神经炎症
小胶质细胞
神经病理学
吞噬作用
神经科学
免疫系统
转基因小鼠
脂多糖
β淀粉样蛋白
淀粉样蛋白(真菌学)
阿尔茨海默病
生物
医学
转基因
药理学
细胞生物学
免疫学
炎症
疾病
病理
生物化学
基因
作者
Yingxia Liang,David Y.W. Lee,Sherri Zhen,Haoqi Sun,Biyue Zhu,Jing Liu,Dan Lei,Chih‐Chung Lin,Siyi Zhang,Nicholas A. Jacques,Luisa Quinti,Chongzhao Ran,Changning Wang,Ana Griciuc,Se Hoon Choi,Rong Hua Dai,Thomas Efferth,Rudolph E. Tanzi,Can Zhang
出处
期刊:Phytomedicine
[Elsevier]
日期:2022-05-13
卷期号:104: 154158-154158
被引量:5
标识
DOI:10.1016/j.phymed.2022.154158
摘要
Based on the complex pathology of AD, a single chemical approach may not be sufficient to deal simultaneously with multiple pathways of amyloid-tau neuroinflammation. A polydrug approach which contains multiple bioactive components targeting multiple pathways in AD would be more appropriate. Here we focused on a Chinese medicine (HLXL), which contains 56 bioactive natural products identified in 11 medicinal plants and displays potent anti-inflammatory and immuno-modulatory activity.We investigated the neuroimmune and neuroinflammation mechanisms by which HLXL may attenuate AD neuropathology. Specifically, we investigated the effects of HLXL on the neuropathology of AD using both transgenic mouse models as well as microglial cell-based models.The 5XFAD transgenic animals and microglial cell models were respectively treated with HLXL and Aβ42, and/or lipopolysaccharide (LPS), and then analyzed focusing on microglia mediated Aβ uptake and clearance, as well as pathway changes.We showed that HLXL significantly reduced amyloid neuropathology by upregulation of microglia-mediated phagocytosis of Aβ both in vivo and in vitro. HLXL displayed multi-modal mechanisms regulating pathways of phagocytosis and energy metabolism.Our results may not only open a new avenue to support pharmacologic modulation of neuroinflammation and the neuroimmune system for AD intervention, but also identify HLXL as a promising natural medicine for AD.It is conceivable that the traditional wisdom of natural medicine in combination with modern science and technology would be the best strategy in developing effective therapeutics for AD.
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