首页> 外文期刊>JPEN. Journal of parenteral and enteral nutrition. >Milk Fat Globule Membrane Ameliorates Necrotizing Enterocolitis in Neonatal Rats and Suppresses Lipopolysaccharide-Induced Inflammatory Response in IEC-6 Enterocytes
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Milk Fat Globule Membrane Ameliorates Necrotizing Enterocolitis in Neonatal Rats and Suppresses Lipopolysaccharide-Induced Inflammatory Response in IEC-6 Enterocytes

机译:乳脂肪球膜在新生大鼠中改善坏死性小肠结肠炎,抑制IEC-6肠细胞中的脂多糖诱导的炎症反应

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Background Evidence has provided support for the beneficial effects of milk fat globule membrane (MFGM) on inflammation in the intestinal tract. The objective of this study was to investigate the effects of MFGM on a rat model of necrotizing enterocolitis (NEC) and its potential mechanism of action. Methods Sixty-two newborn Sprague Dawley rats were randomly divided into 4 experimental groups: Breast-fed normal, formula fed (FF), FF + 6 g/L MFGM, and FF + 12 g/L MFGM. The FF rats and the FF rats supplemented with MFGM were exposed to asphyxia/cold stress to induce NEC. Body weight, histological score, survival time, oxidative stress injury, enterocyte proliferation/apoptosis, and inflammatory response were assessed. Meanwhile, lipopolysaccharide (LPS)-stimulated IEC-6 enterocytes were used as a model to test the anti-inflammatory effects of MFGM. Results Supplementation with 12 g/L MFGM alleviated body weight loss, reduced the incidence of NEC, increased the survival rate, and attenuated the severity of bowel damage in the NEC rat model. Furthermore, 12 g/L MFGM administration inhibited the protein expression of toll-like receptor 4 (TLR4) in the animal model. In IEC-6 enterocytes, the upregulation of TLR4, myeloid differentiation primary response gene 88 (MyD88), phosphorylated nuclear factor-kappa B (NF-kappa B) p65 subunit, and the nuclear translocation of NF-kappa Bp65 induced by LPS was partially inhibited by MFGM pretreatment. Conclusion Our findings suggested that MFGM has beneficial effects on neonatal rats with NEC by suppressing inflammation via the TLR4/MyD88/NF-kappa B pathway.
机译:背景技术证据已经为牛奶脂肪球膜(MFGM)对肠道炎症的有益作用提供了支持。本研究的目的是探讨MFGM对坏死性小肠结肠炎(NEC)大鼠模型的影响及其潜在的作用机制。方法将六十二次新生儿铲达德利大鼠随机分为4种实验组:乳腺喂养正常,配方喂养(FF),FF + 6g / L MFGM,FF + 12g / L MFGM。 FF大鼠和补充有MFGM的FF大鼠暴露于窒息/冷应激以诱导NEC。评估体重,组织学评分,存活时间,氧化应激损伤,肠细胞增殖/凋亡和炎症反应。同时,使用脂多糖(LPS)刺激的IEC-6肠细胞作为测试MFGM的抗炎作用的模型。结果补充12克/升MFGM缓解体重减轻,降低了NEC的发生率,增加了生存率,并减弱了NEC大鼠模型中肠损伤的严重程度。此外,12g / L MFGM给药抑制动物模型中Toll样受体4(TLR4)的蛋白质表达。在IEC-6肠细胞中,TLR4,骨髓分化初级反应基因88(MYD88),磷酸化核因子-Kappa(NF-Kappa B)P65亚基的上调,LPS诱导的NF-Kappa BP65的核转位由MFGM预处理抑制。结论我们的研究结果表明,MFGM通过抑制通过TLR4 / MyD88 / NF-Kappa B途径抑制炎症对新生大鼠的有益作用。

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