Neurodegenerative disorders and ischemic brain diseases

被引:273
作者
Mattson, MP [1 ]
Duan, W [1 ]
Pedersen, WA [1 ]
Culmsee, C [1 ]
机构
[1] NIA, Neurosci Lab, Baltimore, MD 21224 USA
关键词
Alzheimer's disease; caspases; mitochondrial permeability transition; neurotrophic factors; oxidative stress; Parkinson's disease; telomerase;
D O I
10.1023/A:1009676112184
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Degeneration and death of neurons is the fundamental process responsible for the clinical manifestations of many different neurological disorders of aging, incuding Alzheimer's disease, Parkinson's disease and stroke. The death of neurons in such disorders involves apoptotic biochemical cascades involving upstream effectors (Par-4, p53 and pro-apoptotic Bcl-2 family members), mitochondrial alterations and caspase activation. Both genetic and environmental factors, and the aging process itself, contribute to intiation of such neuronal apoptosis. For example, mutations in the amyloid precursor protein and presenilin genes can cause Alzheimer's disease, while head injury is a risk factor for both Alzheimer's and Parkinson's diseases. At the cellular level, neuronal apoptosis in neurodegenerative disorders may be triggered by oxidative stress, metabolic compromise and disruption of calcium homeostasis. Neuroprotective (anti-apoptotic) signaling pathways involving neurotrophic factors, cytokines and "conditioning responses" can counteract the effects of aging and genetic predisposition in experimental models of neurodegenerative disorders. A better understanding of the molecular underpinnings of neuronal death is leading directly to novel preventative and therapeutic approaches to neurodegenerative disorders.
引用
收藏
页码:69 / 81
页数:13
相关论文
共 156 条
  • [41] 2-D
  • [42] Prostate apoptosis response-4 production in synaptic compartments following apoptotic and excitotoxic insults: Evidence for a pivotal role in mitochondrial dysfunction and neuronal degeneration
    Duan, WZ
    Rangnekar, VM
    Mattson, MP
    [J]. JOURNAL OF NEUROCHEMISTRY, 1999, 72 (06) : 2312 - 2322
  • [43] Increased amyloid-beta 42(43) in brains of mice expressing mutant presenilin 1
    Duff, K
    Eckman, C
    Zehr, C
    Yu, X
    Prada, CM
    Pereztur, J
    Hutton, M
    Buee, L
    Harigaya, Y
    Yager, D
    Morgan, D
    Gordon, MN
    Holcomb, L
    Refolo, L
    Zenk, B
    Hardy, J
    Younkin, S
    [J]. NATURE, 1996, 383 (6602) : 710 - 713
  • [44] Attenuation of delayed neuronal death after mild focal ischemia in mice by inhibition of the caspase family
    Endres, H
    Namura, S
    Skimizu-Sasamata, M
    Waeber, C
    Zhang, L
    Gómez-Isla, T
    Hyman, BT
    Moskowitz, MA
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (03) : 238 - 247
  • [45] Neuroprotective effects of gelsolin during murine stroke
    Endres, M
    Fink, K
    Zhu, JM
    Stagliano, NE
    Bondada, V
    Geddes, JW
    Azuma, T
    Mattson, MP
    Kwiatkowski, DJ
    Moskowitz, MA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (03) : 347 - 354
  • [46] Fischer P P, 1999, J Community Health Nurs, V16, P191, DOI 10.1207/S15327655JCHN1603_5
  • [47] Further evolution toward effective therapy for acute ischemic stroke
    Fisher, M
    Bogousslavsky, J
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (16): : 1298 - 1303
  • [48] FU W, 2000, IN PRESS J MOL NEURO, V14
  • [49] Anti-apoptotic role of telomerase in pheochromocytoma cells
    Fu, WM
    Begley, JG
    Killen, MW
    Mattson, MP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (11) : 7264 - 7271
  • [50] Cytosolic redistribution of cytochrome c after transient focal cerebral ischemia in rats
    Fujimura, M
    Morita-Fujimura, Y
    Murakami, K
    Kawase, M
    Chan, PH
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (11) : 1239 - 1247