Wuwei Kushen Changrong capsule alleviates DSS-induced colitis in mice via inhibition of NLRP3 inflammasome and STAT3 pathway.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Frontiers in Pharmacology Pub Date : 2024-09-12 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1423012
Mingjun Chen, Yang Feng, Dan Luo, Chen Zhang, Jing Zhou, Hengheng Dai, Mingxiong Lin, ZhanQi Tong
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Abstract

Purpose: Wuwei Kushen Changrong capsule (Composite Sophora Colon-soluble Capsule, CSCC) is a Chinese patent medicine developed to treat ulcerative colitis. Studies highlight CSCC potential efficacy for ulcerative colitis (UC) but unclear mechanism limits its widely treatment for patients. We aimed to investigate the anti-colitis efficacy of CSCC and explore the mechanism by which GPR43 inhibits the NLRP3/STAT3 signaling pathway, thereby mediating the protective effects of CSCC on the intestinal barrier.

Methods: The protective effects of CSCC were evaluated in a murine ulcerative colitis model induced by 3% DSS. Assessments included body weight, Disease Activity Index (DAI) score, colon length, and histopathological score. Colon tissue, cell function, and immune-inflammatory status were evaluated using immunohistochemistry, immunofluorescence, ELISA, and real-time fluorescence quantitative PCR (RT-PCR). Protein expression levels of relevant pathways and receptors were measured using Western blot. All experiments were repeated.

Results: CSCC protected mice from DSS-induced colitis by upregulating Gpr43, promoting the expression of ZO-1 and Occludin tight junction proteins. Mechanistically, CSCC inhibits the MEK4/JNK1/STAT3 activation pathway, consequently suppressing the STAT3/NLRP3/IL-1β pathway and inhibiting the production of inflammatory factors such as IL-17A.

Conclusion: The mechanisms through which CSCC protects against DSS-induced colitis may include upregulating Gpr43, inhibiting the STAT3/NLRP3 pathway, and suppressing inflammation factors like IL-17A. These findings highlight the mechanisms underlying CSCC's anti-colitis effects and suggest its potential as a therapeutic candidate for managing the progression of UC.

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武威苦参长荣胶囊通过抑制NLRP3炎性体和STAT3通路缓解DSS诱导的小鼠结肠炎
目的:无为苦参长荣胶囊(复方槐花结肠溶胶囊,CSCC)是一种用于治疗溃疡性结肠炎的中成药。研究表明,长荣胶囊对溃疡性结肠炎(UC)具有潜在疗效,但由于机制不清,其治疗范围有限。我们旨在研究CSCC的抗结肠炎功效,并探索GPR43抑制NLRP3/STAT3信号通路,从而介导CSCC对肠屏障保护作用的机制:方法:在 3% DSS 诱导的小鼠溃疡性结肠炎模型中评估 CSCC 的保护作用。评估包括体重、疾病活动指数(DAI)评分、结肠长度和组织病理学评分。使用免疫组化、免疫荧光、酶联免疫吸附和实时荧光定量 PCR(RT-PCR)对结肠组织、细胞功能和免疫炎症状态进行了评估。采用 Western 印迹法测定了相关通路和受体的蛋白表达水平。所有实验均重复进行:结果:CSCC通过上调Gpr43、促进ZO-1和Occludin紧密连接蛋白的表达,保护小鼠免受DSS诱导的结肠炎的影响。从机制上讲,CSCC抑制了MEK4/JNK1/STAT3活化途径,从而抑制了STAT3/NLRP3/IL-1β途径,抑制了IL-17A等炎症因子的产生:结论:CSCC保护DSS诱导的结肠炎的机制可能包括上调Gpr43、抑制STAT3/NLRP3通路和抑制IL-17A等炎症因子。这些发现强调了 CSCC 抗结肠炎作用的机制,并表明 CSCC 有可能成为控制 UC 病程进展的候选疗法。
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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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