Brain, Vol. 125, No. 6, 1196-1209,
June 2002
© 2002 Guarantors of Brain
Dependence of subthalamic nucleus oscillations on movement and dopamine in Parkinson’s disease
1 Department of Physiology, 2 The Toronto Western Research Institute, The Toronto Western Hospital, 3 Department of Surgery, The Toronto Western Hospital and 4 Department of Medicine, The Toronto Western Hospital, University of Toronto, Toronto, Canada
Correspondence to: J. O. Dostrovsky, Department of Physiology, Room 3305, Medical Sciences Building, 1 King’s College Circle, University of Toronto, Toronto, Ontario M5S 1A8, Canada E-mail: j.dostrovsky{at}utoronto.ca
Local field potentials and pairs of neurones in the subthalamic nucleus (STN) of patients with Parkinson’s disease show high-frequency oscillations (HFOs) at 15–30 Hz. This study explores how these HFOs are modulated by voluntary movements and by dopaminergic medication. We examined 15 patients undergoing implantation of bilateral deep brain stimulating electrodes using microelectrode recordings of pairs of STN neurones (eight patients) and macroelectrode recordings of local field potentials from the STN (14 patients). Synchronized HFOs between STN neurones were observed in 28 out of 37 pairs in five patients who had tremor in the operating room and none of 45 pairs in three patients who did not. In two of the three non-tremulous patients, HFOs in the frequency spectra of local field potentials were detected but were weaker than in those patients with tremor. Active movement suppressed synchronized HFOs in three out of five pairs of neurones, independent of changes in firing rate. HFOs observed in the local field potentials in nine out of 14 patients were reduced with voluntary movement in six of the eight patients tested. Dopaminergic medication decreased the incidence of synchronized HFOs in STN neurone pairs, reduced HFO synchrony in a pair of tremor cells concurrent with a reduction in firing rate and limb tremor, and decreased HFOs of local field potentials in the STN. These results demonstrate that HFO synchronization in the STN is reduced by voluntary movements and by exogenous dopaminergic medication. A mechanism for neuronal oscillatory synchronization in basal ganglia is proposed. It is suggested that the firing of STN neurones can be synchronized by 15–30 Hz cortical beta oscillatory activity, particularly when dopamine deficiency results in a higher background firing rate of STN neurones, and that this synchronization contributes to parkinsonian pathophysiology.
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