## Abstract The original article to which this Erratum refers has been published in __Movement__ Disorders 2005;20(3)306–314.
Multiple small doses of levodopa plus entacapone produce continuous dopaminergic stimulation and reduce dyskinesia induction in MPTP-treated drug-naïve primates
✍ Scribed by Lance A. Smith; Michael J. Jackson; Ghassan Al-Barghouthy; Sarah Rose; Mikko Kuoppamaki; Warren Olanow; Peter Jenner
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 115 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0885-3185
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✦ Synopsis
Abstract
Long‐acting dopamine agonist drugs induce a lower incidence of dyskinesia in MPTP‐treated primates and patients with Parkinson's disease compared to pulsatile treatment with levodopa, supporting the concept of continuous dopaminergic stimulation as a means of dyskinesia avoidance. We examined the effects of L‐dopa administered with or without the COMT inhibitor entacapone on dyskinesia induction in previously untreated MPTP‐treated common marmosets. Administration of L‐dopa (12.5 mg/kg p.o.) plus carbidopa twice daily produced fluctuating improvement in motor behavior coupled with dyskinesia. Coadministration with entacapone produced similar patterns of motor improvement and dyskinesia that were not different from that produced by L‐dopa alone. Treatment with L‐dopa (6.25 mg/kg p.o.) plus carbidopa four times daily reversed motor disability and induced dyskinesia in a manner that was not different from the twice‐daily treatment regimens. However, coadministration with entacapone produced more continuous improvement in locomotor activity with less dyskinesia than animals treated with L‐dopa four times daily alone. These data support the notion that pulsatile stimulation contributes to the development of dyskinesia and suggests that more frequent dosing of L‐dopa plus entacapone may be a useful treatment strategy for patients in the early stages of Parkinson's disease. © 2004 Movement Disorder Society
📜 SIMILAR VOLUMES
## Abstract Levodopa (L‐dopa) consistently primes basal ganglia for the appearance of dyskinesia in parkinsonian patients and 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine hydrochloride (MPTP) ‐treated primates. This finding may reflect its relatively short duration of effects resulting in pulsatile