Abstract

Introduction: Striatal dopamine depletion disrupts basal ganglia function and causes Parkinson’s disease (PD). The pathophysiology of the dopamine-dependent relationship between basal ganglia signaling and motor control, however, is not fully understood. We obtained simultaneous recordings of local field potentials (LFPs) from the subthalamic nucleus (STN) and electromyograms (EMGs) in patients with PD to investigate the impact of dopaminergic state and movement on long-range beta functional connectivity between basal ganglia and lower motor neurons.Methods: Eight PD patients were investigated 3 months after implantation of a deep brain stimulation (DBS)-system capable of recording LFPs via chronically-implanted leads (Medtronic, ACTIVA PC+S®). We analyzed STN spectral power and its coherence with EMG in the context of two different movement paradigms (tonic wrist extension vs. alternating wrist extension and flexion) and the effect of levodopa (L-Dopa) intake using an unbiased data-driven approach to determine regions of interest (ROI).Results: Two ROIs capturing prominent coherence within a grand average coherogram were identified. A trend of a dopamine effect was observed for the first ROI (50–150 ms after movement start) with higher STN-EMG coherence in medicated patients. Concerning the second ROI (300–500 ms after movement start), an interaction effect of L-Dopa medication and movement task was observed with higher coherence in the isometric contraction task compared to alternating movements in the medication ON state, a pattern which was reversed in L-Dopa OFF.Discussion: L-Dopa medication may normalize functional connectivity between remote structures of the motor system with increased upper beta coherence reflecting a physiological restriction of the amount of information conveyed between remote structures. This may be necessary to maintain simple movements like isometric contraction. Our study adds dynamic properties to the complex interplay between STN spectral beta power and the nucleus’ functional connectivity to remote structures of the motor system as a function of movement and dopaminergic state. This may help to identify markers of neuronal activity relevant for more individualized programming of DBS therapy.

Highlights

  • Striatal dopamine depletion disrupts basal ganglia function and causes Parkinson’s disease (PD)

  • subthalamic nucleus (STN) spectral power and STN-motor cortex coherence in the beta band decreased compared to baseline prior to and during movement in unmedicated PD patients (Talakoub et al, 2016). These two studies have explicitly looked at dynamic changes of STN oscillatory activity and STN-cortex coherence to be dependent on movement activity. This is of considerable significance given that increased beta oscillations in motor cortex and basal ganglia have been associated with immutability and steady state in motor activity while being modulated during movement change (Brittain and Brown, 2014) the analysis of dynamic changes in oscillatory beta band activity and coherence between relay structures of the motor circuit may be relevant in the process of defining physiological read-out parameters for on demand stimulation systems as closed loop techniques

  • We investigated patients implanted with the ACTIVA PC+S (Medtronic Inc., Minneapolis, MN, USA), a deep brain stimulation (DBS) device that is capable of recording local field potentials (LFPs) activity from chronically implanted STN leads, and studied the effect of motor task and dopaminergic state on the modulation of beta band activity using an event-related approach in PD patients

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Summary

Introduction

Striatal dopamine depletion disrupts basal ganglia function and causes Parkinson’s disease (PD). The pathophysiology of the dopamine-dependent relationship between basal ganglia signaling and motor control, is not fully understood. We obtained simultaneous recordings of local field potentials (LFPs) from the subthalamic nucleus (STN) and electromyograms (EMGs) in patients with PD to investigate the impact of dopaminergic state and movement on long-range beta functional connectivity between basal ganglia and lower motor neurons

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