期刊
NEUROSCIENCE LETTERS
卷 639, 期 -, 页码 36-42出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2016.12.064
关键词
Alzheimer's disease; beta-amyloid; Formononetin; APP; ER alpha; PI3K/Akt
资金
- National Natural Science Foundation of China [31360258]
- Guangdong Provincial Natural Science Foundation [2015A030313047, 2015A030313077]
Amyloid beta (A beta) is the main component of the amyloid plaques that accumulate in the brains of Alzheimer patients. Here, we reported the protective role of Formononetin (Form) against A beta(25-35)-induced neurotoxicity in HT22 cells. We found that Form significantly increased the viability of HT22 cells but decreased the cell apoptosis when challenging with A beta(25-35). The inhibitory effects of Form were associated with PI3K/Akt signaling pathway as PI3K inhibitor (LY294002) or ER alpha specific inhibitor (MPP) blocked the effects. Form also accelerated the non-amyloidogenic process of amyloid precursor protein (APP) by enhancing alpha-secretase activity and sAPP alpha release. Altogether, our findings may provide a novel therapeutic target to treat AD sufferers. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
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