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Effect of taurine on oxidative stress and apoptosis-related protein expression in trinitrobenzene sulphonic acid-induced colitis

机译:牛磺酸对三硝基苯磺酸所致结肠炎氧化应激及凋亡相关蛋白表达的影响

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摘要

Ulcerative colitis (UC) is a multi-factorial inflammatory disease of the colon and rectum. The present study was undertaken to investigate the effect of taurine, an anti-oxidant amino acid, on oxidative stress and the expression of apoptosis-related proteins, pro-apoptotic Bax and anti-apoptotic B cell lymphoma-2 (Bcl-2) in colon tissue in rats with 2,4,6-trinitrobenzene sulphonic acid (TNBS)-induced colitis. Rats received taurine (1·5% w/v) in drinking water for 15 days before and 15 days after administration of TNBS solution. Then, colonic myeloperoxidase (MPO) activity, malondialdehyde (MDA) and glutathione (GSH) levels, and Bax and Bcl-2 expression were measured. TNBS-induced colitis caused significantly increased MPO activity and MDA levels and decreased GSH levels in colon tissue compared to controls. Increase in Bax expression and decrease in Bcl-2 expression were detected in colon of rats with TNBS-induced colitis. Taurine treatment was associated with amelioration in macroscopic and microscopic colitis scores, decreased colonic MPO activity and MDA levels and increased GSH levels in TNBS-induced colitis. In addition, taurine reduced the expression of Bax and prevented the loss of Bcl-2 proteins in colon tissue of rats with TNBS-induced colitis. The results of this study show that taurine administration may exert beneficial effects in UC by decreasing inflammatory reactions, oxidative stress and apoptosis.
机译:溃疡性结肠炎(UC)是结肠和直肠的多因素炎症。本研究旨在研究牛磺酸(一种抗氧化氨基酸)对大鼠体内氧化应激和凋亡相关蛋白,促凋亡Bax和抗凋亡B细胞淋巴瘤2(Bcl-2)表达的影响。 2,4,6-三硝基苯磺酸(TNBS)诱导的结肠炎在大鼠结肠组织中的作用。在给予TNBS溶液之前和之后15天,大鼠在饮用水中接受牛磺酸(1·5%w / v)。然后,测量结肠髓过氧化物酶(MPO)活性,丙二醛(MDA)和谷胱甘肽(GSH)水平,以及Bax和Bcl-2表达。与对照组相比,TNBS引起的结肠炎导致结肠组织中MPO活性和MDA水平显着提高,而GSH水平降低。在TNBS诱导的结肠炎大鼠结肠中检测到Bax表达增加和Bcl-2表达减少。牛磺酸治疗与宏观和微观结肠炎评分的改善,TNBS诱发的结肠炎结肠MPO活性和MDA水平降低以及GSH水平升高相关。此外,牛磺酸可降低TNBS引起的结肠炎大鼠结肠组织中Bax的表达并防止Bcl-2蛋白的丢失。这项研究的结果表明,牛磺酸给药可通过减少炎症反应,氧化应激和细胞凋亡在UC中发挥有益作用。

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