Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jenner, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jenner, P.
NEUROLOGY 2005;65:S3-S5
© 2005 American Academy of Neurology

Neurology supplements are not peer-reviewed.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.

A novel dopamine agonist for the transdermal treatment of Parkinson’s disease

Peter Jenner, DSc, FRPharmS

From the Neurodegenerative Diseases Research Centre, Guy’s, King’s and St Thomas’ School of Biomedical Sciences, King’s College, London, United Kingdom.

Address correspondence to Dr. Peter Jenner, NDRG,GKT School of Biomedical Sciences, King’s 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 Parkinson’s 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.




This article has been cited by other articles:


Home page
The Annals of PharmacotherapyHome page
M. Y Splinter
Rotigotine: Transdermal Dopamine Agonist Treatment of Parkinson's Disease and Restless Legs Syndrome
Ann. Pharmacother., February 1, 2007; 41(2): 285 - 295.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
R. F. Pfeiffer
A promising new technology for Parkinson's disease
Neurology, July 26, 2005; 65(2_suppl_1): S6 - S10.
[Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 by AAN Enterprises, Inc.