Ngo Fung Yin, Wang Weiwei, Chen Qilei, Zhao Jia, Chen Hubiao, Gao Jin-Ming, Rong Jianhui
School of Chinese Medicine, The University of Hong Kong, Hong Kong 999077, China.
Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling 712100, China.
Oxid Med Cell Longev. 2020 Aug 31;2020:5780703. doi: 10.1155/2020/5780703. eCollection 2020.
Aberrant microglial activation drives neuroinflammation and neurodegeneration in Alzheimer's disease (AD). The present study is aimed at investigating whether the herbal formula Qi-Fu-Yin (QFY) could inhibit the inflammatory activation of cultured BV-2 microglia. A network pharmacology approach was employed to predict the active compounds of QFY, protein targets, and affected pathways. The representative pathways and molecular functions of the targets were analyzed by Gene Ontology (GO) and pathway enrichment. A total of 145 active compounds were selected from seven herbal ingredients of QFY. Targets (e.g., MAPT, APP, ACHE, iNOS, and COX-2) were predicted for the selected active compounds based on the relevance to AD and inflammation. As a validation, fractions were sequentially prepared by aqueous extraction, ethanolic precipitation, and HPLC separation, and assayed for downregulating two key proinflammatory biomarkers iNOS and COX-2 in lipopolysaccharide- (LPS-) challenged BV-2 cells by the Western blotting technique. Moreover, the compounds of QFY in 90% ethanol downregulated iNOS in BV-2 cells but showed no activity against COX-2 induction. Among the herbal ingredients of QFY, Angelicae Sinensis Radix and Ginseng Radix et Rhizoma contributed to the selective inhibition of iNOS induction. Furthermore, chemical analysis identified ginsenosides, especially Rg3, as antineuroinflammatory compounds. The herbal formula QFY may ameliorate neuroinflammation via downregulating iNOS in microglia.
异常的小胶质细胞激活会引发阿尔茨海默病(AD)中的神经炎症和神经退行性变。本研究旨在探究中药方剂芪附饮(QFY)是否能抑制培养的BV-2小胶质细胞的炎症激活。采用网络药理学方法预测QFY的活性成分、蛋白质靶点及受影响的信号通路。通过基因本体论(GO)和通路富集分析靶点的代表性信号通路和分子功能。从QFY的七种草药成分中筛选出145种活性成分。根据与AD和炎症的相关性,预测所选活性成分的靶点(如MAPT、APP、ACHE、iNOS和COX-2)。作为验证,通过水提取、乙醇沉淀和高效液相色谱分离依次制备组分,并采用蛋白质印迹技术检测其对脂多糖(LPS)刺激的BV-2细胞中两种关键促炎生物标志物iNOS和COX-2的下调作用。此外,QFY的90%乙醇提取物中的化合物可下调BV-2细胞中的iNOS,但对COX-2的诱导无活性。在QFY的草药成分中,当归和人参有助于选择性抑制iNOS的诱导。此外,化学分析确定人参皂苷,尤其是Rg3,为抗神经炎症化合物。中药方剂QFY可能通过下调小胶质细胞中的iNOS来改善神经炎症。