%0 Journal Article %T Ropinirole Implants Reverse MPTP-Induced Parkinsonism in Rhesus Monkeys %A Steven J. Siegel %A Lauren Nagy %A Torben Skarsfeldt %A Mark Pierce %A Carol O¡¯ Neill %A Robert Lin %A Lori Langhamer %A Jeffery H. Kordower %J Pharmacology & Pharmacy %P 1-8 %@ 2157-9431 %D 2013 %I Scientific Research Publishing %R 10.4236/pp.2013.43A001 %X

Purpose: We compared efficacy and side effects of ropinirole implants with oral ropinirole in parkinsonian monkeys. Methods: Twenty monkeys received injections of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-hydrochloride (MPTP) to render them parkinsonian. Monkeys were then placed into 3 groups based upon clinical rating scores (CRS). Group 1 received oral ropinirole and placebo implants. Group 2 receivedropinirole implants that released 1/9th of the animals¡¯ optimal daily oral dose and oral placebo. Group 3 received placebo implants and oral placebo. Monkeys were assessed for pharmacokinetic data, CRS, Global Dyskinesia Rating Scale, and skin irritation. Results: For the ropinirole implant group, the activity pattern was similar to that seen pre-MPTP; which extended through the weekends and was greater than control treated parkinsonian monkeys. Oral ropinirole yielded a high degree of variability for activity, with values following oral dosing being higher than the pre-MPTP periodbut levels similar to placebo treated parkinsonian animals during weekends, which were excluded from oral dosing. Implants and oral treatment achieved significant improvement in CRS between 11 - 60 days and 4 - 60 days respectively. Conclusion: Low dose ropinirole implants have the potential to provide continuous clinical improvement in bradykinesia with fewer ¡°off periods¡± and lower risk for medication-induced psychosis than oral medication.

%K Ropinirole %K Implant %K Parkinson¡¯s Disease %K MPTP %K Pharmacokinetic %K Dyskinesia %U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=33495