4.3 Review

Synaptic vulnerability in neurodegenerative disease

Journal

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01.jnen.0000228202.35163.c4

Keywords

Alzheimer disease; Huntington disease; motor neuron disease; neurodegeneration; prion; stroke; synapse

Funding

  1. Biotechnology and Biological Sciences Research Council [BB/D001722/1] Funding Source: researchfish
  2. Biotechnology and Biological Sciences Research Council [BB/D001722/1] Funding Source: Medline

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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.

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