Brain Advance Access originally published online on August 22, 2003
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Brain, Vol. 126, No. 10, 2153-2163,
October 2003
© 2003 Guarantors of Brain
doi: 10.1093/brain/awg229
300-Hz subthalamic oscillations in Parkinsons disease
1 Department of Neurological Sciences, Università di Milano, IRCCS Ospedale Maggiore di Milano, 2 Department of Biomedical Engineering, Politecnico di Milano, 3 Department of Clinical Neurology, Ospedale San Paolo, Milano, Italy and 4 School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA *These two authors equally contributed to this work.
Correspondence to: Professor Alberto Priori, Dipartimento di Scienze Neurologiche, Clinica Neurologica, Padiglione Ponti, Ospedale Maggiore Policlinico, Via F. Sforza 35, Milano, 20122, Italy E-mail: alberto.priori{at}unimi.it
Despite several studies and models, much remains unclear about how the human basal ganglia operate. Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is an effective treatment for complicated Parkinsons disease, but how DBS acts also remains unknown. The clinical benefit of DBS at frequencies >100 Hz suggests the possible importance of neural rhythms operating at frequencies higher than the range normally considered for basal ganglia processing (<100 Hz). The electrodes implanted for DBS also offer the opportunity to record neural activity from the human basal ganglia. This study aimed to assess whether oscillations at frequencies >100 Hz operate in the human STN. While recording local field potentials from the STN of nine patients with Parkinsons disease through DBS electrodes, we found a dopamine- and movement-dependent 300-Hz rhythm. At rest, and in the absence of dopaminergic medication, in most cases (eight out of 11 nuclei) the 1001000 Hz band showed no consistent rhythm. Levodopa administration elicited (or markedly increased) a 300-Hz rhythm at rest [(mean ± SD) central frequency: 319 ± 33 Hz; bandwidth: 72 ± 21 Hz; power increase (after medication before medication)/before medication: 1.30 ± 1.25; n = 11, P = 0.00098]. The 300-Hz rhythm was also increased by apomorphine, but not by orphenadrine. The 300-Hz rhythm was modulated by voluntary movement. Before levodopa administration, movement-related power increase in the 300-Hz rhythm was variably present in different subjects, whereas after levodopa it became a robust phenomenon [before 0.014 ± 0.014 arbitrary units (AU), after 0.178 ± 0.339 AU; n = 8, P = 0.0078]. The dopamine-dependent 300-Hz rhythm probably reflects a bistable compound nuclear activity and supports high-resolution information processing in the basal ganglia circuit. An absent 300-Hz subthalamic rhythm could be a pathophysiological clue in Parkinsons disease. The 300-Hz rhythm also provides the rationale for an excitatoryand not only inhibitoryinterpretation of DBS mechanism of action in humans.
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