The Amyloid Cascade Hypothesis in Alzheimer's Disease: It's Time to Change Our Mind

被引:258
作者
Ricciarelli, Roberta [1 ]
Fedele, Ernesto [2 ,3 ]
机构
[1] Univ Genoa, Sect Gen Pathol, Dept Expt Med, Genoa, Italy
[2] Univ Genoa, Sect Pharmacol & Toxicol, Dept Pharm, Genoa, Italy
[3] Univ Genoa, Ctr Excellence Biomed Res, Genoa, Italy
关键词
Alzheimer's disease; beta amyloid; clinical trials; LTP; memory; anti-amyloid therapy; HIPPOCAMPAL SYNAPTIC PLASTICITY; CYCLIC ADENOSINE-MONOPHOSPHATE; GAMMA-SECRETASE INHIBITOR; ACTIVATED RECEPTOR-GAMMA; LONG-TERM POTENTIATION; A-BETA; PRECURSOR PROTEIN; TRANSGENIC MICE; MOUSE MODELS; NEUROFIBRILLARY DEGENERATION;
D O I
10.2174/1570159X15666170116143743
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Since its discovery in 1984, the beta amyloid peptide has treaded the boards of neurosciences as the star molecule in Alzheimer's disease pathogenesis. In the last decade, however, this vision has been challenged by evidence-based medicine showing the almost complete failure of clinical trials that experimented anti-amyloid therapies with great hopes. Moreover, data have accumulated which clearly indicate that this small peptide plays a key role in the physiological processes of memory formation. In the present review, we will discuss the different aspects of the amyloid cascade hypothesis, highlighting its pros and cons, and we will analyse the results of the therapeutic approaches attempted to date that should change the direction of Alzheimer's disease research in the future.
引用
收藏
页码:926 / 935
页数:10
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