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
  • [1] Alam ZI, 1997, J NEUROCHEM, V69, P1326
  • [2] Oxidative DNA damage in the parkinsonian brain: An apparent selective increase in 8-hydroxyguanine levels in substantia nigra
    Alam, ZI
    Jenner, A
    Daniel, SE
    Lees, AJ
    Cairns, N
    Marsden, CD
    Jenner, P
    Halliwell, B
    [J]. JOURNAL OF NEUROCHEMISTRY, 1997, 69 (03) : 1196 - 1203
  • [3] Bcl-x1 bax interaction after transient global ischemia
    Antonawich, FJ
    Krajewski, S
    Reed, JC
    Davis, JN
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (08) : 882 - 886
  • [4] The burden of dementia - A medical and research perspective
    Antuono, P
    Beyer, J
    [J]. THEORETICAL MEDICINE AND BIOETHICS, 1999, 20 (01) : 3 - 13
  • [5] Expression of interleukin-1 beta converting enzyme gene family and bcl-2 gene family in the rat brain following permanent occlusion of the middle cerebral artery
    Asahi, M
    Hoshimaru, M
    Uemura, Y
    Tokime, T
    Kojima, M
    Ohtsuka, T
    Matsuura, N
    Aoki, T
    Shibahara, K
    Kikuchi, H
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (01) : 11 - 18
  • [6] TUMOR-NECROSIS-FACTOR-ALPHA AND TUMOR-NECROSIS-FACTOR-BETA PROTECT NEURONS AGAINST AMYLOID BETA-PEPTIDE TOXICITY - EVIDENCE FOR INVOLVEMENT OF A KAPPA-B-BINDING FACTOR AND ATTENUATION OF PEROXIDE AND CA2+ ACCUMULATION
    BARGER, SW
    HORSTER, D
    FURUKAWA, K
    GOODMAN, Y
    KRIEGLSTEIN, J
    MATTSON, MP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) : 9328 - 9332
  • [7] Barger SW, 1996, MOL BRAIN RES, V40, P116
  • [8] Ischemic preconditioning and brain tolerance - Temporal histological and functional outcomes, protein synthesis requirement, and interleukin-1 receptor antagonist and early gene expression
    Barone, FC
    White, RF
    Spera, PA
    Ellison, J
    Currie, RW
    Wang, XK
    Feuerstein, GZ
    [J]. STROKE, 1998, 29 (09) : 1937 - 1950
  • [9] Altered calcium homeostasis and mitochondrial dysfunction in cortical synaptic compartments of presenilin-1 mutant mice
    Begley, JG
    Duan, WZ
    Chan, S
    Duff, K
    Mattson, MP
    [J]. JOURNAL OF NEUROCHEMISTRY, 1999, 72 (03) : 1030 - 1039
  • [10] Effects of different schedules of MPTP administration on dopaminergic neurodegeneration in mice
    Bezard, E
    Dovero, S
    Bioulac, B
    Gross, C
    [J]. EXPERIMENTAL NEUROLOGY, 1997, 148 (01) : 288 - 292