Rasagiline: A novel anti-Parkinsonian monoamine oxidase-B inhibitor with neuroprotective activity

被引:147
作者
Weinreb, Orly [1 ]
Amit, Tamar [1 ]
Bar-Am, Orit [1 ]
Youdim, Moussa B. H. [1 ]
机构
[1] Technion Israel Inst Technol, Rappaport Fac Med, Eve Topf Ctr Excellence Neurodegenerat Dis, IL-31096 Haifa, Israel
关键词
Rasagiline; 1-(R)-aminoindan; Selegiline; Monoamine oxidase-A and -B; Parkinson's disease; Neurodegeneration; Neuroprotection; Neurorestoration; Mitochondria; Bcl-2 family proteins; Protein kinase C; Neurotrophic factors; AMYLOID PRECURSOR PROTEIN; MONO-AMINE OXIDASE; MPTP-INDUCED NEUROTOXICITY; MAO-B; CELL-DEATH; KINASE-C; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; NEUROTROPHIC FACTOR; L-DEPRENYL; SELECTIVE INHIBITORS;
D O I
10.1016/j.pneurobio.2010.06.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rasagiline (N-propargyl-1-(R)-aminoindan) is a novel, highly potent irreversible monoamine oxidase (MAO)-B inhibitor, anti-Parkinsonian drug. Rasagiline is effective as monotherapy or adjunct to L-Dopa for patients with early and late Parkinson's disease (PD). Its S-isomer, TVP1022 is thousand times less potent as an MAO-B inhibitor. However, both compounds have similar molecular mechanisms of neuroprotection in neuronal cell cultures and animal neurodegenerative models, indicating that the neuroprotective effect of rasagiline does not depend on inhibition of MAO-B, but rather is associated with the N-propargyl moiety, which promotes mitochondrial viability and stabilizes permeability transition by regulating Bcl-2 family proteins. Novel findings demonstrated that the major metabolite of rasagiline, 1-(R)-aminoindan has antioxidant and neuroprotective capabilities and thus, may contribute to the overt activity of its parent compound, rasagiline. This paper will review the earlier and present studies in the development of rasagiline for treatment of PD and discuss its pharmacology and applicable mechanism of action. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:330 / 344
页数:15
相关论文
共 138 条
[1]  
Abu-Raya S, 1999, J NEUROSCI RES, V58, P456, DOI 10.1002/(SICI)1097-4547(19991101)58:3<456::AID-JNR12>3.0.CO
[2]  
2-S
[3]   Neuroprotective and neurotoxic effects of monoamine oxidase-B inhibitors and derived metabolites under ischemia in PC12 cells [J].
Abu-Raya, S ;
Tabakman, R ;
Blaugrund, E ;
Trembovler, V ;
Lazarovici, P .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 434 (03) :109-116
[4]   Mitochondrial permeability transition mediates apoptosis induced by N-methyl(R)salsolinol, an endogenous neurotoxin, and is inhibited by Bcl-2 and rasagiline, N-propargyl-1(R)-aminoindan [J].
Akao, Y ;
Maruyama, W ;
Shimizu, S ;
Yi, H ;
Nakagawa, Y ;
Shamoto-Nagai, M ;
Youdim, MBH ;
Tsujimoto, Y ;
Naoi, M .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (04) :913-923
[5]   An anti-Parkinson's disease drug, N-propargyl-1(R)-aminoindan (rasagiline), enhances expression of anti-apoptotic Bcl-2 in human dopaminergic SH-SY5Y cells [J].
Akao, Y ;
Maruyama, W ;
Yi, H ;
Shamoto-Nagai, M ;
Youdim, MBH ;
Naoi, M .
NEUROSCIENCE LETTERS, 2002, 326 (02) :105-108
[6]   TURNOVER OF BRAIN MONOAMINE-OXIDASE MEASURED INVIVO BY POSITRON EMISSION TOMOGRAPHY USING L-[C-11]DEPRENYL [J].
ARNETT, CD ;
FOWLER, JS ;
MACGREGOR, RR ;
SCHLYER, DJ ;
WOLF, AP ;
LANGSTROM, B ;
HALLDIN, C .
JOURNAL OF NEUROCHEMISTRY, 1987, 49 (02) :522-527
[7]   CDNA CLONING OF HUMAN-LIVER MONOAMINE OXIDASE-A AND OXIDASE-B - MOLECULAR-BASIS OF DIFFERENCES IN ENZYMATIC-PROPERTIES [J].
BACH, AWJ ;
LAN, NC ;
JOHNSON, DL ;
ABELL, CW ;
BEMBENEK, ME ;
KWAN, SW ;
SEEBURG, PH ;
SHIH, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4934-4938
[8]  
BAKER GB, 1976, BRIT J PHARMACOL, V58, pP420
[9]   Contrasting neuroprotective and neurotoxic actions of respective metabolites of anti-Parkinson drugs rasagiline and selegiline [J].
Bar Am, O ;
Amit, T ;
Youdim, MBH .
NEUROSCIENCE LETTERS, 2004, 355 (03) :169-172
[10]   Regulation of Bcl-2 family proteins, neurotrophic factors, and APP processing in the neurorescue activity of propargylamine [J].
Bar-Am, O ;
Weinreb, O ;
Amit, T ;
Youdim, MBH .
FASEB JOURNAL, 2005, 19 (11) :1899-+