Present address: Lilly USA, Lilly Corporate Center, Indianapolis, IN 46285, USA.
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Anti-dyskinetic mechanisms of amantadine and dextromethorphan in the 6-OHDA rat model of Parkinson’s disease: role of NMDA vs. 5-HT1A receptors
Article first published online: 3 AUG 2012
DOI: 10.1111/j.1460-9568.2012.08243.x
© 2012 The Authors. European Journal of Neuroscience © 2012 Federation of European Neuroscience Societies and Blackwell Publishing Ltd
Additional Information
How to Cite
Paquette, M. A., Martinez, A. A., Macheda, T., Meshul, C. K., Johnson, S. W., Berger, S. P. and Giuffrida, A. (2012), Anti-dyskinetic mechanisms of amantadine and dextromethorphan in the 6-OHDA rat model of Parkinson’s disease: role of NMDA vs. 5-HT1A receptors. European Journal of Neuroscience, 36: 3224–3234. doi: 10.1111/j.1460-9568.2012.08243.x
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Present address: Lilly USA, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Publication History
- Issue published online: 5 NOV 2012
- Article first published online: 3 AUG 2012
- Received 27 March 2012, revised 19 June 2012, accepted 3 July 2012
- Abstract
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Keywords:
- 6-hydroxydopamine;
- dyskinesia;
- L-DOPA;
- Parkinson’s disease;
- serotonin
Abstract
Amantadine and dextromethorphan suppress levodopa (L-DOPA)-induced dyskinesia (LID) in patients with Parkinson’s disease (PD) and abnormal involuntary movements (AIMs) in the unilateral 6-hydroxydopamine (6-OHDA) rat model. These effects have been attributed to N-methyl-d-aspartate (NMDA) antagonism. However, amantadine and dextromethorphan are also thought to block serotonin (5-HT) uptake and cause 5-HT overflow, leading to stimulation of 5-HT1A receptors, which has been shown to reduce LID. We undertook a study in 6-OHDA rats to determine whether the anti-dyskinetic effects of these two compounds are mediated by NMDA antagonism and/or 5-HT1A agonism. In addition, we assessed the sensorimotor effects of these drugs using the Vibrissae-Stimulated Forelimb Placement and Cylinder tests. Our data show that the AIM-suppressing effect of amantadine was not affected by the 5-HT1A antagonist WAY-100635, but was partially reversed by the NMDA agonist d-cycloserine. Conversely, the AIM-suppressing effect of dextromethorphan was prevented by WAY-100635 but not by d-cycloserine. Neither amantadine nor dextromethorphan affected the therapeutic effects of L-DOPA in sensorimotor tests. We conclude that the anti-dyskinetic effect of amantadine is partially dependent on NMDA antagonism, while dextromethorphan suppresses AIMs via indirect 5-HT1A agonism. Combined with previous work from our group, our results support the investigation of 5-HT1A agonists as pharmacotherapies for LID in PD patients.