重组人三叶因子3改善实验性坏死性小肠结肠炎肠损伤的抗炎作用。

International Journal of Peptides Pub Date : 2014-01-01 Epub Date: 2014-02-12 DOI:10.1155/2014/634135
Lei Shi, Pang-Hu Zhou, Juan-Li Xi, Hong-Gang Yu, Bing-Hong Zhang
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引用次数: 17

摘要

的目标。重组人三叶因子3(肠三叶因子)已被认为对坏死性小肠结肠炎(NEC)有部分保护作用,但这种保护的机制尚未明确。我们研究了rhTFF3的保护作用是否是抗炎反应的结果。方法。第4天处死大鼠,取回肠远端进行形态学研究和免疫组化检测NF- κ B (p65),并采用ELISA试剂盒检测肠组织中IL-1 β、IL-6和IL-10的含量。结果。新生儿NEC中IL-1 β、IL-6、IL-10均显著高于正常组。正常组与NEC组比较,IL-1 β、IL-6显著降低,IL-10显著升高。在NEC模型中,免疫组化染色显示NF- κ B (p65)呈强棕色,分布于肠上皮。rhTFF3显著降低NEC模型中NF- κ B (p65)的免疫反应性。结论。注射rhTFF3后,肠道炎症得到改善。rhTFF3可能通过抑制炎症反应来保护新生大鼠NEC模型的肠道损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recombinant human trefoil factor 3 ameliorates bowel injury: its anti-inflammatory effect on experimental necrotizing enterocolitis.

Recombinant human trefoil factor 3 ameliorates bowel injury: its anti-inflammatory effect on experimental necrotizing enterocolitis.

Recombinant human trefoil factor 3 ameliorates bowel injury: its anti-inflammatory effect on experimental necrotizing enterocolitis.

Recombinant human trefoil factor 3 ameliorates bowel injury: its anti-inflammatory effect on experimental necrotizing enterocolitis.

Aim. Recombinant human trefoil factor 3 (intestinal trefoil factor) has been suggested to be partially protective against necrotizing enterocolitis (NEC), but the mechanisms of this protection have not been defined. We investigated whether the protective effects of rhTFF3 are the result of an anti-inflammatory response. Methods. The rats were killed on day 4, the distal ileum was harvested for morphological studies and immunohistochemistry for NF- κ B (p65), and the amounts of IL-1 β , IL-6, and IL-10 in the intestinal tissue were measured using commercial ELISA assay kits. Results. In the neonatal NEC, IL-1 β , IL-6, and IL-10 were significantly higher than in normal group. In normal group, IL-1 β and IL-6 were significantly decreased, and the amount of IL-10 was markedly increased compared with NEC group. In the NEC model, immunohistochemical staining for NF- κ B (p65) was demonstrated to be of a strong brown color and was distributed in the intestinal epithelium. Treatment with rhTFF3 significantly decreased the immunoreactivity of NF- κ B (p65) in the NEC model. Conclusions. Intestinal inflammation was ameliorated after rhTFF3 was injected. rhTFF3 may protect against the intestinal injury of the neonatal rat NEC model by suppression of the inflammatory response.

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