[活血疏风颗粒通过TLR4/NF-κB炎症通路减轻慢性偏头痛小鼠中枢致敏]。

Q3 Medicine
Xiaotao Liang, Yifan Xiong, Xueqi Liu, Xiaoshan Liang, Xiaoyu Zhu, Wei Xie
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引用次数: 0

摘要

目的:探讨活血疏风颗粒(HXSFG)减轻慢性偏头痛小鼠模型中枢致敏的作用机制。方法:通过文献查阅分析其主要化学成分,并通过生物信息学分析探讨其药理作用机制。采用隔日(5次)腹腔注射硝酸甘油(10 mg/kg)建立CM雄性C57BL/6J小鼠模型,采用Von Frey试验和热板仪评价低、高剂量HXSFG灌胃或腹腔注射托吡酯改善中枢致敏的效果;RT-qPCR、Western blotting、免疫荧光染色检测各组炎症因子、TLR4/NF - κB信号通路蛋白表达及c-Fos、CGRP活化的变化。结果:网络药理学分析表明,黄芪多糖缓解CM的主要有效成分为刺芒柄花素、芍药苷、槲皮素和丹参酮。基因本体(Gene Ontology, GO)富集分析鉴定出492个GO条目,包括366个生物过程、46个细胞成分和80个分子功能。KEGG通路富集分析表明,toll样受体和NF - κB信号通路在HXSFG对CM的治疗作用中起关键作用。在CM小鼠模型中,托吡酯和HXSFG治疗均可缓解中枢致敏症状,小鼠的机械和热痛阈值得到改善。HXSFG显著降低小鼠模型c-Fos和CGRP的表达,改善炎症标志物,下调TLR4、p-NF - κB、IL-1β和TNF - α蛋白的表达。结论:HXSFG通过调节炎症通路和抑制TLR4/ NF-κB信号通路,有效减轻CM小鼠的中枢致敏,提示其可能作为CM的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Huoxue Shufeng Granule alleviates central sensitization in chronic migraine mice via TLR4/NF-κB inflammatory pathway].

Objectives: To investigate the therapeutic mechanism of Huoxue Shufeng Granules (HXSFG) for alleviating central sensitization in a mouse model of chronic migraine (CM).

Methods: We analyzed the main chemical components of HXSFG through literature review and explored their pharmacological mechanisms by bioinformatics analyses. In a male C57BL/6J mouse model of CM established by intraperitoneal injections of nitroglycerin (10 mg/kg) every other day (5 injections), the effects of gavage with low, and high doses of HXSFG or intraperitoneal injections of topiramate for ameliorating central sensitization were evaluated using Von Frey test and a hot plate apparatus; the changes in expressions of inflammatory factors, the proteins in the TLR4/NF‑κB signaling pathway, and activation of c-Fos and CGRP were detected using RT-qPCR, Western blotting and immunofluorescence staining.

Results: Network pharmacology analysis suggested that the main active components in HXSFG for alleviating CM included formononetin, paeoniflorin, quercetin, and tanshinone. Gene Ontology (GO) enrichment analysis identified 492 GO entries, comprising 366 biological processes, 46 cellular components, and 80 molecular functions. KEGG pathway enrichment analysis indicated that the Toll-like receptor and NF‑κB signaling pathways were crucial in mediating the therapeutic effects of HXSFG on CM. In the mouse models of CM, both topiramate and HXSFG treatments alleviated the symptoms of central sensitization, evidenced by improved mechanical and thermal pain thresholds in the mice. HXSFG significantly reduced the expression of c-Fos and CGRP, improved inflammatory markers, and downregulated the expressions of TLR4, p-NF‑κB, IL-1β, and TNF‑α proteins in the mouse models.

Conclusions: HXSFG effectively alleviates central sensitization in CM mice by modulating the inflammatory pathways and inhibiting the TLR4/ NF-κB signaling pathway, suggesting its potential as a therapeutic option for CM.

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来源期刊
南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
208
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