Ginsenoside Rg2 Ameliorates Alzheimer's Disease by Alleviating Neuroinflammation in APP/PS1 Mice.

IF 5.3 2区 医学 Q1 NEUROSCIENCES
Dilida Yeerkenbieke, Yue Guan, Jing Cui, Qianqian Zhang, Gong Wang, Yifa Zhou, Zhiping Li, Chunyue Wang, Di Wang
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Abstract

Introduction: Ginsenoside Rg2 (GRg2), a naturally occurring triterpenoid derived from ginseng rhizomes, exhibits neuroprotective properties. Neuroinflammation is recognized as one of the key pathogenic mechanisms underlying Alzheimer's disease (AD). This research aims to investigate the beneficial effects of GRg2 on AD and explore its potential mechanisms.

Methods: In APP/PS1 mice, cognitive and behavioral assessments were first performed. Subsequently, brain tissue analyses were performed using immunohistochemical analysis and Western blot. A combined analysis of the gut microbiome and metabolomics was conducted to explore potential mechanisms. Finally, key findings were further validated through immunofluorescence and enzymelinked immunosorbent assay.

Results: GRg2 enhanced learning, memory, and cognitive functions. And inhibits the deposition of β- amyloid and phosphorylated tau. GRg2 effectively inhibits the production of Bacteroides and Helicobacter. In addition, it reduced the levels of pyruvaldehyde and trimethylamine N-oxide, metabolites closely related to neuroinflammation. GRg2 effectively inhibited the activation of astrocytes and microglia in the brains of APP/PS1 mice, and also reduced the expression of neuroinflammatory mediators IL-6, IL-1β, and TNF-α.

Discussions: The findings of this study substantiate the neuroprotective efficacy of GRg2, providing a novel therapeutic strategy and theoretical foundation for natural product-based interventions against AD.

Conclusion: GRg2 improves cognitive function and mitigates AD pathology, which is at least partially attributed to its regulation of gut microbiota and metabolites, as well as its anti-neuroinflammatory effects.

人参皂苷Rg2通过减轻APP/PS1小鼠的神经炎症来改善阿尔茨海默病
人参皂苷Rg2 (GRg2)是一种从人参根茎中提取的天然三萜,具有神经保护作用。神经炎症被认为是阿尔茨海默病(AD)的主要致病机制之一。本研究旨在探讨GRg2对AD的有益作用,并探讨其潜在机制。方法:首先对APP/PS1小鼠进行认知和行为评估。随后,使用免疫组织化学分析和Western blot对脑组织进行分析。研究人员对肠道微生物组和代谢组学进行了联合分析,以探索潜在的机制。最后,通过免疫荧光和酶联免疫吸附试验进一步验证了关键发现。结果:GRg2增强了学习、记忆和认知功能。并抑制β-淀粉样蛋白和磷酸化tau蛋白的沉积。GRg2有效抑制拟杆菌和幽门螺杆菌的产生。此外,它还降低了与神经炎症密切相关的代谢物丙酮醛和三甲胺n -氧化物的水平。GRg2能有效抑制APP/PS1小鼠脑内星形胶质细胞和小胶质细胞的活化,降低神经炎症介质IL-6、IL-1β和TNF-α的表达。讨论:本研究结果证实了GRg2的神经保护作用,为基于天然产物的AD干预提供了新的治疗策略和理论基础。结论:GRg2改善认知功能,减轻AD病理,至少部分归因于其调节肠道微生物群和代谢物,以及抗神经炎症作用。
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来源期刊
Current Neuropharmacology
Current Neuropharmacology 医学-神经科学
CiteScore
8.70
自引率
1.90%
发文量
369
审稿时长
>12 weeks
期刊介绍: Current Neuropharmacology aims to provide current, comprehensive/mini reviews and guest edited issues of all areas of neuropharmacology and related matters of neuroscience. The reviews cover the fields of molecular, cellular, and systems/behavioural aspects of neuropharmacology and neuroscience. The journal serves as a comprehensive, multidisciplinary expert forum for neuropharmacologists and neuroscientists.
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