表皮生长因子减少实验性坏死性小肠结肠炎的肝后遗症。

Biology of the neonate Pub Date : 2006-01-01 Epub Date: 2005-11-29 DOI:10.1159/000090015
Melissa D Halpern, Hana Holubec, Jessica A Clark, Tara A Saunders, Catherine S Williams, Katerina Dvorak, Bohuslav Dvorak
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引用次数: 26

摘要

背景与目的:新生儿坏死性小肠结肠炎(NEC)是早产儿最常见的胃肠道疾病。我们最近证明肠/肝轴通过向肠腔释放炎症介质在NEC的病理生理中起重要作用。我们还表明,补充含有表皮生长因子(EGF)的配方可显著降低与实验性NEC相关的回肠病理。在本研究中,我们检测了EGF对NEC新生大鼠模型中肠/肝轴肝脏部分的影响。方法:将新生大鼠分为3个实验组:NEC组,手工喂养无生长因子配方;NEC + EGF,用添加500 ng/ml大鼠EGF的配方手工喂养;所有动物每天2次进行窒息和冷应激,连续4 d形成NEC。结果:EGF受体表达显著(p)。结论:本研究结果表明,EGF可使新生NEC大鼠肝脏细胞因子过量产生正常化,有助于减轻实验性NEC发育过程中的肠道损伤。这些数据表明,在NEC发病过程中,在配方中添加EGF对肠/肝轴有有益的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidermal growth factor reduces hepatic sequelae in experimental necrotizing enterocolitis.

Background and aim: Neonatal necrotizing enterocolitis (NEC) is the most common gastrointestinal disease of premature infants. We recently demonstrated that the gut/liver axis plays an important role in the pathophysiology of NEC through the release of inflammatory mediators into the intestinal lumen. We have also shown that supplementation of formula with epidermal growth factor (EGF) dramatically decreases ileal pathology associated with experimental NEC. In this study, we examined the effects of EGF on the liver portion of the gut/liver axis in the neonatal rat model of NEC.

Methods: Newborn rats were divided into three experimental groups, NEC, hand-fed with growth-factor free formula; NEC + EGF, hand-fed with formula supplemented with 500 ng/ml rat EGF; or DF, dam fed. All animals were exposed to asphyxia and cold stress twice daily for 4 days to develop NEC.

Results: EGF receptor expression was significantly (p

Conclusion: The results of this study indicate that EGF normalizes cytokine overproduction in the liver of neonatal rats with NEC, which contributes to diminished intestinal damage during the development of experimental NEC. These data suggest that supplementation of formula with EGF can have beneficial effects on the gut/liver axis during NEC pathogenesis.

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