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传统药对马齿苋与石榴皮通过IL-6/STAT3/SOCS3通路减轻小鼠葡聚糖硫酸钠诱导的结肠炎。

Traditional herbal pair Portulacae Herba and Granati Pericarpium alleviates DSS-induced colitis in mice through IL-6/STAT3/SOCS3 pathway.

作者信息

Cheng Zhe, Zhou Yi, Xiong Xinyu, Li Lingli, Chen Zekai, Wu Fan, Dong Ruolan, Liu Qiong, Zhao Yan, Jiang Shujun, Yu Qin, Chen Guang

机构信息

Department of Integrated Traditional Chinese and Western Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

Department of Traditional Chinese Medicine, Wuhan Fourth Hospital, Wuhan 430033, China.

出版信息

Phytomedicine. 2024 Apr;126:155283. doi: 10.1016/j.phymed.2023.155283. Epub 2023 Dec 18.

Abstract

BACKGROUND

Portulacae Herba and Granati Pericarpium pair (PGP) is a traditional Chinese herbal medicine treatment for colitis, clinically demonstrating a relatively favorable effect on relieving diarrhea and abnormal stools. However, the underlying mechanism remain uncertain.

PURPOSE

The present study intends to evaluate the efficacy of PGP in treating colitis in mice and investigate its underlying mechanism.

METHODS

The protective effect of PGP against colitis was determined by monitoring body weight, colon length, colon weight, and survival rate in mice. Colonic inflammation was assessed by serum cytokine levels, colonic H&E staining, and local neutrophil infiltration. The reversal of intestinal epithelial barrier damage by PGP was subsequently analyzed with Western blot and histological staining. Furthermore, RNA-seq analysis and molecular docking were performed to identify potential pathways recruited by PGP. Following the hints of the transcriptomic results, the role of PGP through the IL-6/STAT3/SOCS3 pathway in DSS-induced colitis mice was verified by Western blot.

RESULTS

DSS-induced colitis in mice was significantly curbed by PGP treatment. PGP treatment significantly mitigated DSS-induced colitis in mice, as evidenced by improvements in body weight, DAI severity, survival rate, and inflammatory cytokines levels in serum and colon. Moreover, PGP treatment up-regulated the level of Slc26a3, thereby increasing the expressions of the tight junction/adherens junction proteins ZO-1, occludin and E-cadherin in the colon. RNA-seq analysis revealed that PGP inhibits the IL-6/STAT3/SOCS3 pathway at the transcriptional level. Molecular docking indicated that the major components of PGP could bind tightly to the proteins of IL-6 and SOCS3. Meanwhile, the result of Western blot revealed that the IL-6/STAT3/SOCS3 pathway was inhibited at the protein level after PGP administration.

CONCLUSION

PGP could alleviate colonic inflammation and reverse damage to the intestinal epithelial barrier in DSS-induced colitis mice. The underlying mechanism involves the inhibition of the IL-6/STAT3/SOCS3 pathway.

摘要

背景

马齿苋与石榴皮药对(PGP)是一种治疗结肠炎的传统中药,临床显示其在缓解腹泻和大便异常方面效果相对良好。然而,其潜在机制尚不确定。

目的

本研究旨在评估PGP治疗小鼠结肠炎的疗效并探究其潜在机制。

方法

通过监测小鼠体重、结肠长度、结肠重量和存活率来确定PGP对结肠炎的保护作用。通过血清细胞因子水平、结肠苏木精-伊红染色以及局部中性粒细胞浸润来评估结肠炎症。随后用蛋白质印迹法和组织学染色分析PGP对肠道上皮屏障损伤的逆转作用。此外,进行RNA测序分析和分子对接以确定PGP所涉及的潜在途径。根据转录组学结果的提示,通过蛋白质印迹法验证PGP在葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠中通过白细胞介素-6(IL-6)/信号转导和转录激活因子3(STAT3)/细胞因子信号转导抑制因子3(SOCS3)途径发挥的作用。

结果

PGP治疗可显著抑制DSS诱导的小鼠结肠炎。PGP治疗显著减轻了DSS诱导的小鼠结肠炎,体重、疾病活动指数严重程度、存活率以及血清和结肠中炎症细胞因子水平的改善证明了这一点。此外,PGP治疗上调了溶质载体家族26成员3(Slc26a3)的水平,从而增加了结肠中紧密连接/黏附连接蛋白闭锁小带蛋白1(ZO-1)、闭合蛋白和E-钙黏蛋白的表达。RNA测序分析显示PGP在转录水平上抑制IL-6/STAT3/SOCS3途径。分子对接表明PGP的主要成分可与IL-6和SOCS3的蛋白质紧密结合。同时,蛋白质印迹法结果显示PGP给药后IL-6/STAT3/SOCS3途径在蛋白质水平上受到抑制。

结论

PGP可减轻DSS诱导的结肠炎小鼠的结肠炎症并逆转肠道上皮屏障损伤。其潜在机制涉及对IL-6/STAT3/SOCS3途径的抑制。

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