小檗碱
自噬
高磷酸化
认知功能衰退
葛兰素史克-3
τ蛋白
转基因小鼠
PI3K/AKT/mTOR通路
蛋白激酶B
蛋白磷酸酶2
药理学
糖原合酶
化学
阿尔茨海默病
神经科学
痴呆
医学
转基因
激酶
生物
生物化学
内科学
磷酸酶
疾病
磷酸化
信号转导
细胞凋亡
基因
作者
Ying Chen,Yu‐Ling Chen,Yubin Liang,Hong-Da Chen,Xiaoying Ji,Min Huang
标识
DOI:10.1016/j.biopha.2019.109670
摘要
Berberine is a natural isoquinoline alkaloid isolated from the Rhizoma coptidis. Recent advances in research throw more lights of its beneficial role towards Alzheimer's disease (AD), including promoting β-amyloid (Aβ) clearance, as well as inhibiting Aβ production in the triple-transgenic mouse model of Alzheimer's disease (3×Tg AD). However, it remains unclarified if berberine has an effect on tau pathology. According to our study, berberine did not only significantly improve 3×Tg AD mice's spatial learning capacity and memory retentions, but also attenuated the hyperphosphorylation of tau. via modulating the activity of Akt/glycogen synthase kinase-3β and protein phosphatase 2A. Moreover, berberine reduced the level of tau through an autophagy-based route. It promoted autophagic clearance of tau by enhancing the activity of autophagy via the class III PI3K/beclin-1 pathway. Thus, our results suggest that berberine could mitigate cognitive decline by simultaneously targeting the hyperphosphorylation of tau and the autophagic clearance of tau in AD mice. These findings strongly support berberine as a potential drug candidate for AD.
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