Potential conflict of interest: Nothing to report.
Original Article
Stimulation of the subthalamic nucleus and impulsivity: Release your horses†
Article first published online: 2 JUL 2009
DOI: 10.1002/ana.21795
Copyright © 2009 American Neurological Association
Additional Information
How to Cite
Ballanger, B., van Eimeren, T., Moro, E., Lozano, A. M., Hamani, C., Boulinguez, P., Pellecchia, G., Houle, S., Poon, Y. Y., Lang, A. E. and Strafella, A. P. (2009), Stimulation of the subthalamic nucleus and impulsivity: Release your horses. Annals of Neurology, 66: 817–824. doi: 10.1002/ana.21795
- †
Publication History
- Issue published online: 23 DEC 2009
- Article first published online: 2 JUL 2009
- Accepted manuscript online: 2 JUL 2009 12:00AM EST
- Manuscript Accepted: 22 JUN 2009
- Manuscript Revised: 28 MAY 2009
- Manuscript Received: 19 JAN 2009
Funded by
- Canadian Institutes of Health Research (CIHR). Grant Number: MOP-64423
- CIHR New Investigator Research Award
- Canada Research Chair (tier 1) in Neuroscience
- Abstract
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- Cited By
Abstract
Objective
In Parkinson disease (PD) patients, deep brain stimulation (DBS) of the subthalamic nucleus (STN) may contribute to certain impulsive behavior during high-conflict decisions. A neurocomputational model of the basal ganglia has recently been proposed that suggests this behavioral aspect may be related to the role played by the STN in relaying a “hold your horses” signal intended to allow more time to settle on the best option. The aim of the present study was 2-fold: 1) to extend these observations by providing evidence that the STN may influence and prevent the execution of any response even during low-conflict decisions; and 2) to identify the neural correlates of this effect.
Methods
We measured regional cerebral blood flow during a Go/NoGo and a control (Go) task to study the motor improvement and response inhibition deficits associated with STN-DBS in patients with PD.
Results
Although it improved Unified Parkinson Disease Rating Scale motor ratings and induced a global decrease in reaction time during task performance, STN-DBS impaired response inhibition, as revealed by an increase in commission errors in NoGo trials. These behavioral effects were accompanied by changes in synaptic activity consisting of a reduced activation in the cortical networks responsible for reactive and proactive response inhibition.
Interpretation
The present results suggest that although it improves motor functions in PD patients, modulation of STN hyperactivity with DBS may tend at the same time to favor the appearance of impulsive behavior by acting on the gating mechanism involved in response initiation. Ann Neurol 2009;66:817–824

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