New insights into the role and mechanisms of ginsenoside Rg1 in the management of Alzheimer's disease

被引:59
|
作者
Wu, Jiao-Jiao [1 ]
Yang, Yu [1 ]
Wan, Yan [1 ]
Xia, Jia [1 ]
Xu, Jin-Feng [1 ]
Zhang, Li [1 ]
Liu, Dong [1 ]
Chen, Lu [1 ]
Tang, Fei [1 ]
Ao, Hui [1 ,2 ]
Peng, Cheng [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Key Lab Southwestern Chinese Med Resources, Chengdu, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Innovat Inst Chinese Med & Pharm, Chengdu 611137, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Ginsenoside Rg1; Pharmacological effects; AMYLOID PRECURSOR PROTEIN; NF-KAPPA-B; MEMORY IMPAIRMENTS; SIGNALING PATHWAY; OXIDATIVE STRESS; COGNITIVE IMPAIRMENT; TAU PHOSPHORYLATION; ENDOTHELIAL-CELLS; BETA-PEPTIDE; PC12; CELLS;
D O I
10.1016/j.biopha.2022.113207
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Alzheimer's disease (AD) is a common neurodegenerative disorder in the elderly characterized by memory loss and cognitive dysfunction. The pathogenesis of AD is complex. One-targeted anti-AD drugs usually fail to delay AD progression. Traditional Chinese medicine records have documented the use of the roots of Panax ginseng (ginseng roots) and its prescriptions to treat dementia. Ginsenoside Rg1, the main ginsenoside component of ginseng roots, exhibits a certain therapeutic effect in the abovementioned diseases, suggesting its potential in the management of AD. Therefore, we combed the pathogenesis of AD and currently used anti-AD drugs, and reviewed the availability, pharmacokinetics, and pharmaceutic studies of ginsenoside Rg1. This review summarizes the therapeutic effects and mechanisms of ginsenoside Rg1 and its deglycosylated derivatives in AD in vivo and in vitro. The main mechanisms include improvement in Ap and Tau pathologies, regulation of synaptic function and intestinal microflora, and reduction of inflammation, oxidative stress, and apoptosis. The underlying mechanisms mainly involve the regulation of PKC, MAPK, PI3K/Akt, CDK5, GSK-3 beta, BDNF/TrkB, PKA/CREB, FGF2/Akt, p21WAF1/CIP1, NF-0, NLRP1, TLR3, and TLR4 signaling pathways. As the effects and underlying mechanisms of ginsenoside Rg1 on AD have not been systematically reviewed, we have provided a comprehensive review and shed light on the future directions in the utilization of ginsenoside Rg1 and ginseng roots as well as the development of anti-AD drugs.
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页数:21
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