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

机译:雷公藤甲素对白介素6的抑制作用可预防溃疡性结肠炎小鼠模型的炎症

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摘要

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.
机译:本研究旨在评估在硫酸葡聚糖硫酸钠(DSS)诱导的溃疡性结肠炎(UC)小鼠模型中白介素(IL)-6的表达及其与雷公藤内酯(TL)的抗结肠炎作用的潜在关系。通过ELISA测量血清IL-6水平。结肠黏膜标本中IL-6基因表达水平通过逆转录定量PCR进行评估,蛋白质表达通过Western blot分析和免疫组化进行评估。 IL-6的表达在正常对照动物的粘膜标本中较弱,而在DSS诱导的小鼠中则上调。在用TL(0.4和0.6 mg / kg),地塞米松或美沙拉嗪处理的模型小鼠中,与用生理盐水或丙二醇处理的模型小鼠相比,IL-6表达显着降低(P <0.05),而在用0.2 mg的TL处理时/ kg没有引起任何明显的抑制作用。 TL(0.4 mg / kg和0.6 mg / kg),美沙拉嗪和地塞米松治疗之间在IL-6表达或组织学评分方面无显着差异(P> 0.05)。本研究的结果表明IL-6在UC小鼠模型中过表达,并参与疾病进展。另外,TL通过抑制IL-6表达在UC中发挥治疗作用。

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