Synaptic vulnerability in neurodegenerative disease

被引:152
|
作者
Wishart, Thomas M.
Parson, Simon H. [1 ]
Gillingwater, Thomas H.
机构
[1] Univ Leeds, Fac Biol Sci, Inst Membrane & Syst Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Edinburgh, Sch Med, Ctr Integrat Physiol, Edinburgh EH8 9YL, Midlothian, Scotland
[3] Univ Edinburgh, Sch Med, Ctr Res Neurosci, Edinburgh EH8 9YL, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
Alzheimer disease; Huntington disease; motor neuron disease; neurodegeneration; prion; stroke; synapse;
D O I
10.1097/01.jnen.0000228202.35163.c4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Recent developments in our understanding of the pathophysiological mechanisms underlying degeneration in both the central and peripheral nervous systems have highlighted the critical role that synapses play in the instigation and progression of neuronal loss. In fact, several lines of evidence suggest that previous attempts to delay the onset and progression of clinical symptoms in a broad range of neurodegenerative diseases may have been unsuccessful as a result of a failure to protect synaptic cornpartments. As a result, the synapse needs to be viewed as an important target for the development of novel protective treatments aimed at preventing or slowing disease progression. We summarize important findings from human studies and animal models demonstrating common synaptic vulnerability across several neurodegenerative diseases. We also discuss recent developments in our understanding of degenerative mechanisms that are known to be localized to synapses and suggest potential ways to harness this understanding to develop synaptoprotective strategies for neurodegenerative disease.
引用
收藏
页码:733 / 739
页数:7
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