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Time-dependent expression of endothelin-1 in lungs and the effects of TNF-α blocking peptide on acute lung injury in an endotoxemic rat model

机译:内毒素血症大鼠模型中肺内皮内皮素-1的时间依赖性表达及TNF-α阻断肽对急性肺损伤的影响

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Endothelin (ET)-1 is a potent vasoconstrictor that has been implicated in the pathogenesis of a number of diseases, and some studies suggest that circulating ET-1 is elevated in sepsis. The present study investigated whether ET plays a role in sepsis-mediated acute lung injury and whether its expression could be down regulated by blockade of TNF-α in septic lung. Male Wistar rats at 8 weeks of age were administered with either saline or lipopolysaccharide (LPS) at different time points (1, 3, 6 and 10 h) and various tests were then performed. The features of acute lung injury were observed at 1 h after LPS administration, which gradually became severe with time. Systolic and diastolic pressures were reduced just about one hour after LPS administration, whereas pulmonary TNF-α levels were significantly increased at various time points after LPS administration. LPS induced a time-dependent expression of ET-1 and ETA receptor in the lungs compared to control, peaking and incre sing by 3 fold at 6 h after induction of endotoxemia, whereas levels of ETB receptor, which has vasodilating effects, were remarkably down regulated time-dependently. We conclude that time-dependent increase of ET-1 and ETA receptor with the down regulation of ETB receptor may play a role in the pathogenesis of acute lung injury in endotoxemia. Finally, treatment of LPS-administered rats with TNF-α blocking peptide for three hours significantly suppressed levels of pulmonary ET-1. These data taken together, led us to conclude that differential alteration in ET expression and its receptors may be mediated by TNF-α and may, in part, account for the pathogenesis of acute lung injury in endotoxemia.
机译:内皮素(ET)-1是一种有效的血管收缩剂,与多种疾病的发病机制有关,一些研究表明脓毒症中循环ET-1升高。本研究调查了ET是否在败血症介导的急性肺损伤中发挥作用,以及其表达是否可被脓毒症肺中的TNF-α阻断而下调。在不同的时间点(1、3、6和10小时)给8周龄的雄性Wistar大鼠注射生理盐水或脂多糖(LPS),然后进行各种测试。 LPS给药后1小时观察到急性肺损伤的特征,随着时间的推移逐渐严重。 LPS给药后约一小时收缩压和舒张压降低,而LPS给药后不同时间点肺TNF-α水平显着升高。与内毒素血症诱导后的6小时相比,LPS诱导肺中ET-1和ETA受体的表达呈时间依赖性,在对照中达到峰值并增加3倍,而具有血管舒张作用的ETB受体水平则显着下降随时间而变化。我们得出结论,ET-1和ETA受体的时间依赖性增加与ETB受体的下调可能在内毒素血症急性肺损伤的发病机理中起作用。最后,用TNF-α阻断肽对LPS给药的大鼠进行3小时的治疗可显着抑制肺ET-1的水平。这些数据加在一起,使我们得出结论,ET表达及其受体的差异性改变可能是由TNF-α介导的,并且可能部分解释了内毒素血症急性肺损伤的发病机制。

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