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首页> 外文期刊>American Journal of Physiology >Development of an animal model of chronic alcohol-induced pancreatitis in the rat.
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Development of an animal model of chronic alcohol-induced pancreatitis in the rat.

机译:大鼠慢性酒精性胰腺炎动物模型的开发。

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This study was designed to develop an animal model of alcoholic pancreatitis and to test the hypothesis that the dose of ethanol and the type of dietary fat affect free radical formation and pancreatic pathology. Female Wistar rats were fed liquid diets rich in corn oil (unsaturated fat), with or without a standard or high dose of ethanol, and medium-chain triglycerides (saturated fat) with a high dose of ethanol for 8 wk enterally. The dose of ethanol was increased as tolerance developed, which allowed approximately twice as much alcohol to be delivered in the high-dose group. Serum pancreatic enzymes and histology were normal after 4 wk of diets rich in unsaturated fat, with or without the standard dose of ethanol. In contrast, enzyme levels were elevated significantly by the high ethanol dose. Increases were blunted significantly by dietary saturated fat. Fibrosis and collagen alpha1(I) expression in the pancreas were not detectable after 4 wk of enteral ethanol feeding; however, they were enhanced significantly by the high dose after 8 wk. Furthermore, radical adducts detected by electron spin resonance were minimal with the standard dose; however, the high dose increased carbon-centered radical adducts as well as 4-hydroxynonenal, an index of lipid peroxidation, significantly. Radical adducts were also blunted by approximately 70% by dietary saturated fat. The animal model presented here is the first to demonstrate chronic alcohol-induced pancreatitis in a reproducible manner. The key factors responsible for pathology are the amount of ethanol administered and the type of dietary fat.
机译:这项研究旨在开发酒精性胰腺炎的动物模型,并测试乙醇剂量和饮食脂肪类型影响自由基形成和胰腺病理的假设。给雌性Wistar大鼠喂食富含玉米油(不饱和脂肪),有或没有标准或高剂量乙醇的流质饮食,肠内含8周高剂量乙醇的中链甘油三酸酯(饱和脂肪)。乙醇的剂量随着耐受性的发展而增加,这使得高剂量组中的酒精输送量约为两倍。富含或不含标准剂量乙醇的不饱和脂肪饮食4周后,血清胰腺酶和组织学正常。相反,高乙醇剂量可显着提高酶水平。饮食中的饱和脂肪明显抑制了脂肪的增加。肠内饲喂乙醇4周后,未检测到胰腺中的纤维化和胶原α1(I)表达。但是,经过8周的高剂量后,它们显着增强。此外,在标准剂量下,通过电子自旋共振检测到的自由基加合物最小。然而,高剂量显着增加了以碳为中心的自由基加合物以及4-羟基壬烯醛(脂质过氧化的指数)。饮食中的饱和脂肪也使自由基加合物的含量降低了约70%。这里介绍的动物模型是第一个以可再现的方式证明慢性酒精性胰腺炎的动物模型。造成病理的关键因素是乙醇的摄入量和饮食脂肪的类型。

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