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首页> 外文期刊>Human and Experimental Toxicology >Anti-inflammatory, antioxidant and anti-apoptotic activity of diosmin in acetic acid-induced ulcerative colitis
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Anti-inflammatory, antioxidant and anti-apoptotic activity of diosmin in acetic acid-induced ulcerative colitis

机译:乙酸诱导的溃疡性结肠炎中脱辛蛋白的抗炎,抗氧化和抗凋亡活性

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摘要

Ulcerative colitis (UC) is a chronic inflammatory disease affecting colon. The primary symptoms of UC are diarrhoea with blood and mucus and sometimes associated with pain. Aim: This study aimed to evaluate the effects of diosmin (DIO) on UC. Methods: UC was induced in rats by rectal administration of acetic acid (AA). The degree of mucosal ulceration and damage was determined by evaluating the disease activity index (DAI) and colon damage index scores. Inflammation, oxidative stress and apoptotic responses were determined by measuring the levels of tumour necrosis factor-α (TNF-α), cyclooxygenase-2 (COX-II), malondialdehyde (MDA) and reduced glutathione (GSH) in addition to myeloperoxidase (MPO) activity and caspase-3 expression. Results: The results of this study indicate that AA caused increase in DAI and colon damage index scores. Also, markers of inflammation (TNF-α, COX-II and MPO) and oxidative stress (MDA and reduced GSH) were significantly elevated. These changes were associated with increases in colon caspase-3 expression. Treatment of rats with two doses of DIO produced a dose-dependent decline in DAI and colon damage index scores. Also, DIO resulted in significant reduction of inflammatory and oxidative stress markers as well as reduced the expression of caspase-3. Conclusion: DIO therapy decreased UC development depending on its ability to decreases inflammation, oxidative stress and apoptosis in rat colon.
机译:溃疡性结肠炎(UC)是一种影响结肠的慢性炎症疾病。 UC的主要症状是血液和粘液的腹泻,有时与疼痛有关。目的:本研究旨在评估二孢子(DIO)对UC的影响。方法:通过直肠施用乙酸(AA)在大鼠中诱导UC。通过评估疾病活动指数(DAI)和结肠损伤指数评分来确定粘膜溃疡和损伤程度。通过测量肌髓氧化酶(MPO)除了测量肿瘤坏死因子-α(TNF-α),环氧氧酶-2(COX-II),丙二醛(MDA)和降低的谷胱甘肽(GSH)的肿瘤坏死因子-α(TNF-α)和还原谷胱甘肽(GSH)而确定炎症,氧化应激和凋亡反应。(MPO )活性和caspase-3表达。结果:该研究的结果表明,AA造成傣族和结肠损伤指数评分的增加。而且,炎症(TNF-α,COX-II和MPO)和氧化应激(MDA和减少GSH)的标记显着升高。这些变化与结肠Caspase-3表达的增加有关。用两剂DIO治疗大鼠产生的DAI和结肠损伤指数评分的剂量依赖性下降。此外,DIO导致炎性和氧化应激标记物的显着降低,以及降低Caspase-3的表达。结论:DIO治疗根据其降低炎症,氧化应激和大鼠结肠凋亡的能力降低了UC开发。

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