hz/1.35V, 130 Hz/2V, 60 Hz/2V). During 130 Hz/2V DBS, baseline (no DBS) STN alpha (8 – 12 Hz) and beta (13 – 35 Hz) band power decreased (N=14, P < 0.001 for both), whereas during 60 Hz/2V DBS, alpha band and peak frequency power increased (P = 0.012, P = 0.007, respectively). The effect of 60 Hz/2V DBS opposed that of power-equivalent (130 Hz/1.35V) DBS (alpha: P < 0.001, beta: P = 0.006). These results show that intra-operative 60 Hz STN DBS amplified whereas 130 Hz STN DBS attenuated resting state neural synchrony in PD; the effects were frequency-specific. We demonstrate that neurostimulation may be useful as a tool to selectively modulate resting state resonant bands of neural synchrony and to investigate its influence on motor and non-motor behaviors in PD and other neuropsychiatric diseases.
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spelling pubmed-43738182015-03-27 Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease Blumenfeld, Zack Velisar, Anca Miller Koop, Mandy Hill, Bruce C. Shreve, Lauren A. Quinn, Emma J. Kilbane, Camilla Yu, Hong Henderson, Jaimie M. Brontë-Stewart, Helen PLoS One Research Article High frequency subthalamic nucleus (STN) deep brain stimulation (DBS) improves the cardinal motor signs of Parkinson’s disease (PD) and attenuates STN alpha/beta band neural synchrony in a voltage-dependent manner. While there is a growing interest in the behavioral effects of lower frequency (60 Hz) DBS, little is known about its effect on STN neural synchrony. Here we demonstrate for the first time that during intra-operative 60 Hz STN DBS, one or more bands of resting state neural synchrony were amplified in the STN in PD. We recorded intra-operative STN resting state local field potentials (LFPs) from twenty-eight STNs in seventeen PD subjects after placement of the DBS lead (model 3389, Medtronic, Inc.) before and during three randomized neurostimulation sets (130 Hz/1.35V, 130 Hz/2V, 60 Hz/2V). During 130 Hz/2V DBS, baseline (no DBS) STN alpha (8 – 12 Hz) and beta (13 – 35 Hz) band power decreased (N=14, P < 0.001 for both), whereas during 60 Hz/2V DBS, alpha band and peak frequency power increased (P = 0.012, P = 0.007, respectively). The effect of 60 Hz/2V DBS opposed that of power-equivalent (130 Hz/1.35V) DBS (alpha: P < 0.001, beta: P = 0.006). These results show that intra-operative 60 Hz STN DBS amplified whereas 130 Hz STN DBS attenuated resting state neural synchrony in PD; the effects were frequency-specific. We demonstrate that neurostimulation may be useful as a tool to selectively modulate resting state resonant bands of neural synchrony and to investigate its influence on motor and non-motor behaviors in PD and other neuropsychiatric diseases. Public Library of Science 2015-03-25 /pmc/articles/PMC4373818/ /pubmed/25807463 http://dx.doi.org/10.1371/journal.pone.0121067 Text en © 2015 Blumenfeld et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Blumenfeld, Zack
Velisar, Anca
Miller Koop, Mandy
Hill, Bruce C.
Shreve, Lauren A.
Quinn, Emma J.
Kilbane, Camilla
Yu, Hong
Henderson, Jaimie M.
Brontë-Stewart, Helen
Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease
title Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease
title_full Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease
title_fullStr Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease
title_full_unstemmed Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease
title_short Sixty Hertz Neurostimulation Amplifies Subthalamic Neural Synchrony in Parkinson’s Disease
title_sort sixty hertz neurostimulation amplifies subthalamic neural synchrony in parkinson’s disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373818/
https://www.ncbi.nlm.nih.gov/pubmed/25807463
http://dx.doi.org/10.1371/journal.pone.0121067
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