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The Therapeutic Effect of Shark Liver Oil in a Rat Model of Acetic Acid-Induced Ulcerative Colitis

机译:鲨鱼肝油在醋酸诱导溃疡性结肠炎大鼠模型中的治疗作用

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Ulcerative colitis (UC) is one of the most well-known types of inflammatory bowel disease that manifests as recurrent inflammation of rectum and colon. The goal of this study is to evaluate the protective effects of shark liver oil (SLO) on acetic acid-induced ulcerative colitis in rats. Eighty induced UC rats were randomly divided into ten equal groups and received the following treatments for seven days: 1?ml of normal saline rectally, 1?ml of gel base (carboxymethyl cellulose) rectally, 10?mg/kg of Asacol rectally, 10?mg/kg of mesalazine orally, 5% gel form of SLO rectally, 10% gel form of SLO rectally, 200?mg of SLO orally, and 400?mg of SLO orally. We examined the oxidative stress indices, histopathological features, and body weight changes, as well as the function of the liver and kidneys at the end of treatment. Administration of 10% rectal and 400?mg oral SLO resulted in a significant weight gain. Also, glutathione peroxidase activity was significantly higher in 5% and 10% SLO-treated groups, and elevated superoxide dismutase activity in rats that received 5% SLO was observed compared to negative control and Asacol groups. While no significant changes were observed in most of the kidney and liver function markers, higher levels of aspartate aminotransferase were detected in the group that received 400?mg SLO orally compared to negative control and Asacol groups. Many histopathological signs of improvement were observed in mesalazine, Asacol, and SLO groups. There were no significant changes detected in the mean rank among different groups. Our data indicate that SLO supplementation could improve the amelioration of acetic acid-induced UC in rats due to its antioxidant effects.
机译:溃疡性结肠炎(UC)是最着名的炎症性炎症疾病之一,表现为直肠和结肠的复发性炎症。本研究的目标是评估鲨鱼肝油(SLO)对大鼠醋酸诱导的溃疡性结肠炎的保护作用。将80只诱导的UC大鼠随机分为十个相等的基团,并在七天内接受以下处理:1?ml常规盐水直肠,1?ml凝胶碱(羧甲基纤维素)直肠,10?Mg / kg浅藻醇直肠,10 ?Mg / kg甲烷​​嗪口服,5%凝胶形式的Slo直肠,10%凝胶形式的Slo直肠,200〜Mg Slo口服,400毫克口服。我们检查了氧化应激指数,组织病理学特征和体重变化,以及肝脏和肾脏在治疗结束时的功能。施用10%的直肠和400毫克口服SLO导致重量增加。此外,在5%和10%的SLO处理基团中,谷胱甘肽过氧化物酶活性显着升高,并且与阴性对照和asacol基团相比,观察到接受5%SLO的大鼠的超氧化物歧化酶活性升高。虽然在大多数肾脏和肝功能标记中没有观察到显着的变化,但在与阴性对照和asacol基团相比,在将400×mg slo的基团中检测到更高水平的天冬氨酸氨基转移酶。在甲烷嗪,asacol和Slo组中观察到许多组织病理学迹象。在不同组之间的平均等级中没有检测到显着变化。我们的数据表明,由于其抗氧化效应,SLO补充可以改善乙酸诱导的UC的改善。

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