In vivo reversal of amyloid-β lesions in rat brain

被引:73
作者
Sigurdsson, EM
Permanne, B
Soto, C
Wisniewski, T
Frangione, B
机构
[1] NYU, Med Ctr, Dept Pathol, New York, NY 10016 USA
[2] NYU, Med Ctr, Dept Neurol, New York, NY 10016 USA
关键词
Alzheimer disease; amygdala; amyloid-beta; cell shrinkage; interleukin-1; beta; microglia; therapy;
D O I
10.1093/jnen/59.1.11
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cerebral amyloid-beta (A beta) deposition is central to the neuropathological definition of Alzheimer disease (AD) with A beta related toxicity being linked to its beta-sheet conformation and/or aggregation. We show that a beta-sheet breaker peptide (iA beta 5) dose-dependently and reproducibly induced in vivo disassembly of fibrillar amyloid deposits, with control peptides having no effect. The iA beta 5-induced disassembly prevented and/or reversed neuronal shrinkage caused by A beta and reduced the extent of interleukin-1 beta positive microglia-like cells that surround the A beta deposits. These findings suggest that beta-sheet breakers, such as iA beta 5 or similar peptidomimetic compounds, may be useful for reducing the size and/or number of cerebral amyloid plaques in A beta, and subsequently diminishing A beta-related histopathology.
引用
收藏
页码:11 / 17
页数:7
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