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Disruption of the pacemaker activity of interstitial cells of Cajal via nitric oxide contributes to postoperative ileus

机译:通过一氧化氮通过一氧化氮的CAJAL间质细胞的起搏器活性的破坏有助于术后inleus

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Abstract Background Interstitial cells of Cajal ( ICC ) serve as intestinal pacemakers. Postoperative ileus ( POI ) is a gastrointestinal motility disorder that occurs following abdominal surgery, which is caused by inflammation‐induced dysfunction of smooth muscles and enteric neurons. However, the participation of ICC in POI is not well understood. In this study, we investigated the functional changes of ICC in a mouse model of POI . Methods Intestinal manipulation ( IM ) was performed to induce POI . At 24?h or 48?h after IM , the field potential of the intestinal tunica muscularis was investigated. Tissues were also examined by immunohistochemistry and electron microscopic analysis. Key Results Gastrointestinal transit was significantly decreased with intestinal tunica muscularis inflammation at 24?h after IM , which was ameliorated at 48?h after IM . The generation and propagation of pacemaker potentials were disrupted at 24?h after IM and recovered to the control level at 48?h after IM . ICC networks, detected by c‐Kit immunoreactivity, were remarkably disrupted at 24?h after IM . Electron microscopic analysis revealed abnormal vacuoles in the ICC cytoplasm. Interestingly, the ICC networks recovered at 48?h after IM . Administration of aminoguanidine, an inducible nitric oxide synthase inhibitor, suppressed the disruption of ICC networks. Ileal smooth muscle tissue cultured in the presence of nitric oxide donor, showed disrupted ICC networks. Conclusions and Inferences The generation and propagation of pacemaker potentials by ICC are disrupted via nitric oxide after IM , and this disruption may contribute to POI . When inflammation is ameliorated, ICC can recover their pacemaker function.
机译:Cajal(ICC)的抽象背景间质细胞用作肠道士起搏器。术后Ileus(POI)是腹部手术后发生的胃肠动力障碍,这是由炎症诱导的光滑肌和肠道神经元引起的。但是,ICC在POI中的参与并不了解。在这项研究中,我们调查了POI小鼠模型中ICC的功能变化。方法进行肠道操纵(IM)以诱导POI。在IM之后,在24?H或48?H时,研究了肠道肌肉肌肉的田间潜力。还通过免疫组织化学和电子显微镜分析检查组织。在IM后24μl肠道肌肉炎症下,胃肠道转换的胃肠道转换显着降低,在IM后48℃改善。在IM后,起搏器电位的产生和繁殖在24μl下发,并在IM后在48℃下恢复到控制水平。通过C-kit免疫反应检测的ICC网络在IM后24℃下显着破坏。电子显微镜分析显示ICC细胞质中的异常泡沫。有趣的是,ICC网络在IM后48次恢复。氨基胍施用诱导型一氧化氮合酶抑制剂,抑制了ICC网络的破坏。在存在一氧化氮供体存在下培养的髂骨平滑肌组织显示出破坏的ICC网络。结论和推论在IMC之后通过一氧化物的起搏器电位的产生和繁殖,并且这种破坏可能有助于POI。当炎症改善时,ICC可以恢复起搏器功能。

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