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  4. The genesis and functional consequences of cortico-subthalamic beta augmentation and excessive subthalamic burst discharges after dopaminergic deprivation
 
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The genesis and functional consequences of cortico-subthalamic beta augmentation and excessive subthalamic burst discharges after dopaminergic deprivation

Journal
Experimental neurology
Journal Volume
356
Start Page
114153
ISSN
0014-4886
Date Issued
2022-10
Author(s)
HSING-JUNG LAI  
Deng, Chuan-Rou
Wang, Ren-Wei
Lee, Lan-Hsin Nancy
CHUNG-CHIN KUO  
DOI
10.1016/j.expneurol.2022.114153
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/615926
URL
https://api.elsevier.com/content/abstract/scopus_id/85134250350
Abstract
The cardinal electrophysiological signs in Parkinson's disease (PD) include augmented beta oscillations in the motor cortex-subthalamic nucleus (MC-STN) axis and excessive burst discharges in STN. We have shown that excessive STN burst discharges have a direct causal relation with the locomotor deficits in PD. To investigate the correlation between the two cardinal signs, we characterized the courses of development of the electrophysiological abnormalities in the hemiparkinsonian rat model. The loss of dopaminergic neurons develops fast, and is histologically completed within 4-7 days of the lesion. The increase in STN burst discharges is limited to the lesioned side, and follows a very similar course. In contrast, beta augmentation has a bilateral presentation, and requires 14-21 days for full development. Behaviorally, the gross locomotor deficits in open field test and limb akinesia in stepping test match the foregoing fast and slow time courses, respectively. A further look into the spike entrainment shows that the oscillations in local field potential (LFP) of the MC effectively entrain the multi-unit (MU) spikes of MC, STN and entopeduncular nucleus (EPN), a rat homolog of human globus pallidus interna (GPi), whereas the LFP of STN or EPN (GPi) cannot entrain the spikes in MC. We conclude that excessive STN burst discharges are a direct consequence, whereas beta augmentation is probably a secondary or adaptive changes in the cortico-subcortical re-entrant loops, to dopaminergic deprivation. Beta augmentation is therefore not so consistently present as excessive STN burst discharges, but could signal more delicate derangements at the level of cortical programming in PD.
Subjects
Limb akinesia; Local field potential; Locomotor dysfunction; Parkinson's disease; STN burst discharges; beta oscillation
SDGs

[SDGs]SDG3

Type
journal article

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