Interrogating basal ganglia reinforcement with deep brain stimulation in Parkinson’s disease.
ReinforceBG aims to explore dopamine's role in Parkinson's disease through advanced neuromodulation techniques to enhance understanding and develop innovative treatments for motor and cognitive symptoms.
Projectdetails
Introduction
Dopamine and the basal ganglia have been conserved over more than 500 million years of evolution. They are fundamental to animal and human behaviour. Parkinson's disease (PD) is associated with the loss of dopaminergic innervation to the basal ganglia. Over 6 million people suffer from the debilitating symptoms of PD that span disturbance of emotion, cognition, and movement.
Need for Understanding
There is a pressing need to understand the pathogenesis of these symptoms, but an integrated account of dopamine and basal ganglia function is lacking. This constitutes a significant roadblock to scientific and therapeutic advances.
Novel Hypothesis
To overcome this roadblock, ReinforceBG poses the novel unconventional hypothesis that loss of dopamine in PD does not impair movement per se but leads to chronic negative reinforcement of neural population dynamics. Conversely, in the healthy state, transient dopamine signals may stabilize cortex-basal ganglia activity to facilitate reentry and refinement of cortical output.
Research Approach
To address this hypothesis, ReinforceBG will combine invasive electrocorticography and local field potential recordings with closed-loop deep brain stimulation in PD patients.
Aims of the Project
- Aim 1: Investigate how basal ganglia pathways coordinate neuromuscular adaptation.
- Aim 2: Shed light on basal ganglia reinforcement in multiple behavioural domains, including movement, gait, speech, and spatial navigation in virtual reality.
- Aim 3: Develop a neuroprosthetic brain-computer interface that aims to modulate basal ganglia reinforcement.
Innovative Perspective
ReinforceBG deviates from outdated models on pro- vs. antikinetic Go and NoGo pathways and promises a holistic reinforcement-centered view of basal ganglia function.
Future Implications
It will leverage the unprecedented spatiotemporal precision of neuromodulation for the development of an innovative brain circuit intervention that modulates neural reinforcement in real time. This opens new horizons for the interdisciplinary treatment of brain disorders affecting the dopaminergic system.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.499.580 |
Totale projectbegroting | € 1.499.580 |
Tijdlijn
Startdatum | 1-3-2023 |
Einddatum | 29-2-2028 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- CHARITE - UNIVERSITAETSMEDIZIN BERLINpenvoerder
Land(en)
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Vergelijkbare projecten uit andere regelingen
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Opto-Electronic Neural Connectoid Model Implemented for Neurodegenerative DiseaseThe project aims to develop a novel human brain-organoid model, called connectoids, to replace animal testing for Parkinson's disease, enhancing therapy monitoring and reducing societal burdens. | EIC Pathfinder | € 2.992.203 | 2022 | Details |
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Adpative DBSAlphaDBS enhances DBS treatment for Parkinson's by using adaptive stimulation based on local field potentials to optimize energy delivery in real-time. | EIC Accelerator | € 2.499.999 | 2023 | Details |
Opto-Electronic Neural Connectoid Model Implemented for Neurodegenerative Disease
The project aims to develop a novel human brain-organoid model, called connectoids, to replace animal testing for Parkinson's disease, enhancing therapy monitoring and reducing societal burdens.
Atlas of the Human Deep Brain Nuclei, Connections, and Vasculature
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Adpative DBS
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