A focus on the synapse for neuroprotection in Alzheimer disease and other dementias

被引:276
作者
Coleman, P
Federoff, H
Kurlan, R
机构
[1] Univ Rochester, Sch Med, Dept Neurol, Rochester, NY 14642 USA
[2] Univ Rochester, Sch Med, Ctr Aging & Dev Biol, Rochester, NY 14642 USA
关键词
D O I
10.1212/01.WNL.0000140626.48118.0A
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Synaptic dysfunction and failure are processes that occur early in Alzheimer disease ( AD) and are important targets for protective treatments to slow AD progression and preserve cognitive and functional abilities. Synaptic loss is the best current pathologic correlate of cognitive decline, and synaptic dysfunction is evident long before synapses and neurons are lost. Once synaptic function fails, even in the setting of surviving neurons, there may be little chance of effectively interfering with the disease process. This review emphasizes the importance of preserving synaptic structure and function (i.e., "synaptoprotection") in AD. Such "synaptoprotective" therapy will probably need to be administered at a critical early time point, perhaps years before onset of clinical symptoms.
引用
收藏
页码:1155 / 1162
页数:8
相关论文
共 133 条
  • [1] STRUCTURAL PLASTICITY OF SYNAPSES IN ALZHEIMERS-DISEASE
    ADAMS, IM
    [J]. MOLECULAR NEUROBIOLOGY, 1991, 5 (2-4) : 411 - 419
  • [2] BDNF-triggered events in the rat hippocampus are required for both short- and long-term memory formation
    Alonso, M
    Vianna, MRM
    Depino, AM
    Souza, TME
    Pereira, P
    Szapiro, G
    Viola, H
    Pitossi, F
    Izquierdo, I
    Medina, JH
    [J]. HIPPOCAMPUS, 2002, 12 (04) : 551 - 560
  • [3] β-amyloid neurotoxicity is exacerbated during glycolysis inhibition and mitochondrial impairment in the rat hippocampus in vivo and in isolated nerve terminals:: Implications for Alzheimer's disease
    Arias, C
    Montiel, T
    Quiroz-Báez, R
    Massieu, L
    [J]. EXPERIMENTAL NEUROLOGY, 2002, 176 (01) : 163 - 174
  • [4] Microglial activation by Alzheimer amyloid precursor protein and modulation by apolipoprotein E
    Barger, SW
    Harmon, AD
    [J]. NATURE, 1997, 388 (6645) : 878 - 881
  • [5] Activation of microglia by secreted amyloid precursor protein evokes release of glutamate by cystine exchange and attenuates synaptic function
    Barger, SW
    Basile, AS
    [J]. JOURNAL OF NEUROCHEMISTRY, 2001, 76 (03) : 846 - 854
  • [6] Hippocampal brain-derived neurotrophic factor gene regulation by exercise and the medial septum
    Berchtold, NC
    Kesslak, JP
    Cotman, CW
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 68 (05) : 511 - 521
  • [7] MORPHOLOGICAL ADAPTIVE RESPONSE OF THE SYNAPTIC JUNCTIONAL ZONES IN THE HUMAN DENTATE GYRUS DURING AGING AND ALZHEIMERS-DISEASE
    BERTONIFREDDARI, C
    FATTORETTI, P
    CASOLI, T
    MEIERRUGE, W
    ULRICH, J
    [J]. BRAIN RESEARCH, 1990, 517 (1-2) : 69 - 75
  • [8] BertoniFreddari C, 1996, ANAL QUANT CYTOL, V18, P209
  • [9] ENLARGEMENT OF SYNAPTIC SIZE AS A COMPENSATIVE REACTION IN AGING AND DEMENTIA
    BERTONIFREDDARI, C
    FATTORETTI, P
    PIERONI, M
    MEIERRUGE, W
    ULRICH, J
    [J]. PATHOLOGY RESEARCH AND PRACTICE, 1992, 188 (4-5) : 612 - 615
  • [10] CHARACTERIZATION OF NERVE GROWTH-FACTOR (NGF) RELEASE FROM HIPPOCAMPAL-NEURONS - EVIDENCE FOR A CONSTITUTIVE AND AN UNCONVENTIONAL SODIUM-DEPENDENT REGULATED PATHWAY
    BLOCHL, A
    THOENEN, H
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1995, 7 (06) : 1220 - 1228