Monoamine oxidase-B inhibitors in the treatment of Alzheimers disease

被引:172
作者
Thomas, T [1 ]
机构
[1] Woodlands Med & Res Ctr, Oldsmar, FL 34677 USA
关键词
MAO-B inhibitors; L-deprenyl; selegiline; Alzheimer's disease; Parkinson's disease; amyloid-beta toxicity; endothelium; nitric oxide; neuroprotection; cerebral blood flow;
D O I
10.1016/S0197-4580(00)00100-7
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The monoamine oxidase-B (MAO-B) inhibitor L-deprenyl (Selegiline) is effective in treating Parkinson's disease and possibly Alzheimer's disease, with a concomitant extension of life span. It has been suggested that the therapeutic efficacy of L-deprenyl may involve actions other than the inhibition of the enzyme MAO-B. This article reviews some novel actions of L-deprenyl and suggests that stimulation of nitric oxide (NO) production could be central to the action of the drug. L-Deprenyl induced rapid increases in NO production in brain tissue and cerebral blood vessels. In vitro or in vivo application of L-deprenyl produced vasodilatation. The drug also protected the vascular endothelium from the toxic effects of amyloid-beta peptide. Because NO modulates activities including cerebral blood flow and memory, and reduced NO production has been observed in AD brain, stimulation of NO production by L-deprenyl could contribute to the enhancement of cognitive function in AD. MAO-B inhibitors are unique in that they exert protective effects on both vascular and neuronal tissue and thus warrant further consideration in the treatment of vascular and neurodegenerative diseases associated with aging. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:343 / 348
页数:6
相关论文
共 43 条
[1]   INCREASED ACTIVITY OF BRAIN AND PLATELET MONOAMINE-OXIDASE IN DEMENTIA OF ALZHEIMER TYPE [J].
ADOLFSSON, R ;
GOTTFRIES, CG ;
ORELAND, L ;
WIBERG, A ;
WINBLAD, B .
LIFE SCIENCES, 1980, 27 (12) :1029-1034
[2]  
Barrett J S, 1996, Am J Ther, V3, P688, DOI 10.1097/00045391-199610000-00004
[3]   INCREASED LIFE EXPECTANCY RESULTING FROM ADDITION OF L-DEPRENYL TO MADOPAR TREATMENT IN PARKINSONS-DISEASE - A LONGTERM STUDY [J].
BIRKMAYER, W ;
KNOLL, J ;
RIEDERER, P ;
YOUDIM, MBH ;
HARS, V ;
MARTON, J .
JOURNAL OF NEURAL TRANSMISSION, 1985, 64 (02) :113-127
[4]   A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS [J].
BLISS, TVP ;
COLLINGRIDGE, GL .
NATURE, 1993, 361 (6407) :31-39
[5]   NITRIC-OXIDE, A NOVEL NEURONAL MESSENGER [J].
BREDT, DS ;
SNYDER, SH .
NEURON, 1992, 8 (01) :3-11
[6]   L-DEPRENYL IN THE TREATMENT OF MILD DEMENTIA OF THE ALZHEIMER-TYPE - RESULTS OF A 15-MONTH TRIAL [J].
BURKE, WJ ;
ROCCAFORTE, WH ;
WENGEL, SP ;
BAYER, BL ;
RANNO, AE ;
WILLCOCKSON, NK .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 1993, 41 (11) :1219-1225
[7]   Cerebrovascular disease and threshold for dementia in the early stages of Alzheimer's disease [J].
Esiri, MM ;
Nagy, Z ;
Smith, MZ ;
Barnetson, L ;
Smith, AD .
LANCET, 1999, 354 (9182) :919-920
[8]   NITRIC-OXIDE AND THE CEREBRAL-CIRCULATION [J].
FARACI, FM ;
BRIAN, JE .
STROKE, 1994, 25 (03) :692-703
[9]   L-deprenyl in Alzheimer's disease - Cognitive and behavioral effects [J].
Freedman, M ;
Rewilak, D ;
Xerri, T ;
Cohen, S ;
Gordon, AS ;
Shandling, M ;
Logan, AG .
NEUROLOGY, 1998, 50 (03) :660-668
[10]   Neuronal sparing and behavioral effects of the antiapoptotic drug, (-)Deprenyl, following kainic acid administration [J].
Gelowitz, DL ;
Paterson, IA .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1999, 62 (02) :255-262