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乌索酸对葡聚糖硫酸钠诱导的结肠炎和脂多糖刺激的巨噬细胞的抗炎特性。

Anti-inflammatory properties of uvaol on DSS-induced colitis and LPS-stimulated macrophages.

作者信息

Du Shi-Yun, Huang Hai-Feng, Li Xian-Qian, Zhai Li-Xiang, Zhu Qin-Chang, Zheng Kai, Song Xun, Xu Chen-Shu, Li Chen-Yang, Li Ying, He Zhen-Dan, Xiao Hai-Tao

机构信息

1School of Pharmaceutical Sciences, Guangdong Key Laboratory for Genome Stability & Human Disease Prevention, Shenzhen Key Laboratory of Novel Natural Health Care Products, Innovation Platform for Natural Small Molecule Drugs, Engineering Laboratory of Shenzhen Natural Small Molecule Innovative Drugs, Health Science Center, Shenzhen University, Shenzhen, 518060 China.

2The Key Laboratory of Pharmacology and Druggability for Natural Medicines, Department of Education, Guizhou Medical University, Guiyang, 550025 Guizhou China.

出版信息

Chin Med. 2020 May 7;15:43. doi: 10.1186/s13020-020-00322-0. eCollection 2020.

Abstract

BACKGROUND

leaves are used as a kind of phytomedicine and the main ingredient in some traditional Chinese medicine products for the relief of colitis. To understand the bioactive constituents of L., we did a phytochemistry study and investigated anti-Inflammatory effects of compounds and explored the underlying mechanisms.

METHODS

We isolated compounds from ethanol extract of L. leaf and detected the most effective compound by NO inhibition assay. We investigated anti-Inflammatory effects on dextran sulfate sodium (DSS)-induced colitis mice and lipopolysaccharide (LPS)-stimulated RAW264.7 cells. The disease activity index was determined by scores of body weight loss, diarrhea and rectal bleeding; histological damage was analyzed by H&E staining; macrophages change in the colon were analyzed by immunohistochemistry (IHC); myeloperoxidase activity was measured by myeloperoxidase assay kits; levels of proinflammatory cytokines were determined by qPCR and ELISA; protein production such as COX-2, iNOS, STAT3 and ERK1/2 were determined by western blotting.

RESULTS

We isolated uvaol from ethanol extract of L. leaf and found uvaol has excellent potential of inhibiting NO production. We further found uvaol could attenuate disease activity index (DAI), colon shortening, colon injury, and colonic myeloperoxidase activity in DSS-induced colitis mice. Moreover, uvaol significantly reduces mRNA expression and production of pro-inflammatory cytokines (TNF-α, IL-6, IL-1β, and MCP-1) and infiltration of macrophages in colonic tissues of colitis mice. Studies on LPS challenged murine macrophage RAW246.7 cells also revealed that uvaol reduces mRNA expression and production of pro-inflammatory cytokines and mediators. Mechanically, uvaol inhibits the pro-inflammatory ERK/STAT3 axis in both inflamed colonic tissues and macrophages.

CONCLUSIONS

leaf contains uvaol and uvaol has potent anti-inflammatory effects on DSS-induced experimental colitis and LPS-stimulated RAW264.7 macrophage cells. These results suggest uvaol is a prospective anti-inflammatory agent for colonic inflammation.

摘要

背景

树叶被用作一种植物药,也是一些用于缓解结肠炎的中药产品的主要成分。为了解某植物的生物活性成分,我们进行了植物化学研究,研究了化合物的抗炎作用并探索其潜在机制。

方法

我们从某植物叶的乙醇提取物中分离化合物,并通过一氧化氮抑制试验检测最有效的化合物。我们研究了对葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠和脂多糖(LPS)刺激的RAW264.7细胞的抗炎作用。通过体重减轻、腹泻和直肠出血评分确定疾病活动指数;通过苏木精和伊红(H&E)染色分析组织学损伤;通过免疫组织化学(IHC)分析结肠中巨噬细胞的变化;通过髓过氧化物酶检测试剂盒测量髓过氧化物酶活性;通过定量聚合酶链反应(qPCR)和酶联免疫吸附测定(ELISA)测定促炎细胞因子水平;通过蛋白质印迹法测定COX-2、诱导型一氧化氮合酶(iNOS)、信号转导和转录激活因子3(STAT3)和细胞外信号调节激酶1/2(ERK1/2)等蛋白质的产生。

结果

我们从某植物叶的乙醇提取物中分离出羽扇豆醇,并发现羽扇豆醇具有出色的抑制一氧化氮产生的潜力。我们进一步发现羽扇豆醇可以减轻DSS诱导的结肠炎小鼠的疾病活动指数(DAI)、结肠缩短、结肠损伤和结肠髓过氧化物酶活性。此外,羽扇豆醇显著降低结肠炎小鼠结肠组织中促炎细胞因子(肿瘤坏死因子-α、白细胞介素-6、白细胞介素-1β和单核细胞趋化蛋白-1)的mRNA表达和产生以及巨噬细胞的浸润。对LPS刺激的小鼠巨噬细胞RAW246.7细胞的研究还表明,羽扇豆醇降低促炎细胞因子和介质的mRNA表达和产生。从机制上讲,羽扇豆醇在炎症结肠组织和巨噬细胞中均抑制促炎ERK/STAT3轴。

结论

某植物叶含有羽扇豆醇,羽扇豆醇对DSS诱导的实验性结肠炎和LPS刺激后的RAW264.7巨噬细胞具有强大的抗炎作用。这些结果表明羽扇豆醇是一种用于结肠炎症的前瞻性抗炎剂。

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