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High‐Frequency Oscillations in the Pallidum: A Pathophysiological Biomarker in Parkinson's Disease?
Author(s) -
Johnson Luke A.,
Aman Joshua E.,
Yu Ying,
Escobar Sanabria David,
Wang Jing,
Hill Meghan,
Dharnipragada Rajiv,
Patriat Remi,
Fiecas Mark,
Li Laura,
Schrock Lauren E.,
Cooper Scott E.,
Johnson Matthew D.,
Park Michael C.,
Harel Noam,
Vitek Jerrold L.
Publication year - 2021
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.28566
Subject(s) - subthalamic nucleus , parkinson's disease , neuroscience , basal ganglia , deep brain stimulation , parkinsonism , dopaminergic , pathophysiology , local field potential , psychology , globus pallidus , mptp , medicine , dopamine , central nervous system , disease
Background Abnormal oscillatory neural activity in the beta‐frequency band (13–35 Hz) is thought to play a role in Parkinson's disease (PD); however, increasing evidence points to alterations in high‐frequency ranges (>100 Hz) also having pathophysiological relevance. Objectives Studies have found that power in subthalamic nucleus (STN) high‐frequency oscillations is increased with dopaminergic medication and during voluntary movements, implicating these brain rhythms in normal basal ganglia function. The objective of this study was to investigate whether similar signaling occurs in the internal globus pallidus (GPi), a nucleus increasingly used as a target for deep brain stimulation (DBS) for PD. Methods Spontaneous and movement‐related GPi field potentials were recorded from DBS leads in 5 externalized PD patients on and off dopaminergic medication, as well as from 3 rhesus monkeys before and after the induction of parkinsonism with the neurotoxin 1‐methyl‐4‐phenyl‐1,2,3,6 tetrahydropyridine. Results In the parkinsonian condition, we identified a prominent oscillatory peak centered at 200–300 Hz that increased during movement. In patients the magnitude of high‐frequency oscillation modulation was negatively correlated with bradykinesia. In monkeys, high‐frequency oscillations were mostly absent in the naive condition but emerged after the neurotoxin 1‐methyl‐4‐phenyl‐1,2,3,6 tetrahydropyridine. In patients, spontaneous high‐frequency oscillations were significantly attenuated on‐medication. Conclusions Our findings provide evidence in support of the hypothesis that exaggerated, movement‐modulated high‐frequency oscillations in the GPi are pathophysiological features of PD. These findings suggest that the functional role(s) of high‐frequency oscillations may differ between the STN and GPi and motivate additional investigations into their relationship to motor control in normal and diseased states.