Literature DB >> 18072817

Spotlight on rasagiline in Parkinson's disease.

Vicki Oldfield1, Gillian M Keating, Caroline M Perry.   

Abstract

Rasagiline (Azilect) is a novel, selective, irreversible second-generation inhibitor of monoamine oxidase type B (MAO-B). It is administered orally once daily and is approved in the US, Canada, Mexico, Israel and the EU for use as monotherapy and as adjunct therapy in the treatment of Parkinson's disease. Results of well designed clinical studies indicate that rasagiline is effective as initial monotherapy and improves Parkinson's symptomatology in patients with early Parkinson's disease. In addition, when administered in conjunction with levodopa, in patients with moderate to advanced disease and motor fluctuations, rasagiline reduces mean daily 'off' time and increases daily 'on' time without troublesome dyskinesias, compared with controls. Rasagiline is generally well tolerated as monotherapy and adjunctive therapy and is administered once daily. Thus, rasagiline, administered as a simple and convenient dosage regimen, is a well tolerated and effective option for monotherapy in patients with early Parkinson's disease and for adjunctive therapy in patients with moderate to advanced disease.

Entities:  

Year:  2008        PMID: 18072817     DOI: 10.2165/00023210-200822010-00007

Source DB:  PubMed          Journal:  CNS Drugs        ISSN: 1172-7047            Impact factor:   5.749


  41 in total

1.  Pharmacology of rasagiline (N-propargyl-1R-aminoindan).

Authors:  J P Finberg; I Lamensdorf; M Weinstock; M Schwartz; M B Youdim
Journal:  Adv Neurol       Date:  1999

2.  A controlled trial of rasagiline in early Parkinson disease: the TEMPO Study.

Authors: 
Journal:  Arch Neurol       Date:  2002-12

Review 3.  The therapeutic potential of monoamine oxidase inhibitors.

Authors:  Moussa B H Youdim; Dale Edmondson; Keith F Tipton
Journal:  Nat Rev Neurosci       Date:  2006-04       Impact factor: 34.870

4.  The anti-Parkinson drug rasagiline and its cholinesterase inhibitor derivatives exert neuroprotection unrelated to MAO inhibition in cell culture and in vivo.

Authors:  M B Youdim; A Wadia; W Tatton; M Weinstock
Journal:  Ann N Y Acad Sci       Date:  2001-06       Impact factor: 5.691

5.  Rasagiline mesylate, a new MAO-B inhibitor for the treatment of Parkinson's disease: a double-blind study as adjunctive therapy to levodopa.

Authors:  J M Rabey; I Sagi; M Huberman; E Melamed; A Korczyn; N Giladi; R Inzelberg; R Djaldetti; C Klein; G Berecz
Journal:  Clin Neuropharmacol       Date:  2000 Nov-Dec       Impact factor: 1.592

6.  Tolerability, safety, pharmacodynamics, and pharmacokinetics of rasagiline: a potent, selective, and irreversible monoamine oxidase type B inhibitor.

Authors:  John J Thébault; Michel Guillaume; Ruth Levy
Journal:  Pharmacotherapy       Date:  2004-10       Impact factor: 4.705

7.  Rasagiline, a monoamine oxidase-B inhibitor, protects NGF-differentiated PC12 cells against oxygen-glucose deprivation.

Authors:  S Abu-Raya; E Blaugrund; V Trembovler; E Shilderman-Bloch; E Shohami; P Lazarovici
Journal:  J Neurosci Res       Date:  1999-11-01       Impact factor: 4.164

8.  Neuroprotective effect of rasagiline in a rodent model of Parkinson's disease.

Authors:  F Blandini; M T Armentero; R Fancellu; E Blaugrund; G Nappi
Journal:  Exp Neurol       Date:  2004-06       Impact factor: 5.330

9.  Contrasting neuroprotective and neurotoxic actions of respective metabolites of anti-Parkinson drugs rasagiline and selegiline.

Authors:  Orit Bar Am; Tamar Amit; Moussa B H Youdim
Journal:  Neurosci Lett       Date:  2004-01-30       Impact factor: 3.046

10.  Anti-apoptotic function of propargylamine inhibitors of type-B monoamine oxidase.

Authors:  M Naoi; W Maruyama; M B H Youdim; P Yu; A A Boulton
Journal:  Inflammopharmacology       Date:  2003       Impact factor: 4.473

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