Ginsenosides Rg1, Rb1 and rare ginsenosides: Promising candidate agents for Parkinson's disease and Alzheimer's disease and network pharmacology analysis

被引:0
作者
Jiang, Mingchun [1 ,2 ]
Chi, Jiaxin [1 ]
Qiao, Yifan [1 ]
Wang, Jinpeng [1 ]
Zhang, Zhixin [3 ]
Liu, Jia [1 ]
Sheng, Xinhao [1 ]
Yuan, Liangjie [1 ,2 ]
机构
[1] Shandong First Med Univ & Shandong Acad Med Sci, Sch Clin Med & Basic Med Sci, Jinan 250000, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Shandong First Med Univ, Affiliated Hosp 2, Tai An 271000, Peoples R China
[3] Shandong First Med Univ & Shandong Acad Med Sci, Sch Pharm, Jinan 250000, Peoples R China
关键词
Ginsenoside; Neurodegenerative disorder; Parkinson's disease; Alzheimer's disease; Network pharmacology; ALPHA-SYNUCLEIN; PC12; CELLS; AMYLOID-BETA; TAU-HYPERPHOSPHORYLATION; NEURONAL DEGENERATION; OXIDATIVE STRESS; MOUSE MODEL; RAT MODEL; PROTECTS; NEUROINFLAMMATION;
D O I
10.1016/j.phrs.2025.107578
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ginseng has been commonly used as a traditional Chinese medicine in Asian countries for thousands of years. Ginsenosides are the main pharmacologically active ingredients isolated from ginseng and have neuroprotective effects in the treatment of neurodegenerative disorders, such as Parkinson's disease (PD) and Alzheimer's disease (AD). To summarise and investigate the protective roles of ginsenosides and their underlying mechanisms in PD and AD, we used "Ginsenoside", "Parkinson's disease", "Alzheimer's disease", "anti-inflammatory", "antioxidant", and "apoptosis" as keywords to search and extract relevant literature information from scientific databases such as Elsevier, PubMed, and Google Scholar databases. In particular, we used network pharmacology to identify the potential targets of ginsenosides Rg1 and Rb1 in PD and AD. By analysing the existing research advances and network pharmacology results, we found that the neuroprotective effects of ginsenosides, primarily mediated through anti-inflammation, anti-apoptosis and anti-oxidative stress, etc, may be associated with the PI3K/Akt, BDNF/TrkB, MAPKs, NF-kappa B, Nrf2 and Wnt/beta-catenin signalling pathways. This review systematically summarises the different roles and mechanisms of ginsenosides Rg1, Rb1, and rare ginsenosides in PD and AD and provides new strategies for the treatment of neurodegenerative disorders. Network pharmacology provides a new research paradigm for the treatment of PD and AD using Rg1 and Rb1.
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