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The pharmacodynamic active components study of Tibetan medicine Gentianopsis paludosa on ulcerative colitis fibrosis

机译:藏药龙莲族术治疗溃疡性结肠炎纤维化的药效学活性成分研究

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The current study focused on the pharmacodynamic activity components of Gentianopsis paludosa against ulcerative colitis (UC) fibrosis including symptoms of intestinal diarrhea and inflammatory. Trinitro-benzene-sulfonic acid induced UC model rats were gavaged with gradient polarity extracts respectively from-ethanol-extract of Gentianopsis paludosa. Masson staining and qRT-PCR methods were respectively used to assess the degree of UC fibrosis and detect the mRNA expressions of collagen I, collagen III, a-smooth muscle actin (alpha-SIVIA) and E-cadherin in colon tissue. Separated by silica gel column chromatography, further screening was conducted until active components appeared. Infrared, nuclear magnetic resonance, mass spectroscopy and ultraviolet methods were applied to confirm active components' structures. The results indicated that the expression of collagen I, collagen III and alpha-SMA mRNA in the colon tissues of acetidin group rats was obviously depressed compared with control groups while E-cadherin displayed just opposite. Dyed in blue indicating UC fibrosis degree, the area of acetidin group was less than that other experimental groups. Four components: (1,8-Dihydroxy-3,7-Dimethoxyxanthones, 1-hydroxy-3,7,8-Trimethoxyxanthones, 1,7-Dihydroxy-3,8-Dimethoxyxanthones and 1-hydroxy-3,7-Dimethoxyxanthones), were obtained from acetidin group and all of which have a significant equivalence to Gentianopsis paludosa on the therapeutic effect of UC fibrosis. Our findings revealed the activity components for clinical application history of Gentianopsis paludosa and provided a preliminary foundation for further new drug research and exploitation. (C) 2017 Elsevier B.V. All rights reserved.
机译:目前的研究侧重于杜兰甘蓝宫(UC)纤维化的药效学活性组分,包括肠道腹泻和炎症的症状。三腈 - 苯磺酸诱导的UC模型大鼠分别从龙莲草紫杉醇提取物中加长梯度极性提取物。分别用于评估UC纤维化程度的Masson染色和QRT-PCR方法,并检测结肠组织中胶原I,胶原III,A-平滑肌肌动蛋白(Alpha-Sivia)和E-Cadherin的mRNA表达。用硅胶柱色谱分离,进行进一步筛选直至出现活性组分。施用红外,核磁共振,质谱和紫外线方法以确认有源组分的结构。结果表明,与对照组相比,胰蛋白酶I,胶原III和α-SMA mRNA的表达明显抑制了对照组,而E-Cadherin恰好相反。以蓝色染色表明UC纤维化度,醋替辛基团的面积小于其他实验组。四种组分:( 1,8-二羟基-3,7-二甲氧基吡啶,1-羟基-3,7,8-三甲氧基吡喃酮,1,7-二羟基-3,8-二甲氧基吡啶和1-羟基-3,7-二甲氧基杂散) ,从醋Etidin基团获得,所有这些都对UC纤维化的治疗作用进行了龙莲族病症alpiopsis paludosa。我们的研究结果揭示了Gentianopsis Paludosa临床应用历史的活性组分,为进一步的新药物研究和剥削提供了初步基础。 (c)2017 Elsevier B.v.保留所有权利。

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