槲皮素能否通过抑制NLRP3炎性体通路来预防阿尔茨海默病的易感因素?

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Azza S Awad, Bassant M El-Mokadem, Miar M Sherif, Abeer Bishr
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引用次数: 0

摘要

目的:大脑及其认知功能最容易受到应激的影响,已知应激可促进阿尔茨海默病(AD)的病理表现。本研究旨在通过研究NLRP3炎性体通路,探讨2周的限制性应激(RS)的作用,以及槲皮素剂量依赖性对AD早期发病的保护作用。方法:将大鼠分为4组:对照组(Con)、诱导组(Ind),其中诱导组每天6 h,持续2周,低剂量和高剂量Q (Q1+Ind和Q2+Ind)分别在诱导RS前给予相同时间。通过行为测试来评估认知功能。主要发现:高剂量的Q对NLRP3炎症小体通路、氧化应激、磷酸化tau蛋白和β淀粉样蛋白(Aβ)的抑制作用更强,2周的RS显著激活了这些蛋白,这些结果支持了组织病理学检查中细胞结构的改善和认知功能的增强,两剂量的Q显示了它们的保护作用。结论:这证明Q保护大脑免受2周RS诱导的AD的初始发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can Quercetin protect against the pre-disposing factors for Alzheimer's disease via inhibiting NLRP3 inflammasome pathway?

Objectives: The brain and its cognitive functions are most liable to stress, where it is known to promote the pathological manifestation of Alzheimer's disease (AD). This study aimed to investigate the effect of a 2-week-period of restraint stress (RS), as well as the protective effect of Quercetin in a dose-dependent manner against the early start of AD via studying the NLRP3 inflammasome pathway.

Methods: The rats were divided into four groups: control (Con), induction (Ind), where 6 h/day for 2 weeks of RS was induced, low and high doses of Q (Q1+Ind and Q2+Ind, respectively), which were administered before the induction of RS for the same period. Behavioral tests were performed to assess the cognitive functions.

Key findings: The higher dose of Q has shown more inhibition of the NLRP3 inflammasome pathway, oxidative stress, as well as the phosphorylated-tau and amyloid-β (Aβ) protein, which were significantly fired up by the 2 weeks of RS. These results were backed with the improved cellular structure in the histopathological examination and enhanced cognitive functions, where the two doses of Q have shown their protective effect.

Conclusions: This proves that Q shielded the brain against the initial pathogenesis of AD, induced by 2 weeks of RS.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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