联合服用梓醇、葛根素、天麻素和龙脑香酚可调节 Tlr4/Myd88/NF-κB 信号通路,缓解阿尔茨海默病的小胶质细胞炎症。

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2024-10-31 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1492237
Huijing Ren, Ling Tang, Zhiying Yuan, Yang Liu, Xuejiao Zhou, Xiao Xiao, Xingyu Wu, Weihai Chen, Yi Chen, Hongjin Wang, Qiang Xue, Xiaoyu Xu
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种渐进性神经退行性疾病,影响着全球数百万人,目前尚无有效的治疗方法。近几十年来,各种传统中药(TCM)及其有效成分在细胞和动物模型中显示出减轻阿尔茨海默病发病机制的潜力。然而,对于在实践中通常使用的中药配方的效果研究较少。本研究旨在探讨由4种中药成分(梓醇、葛根素、天麻素和龙胆泻肝素)组成的几种配方对链脲佐菌素(STZ)诱导的细胞和大鼠AD模型的治疗效果。实验采用新物体识别(NOR)、高架迷宫(EMP)和莫里斯水迷宫(MWM)测试评估大鼠的认知功能。利用高尔基体染色、血涂片和伊红(HE)染色以及尼氏染色分析评估海马组织的生理机能。基因表达谱采用转录组学和反转录定量聚合酶链反应分析,蛋白质表达水平则采用免疫印迹、免疫组织化学和免疫荧光测定。细胞因子的产生采用酶联免疫吸附测定法进行评估。结果表明,联合使用这四种成分(CPGB)对 AD 细胞模型具有卓越的缓解作用,这体现在促炎细胞因子产生减少和 Aβ 蛋白沉积减少上。进一步的体内和体外实验证实,不同剂量的 CPGB 配方能有效改善 STZ 诱导的认知障碍,如 NOR、MWM 和 EMP 测试所示,以及海马组织和三维脑神经血管单元(3D-NVU)模型的病理变化,包括减少 Aβ 蛋白沉积和斑块形成。转录组测序和分析确定了海马组织中因STZ和CPGB处理而导致表达水平显著改变的35个基因,这些基因富集在Tlr4/Myd88/NF-κB信号通路中。在 3D-NVU 模型中,对这一通路的干扰极大地影响了 CPGB 的治疗效果。总之,这些研究结果表明,通过调节Tlr4/Myd88/NF-κB信号通路,联合应用梓醇、葛根素、天麻素和龙胆紫对AD具有卓越的治疗效果。这项研究加强了中医药治疗AD的理论基础,为缓解和治疗AD提供了新的见解和参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined administration of catalpol, puerarin, gastrodin, and borneol modulates the Tlr4/Myd88/NF-κB signaling pathway and alleviates microglia inflammation in Alzheimer's disease.

Alzheimer's Disease (AD) is a progressive neurodegenerative disorder affecting millions of people worldwide, with no effective treatment currently available. In recent decades, various traditional Chinese medicines (TCMs) and their active ingredients have shown the potential to attenuate the pathogenesis of AD in cellular and animal models. However, the effects of TCM formulas, which are typically administered in practice, have been less studied. This study aims to investigate the therapeutic effects of several formulas consisting of 4 components herbal components: catalpol, puerarin, gastrodin, and borneol, on streptozotocin (STZ)-induced AD models in cells and rats. The new object recognition (NOR), elevated plus maze (EMP), and Morris water maze (MWM) tests were used to evaluate the cognitive functions of rats. Golgi staining, Haematoxylin and Eosin (HE) staining, and Nissl staining analyses were employed assess the physiology of hippocampal tissues. Gene expression profiles were analyzed used transcriptomics and reverse transcription quantitative polymerase chain reaction analysis, while protein expression levels were determined using immunoblotting, immunohistochemical, and immunofluorescence. The production of cytokines was evaluated with enzyme-linked immunosorbent assay. The results demonstrated that the combined administration of these 4 components (CPGB) had superior mitigating effects on AD cell model, as evidenced by the reduced pro-inflammatory cytokine production and decreased deposition of Aβ protein. Further in vivo and in vitro experiments confirmed that varying doses of CPGB formula effectively ameliorated STZ-induced cognitive deficits, as shown by NOR, MWM, and EMP tests, as well as pathological changes in hippocampal tissues and a 3-dimensional brain neurovascular unit (3D-NVU) model, including decreased deposition of Aβ protein and formation of plaques. Transcriptome sequencing and analysis identified 35 genes with significantly altered expression levels due to STZ and CPGB treatment in hippocampal tissues, which were enriched in the Tlr4/Myd88/NF-κB signaling pathway. Interference with this pathway significantly influenced the therapeutic effects of CPGB in the 3D-NVU model. Collectively, these findings suggest that the combined administration of catalpol, puerarin, gastrodin, and borneol offers superior therapeutic effects on AD by modulating the Tlr4/Myd88/NF-κB signaling pathway. This study strengthens the theoretical foundation for using TCMs to treat AD, proving new insights and references for alleviating and treating AD.

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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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