Movement-related changes in pallidocortical synchrony differentiate action execution and observation in humans.
Action observation
Beta oscillations
Deep brain stimulation
Motor control
Parkinson disease
Journal
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
ISSN: 1872-8952
Titre abrégé: Clin Neurophysiol
Pays: Netherlands
ID NLM: 100883319
Informations de publication
Date de publication:
08 2021
08 2021
Historique:
received:
01
09
2020
revised:
02
02
2021
accepted:
15
03
2021
pubmed:
14
5
2021
medline:
12
10
2021
entrez:
13
5
2021
Statut:
ppublish
Résumé
Suppression of local and network alpha and beta oscillations in the human basal ganglia-thalamocortical (BGTC) circuit is a prominent feature of movement, including suppression of local alpha/beta power, cross-region beta phase coupling, and cortical and subcortical phase-amplitude coupling (PAC). We hypothesized that network-level coupling is more directly related to movement execution than local power changes, given the role of pathological network hypersynchrony in movement disorders such as Parkinson disease (PD). Understanding the specificity of these movement-related signals is important for designing novel therapeutics. We recorded globus pallidus internus (GPi) and motor cortical local field potentials during movement execution, passive movement observation and rest in 12 patients with PD undergoing deep brain stimulator implantation. Local alpha/beta power is suppressed in the globus pallidus and motor cortex during both action execution and action observation, although less so during action observation. In contrast, pallidocortical phase synchrony and GPi and motor cortical alpha/beta-gamma PAC are suppressed only during action execution. The functional dissociation across tasks in pallidocortical network activity suggests a particularly important role of network coupling in motor execution. Network level recordings provide important specificity in differentiating motor behavior and may provide significant value for future closed loop therapies.
Identifiants
pubmed: 33980469
pii: S1388-2457(21)00521-6
doi: 10.1016/j.clinph.2021.03.037
pmc: PMC8286311
mid: NIHMS1696686
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
1990-2001Subventions
Organisme : NINDS NIH HHS
ID : R01 NS097782
Pays : United States
Organisme : NINDS NIH HHS
ID : R25 NS065723
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS098961
Pays : United States
Informations de copyright
Copyright © 2021 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Conflict of Interest Statement MM is currently employed by Boston Scientific; work was done while she was employed at UCLA. NP receives grant support from Medtronic and Boston Scientific and consultant fees from Abbott and Boston Scientific.
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