郑晨娜, 段训威, 贾东方, 罗彩林, 汪宁卿, 杨会勇, 刁勇. 重组人组织激肽释放酶结合蛋白对小鼠溃疡性结肠炎的抗炎作用J. 药学学报, 2016,51(7): 1077-1082. doi: 10.16438/j.0513-4870.2015-1167
引用本文: 郑晨娜, 段训威, 贾东方, 罗彩林, 汪宁卿, 杨会勇, 刁勇. 重组人组织激肽释放酶结合蛋白对小鼠溃疡性结肠炎的抗炎作用J. 药学学报, 2016,51(7): 1077-1082. doi: 10.16438/j.0513-4870.2015-1167
ZHENG Chen-na, DUAN Xun-wei, JIA Dong-fang, LUO Cai-lin, WANG Ning-qing, YANG Hui-yong, DIAO Yong. Anti-inflammatory effect of recombinant human kallistatin in ulcerative colitis of miceJ. Acta Pharmaceutica Sinica, 2016,51(7): 1077-1082. doi: 10.16438/j.0513-4870.2015-1167
Citation: ZHENG Chen-na, DUAN Xun-wei, JIA Dong-fang, LUO Cai-lin, WANG Ning-qing, YANG Hui-yong, DIAO Yong. Anti-inflammatory effect of recombinant human kallistatin in ulcerative colitis of miceJ. Acta Pharmaceutica Sinica, 2016,51(7): 1077-1082. doi: 10.16438/j.0513-4870.2015-1167

重组人组织激肽释放酶结合蛋白对小鼠溃疡性结肠炎的抗炎作用

Anti-inflammatory effect of recombinant human kallistatin in ulcerative colitis of mice

  • 摘要: 本文考察了重组人组织激肽释放酶结合蛋白(kallistatin, Kal)对溃疡性结肠炎(UC)小鼠模型的体内抗炎效果。采用4%葡聚糖酸钠(DSS)建立小鼠UC模型,随机分为模型组与Kal高、中、低剂量治疗组及柳氮磺胺吡啶(SASP)治疗组,并与正常对照组比较。测定6组间小鼠体重、结肠长度及病变组织炎症因子及IL-10和TNF-α水平变化,并进行组织损伤评分。结果显示,与模型组相比,Kal高剂量治疗组和SASP治疗组的组织损伤评分、MPO/MDA/TNF-α水平均显著降低,而小鼠体重、IL-10水平和SOD活性则显著提高,趋近于正常对照组,经过Kal治疗后小鼠溃疡性结肠炎得到了明显的改善,且呈剂量依赖性。因此,本研究揭示了Kal可以改善小鼠溃疡性结肠炎,可能与其参与调控炎性细胞因子IL-10、TNF-α水平及具有一定抗氧化能力有关。

     

    Abstract: This study was designed to evaluate the anti-inflammatory effect of recombinant human kallistatin (Kal) on ulcerative colitis (UC) in the mouse model. Acute colitis was induced by administration of 4% dextran sodium suffate (DSS) to KM mice for 7 days. The mice were then randomized into 5 groups:model control, Kal 0.2 mg·kg-1·d-1, 1.0 mg·kg-1·d-1 and 2.0 mg·kg-1·d-1 group, salazosulfapyridine (SASP) group. Ten age-matched normal KM mouse were administered with saline in the normal control. The weight, colon length, inflammation factor (MPO/SOD/MDA) and TNF-α/IL-10 levels among the five groups of mice were determined. The results showed that histological index score and MPO/MDA/TNF-α levels of high-dose Kal treatment group and SASP group were significantly lower compared with the model group (P<0.01), but the weight, colon length, IL-10 level and SOD activity were significant higher than the model group (P<0.01), approaching the normal group. These parameters showed that Kal can significantly relieve the UC state in a dose-dependent manner. This study demonstrates that Kal significantly remits UC in mice, and participates in the regulation of inflammatory cytokines TNF-α/IL-10 levels and has some antioxidant activity.

     

/

返回文章
返回