结合网络药理学和实验验证研究人参首乌汤改善阿尔茨海默病的作用和机制

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-12-01 Epub Date: 2024-10-17 DOI:10.1080/13880209.2024.2415660
Jing-Jing Liu, Jian-Bo Yang, Ying Wang, Xiao-Ru Hu, Ya-Dan Wang, Li-Xing Nie, Feng Wei, Jian-Dong Yu, Ling-Wen Yao, Bei-Lei Xu, Shuang-Cheng Ma, Hong-Yu Jin
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引用次数: 0

摘要

背景:人参首乌汤(RSSW)治疗阿尔茨海默病(AD)的机制尚不清楚:材料与方法:10只SAMR1小鼠和40只SAMP小鼠:将10只SAMR1小鼠和40只SAMP8小鼠分为5组:对照组(SAMR1)、模型组(SAMP8)、阳性药物组(多奈哌齐,1.3 mg/kg/d)和RSSW组(低剂量,117 mg/kg/d;高剂量,234 mg/kg/d)。从 6 个月大开始,胃内给药,共 60 天。随后,利用新物体识别测试和莫里斯水迷宫测试评估了快速衰老小鼠记忆力的改善情况。通过对吸收的血液成分的鉴定和网络药理学分析,确定了参与治疗AD的有效成分和潜在靶点。最后,还利用免疫印迹法和酶联免疫吸附法检测了与AD相关的生物指标:结果:我们的研究结果表明,RSSW能有效改善SAMP8小鼠的记忆障碍,抑制tau过度磷酸化,减少β-淀粉样蛋白斑块沉积。RSSW中30种吸收的血液成分被鉴定出来,发现了96个在缓解AD中起关键作用的主要靶点。值得注意的是,所获得的主要靶点高度富集于SIRT1介导的信号通路中。随后的实验验证证实,RSSW 能激活 SIRT1/NF-κB、SIRT1/AMPK 和 SIRT1/p53 信号级联。通过分子对接,预测出了九种潜在的活性成分:我们的研究结果表明了RSSW治疗AD的机制,即通过减少大脑皮层组织炎症和细胞凋亡来改善记忆损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrating network pharmacology and experimental validation to investigate the effects and mechanism of Renshen Shouwu decoction for ameliorating Alzheimer's disease.

Context: The mechanism of Renshen Shouwu Decoction (RSSW) in treating Alzheimer's disease (AD) remains unknown.

Objective: This study investigates the effects and mechanism of RSSW for ameliorating AD.

Materials and methods: Ten SAMR1 mice and 40 SAMP8 mice were divided into five groups: control (SAMR1), model (SAMP8), positive drug (Donepezil, 1.3 mg/kg/d), and RSSW (Low-dose, 117 mg/kg/d; High-dose, 234 mg/kg/d). Starting from 6 months of age, the medications were administered intragastrically for a total of 60 days. Subsequently, memory improvement in rapidly aging mice was assessed using the novel object recognition test and Morris water maze test. Through the identification of absorbed blood components and analysis of network pharmacology, active ingredients and potential targets involved in the treatment of AD were identified. Finally, AD-related biological indicators were detected using western blotting and ELISA.

Result: Our results demonstrated that RSSW effectively ameliorated memory impairments, inhibited tau hyperphosphorylation, and reduced β-amyloid plaque deposition in SAMP8 mice. Thirty absorbed blood components in RSSW were identified, revealing identified 96 major targets that play a key role in alleviating AD. Notably, the obtained main targets were highly enriched in SIRT1-mediated signaling pathways. Subsequent experimental validation confirmed that RSSW activated the SIRT1/NF-κB, SIRT1/AMPK, and SIRT1/p53 signaling cascades. Nine potential active ingredients were predicted through molecular docking.

Discussion and conclusions: Our research findings suggest the mechanism of RSSW treatment for AD, which ameliorates memory impairments by reducing cortical tissue inflammation and apoptosis.

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CiteScore
7.20
自引率
4.30%
发文量
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