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紫荆花通过调节抗氧化和炎症介质对乙酸诱导的溃疡性结肠炎的保护作用。

Protective effect of Bauhinia tomentosa on acetic acid induced ulcerative colitis by regulating antioxidant and inflammatory mediators.

机构信息

Department of Biotechnology, Karunya University, Karunya Nagar, Coimbatore, Tamil Nadu, India.

出版信息

Int Immunopharmacol. 2013 May;16(1):57-66. doi: 10.1016/j.intimp.2013.03.008. Epub 2013 Mar 26.

Abstract

Inflammatory bowel diseases (IBD), including Crohn's disease and Ulcerative colitis (UC), are life-long and recurrent disorders of the gastrointestinal tract with unknown etiology. The present study is designed to evaluate the ameliorative effect of Bauhinia tomentosa during ulcerative colitis (UC). Three groups of animals (n=6) were treated with B. tomentosa (5, 10, 20 mg/kg B.wt respectively) for 5 consecutive days before induction of UC. UC was induced by intracolonic injection of 3% acetic acid. The colonic mucosal injury was assessed by macroscopic scoring and histological examination. Furthermore, the mucosal content of lipid peroxidation (LPO), reduced glutathione (GSH), nitric oxide (NO), glutathione peroxidase (GPx) and superoxide dismutase (SOD) activity confirms that B. tomentosa could significantly inhibit colitis in a dose dependent manner. The myeloperoxidase (MPO), tumor necrosis factor (TNF-α), inducible nitric oxide synthase (iNOS) expression studies and lactate dehydrogenase (LDH) assay also supported that B. tomentosa could significantly inhibit experimental colitis. The effect was comparable to the standard drug sulfasalazine. Colonic mucosal injury parallels with the result of histological and biochemical evaluations. The extracts obtained from B. tomentosa possess active substances, which exert marked protective effects in acute experimental colitis, possibly by regulating the antioxidant and inflammatory mediators.

摘要

炎症性肠病(IBD),包括克罗恩病和溃疡性结肠炎(UC),是一种终生且反复发作的胃肠道疾病,其病因不明。本研究旨在评估羊蹄甲在溃疡性结肠炎(UC)中的改善作用。三组动物(n=6)分别在 UC 诱导前连续 5 天给予羊蹄甲(5、10、20mg/kg BW 体重)。通过直肠内注射 3%乙酸诱导 UC。通过宏观评分和组织学检查评估结肠黏膜损伤。此外,黏膜中脂质过氧化(LPO)、还原型谷胱甘肽(GSH)、一氧化氮(NO)、谷胱甘肽过氧化物酶(GPx)和超氧化物歧化酶(SOD)活性的黏膜含量证实,羊蹄甲可以在剂量依赖性的方式下显著抑制结肠炎。髓过氧化物酶(MPO)、肿瘤坏死因子(TNF-α)、诱导型一氧化氮合酶(iNOS)表达研究和乳酸脱氢酶(LDH)测定也支持羊蹄甲能显著抑制实验性结肠炎。其作用与标准药物柳氮磺胺吡啶相当。结肠黏膜损伤与组织学和生化评估的结果平行。羊蹄甲提取物中含有活性物质,这些物质可能通过调节抗氧化剂和炎症介质,对急性实验性结肠炎发挥显著的保护作用。

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