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雷公藤内酯醇抑制白细胞介素6可预防溃疡性结肠炎小鼠模型中的炎症。

Interleukin 6 inhibition by triptolide prevents inflammation in a mouse model of ulcerative colitis.

作者信息

Zhang Haifeng, Chen Weichang

机构信息

Department of Gastroenterology, The First Affiliated Hospital of Soochow University, Soochow, Jiangsu 215006, P.R. China.

Department of Infectious Diseases, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, P.R. China.

出版信息

Exp Ther Med. 2017 Sep;14(3):2271-2276. doi: 10.3892/etm.2017.4778. Epub 2017 Jul 11.

Abstract

The present study aimed to assess interleukin (IL)-6 expression in a murine model of ulcerative colitis (UC) induced by dextran sulfate sodium (DSS) and its potential association with the anti-colitis effects of triptolide (TL). Serum IL-6 levels were measured by ELISA. IL-6 gene expression levels in colonic mucosa specimens were assessed by reverse-transcription quantitative PCR and protein expression was evaluated by western blot analysis and immunohistochemistry. The expression of IL-6 was weak in mucosa specimens from normal control animals and upregulated in DSS-induced mice. In model mice treated with TL (0.4 and 0.6 mg/kg), dexamethasone or mesalazine, IL-6 expression was significantly reduced compared with that in model mice treated with normal saline or propylene glycol (P<0.05), while TL at 0.2 mg/kg did not elicit any significant inhibitory effect. There was no significant difference among TL (0.4 mg/kg and 0.6 mg/kg), mesalazine and dexamethasone treatments (P>0.05) in terms of IL-6 expression or histological score. The results of the present study indicated that IL-6 was overexpressed in a mouse model of UC and was involved in disease progression. In addition, TL exerted therapeutic effects in UC through inhibition of IL-6 expression.

摘要

本研究旨在评估硫酸葡聚糖钠(DSS)诱导的溃疡性结肠炎(UC)小鼠模型中白细胞介素(IL)-6的表达及其与雷公藤内酯醇(TL)抗结肠炎作用的潜在关联。采用酶联免疫吸附测定(ELISA)法检测血清IL-6水平。通过逆转录定量聚合酶链反应评估结肠黏膜标本中IL-6基因表达水平,采用蛋白质印迹分析和免疫组织化学评估蛋白质表达。正常对照动物的黏膜标本中IL-6表达较弱,而在DSS诱导的小鼠中上调。在用TL(0.4和0.6mg/kg)、地塞米松或美沙拉嗪治疗的模型小鼠中,与用生理盐水或丙二醇治疗的模型小鼠相比,IL-6表达显著降低(P<0.05),而0.2mg/kg的TL未产生任何显著的抑制作用。在IL-6表达或组织学评分方面,TL(0.4mg/kg和0.6mg/kg)、美沙拉嗪和地塞米松治疗之间无显著差异(P>0.05)。本研究结果表明,IL-6在UC小鼠模型中过度表达并参与疾病进展。此外,TL通过抑制IL-6表达在UC中发挥治疗作用。

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