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Key Molecular Mechanisms of Chaiqinchengqi Decoction in Alleviating the Pulmonary Albumin Leakage Caused by Endotoxemia in Severe Acute Pancreatitis Rats

机译:柴芹cheng芪汤减轻重症急性胰腺炎大鼠内毒素血症引起的肺白蛋白渗漏的关键分子机制

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摘要

To reveal the key molecular mechanisms of Chaiqinchengqi decoction (CQCQD) in alleviating the pulmonary albumin leakage caused by endotoxemia in severe acute pancreatitis (SAP) rats. Rats models of SAP endotoxemia-induced acute lung injury were established, the studies in vivo provided the important evidences that the therapy of CQCQD significantly ameliorated the increases in plasma levels of lipopolysaccharide (LPS), sCd14, and Lbp, the elevation of serum amylase level, the enhancements of systemic and pulmonary albumin leakage, and the depravation of airways indicators, thus improving respiratory dysfunction and also pancreatic and pulmonary histopathological changes. According to the analyses of rats pulmonary tissue microarray and protein-protein interaction network, c-Fos, c-Src, and p85α were predicted as the target proteins for CQCQD in alleviating pulmonary albumin leakage. To confirm these predictions, human umbilical vein endothelial cells were employed in in vitro studies, which provide the evidences that (1) LPS-induced paracellular leakage and proinflammatory cytokines release were suppressed by pretreatment with inhibitors of c-Src (PP1) or PI3K () or by transfection with siRNAs of c-Fos; (2) fortunately, CQCQD imitated the actions of these selective inhibitions agents to inhibit LPS-induced high expressions of p-Src, p-p85α, and c-Fos, therefore attenuating paracellular leakage and proinflammatory cytokines release.
机译:揭示柴琴城七汤减轻严重急性胰腺炎(SAP)大鼠内毒素血症引起的肺白蛋白渗漏的关键分子机制。建立了SAP内毒素血症引起的急性肺损伤大鼠模型,体内研究提供了重要的证据,表明CQCQD的治疗显着改善了血浆脂多糖(LPS),sCd14和Lbp的升高,血清淀粉酶水平的升高,全身和肺白蛋白渗漏的增强以及气道指标的恶化,从而改善呼吸功能障碍以及胰腺和肺组织病理学变化。通过对大鼠肺组织芯片和蛋白质-蛋白质相互作用网络的分析,预测c-Fos,c-Src和p85α是减轻肺白蛋白渗漏的CQCQD的目标蛋白质。为了证实这些预测,在体外研究中使用了人脐静脉内皮细胞,这些证据提供了以下证据:(1)预处理c-Src(PP1)或PI3K抑制剂可抑制LPS诱导的旁细胞渗漏和促炎性细胞因子释放( )或通过c-Fos的siRNA转染; (2)幸运的是,CQCQD模仿了这些选择性抑制剂的作用,以抑制LPS诱导的p-Src,p-p85α和c-Fos的高表达,从而减弱了细胞旁渗漏和促炎细胞因子的释放。

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