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| Neurology supplements are not peer-reviewed. Information contained in Neurology supplements represent the opinions of the authors and are not endorsed by nor do they reflect the views of the American Academy of Neurology, Editor-in-Chief, or Associate Editors of Neurology. |
From the Neurodegenerative Diseases Research Centre, Guys, Kings and St Thomas School of Biomedical Sciences, Kings College, London, United Kingdom.
Address correspondence to Dr. Peter Jenner, NDRG,GKT School of Biomedical Sciences, Kings College, London SE1 1UL,UK; e-mail: peter.jenner{at}kcl.ac.uk
Rotigotine is a non-ergot, enantio-selective, D3/D2/D1 dopamine (DA) agonist drug that is effective in classical models of Parkinsons disease (PD), including the reserpinised mouse, the 6-hydroxydopamine-lesioned rat, and the MPTP-treated primate. It is active after oral administration but shows high clearance and a relatively short duration of effect. However, rotigotine is also effective after transdermal application in 6-hydroxydopamine-lesioned rats and MPTP-treated monkeys, in both of which the duration of effect is markedly enhanced. The pharmacologic properties of rotigotine suggest that it has the characteristics necessary to form the basis of a transdermal treatment for the control of motor symptoms of PD.
Publication of this supplement was supported by an educational grant from Schwarz Pharma. The sponsor has provided P.J. with the following support: an honorarium for his participation in this project, honoraria during his career, and grant support.
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