Use Chou's 5-steps Rule to Study the Mechanism of Uncaria Rhynchophylla for Treating Alzheimer's Disease Based on Network Pharmacology

Meng Fang, Peng Zeng, Jinglou Chen, Han Zhao, Haiping Wang, Jing Guo
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Abstract

Objective: To tentatively investigate the mechanism of uncaria rhynchophylla (UR) in treatment of Alzheimer's disease (AD). Methods: The targets and pathways of UR against AD were obtained from network pharmacology analysis. Results: We analyzed and obtained 7 active ingredients of UR, 29 targets of UR for treatment of AD, of which 26.9% targets were protein-modifying enzymes. The core active ingredients of UR were C3, C6, C7 and C5. The core targets of UR in the treatment of AD are AKT1, CASP3 and MTOR. The enrichment analysis of GO biological process suggests that the biological function of UR in the treatment of AD mainly involves regulation of neurotransmitter levels, rhythmic process, cellular response to nitrogen compound, calcium ion transport, response to toxic substance, response to oxygen levels, maintenance of location, positive regulation of cell death, and apoptotic signaling pathway, etc. KEGG pathway enrichment analysis showed that the most significant enrichment signaling pathways were neuroactive ligand-receptor interaction, calcium signaling pathway, cAMP signaling pathway, PI3K-Akt signaling pathway and so on. Conclusion: UR against AD may be related to its multiple components, multiple targets and biological functions. This study can provide a theoretical basis for further experimental and clinical research.
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基于网络药理学的周氏五步法研究钩藤治疗阿尔茨海默病的作用机制
目的:初步探讨钩尾虫(uncaria rhynchophyla, UR)治疗阿尔茨海默病(Alzheimer's disease, AD)的作用机制。方法:通过网络药理学分析获得UR抗AD的靶点和通路。结果:我们分析得到了UR的7种有效成分,获得了UR治疗AD的靶点29个,其中26.9%的靶点为蛋白修饰酶。UR的核心活性成分为C3、C6、C7和C5。UR治疗AD的核心靶点是AKT1、CASP3和MTOR。氧化石墨烯生物过程富集分析提示,尿酸治疗AD的生物学功能主要包括调节神经递质水平、节律过程、细胞对氮化合物的反应、钙离子转运、对有毒物质的反应、对氧水平的反应、位置维持、对细胞死亡的正向调节、凋亡信号通路等。KEGG通路富集分析显示,富集最显著的信号通路为神经活性配体-受体相互作用、钙信号通路、cAMP信号通路、PI3K-Akt信号通路等。结论:UR抗AD可能与其多组分、多靶点及生物学功能有关。本研究可为进一步的实验和临床研究提供理论依据。
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