竹骨丸通过激活il - 22/JAK1/STAT3信号通路减轻NAFLD

IF 2.2 4区 生物学 Q3 CELL BIOLOGY
Tong Wang, Xiaobo Zhang, Tao Shen, Zubing Zhou
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引用次数: 0

摘要

本研究旨在探讨助瘀丸对非酒精性脂肪性肝病(NAFLD)的降脂、抗炎和抗氧化作用,并确定其治疗作用是否通过调节IL-22/JAK1/STAT3信号通路介导。动物实验采用高脂饲料喂养C57BL/6小鼠17周,建立NAFLD模型。将患者随机分为对照组、竹瘀丸治疗组和阳性对照组,干预时间为6周。采集小鼠肝组织和血清,进行血脂和肝酶活性生化分析。肝切片进行HE染色和油红O染色,观察组织病理变化和脂质积累情况。ELISA法定量炎症因子水平,DCFH-DA和MitoSOX染色法检测肝脏活性氧(ROS)水平。在细胞实验中,以小鼠肝细胞AML-12为模型,用游离脂肪酸处理细胞模拟NAFLD微环境。ELISA检测炎症因子表达变化,检测细胞ROS和线粒体ROS水平。此外,利用siRNA技术沉默IL-22,并通过Colivelin激活JAK/STAT信号通路。观察细胞内脂质沉积和ROS信号的变化,WB法检测IL-22/JAK1/STAT3信号通路相关蛋白的表达变化。动物实验中,小鼠血清生化指标检测结果显示,竹骨丸能有效降低ALT、AST、TC、TG、LDL-C、HDL-C水平。HE和油红O染色显示逐瘀丸明显减轻肝脏脂质积聚和炎症浸润。炎症因子检测结果显示,逐瘀丸可显著降低小鼠血清中促炎因子IL-6、TNF-α、IL-1 β、MCP-1水平,升高IL-22表达。DCFH-DA和MitoSOX染色法结果显示,竹骨丸能显著降低NAFLD小鼠肝组织中ROS水平。体外实验表明,珠瘀丸可显著降低NAFLD细胞模型中促炎因子IL-6、TNF-α、IL-1 β、MCP-1水平,升高IL-22表达,显著降低ROS水平,升高p-JAK1蛋白、p-STAT3蛋白、BCL-2蛋白表达,降低BAX蛋白表达。sirna介导的IL-22沉默显著减弱了助瘀丸减少脂质沉积和增强抗氧化防御的治疗作用,也降低了其激活IL-22/JAK1/STAT3信号通路的能力。同时,STAT3激活剂Colivelin能够部分逆转IL-22沉默的影响。助瘀丸可调节脂质代谢,抑制炎症反应,减轻氧化应激,激活IL-22/JAK1/STAT3/BCL-2信号通路,改善NAFLD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zhuyu pill mitigates NAFLD through activation of IL22/JAK1/STAT3 signaling pathway

This study aims to investigate the lipid-lowering, anti-inflammatory, and antioxidant effects of Zhuyu Pill in non-alcoholic fatty liver disease (NAFLD), and to determine whether its therapeutic action is mediated through modulation of the IL-22/JAK1/STAT3 signaling pathway. In animal experiments, C57BL/6 mice were fed a high-fat diet for 17 weeks to induce a NAFLD model. They were randomly divided into a control group, a Zhuyu Pill treatment group, and a positive control group, and the intervention lasted for 6 weeks. Mouse liver tissue and serum were collected for biochemical analysis of blood lipids and liver enzyme activities. Liver sections were processed for HE staining and Oil Red O staining to evaluate histopathological changes and lipid accumulation. ELISA was employed to quantify inflammatory factor levels, while DCFH-DA and MitoSOX staining used to detect reactive oxygen species (ROS) in the liver. In cell experiments, mouse liver cells AML-12 were used as a model, and cells were treated with free fatty acids to simulate the NAFLD microenvironment. ELISA was used to detect changes in the expression of inflammatory factors and detecting the levels of cellular ROS and mitochondrial ROS. In addition, siRNA technology was used to silence IL-22 and activate the JAK/STAT signaling pathway with Colivelin. The changes in lipid deposition and ROS signaling in cells were observed, and the expression changes of IL-22/JAK1/STAT3 signaling pathway related proteins were detected by WB method. In animal experiments, the detection results of serum biochemical indicators in mice showed that Zhuyu Pill can effectively reduce the levels of ALT, AST, TC, TG, LDL-C, and HDL-C. HE and Oil Red O staining revealed that Zhuyu Pill markedly alleviated hepatic lipid accumulation and inflammatory infiltration. The results of inflammatory factors showed that treatment with Zhuyu Pill significantly reduced the levels of pro-inflammatory factors IL-6, TNF-α, IL-1 β, and MCP-1 in mouse serum, while increasing the expression of IL-22. The results of DCFH-DA and MitoSOX staining methods showed that Zhuyu Pill could significantly reduce the level of ROS in the liver tissue of NAFLD mice. In vitro experiments showed that treatment with Zhuyu Pill significantly reduced the levels of pro-inflammatory cytokines IL-6, TNF-α, IL-1 β, and MCP-1 in NAFLD cell models, increased the expression of IL-22, significantly reduced ROS levels, increased the expression of p-JAK1 protein, p-STAT3 protein, BCL-2 protein, and reduced the expression of BAX protein. SiRNA-mediated IL-22 silencing markedly attenuated the therapeutic effects of Zhuyu Pill on reducing lipid deposition and enhancing antioxidant defense, and also diminished its ability to activate the IL-22/JAK1/STAT3 signaling pathway. Meanwhile, STAT3 activator Colivelin was able to partially reverse the effects of IL-22 silencing. Zhuyu Pill can regulate lipid metabolism, inhibit inflammatory response, alleviate oxidative stress, and activate the IL-22/JAK1/STAT3/BCL-2 signaling pathway to improve NAFLD.

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来源期刊
Journal of Molecular Histology
Journal of Molecular Histology 生物-细胞生物学
CiteScore
5.90
自引率
0.00%
发文量
68
审稿时长
1 months
期刊介绍: The Journal of Molecular Histology publishes results of original research on the localization and expression of molecules in animal cells, tissues and organs. Coverage includes studies describing novel cellular or ultrastructural distributions of molecules which provide insight into biochemical or physiological function, development, histologic structure and disease processes. Major research themes of particular interest include: - Cell-Cell and Cell-Matrix Interactions; - Connective Tissues; - Development and Disease; - Neuroscience. Please note that the Journal of Molecular Histology does not consider manuscripts dealing with the application of immunological or other probes on non-standard laboratory animal models unless the results are clearly of significant and general biological importance. The Journal of Molecular Histology publishes full-length original research papers, review articles, short communications and letters to the editors. All manuscripts are typically reviewed by two independent referees. The Journal of Molecular Histology is a continuation of The Histochemical Journal.
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