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Subcortical short‐term plasticity elicited by deep brain stimulation
OBJECTIVE: To investigate local short‐term neuroplasticity elicited by subthalamic, thalamic, and pallidal deep brain stimulation (DBS) for movement disorders. METHODS: During DBS surgery, we delivered pairs of stimulus pulses with both circular and directional leads across 90 interstimulus interval...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108424/ https://www.ncbi.nlm.nih.gov/pubmed/33826240 http://dx.doi.org/10.1002/acn3.51275 |
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author | Awad, Mohammad Z. Vaden, Ryan J. Irwin, Zachary T. Gonzalez, Christopher L. Black, Sarah Nakhmani, Arie Jaeger, Byron C. Bentley, J. Nicole Guthrie, Barton L. Walker, Harrison C. |
author_facet | Awad, Mohammad Z. Vaden, Ryan J. Irwin, Zachary T. Gonzalez, Christopher L. Black, Sarah Nakhmani, Arie Jaeger, Byron C. Bentley, J. Nicole Guthrie, Barton L. Walker, Harrison C. |
author_sort | Awad, Mohammad Z. |
collection | PubMed |
description | OBJECTIVE: To investigate local short‐term neuroplasticity elicited by subthalamic, thalamic, and pallidal deep brain stimulation (DBS) for movement disorders. METHODS: During DBS surgery, we delivered pairs of stimulus pulses with both circular and directional leads across 90 interstimulus intervals in 17 participants and recorded local field potentials from unused contacts on the implanted electrode array. We removed the stimulus artifact, validated the neural origin of the underlying signals, and examined short‐term plasticity as a function of interstimulus interval and DBS target, using linear mixed effects models. RESULTS: DBS evokes short latency local field potentials that are readily detected with both circular and directional leads at all stimulation targets (0.31 ± 0.10 msec peak latency, mean ± SD). Peak amplitude, area, and latency are modified strongly by interstimulus interval (P < 0.001) and display absolute and relative refractory periods (0.56 ± 0.08 and 2.94 ± 1.05 msec, respectively). We also identified later oscillatory activity in the subthalamic‐pallidal circuit (4.50 ± 1.11 msec peak latency) that displays paired pulse facilitation (present in 5/8 subthalamic, 4/5 pallidal, and 0/6 thalamic trajectories, P = 0.018, Fisher’s exact test), and correlates with resting beta frequency power (P < 0.001), therapeutic DBS frequencies, and stimulation sites chosen later for therapy in the ambulatory setting (P = 0.031). INTERPRETATION: Paired DBS pulses synchronize local circuit electrophysiology and elicit short‐term neuroplasticity in the subthalamic‐pallidal circuit. Collectively, these responses likely represent the earliest detectable interaction between the DBS pulse and local neuronal tissue in humans. Evoked subcortical field potentials could serve as a predictive biomarker to guide the implementation of next‐generation directional and adaptive stimulation devices. |
format | Online Article Text |
id | pubmed-8108424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81084242021-05-10 Subcortical short‐term plasticity elicited by deep brain stimulation Awad, Mohammad Z. Vaden, Ryan J. Irwin, Zachary T. Gonzalez, Christopher L. Black, Sarah Nakhmani, Arie Jaeger, Byron C. Bentley, J. Nicole Guthrie, Barton L. Walker, Harrison C. Ann Clin Transl Neurol Research Articles OBJECTIVE: To investigate local short‐term neuroplasticity elicited by subthalamic, thalamic, and pallidal deep brain stimulation (DBS) for movement disorders. METHODS: During DBS surgery, we delivered pairs of stimulus pulses with both circular and directional leads across 90 interstimulus intervals in 17 participants and recorded local field potentials from unused contacts on the implanted electrode array. We removed the stimulus artifact, validated the neural origin of the underlying signals, and examined short‐term plasticity as a function of interstimulus interval and DBS target, using linear mixed effects models. RESULTS: DBS evokes short latency local field potentials that are readily detected with both circular and directional leads at all stimulation targets (0.31 ± 0.10 msec peak latency, mean ± SD). Peak amplitude, area, and latency are modified strongly by interstimulus interval (P < 0.001) and display absolute and relative refractory periods (0.56 ± 0.08 and 2.94 ± 1.05 msec, respectively). We also identified later oscillatory activity in the subthalamic‐pallidal circuit (4.50 ± 1.11 msec peak latency) that displays paired pulse facilitation (present in 5/8 subthalamic, 4/5 pallidal, and 0/6 thalamic trajectories, P = 0.018, Fisher’s exact test), and correlates with resting beta frequency power (P < 0.001), therapeutic DBS frequencies, and stimulation sites chosen later for therapy in the ambulatory setting (P = 0.031). INTERPRETATION: Paired DBS pulses synchronize local circuit electrophysiology and elicit short‐term neuroplasticity in the subthalamic‐pallidal circuit. Collectively, these responses likely represent the earliest detectable interaction between the DBS pulse and local neuronal tissue in humans. Evoked subcortical field potentials could serve as a predictive biomarker to guide the implementation of next‐generation directional and adaptive stimulation devices. John Wiley and Sons Inc. 2021-04-07 /pmc/articles/PMC8108424/ /pubmed/33826240 http://dx.doi.org/10.1002/acn3.51275 Text en © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Awad, Mohammad Z. Vaden, Ryan J. Irwin, Zachary T. Gonzalez, Christopher L. Black, Sarah Nakhmani, Arie Jaeger, Byron C. Bentley, J. Nicole Guthrie, Barton L. Walker, Harrison C. Subcortical short‐term plasticity elicited by deep brain stimulation |
title | Subcortical short‐term plasticity elicited by deep brain stimulation |
title_full | Subcortical short‐term plasticity elicited by deep brain stimulation |
title_fullStr | Subcortical short‐term plasticity elicited by deep brain stimulation |
title_full_unstemmed | Subcortical short‐term plasticity elicited by deep brain stimulation |
title_short | Subcortical short‐term plasticity elicited by deep brain stimulation |
title_sort | subcortical short‐term plasticity elicited by deep brain stimulation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108424/ https://www.ncbi.nlm.nih.gov/pubmed/33826240 http://dx.doi.org/10.1002/acn3.51275 |
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