Angesinenolide B, A邻苯二聚体过氧化,通过抑制MAPK/STATs信号通路和ROS产生发挥抗炎作用。

IF 4.1 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2025-02-03 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S501313
Laibin Zhang, Yuan Liu, Huanhuan Wang, Shuangyan Guo, Jieli Lv
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引用次数: 0

摘要

目的:当归烯内酯B (Angesinenolide B, ASB)是一种具有过氧桥的苯酞二聚体,从中药当归中分离得到,具有显著的抗炎作用。本研究的目的是在脂多糖(LPS)刺激的巨噬细胞和cuso4诱导的斑马鱼模型中评估ASB的抗炎功能及其可能的机制。方法:采用Griess法测定lps刺激RAW264.7细胞中促炎介质一氧化氮(NO)水平。ELISA检测肿瘤坏死因子-α (TNF-α)和白细胞介素-6 (IL-6)的生成,qRT-PCR检测TNF-α、IL-6、诱导型NO合成酶(iNOS)和环氧合酶-2 (COX-2) mRNA的表达。采用荧光显微镜和流式细胞术检测ROS的生成。采用Western blot和免疫荧光技术评估ASB对iNOS和COX-2以及NF-κB、MAPK和STATs信号通路的影响。此外,通过分子对接分析验证了ASB与靶蛋白之间的亲和力。在体内,使用荧光探针DCFH-DA研究ROS的生成,并在cuso4诱导的斑马鱼炎症模型中评估TNF-α和IL-6 mRNA的表达。结果:ASB处理可抑制lps刺激的RAW264.7细胞NO、TNF-α、IL-6、ROS水平,抑制iNOS、COX-2蛋白及mRNA表达,下调MAPK、STATs信号通路。此外,ASB有效地减弱了CuSO4诱导的斑马鱼炎症模型中ROS的过量产生和TNF-α和IL-6 mRNA的高表达。结论:ASB可能降低促炎介质和细胞因子水平,减少ROS的产生,下调MAPK和STATs信号通路,从而发挥抗炎作用。这意味着ASB有可能成为治疗炎症的可行方法。
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Angesinenolide B, A Phthalide Dimeric Peroxide, Exerts Anti-Inflammatory Properties by Suppressing MAPK/STATs Signaling Pathways and ROS Production.

Purpose: Angesinenolide B (ASB), a phthalide dimer with a peroxy bridge, is uniquely isolated from Chinese medicine Angelica sinensis radix and demonstrates significant anti-inflammatory properties. The objective of the current study was to evaluate the anti-inflammatory function of ASB and the potential mechanism in lipopolysaccharide (LPS)-stimulated macrophages and CuSO4-induced zebrafish models.

Methods: The level of nitric oxide (NO), a proinflammatory mediator, in LPS-stimulated RAW264.7 cells was quantified using Griess method. ELISA was employed to investigate the generation of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), while qRT-PCR was utilized to analyze the mRNA expressions of TNF-α, IL-6, inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2). Fluorescence microscopy and flow cytometry were employed for the determination of ROS generation. Western blot and immunofluorescence techniques were utilized to assess the impact of ASB on iNOS and COX-2, and on the NF-κB, MAPK and STATs signaling pathways. Moreover, the affinities between ASB and the target proteins were verified by molecular docking analysis. In vivo, ROS generation was explored using fluorescent probe DCFH-DA, and the TNF-α and IL-6 mRNA expressions were also evaluated in CuSO4-induced zebrafish inflammation model.

Results: ASB treatment was found to suppress the levels of NO, TNF-α, IL-6 and ROS, restrain the expressions of iNOS and COX-2 proteins and mRNA, as well as down-regulate MAPK and STATs signaling pathways in LPS-stimulated RAW264.7 cells. Furthermore, the administration of ASB effectively attenuated the overproduction ROS and the high mRNA expressions of TNF-α and IL-6 in a zebrafish model of inflammation induced by CuSO4.

Conclusion: ASB has the potentiality to reduce the levels of proinflammatory mediators and cytokines, decrease ROS production, and also down-regulate the MAPK and STATs signaling pathways, thereby exerting an anti-inflammatory effect. This implies that ASB could potentially serve as a viable approach for addressing inflammatory conditions.

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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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