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首页> 外文期刊>Journal of Translational Medicine >Therapeutic effects of pyrrolidine dithiocarbamate on acute lung injury in rabbits
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Therapeutic effects of pyrrolidine dithiocarbamate on acute lung injury in rabbits

机译:吡咯烷二硫代氨基甲酸酯对家兔急性肺损伤的治疗作用

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Background Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) is an early characteristic of multiple organ dysfunction, responsible for high mortality and poor prognosis in patients. The present study aims to evaluate therapeutic effects and mechanisms of pyrrolidine dithiocarbamate (PDTC) on ALI. Methods Alveolar-arterial oxygen difference, lung tissue edema and compromise, NF-κB activation in polymorphonuclear neutrophil (PMN), and systemic levels of tumor necrosis factor-alpha (TNFa) and intercellular adhesion molecule-1 (ICAM-1) in rabbits induced by the intravenous administration of lipopolysaccharide (LPS) and treated with PDTC. Production of TNFa and IL-8, activation of Cathepsin G, and PMNs adhesion were also measured. Results The intravenous administration of PDTC had partial therapeutic effects on endotoxemia-induced lung tissue edema and damage, neutrophil influx to the lung, alveolar-capillary barrier dysfunction, and high systemic levels of TNFa and ICAM-1 as well as over-activation of NF-κB. PDTC could directly and partially inhibit LPS-induced TNFa hyper-production and over-activities of Cathepsin G. Such inhibitory effects of PDTC were related to the various stimuli and enhanced through combination with PI3K inhibitor. Conclusion NF-κB signal pathway could be one of targeting molecules and the combination with other signal pathway inhibitors may be an alternative of therapeutic strategies for ALI/ARDS.
机译:背景技术急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是多器官功能障碍的早期特征,导致患者高死亡率和预后不良。本研究旨在评估吡咯烷二硫代氨基甲酸酯(PDTC)对ALI的治疗作用和机制。方法诱导的家兔肺泡动脉血氧差异,肺组织水肿和受损,多形核中性粒细胞(PMN)中的NF-κB活化,肿瘤坏死因子-α(TNFa)和细胞间粘附分子-1(ICAM-1)的全身水平通过静脉注射脂多糖(LPS)并用PDTC治疗。还测量了TNFa和IL-8的产生,组织蛋白酶G的激活以及PMN的粘附。结果PDTC的静脉内给药对内毒素血症引起的肺组织水肿和损伤,肺中性粒细胞流入,肺泡-毛细血管屏障功能障碍,全身性TNFa和ICAM-1高以及NF过度活化具有部分治疗作用-κB。 PDTC可以直接和部分抑制LPS诱导的组织蛋白酶G的TNFa过度产生和过度活性。PDTC的这种抑制作用与各种刺激有关,并通过与PI3K抑制剂组合而增强。结论NF-κB信号通路可能是靶向分子之一,与其他信号通路抑制剂的组合可能是ALI / ARDS治疗策略的替代方案。

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