Optimal Formula of Angelica sinensis Ameliorates Memory Deficits in β-amyloid Protein-induced Alzheimer’s Disease Rat Model

疾病 淀粉样β 当归 神经科学 τ蛋白 淀粉样蛋白(真菌学) 阿尔茨海默病 医学 生物 内科学 病理 替代医学 中医药
作者
Huping Wang,Wu H,Chao Ma,Qingtao Zeng,Kai-Min Zhu,Shumei Cui,Hailong Li,Wu Guotai,Zixiang Wu,Jianzheng He
出处
期刊:Current medical science [Springer Science+Business Media]
卷期号:42 (1): 39-47 被引量:3
标识
DOI:10.1007/s11596-022-2528-1
摘要

Angelica (A.) sinensis is used as a traditional medical herb for the treatment of neurodegeneration, aging, and inflammation in Asia. A. sinensis optimal formula (AOF) is the best combination in A. sinensis that has been screened to rescue the cognitive ability in β-amyloid peptide (Aβ25-35)-treated Alzheimer's disease (AD) rats. The objective of this study was to investigate the effect of AOF on the learning and memory of AD rats as well as to explore the underlying mechanisms.Male Wistar rats were infused with Aβ25-35 for AD model induction or saline (negative control). Five groups of AD rats were fed on AOF at 20, 40, or 80 mL/kg every day, donepezil at 0.9 mg/kg every day (positive control), or an equal volume of water (AD model) intragastrically once a day for 4 weeks, while the negative control rats were fed on water. The Morris water maze test was used to evaluate the cognitive function of the rats. The Aβ accumulation, cholinergic levels, and antioxidative ability were detected by ELISA. Additionally, the candidate mechanism was determined by gene sequencing and quantitative real-time polymerase chain reaction.The results showed that AOF administration significantly ameliorated Aβ25-35-induced memory impairment. AOF decreased the levels of amyloid-β precursor protein and Aβ in the hippocampus, rescued the cholinergic levels, increased the activity of superoxide dismutase, and decreased the malondialdehyde level. In addition, AOF inhibited the expression of IL1b, Mpo, and Prkcg in the hippocampus.These experimental findings illustrate that AOF prevents the decrease in cognitive function and Aβ deposits in Aβ25-35-treated rats via modulating neuroinflammation and oxidative stress, thus highlighting a potential therapeutic avenue to promote the co-administration of formulas that act on different nodes to maximize beneficial effects and minimize negative side effects.
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