Biochemical and Therapeutic Effects of Antioxidants in the Treatment of Alzheimer's Disease, Parkinson's Disease, and Amyotrophic Lateral Sclerosis

被引:187
作者
Di Matteo, Vincenzo [1 ]
Esposito, Ennio [1 ]
机构
[1] Consorzio Mario Negri Sud, Ist Ric Farmacol Mario Negri, I-66030 Chieti, Italy
关键词
neurodegeneration; Alzheimer's disease; Parkinson's disease; amyotrophic lateral sclerosis; oxidative stress; nuclear factor kB; antioxidants; polyphenols; neuroprotection; nutritional;
D O I
10.2174/1568007033482959
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Aging is a major risk factor for neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS). An unbalanced overproduction of reactive oxygen species (ROS) may give rise to oxidative stress which can induce neuronal damage, ultimately leading to neuronal death by apoptosis or necrosis. A large body of evidence indicates that oxidative stress is involved in the pathogenesis of AD, PD, and ALS. Several studies have shown that nutritional antioxidants (especially vitamin E and polyphenols) can block neuronal death in vitro, and may have therapeutic properties in animal models of neurodegenerative diseases including AD, PD, and ALS. Morever, clinical data suggest that nutritional antioxidants might exert some protective effect against AD, PD, and ALS. In this paper, the biochemical mechanisms by which nutritional antioxidants can reduce or block neuronal death occurring in neurodegenerative disorders are reviewed. Particular emphasis will be given to the role played by the nuclear transcription factor -kB (NF-kB) in apoptosis, and in the pathogenesis of neurodegenenerative disorders, such as AD, PD, and ALS. The effects of ROS and antioxidants on NF-kB function and their relevance in the pathophysiology of neurodegenerative diseases will also be examined.
引用
收藏
页码:95 / 107
页数:13
相关论文
共 279 条
[1]  
Abe K, 1997, NEUROL RES, V19, P124
[2]  
AGID Y, 1993, ADV NEUROL, V60, P148
[3]   Increased sensitivity of fibroblasts from amyotrophic lateral sclerosis patients to oxidative stress [J].
Aguirre, T ;
Van Den Bosch, L ;
Goetschalckx, K ;
Tilkin, P ;
Mathijs, G ;
Cassiman, JJ ;
Robberecht, W .
ANNALS OF NEUROLOGY, 1998, 43 (04) :452-457
[4]   Protein oxidation in the brain in Alzheimer's disease [J].
Aksenov, MY ;
Aksenova, MV ;
Butterfield, DA ;
Geddes, JW ;
Markesbery, WR .
NEUROSCIENCE, 2001, 103 (02) :373-383
[5]   Oxidative DNA damage in the parkinsonian brain: An apparent selective increase in 8-hydroxyguanine levels in substantia nigra [J].
Alam, ZI ;
Jenner, A ;
Daniel, SE ;
Lees, AJ ;
Cairns, N ;
Marsden, CD ;
Jenner, P ;
Halliwell, B .
JOURNAL OF NEUROCHEMISTRY, 1997, 69 (03) :1196-1203
[6]   N-acetyl-L-cysteine improves survival and preserves motor performance in an animal model of familial amyotrophic lateral sclerosis [J].
Andreassen, OA ;
Dedeoglu, A ;
Klivenyi, P ;
Beal, MF ;
Bush, AI .
NEUROREPORT, 2000, 11 (11) :2491-2493
[7]   Effects of an inhibitor of poly(ADP-ribose) polymerase, desmethylselegiline, trientine, and lipoic acid in transgenic ALS mice [J].
Andreassen, OA ;
Dedeoglu, A ;
Friedlich, A ;
Ferrante, KL ;
Hughes, D ;
Szabo, C ;
Beal, MF .
EXPERIMENTAL NEUROLOGY, 2001, 168 (02) :419-424
[8]  
Anglade P, 1997, HISTOL HISTOPATHOL, V12, P25
[9]   NF-kappa B: Ten years after [J].
Baeuerle, PA ;
Baltimore, D .
CELL, 1996, 87 (01) :13-20
[10]  
BAEUERLE PA, 1994, ANNU REV IMMUNOL, V12, P141, DOI 10.1146/annurev.immunol.12.1.141