首页> 美国卫生研究院文献>BioMed Research International >Glucose-Insulin-Potassium Alleviates Intestinal Mucosal Barrier Injuries Involving Decreased Expression of Uncoupling Protein 2 and NLR Family-Pyrin Domain-Containing 3 Inflammasome in Polymicrobial Sepsis
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Glucose-Insulin-Potassium Alleviates Intestinal Mucosal Barrier Injuries Involving Decreased Expression of Uncoupling Protein 2 and NLR Family-Pyrin Domain-Containing 3 Inflammasome in Polymicrobial Sepsis

机译:葡萄糖-胰岛素-钾缓解了肠道黏膜屏障损伤,涉及解耦蛋白2和含NLR家族-蛋白结构域的3炎性体在多发性脓毒症中的表达减少。

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摘要

Uncoupling protein 2 (UCP2) may be critical for intestinal barrier function which may play a key role in the development of sepsis, and insulin has been reported to have anti-inflammatory effects. Male Sprague-Dawley rats were randomly allocated into five groups: control group, cecal ligation and puncture (CLP) group, sham surgery group, CLP plus glucose-insulin-potassium (GIK) group, and CLP plus glucose and potassium (GK) group. Ileum tissues were collected at 24 h after surgery. Histological and cytokine analyses, intestinal permeability tests, and western blots of intestinal epithelial tight junction component proteins and UCP2 were performed. Compared with CLP group, the CLP + GIK group had milder histological damage, lower levels of cytokines in the serum and ileum tissue samples, and lower UCP2 expression, whereas the CLP + GK group had no such effects. Moreover, the CLP + GIK group exhibited decreased epithelial permeability of the ileum and increased expression of zonula occludens-1, occludin, and claudin-1 in the ileum. The findings demonstrated that the UCP2 and NLR family-pyrin domain-containing 3/caspase 1/interleukin 1β signaling pathway may be involved in intestinal barrier injury and that GIK treatment decreased intestinal barrier permeability. Thus, GIK may be a useful treatment for intestinal barrier injury during sepsis.
机译:解偶联蛋白2(UCP2)对于肠屏障功能可能至关重要,而肠屏障功能可能在败血症的发生中起关键作用,据报道胰岛素具有抗炎作用。将雄性Sprague-Dawley大鼠随机分为五组:对照组,盲肠结扎穿刺(CLP)组,假手术组,CLP加葡萄糖-胰岛素-钾(GIK)组和CLP加葡萄糖和钾(GK)组。手术后24小时收集回肠组织。进行了组织学和细胞因子分析,肠通透性测试以及肠上皮紧密连接成分蛋白和UCP2的蛋白质印迹。与CLP组相比,CLP + GIK组的组织学损伤较轻,血清和回肠组织样品中的细胞因子水平较低,UCP2表达较低,而CLP + GK组则无此作用。此外,CLP + GIK组在回肠中表现出回肠上皮通透性降低和小带闭合蛋白-1,闭合蛋白和claudin-1的表达增加。这些发现表明,UCP2和NLR家族-含pyrin结构域的3 / caspase 1 / interleukin1β信号通路可能与肠屏障损伤有关,而GIK治疗降低了肠屏障通透性。因此,GIK可能是脓毒症中肠屏障损伤的有用治疗方法。

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