Protective Effect of Nigella Sativa on Taurocholate Induced Pancreatitis in Rats

Mehmet Ali Kosekli, O. Ozmen, S. Sahinduran, M. Yılmaz
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Abstract

Introduction: Acute necrotizing pancreatitis with a high mortality rate and the search for treatment continues. We investigated the protective effect of Nigella Sativa (NS), with antioxidant and anti-inflammatory effects, in experimental acute necrotizing pancreatitis. Materials and Methods: Thirty six male Wistar albino rats (weights 180-220 g) were randomised into four groups. Group 1 (Control): Rats were given standard mouse chow. No pro-drug or pancreatic intervention was performed. Group 2 (NS): In addition to their standard diet, rats were given 0.1 ml/100gr of NS orally for 3 days prior to the experiment. Group 3: Necrotizing pancreatitis was induced by retrograde administration of 3% Na-Taurocholate through the distal common bile duct of the rats on on experiment day. Group 4 (NS+ANP): Necrotizing pancreatitis was also formed in rats receiving 0.1ml/100 mg of NS for 3 days. Rats were given high-dose anesthesia 8 hours after the onset of pancreatitis. Immunohistochemical (TNF-a, MDA, MPO, Caspase), histological pancreatitis scoring and biochemical (LDH, Lipase, amylase) analyzes were performed from the blood and pancreatic tissue samples obtained. Results: There was no difference in histopathological, immunohistochemical and biochemical values between Group 1 and Group 2 (p>0.05). There were significiant differences between Group 4 and Group 3 in terms of histopathological, immunohistochemical and biochemical parameters (p<0.001). The pancreatitis findings of the Group 4 were found to be significantly milder than Group 3, which did not receive NS. Conclusion: NS pretreatment alleviates NaTaurocholate-induced experimental pancreatitis. NS firstly studied in experimental models of pancreatitis.
黑草对牛磺胆酸盐诱导大鼠胰腺炎的保护作用
简介:急性坏死性胰腺炎具有高死亡率和治疗的研究仍在继续。我们研究了黑草(Nigella Sativa, NS)对实验性急性坏死性胰腺炎的抗氧化和抗炎保护作用。材料与方法:36只体重180 ~ 220 g的雄性Wistar白化大鼠随机分为4组。第一组(对照组):给予小鼠标准饲料。未进行前药物或胰腺干预。第2组(NS):实验前3天,在标准饮食的基础上,给予0.1 ml/100gr的NS口服。第三组:实验第1天经大鼠胆总管远端逆行给药3% na -牛胆酸钠诱导坏死性胰腺炎。第4组(NS+ANP):给予0.1ml/100 mg NS,连续3天也可形成坏死性胰腺炎。大鼠在胰腺炎发病8小时后给予大剂量麻醉。对获得的血液和胰腺组织样本进行免疫组织化学(TNF-a、MDA、MPO、Caspase)、组织学胰腺炎评分和生化(LDH、脂肪酶、淀粉酶)分析。结果:1组与2组在组织病理学、免疫组化、生化指标上差异无统计学意义(p>0.05)。4组与3组在组织病理学、免疫组化及生化指标上差异有统计学意义(p<0.001)。第4组的胰腺炎症状明显轻于未接受NS治疗的第3组。结论:NS预处理可减轻nataurocholate诱导的实验性胰腺炎。NS首次在胰腺炎实验模型中进行研究。
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