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首页> 外文期刊>The anatomical record: advances in integrative anatomy and evolutionary biology >Comparative Study of Trans-Oral and Trans-Tracheal Intratracheal Instillations in a Murine Model of Acute Lung Injury
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Comparative Study of Trans-Oral and Trans-Tracheal Intratracheal Instillations in a Murine Model of Acute Lung Injury

机译:小鼠急性肺损伤模型中经口和经气管内气管滴注的比较研究

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Animal model is of importance to further elucidate the pathogenesis of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). We envisioned a possibility that there might be the differences in lipopolysaccharide (LPS)-induced acute lung inflammation by the trans-oral and trans-tracheal intratracheal instillations. We compared the LPS-induced early inflammatory responses by these two methods. The evaluative system included bronchoalveolar lavage (BAL) fluid biochemical analysis and differential cell counting, lung wet/dry weight ratio and lung histology. In vitro studies were performed on human bronchial epithelial cell line NCI-H292 and alveolar Type II epithelial cell line A549 stimulated with LPS. Both interleukin (IL)-8 release in the BAL fluid and IL-8 secretions from NCI-H292 and A549 cells were measured. We found that the trans-tracheal intratracheal instillation promoted the LPS-induced cell injury, neutrophil infiltration, and pulmonary edema compared to the trans-oral one. The LPS-induced pathological changes by the trans-oral intratracheal instillation were characterized by pulmonary interstitial edema, but the trans-tracheal intratracheal instillation was exudative pulmonary edema. More IL-8 is produced from A549 cells than from NCI-H292 cells under the treatment of LPS. The increased IL-8 release in the BAL fluid and enhanced inflammatory responses caused by LPS may be due to more LPS delivered into the alveolar spaces by the trans-tracheal intratracheal instillation compared to the trans-oral one. The trans-tracheal intratracheal instillation is proved to be more suitable to establish the murine model of ALI than the trans-oral one and helpful to further elucidate the pathogenesis of ALI/ARDS.
机译:动物模型对于进一步阐明急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)的发病机制至关重要。我们预想了通过经口和经气管内气管内滴注在脂多糖(LPS)诱导的急性肺部炎症中可能存在差异的可能性。我们通过这两种方法比较了LPS诱导的早期炎症反应。该评估系统包括支气管肺泡灌洗液(BAL)的生化分析和差分细胞计数,肺干重比和肺组织学。在人支气管上皮细胞系NCI-H292和LPS刺激的II型肺泡上皮细胞系A549上进行了体外研究。测量了BAL液中的白介素(IL)-8释放以及NCI-H292和A549细胞的IL-8分泌。我们发现,与经口相比,经气管内气管内滴注可促进LPS诱导的细胞损伤,中性粒细胞浸润和肺水肿。经口气管内滴注LPS引起的病理改变的特征是肺间质水肿,而经气管内气管滴注的表现为渗出性肺水肿。在LPS处理下,从A549细胞产生的IL-8比从NCI-H292细胞产生的更多。由BPS引起的BAL液中IL-8释放的增加和炎症反应的增强可能是由于经口气管内气管滴注与经口相比,更多的LPS传递到肺泡腔。经气管内气管滴注被证明比经口的更适合建立ALI的鼠模型,并有助于进一步阐明ALI / ARDS的发病机理。

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