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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Regulation of JAK2/STAT3 and NF-kappa B signal transduction pathways; Veronica polita alleviates dextran sulfate sodium-induced murine colitis
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Regulation of JAK2/STAT3 and NF-kappa B signal transduction pathways; Veronica polita alleviates dextran sulfate sodium-induced murine colitis

机译:jak2 / stat3和nf-κB信号转导途径的调节; Veronica洛丽塔减轻了硫酸葡聚糖钠诱导的鼠结肠炎

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摘要

Ulcerative colitis (UC) is a major inflammatory bowel disease (IBD) has become a worldwide emergent disease. Veronica polita (VP) is a medicinal herb that has strong antioxidant and anti-inflammatory properties. In the present study, we studied the protective effect of VP on dextran sulfate sodium (DSS)-induced experimental colitis in mice. Phytochemical screening of VP extract demonstrated the presence of high total phenolic and flavonoid contents. Compared with the DSS group, VP significantly reduced clinical symptoms with less weight loss, bloody stool, shortening of the colon, and the severity of colitis was considerably inhibited as evidenced by the reduced disease activity index (DAI) and degree of histological damage in the colon and spleen. Also, treatment with VP considerably decreased the nitric oxide (NO) and malondialdehyde (MDA) level. VP remarkably downregulated the expression of tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), inducible nitric oxide synthetase (iNOS) and cyclooxygenase-2 (COX-2) in the colon tissue. Likewise, activation of the signal transducer and activator of transcription 3 (STAT3) and nuclear factor-kappa B (NF-kappa B) was effectively blocked by VP. Taken together, these results demonstrate that VP has an ameliorative effect on colonic inflammation mediated by modulation of oxidative stress and inflammatory mediators by suppressing the JAK2/STAT3 and NF-kappa B signaling pathways.
机译:溃疡性结肠炎(UC)是一种主要的炎症性肠病(IBD)已成为全球急性疾病。 Veronica洛妮塔(vp)是一种药草,具有强抗氧化和抗炎性质。在本研究中,我们研究了VP对硫酸葡聚糖钠(DSS)诱导的小鼠实验性结肠炎的保护作用。 VP提取物的植物化学筛选证明了高总酚类和黄酮含量的存在。与DSS组相比,VP显着降低临床症状,减肥,血腥粪便缩短,结肠缩短,并且显着抑制的严重程度,如减少的疾病活动指数(DAI)和组织学伤害程度证明结肠和脾脏。此外,用VP处理显着降低了一氧化氮(NO)和丙二醛(MDA)水平。 VP显着下调肿瘤坏死因子-α(TNF-α),白细胞介素-1β(IL-1β),白细胞介素-6(IL-6),诱导型一氧化氮合成酶(InOS)和环氧氧酶-2(COX -2)在结肠组织中。同样地,VP有效阻断信号传感器和转录3(STAT3)和核因子-Kappa(NF-Kappa B)的信号传感器和活化剂的激活。总之,这些结果表明,通过抑制JAK2 / STAT3和NF-Kappa B信号通路,VP对通过调节氧化应激和炎症介质介导的结肠炎症的改善作用。

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