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  Shared pathway-specific network mechanisms of dopamine and deep brain stimulation for the treatment of Parkinson's disease

Binns, T. S., Köhler, R. M., Vanhoecke, J., Chikermane, M., Gerster, M., Merk, T., et al. (2024). Shared pathway-specific network mechanisms of dopamine and deep brain stimulation for the treatment of Parkinson's disease. bioRxiv. doi:10.1101/2024.04.14.586969.

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Binns, Thomas S., Author
Köhler, Richard M., Author
Vanhoecke, Jonathan, Author
Chikermane, Meera, Author
Gerster, Moritz1, Author                 
Merk, Timon, Author
Pellegrini, Franziska, Author
Busch, Johannes L., Author
Habets, Jeroen G.V., Author
Cavallo, Alessia, Author
Li, Ningfei, Author
Horn, Andreas, Author
Krause, Patricia, Author
Faust, Katharina, Author
Schneider, Gerd-Helge, Author
Haufe, Stefan, Author
Kühn, Andrea A., Author
Neumann, Wolf-Julian, Author
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1Department Neurology, MPI for Human Cognitive and Brain Sciences, Max Planck Society, ou_634549              

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 Abstract: Deep brain stimulation (DBS) is a brain circuit intervention that can modulate distinct neural pathways for the alleviation of neurological symptoms in patients with brain disorders. In Parkinson’s disease, subthalamic DBS clinically mimics the effect of dopaminergic drug treatment, but the shared pathway mechanisms on cortex – basal ganglia networks are unknown. To address this critical knowledge gap, we combined fully-invasive neural multisite recordings in patients undergoing DBS surgery with MRI-based whole-brain connectomics. Our findings demonstrate that dopamine and DBS exert distinct mesoscale effects through modulation of local neural population synchrony. In contrast, at the macroscale, DBS mimics dopamine in its suppression of excessive interregional network synchrony associated with indirect and hyperdirect cortex – basal ganglia pathways. Our results provide a better understanding of the circuit mechanisms of dopamine and DBS, laying the foundation for advanced closed-loop neurostimulation therapies.

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Language(s): eng - English
 Dates: 2024-04-17
 Publication Status: Published online
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 Identifiers: DOI: 10.1101/2024.04.14.586969
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Title: bioRxiv
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