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首页> 外文期刊>International immunopharmacology >Ameliorative effects of 3,4-oxo-isopropylidene-shikimic acid on experimental colitis and their mechanisms in rats
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Ameliorative effects of 3,4-oxo-isopropylidene-shikimic acid on experimental colitis and their mechanisms in rats

机译:3,4-氧代异亚丙基-草酸对大鼠实验性结肠炎的改善作用及其机制

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The aim of the present study was to investigate the therapeutic effect and mechanism of 3,4-oxo-isopropylidene-shikimic acid (ISA) on 2,4,6- trinitrobenzenesulfonic acid (TNBS)-induced colitis in rats. (50, 100, 200 mg/kg) was administered for 14 days, 1 day after the induction of colitis by TNBS. The colonic injury and inflammation were assessed by macroscopic damage scores and myeloperoxidase (MPO) activity. Malondialdehyde (MDA) and nitric oxide (NO) levels, and superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activities in plasma were measured with biochemical methods. Prostaglandin E2 (PGE2) level in colon was determined by radioimmunoassay. Expressions of inducible nitric oxide synthase (iNOS), cyclo-oxygenase-2 (COX-2), inhibitor kappa B-alpha (IκBα) and nuclear factor kappa B (NF-κB) p65 proteins in the colonic tissue were detected with immunohistochemistry. Enhanced colonic mucosal injury, inflammatory response and oxidative stress were observed in the animals clystered with TNBS, which was manifested as the significant increase in colon mucosal damage index, MPO activity, levels of MDA, NO and PGE2, as well as the expressions of iNOS, COX-2 and NF-κB p65 proteins in the colonic mucosa, and the significant decrease in expressions of IκBα proteins in the colonic mucosa. However, these parameters were found to be significantly ameliorated in rats treated with ISA at given doses, especially at 100 mg/kg and 200 mg/kg. Administration of ISA may have significant therapeutic effects on experimental colitis in rats, probably due to its mechanism of antioxidation, its inhibition of arachidonic acid metabolism and its modulation of the IκBα/NF-κB p65 expression.
机译:本研究的目的是研究3,4-氧代-异亚丙基-ki草酸(ISA)对2,4,6-三硝基苯磺酸(TNBS)诱导的大鼠结肠炎的治疗作用和机制。 TNBS诱发结肠炎后1天(50、100、200 mg / kg)施用14天。通过宏观损伤评分和髓过氧化物酶(MPO)活性评估结肠损伤和炎症。用生化方法测量血浆中丙二醛(MDA)和一氧化氮(NO)的含量,血浆超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的活性。通过放射免疫测定法测定结肠中的前列腺素E2(PGE2)水平。用免疫组织化学方法检测结肠组织中诱导型一氧化氮合酶(iNOS),环氧化酶-2(COX-2),抑制剂κB(IκBα)和核因子κB(NF-κB)p65蛋白的表达。 TNBS灌肠动物观察到结肠黏膜损伤,炎症反应和氧化应激增强,这表现为结肠黏膜损伤指数,MPO活性,MDA,NO和PGE2含量以及iNOS的表达显着增加。 ,结肠黏膜中COX-2和NF-κBp65蛋白的表达,以及结肠黏膜中IκBα蛋白表达的显着降低。但是,发现在给定剂量的ISA处理的大鼠中,尤其是在100 mg / kg和200 mg / kg的大鼠中,这些参数明显改善。 ISA的给药可能对大鼠实验性结肠炎具有显着的治疗作用,这可能是由于其抗氧化的机制,对花生四烯酸代谢的抑制以及对IκBα/NF-κBp65表达的调节。

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