Neuroprotection and mechanisms of ginsenosides in nervous system diseases: Progress and perspectives.
Li ZhouFeilong TanXue ZhangYanhua LiWenjie YinPublished in: IUBMB life (2024)
Ginsenosides are the primary component discernible from ginseng, including Rb1, Rb2, Rd, Rg1, Rg2, and compound K, and so forth. They have been shown to have multiple pharmacological activities. In recent years, more and more studies have been devoted to the neuroprotection of various ginsenosides against neurological diseases and their potential mechanisms. This paper comprehensively summarizes and reviews the neuroprotective effects of various ginsenosides on neurological diseases, especially acute and chronic neurodegenerative diseases, and their mechanisms, as well as their potential therapeutic applications to promote neuroprotection in disease prevention, treatment, and prognosis. Briefly, ginsenosides exert effective neuroprotective effects on neurological conditions, including stroke, Alzheimer's disease, Parkinson's disease, and brain/spinal cord injuries through a variety of molecular mechanisms, including anti-inflammatory, antioxidant, and anti-apoptotic. Among them, some signaling pathways play important roles in related processes, such as PI3K/Akt, TLR4/NF-κB, ROS/TXNIP/NLRP3, HO-1/Nrf2, Wnt/β-catenin, and Ca 2+ pathway. In conclusion, the present study reviews the research progress on the neuroprotective effects of ginsenosides in the last decade, with the aim of furnishing essential theoretical underpinning and effective references for further research and exploration of the multiple medicinal values of Chinese herbal medicines and their small molecule compounds, including ginseng and panax ginseng. Because there is less evidence in the existing clinical studies, future research should be focused on clinical trials in order to truly reflect the clinical value of various ginsenosides for the benefit of patients.
Keyphrases
- cerebral ischemia
- pi k akt
- signaling pathway
- subarachnoid hemorrhage
- brain injury
- cell proliferation
- anti inflammatory
- blood brain barrier
- small molecule
- clinical trial
- spinal cord
- oxidative stress
- end stage renal disease
- cell death
- stem cells
- inflammatory response
- epithelial mesenchymal transition
- nlrp inflammasome
- toll like receptor
- ejection fraction
- chronic kidney disease
- functional connectivity
- risk assessment
- peritoneal dialysis
- spinal cord injury
- lps induced
- cognitive decline
- resting state
- open label
- neuropathic pain
- replacement therapy
- aortic dissection
- reactive oxygen species
- phase ii