Novel approaches to increase synaptic resilience as potential treatments for Alzheimer's disease

被引:10
|
作者
Pham, Andrew Q. [1 ]
Dore, Kim [1 ]
机构
[1] UCSD, Ctr Neural Circuits & Behav, Dept Neurosci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Neuroprotection; Therapeutic strategies; AD model mice; APP; PS1; PSD-95; phosphatases; cofilin; calcineurin; BDNF; APOE2; Klotho; AMYLOID-BETA OLIGOMERS; LONG-TERM DEPRESSION; COGNITIVE DEFICITS; PHYSICAL-EXERCISE; DENDRITIC SPINES; NEUROTROPHIC FACTOR; APOLIPOPROTEIN-E; TG2576; MICE; PROTEIN; KLOTHO;
D O I
10.1016/j.semcdb.2022.03.032
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A significant proportion of brains with Alzheimer's disease pathology are obtained from patients that were cognitively normal, suggesting that differences within the brains of these individuals made them resilient to the disease. Here, we describe recent approaches that specifically increase synaptic resilience, as loss of synapses is considered to be the first change in the brains of Alzheimer's patients. We start by discussing studies showing benefit from increased expression of neurotrophic factors and protective genes. Methods that effectively make dendritic spines stronger, specifically by acting through actin network proteins, scaffolding proteins and inhibition of phosphatases are described next. Importantly, the therapeutic strategies presented in this review tackle Alzheimer's disease not by targeting plaques and tangles, but instead by making synapses resilient to the pathology associated with Alzheimer's disease, which has tremendous potential.
引用
收藏
页码:84 / 92
页数:9
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