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find Keyword "葡聚糖硫酸钠" 2 results
  • Effects of Mast Cell Membrane Stabilizer on Acute Colitis in Rats

    【摘要】 目的 研究肥大细胞膜稳定剂色甘酸二钠(disordium cromoglycate,DC)对葡聚糖硫酸钠(dextran sulfate sodium,DSS)诱导的大鼠急性结肠炎的影响。 方法 出生80~100 d的雄性SD清洁级大鼠30只,体重180~250 g。30只大鼠随机分为3组:正常对照组(A组)、溃疡性结肠炎组(B组)和DC组(C组),每组各10只。B组和C组自由饮用40 g/L DSS溶液(4%) 7 d诱发急性结肠炎,同时C组每天按100 mg/kg腹腔注射DC 1次,A组和B组每天腹腔注射等量的生理盐水。7 d后,处死各组大鼠。对各组大鼠行疾病活动指数评分,结肠组织行大体评分、组织学评分,检测门静脉血一氧化氮浓度,结肠组织髓过氧化物酶活性。 结果 疾病活动指数评分、大体评分、组织学评分、一氧化氮浓度及髓过氧化物酶活性均表现为B组gt;C组gt;A组(Plt;0.05)。 结论 肥大细胞膜稳定剂DC对DSS诱导的大鼠急性结肠炎有一定的保护作用。【Abstract】 Objective To observe the influence of the mast cell memebrane stabilizer, disordium cromoglycate (DC), on dextran sulfate sodium (DSS)-induced colitis in rats. Methods Thirty male Sprague-Dawley (SD) rats aged 80 to 100 days with their weight ranged from 180 to 250 g were randomly divided into 3 groups: normal control group (group A), dextran sulfate sodium group (group B) and disordium cromoglycate group (group C), with 10 rats in each. Rats in group B and C drank 40 g/L DSS solution (4%) for 7 days to induce acute colitis. At the same time, intraperitoneal administration of DC (100 mg/kg) to rats in group C was carried out once a day, while the other two groups of rats were given the same amount of normal saline solution. Disease activity index (DAI), gross and histological evaluation were analyzed. NO concentration of blood from portal vein was measured. Myeloperoxidase (MPO) activity of colonic tissue was detected. Results The experimental data of group C, including DAI, gross evaluation, histological assessment, NO concentration and MPO activity, were all significantly higher than those of group A (Plt;0.05), but lower than those of group B (Plt;0.05). Conclusion Disordium cromoglycate can protect the colon of rats with DSS-induced acute colitis.

    Release date:2016-09-08 09:26 Export PDF Favorites Scan
  • p38丝裂原活化蛋白激酶抑制剂对葡聚糖硫酸钠诱导的溃疡性结肠炎大鼠结肠传输功能的影响

    目的探讨p38丝裂原活化蛋白激酶(p38MAPK)抑制剂在葡聚糖硫酸钠(DSS)诱导的溃疡性结肠炎大鼠肠道动力障碍中的作用。 方法34只Sprague-Dawley大鼠用随机数字表法随机分成4组:正常对照组(正常组,n=8),DSS模型组(DSS组,n=8),DSS+生理盐水(NS)组(DSS+NS组,n=9),DSS+SB203580干预组(SB203580组,n=9)。除正常组外,所有大鼠每日饮用5% DSS溶液,SB203580组大鼠在饮用5%DSS溶液72 h以后,每天予以SB203580(1 mg/kg体质量)进行腹腔注射,观察各组大鼠的疾病活动指数(DAI),以酚红法测定大鼠结肠传输功能。 结果①DSS组和DSS+NS组大鼠的DAI评分明显高于正常组,SB203580组DAI评分明显降低,但仍然高于正常组(P<0.05),DSS组和DSS+NS组之间差异无统计学意义(P>0.05)。②与正常对照组比较,DSS组和DSS+NS组大鼠的结肠传输功能明显延迟,经SB203580干预后,其结肠传输功能明显改善(P<0.05),DSS组和DSS+NS组之间差异无统计学意义(P>0.05)。 结论SB203580能阻断p38MAPK信号转导通路,改善DSS诱导的结肠炎症,从而改善结肠传输功能。

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