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J Neurophysiol 97: 2627-2641, 2007. First published January 10, 2007; doi:10.1152/jn.00443.2006
0022-3077/07 $8.00
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Internal Pallidal Neuronal Activity During Mild Drug-Related Dyskinesias in Parkinson's Disease: Decreased Firing Rates and Altered Firing Patterns

J. I. Lee1,, L. Verhagen Metman2,, S. Ohara3,, P. M. Dougherty4,, J. H. Kim5 and F. A. Lenz5

1Department of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea; 2Rush University Medical Center, Chicago, Illinois; 3Department of Neurosurgery, Kyoto Kizugawa Hospital, Kyoto, Japan; 4Department of Anesthesiology, M.D. Anderson Medical Center, Houston, Texas; 1,3,4,5Department of Neurosurgery, Johns Hopkins University, Baltimore; and 2Experimental Therapeutics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland

Submitted 26 April 2006; accepted in final form 7 January 2007

The neuronal basis of hyperkinetic movement disorders has long been unclear. We now test the hypothesis that changes in the firing pattern of neurons in the globus pallidus internus (GPi) are related to dyskinesias induced by low doses of apomorphine in patients with advanced Parkinson's disease (PD). During pallidotomy for advanced PD, the activity of single neurons was studied both before and after administration of apomorphine at doses just adequate to induce dyskinesias (21 neurons, 17 patients). After the apomorphine injection, these spike trains demonstrated an initial fall in firing from baseline. In nine neurons, the onset of ON was simultaneous with that of dyskinesias. In these spike trains, the initial fall in firing rate preceded and was larger than the fall at the onset of ON with dyskinesias. Among the three neurons in which the onset of ON occurred before that of dyskinesias, the firing rate did not change at the time of onset of dyskinesias. After injection of apomorphine, dyskinesias during ON with dyskinesias often fluctuated between transient periods with dyskinesias and those without. Average firing rates were not different between these two types of transient periods. Transient periods with dyskinesias were characterized by interspike interval (ISI) independence, stationary spike trains, and higher variability of ISIs. A small but significant group of neurons demonstrated recurring ISI patterns during transient periods of ON with dyskinesias. These results suggest that mild dyskinesias resulting from low doses of apomorphine are related to both low GPi neuronal firing rates and altered firing patterns.


Address for reprint requests and other correspondence: F. A. Lenz, Dept. of Neurosurgery, Meyer 8-181. Johns Hopkins Hospital, Baltimore, MD 21287-7713 (E-mail: flenz1{at}jhmi.edu)




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