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Mucosal loss with increased expression of IL-6, IL-8, and COX-2 in a formula-feeding only neonatal rat model of necrotizing enterocolitis

机译:在仅以配方奶喂养的坏死性小肠结肠炎新生大鼠模型中,粘膜丢失并伴随IL-6,IL-8和COX-2表达增加

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Introduction The aim of our study is to establish a reliable neonatal rat model by formula feeding only for evaluation of early surgical intervention on the course of experimental necrotizing enterocolitis (NEC). Material and methods Newborn Sprague-Dawley rats were divided into 50 breast-fed (group 1) and 38 formula fed (Similac/Esbilac, group 2) animals. The pups were sacrificed on the 4th, 5th, and 6th day of life and the terminal intestine examined for macroscopic and histologic changes as well as cytokine expression. Results The histological mucosal damage was significantly higher of group 2 compared to group 1. The area of the vital mucosa of group 2 was significantly (58.57%, p < 0.001) lower compared to group 1 (75.12%). The mRNA expression of the inflammatory cytokines IL-6, IL-8 and COX-2 was significantly 2-, 5- and 10-fold increased in group 2 compared to group 1. Discussion Formula fed newborn rats displayed an inflammatory enterocolitis similar to human NEC. Our study demonstrates a significant loss of mucosa in animals with NEC having increased expression levels of IL-6, IL-8 and COX-2. Mucosal loss appears to be a distinct feature of experimental NEC and has to be correlated with the human disease.
机译:引言我们研究的目的是通过配方喂养建立一个可靠的新生大鼠模型,仅用于评估实验性坏死性小肠结肠炎(NEC)过程中的早期外科手术干预。材料和方法将新生的Sprague-Dawley大鼠分为50只母乳喂养(第1组)和38只配方奶喂养的动物(Similac / Esbilac,第2组)。在生命的第4、5和6天处死幼犬,并检查终肠的宏观和组织学变化以及细胞因子表达。结果与第1组相比,第2组的组织学黏膜损伤明显更高。与第1组(75.12%)相比,第2组的重要粘膜面积明显减少(58.57%,p <0.001)。与第1组相比,第2组中炎性细胞因子IL-6,IL-8和COX-2的mRNA表达分别显着提高了2倍,5倍和10倍。 NEC。我们的研究表明,NEC动物的粘膜明显丧失,其IL-6,IL-8和COX-2的表达水平增加。粘膜丢失似乎是实验性NEC的独特特征,必须与人类疾病相关。

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