Dopamine depletion leads to pathological synchronization of distinct basal ganglia loops in the beta band

Motor symptoms of Parkinson's Disease (PD) are associated with dopamine deficits and pathological oscillation of basal ganglia (BG) neurons in the β range ([12-30] Hz). However, how dopamine depletion affects the oscillation dynamics of BG nuclei is still unclear. With a spiking neurons model,...

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Main Authors: Ahmadipour, M. (Author), Mannella, R. (Author), Mazzoni, A. (Author), Ortone, A. (Author), Vergani, A.A (Author)
Format: Article
Language:English
Published: NLM (Medline) 2023
Subjects:
Online Access:View Fulltext in Publisher
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LEADER 02879nam a2200349Ia 4500
001 10.1371-journal.pcbi.1010645
008 230529s2023 CNT 000 0 und d
020 |a 15537358 (ISSN) 
245 1 0 |a Dopamine depletion leads to pathological synchronization of distinct basal ganglia loops in the beta band 
260 0 |b NLM (Medline)  |c 2023 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1371/journal.pcbi.1010645 
856 |z View in Scopus  |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-85159731574&doi=10.1371%2fjournal.pcbi.1010645&partnerID=40&md5=9f59a8a97799bd6265cda02a9b5937e2 
520 3 |a Motor symptoms of Parkinson's Disease (PD) are associated with dopamine deficits and pathological oscillation of basal ganglia (BG) neurons in the β range ([12-30] Hz). However, how dopamine depletion affects the oscillation dynamics of BG nuclei is still unclear. With a spiking neurons model, we here capture the features of BG nuclei interactions leading to oscillations in dopamine-depleted condition. We highlight that both the loop between subthalamic nucleus (STN) and Globus Pallidus pars externa (GPe) and the loop between striatal fast spiking and medium spiny neurons and GPe display resonances in the β range, and synchronize to a common β frequency through interaction. Crucially, the synchronization depends on dopamine depletion: the two loops are largely independent for high levels of dopamine, but progressively synchronize as dopamine is depleted due to the increased strength of the striatal loop. The model is validated against recent experimental reports on the role of cortical inputs, STN and GPe activity in the generation of β oscillations. Our results highlight the role of the interplay between the GPe-STN and the GPe-striatum loop in generating sustained β oscillations in PD subjects, and explain how this interplay depends on the level of dopamine. This paves the way to the design of therapies specifically addressing the onset of pathological β oscillations. Copyright: © 2023 Ortone et al. 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 credited. 
650 0 4 |a Basal Ganglia 
650 0 4 |a basal ganglion 
650 0 4 |a dopamine 
650 0 4 |a Dopamine 
650 0 4 |a globus pallidus 
650 0 4 |a Globus Pallidus 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a Parkinson disease 
650 0 4 |a Parkinson Disease 
650 0 4 |a physiology 
650 0 4 |a subthalamic nucleus 
650 0 4 |a Subthalamic Nucleus 
700 1 0 |a Ahmadipour, M.  |e author 
700 1 0 |a Mannella, R.  |e author 
700 1 0 |a Mazzoni, A.  |e author 
700 1 0 |a Ortone, A.  |e author 
700 1 0 |a Vergani, A.A.  |e author 
773 |t PLoS computational biology