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The effect of matrix metalloproteinase-3 deficiency on pulmonary surfactant in a mouse model of acute lung injury

机译:基质金属蛋白酶-3缺乏对急性肺损伤小鼠肺表面活性物质的影响

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摘要

The acute respiratory distress syndrome (ARDS) is characterized by arterial hypoxemia accompanied by severe inflammation and alterations to the pulmonary surfactant system. Published data has demonstrated a protective effect of matrix metalloproteinase-3 (Mmp3) deficiency against the inflammatory response associated with ARDS; however, the effect of Mmp3 on physiologic parameters and alterations to surfactant have not been previously studied. It was hypothesized that Mmp3 deficient (Mmp3(-/-)) mice would be protected against lung dysfunction associated with ARDS and maintain a functional pulmonary surfactant system. Wild type (WT) and Mmp3(-/-) mice were subjected to acid-aspiration followed by mechanical ventilation. Mmp3(-/-) mice maintained higher arterial oxygenation compared with WT mice at the completion of ventilation. Significant increase in functional large aggregate surfactant forms were observed in Mmp3(-/-) mice compared with WT mice. These findings further support a role of Mmp3 as an attractive therapeutic target for drug development in the setting of ARDS.
机译:急性呼吸窘迫综合征(ARDS)的特征是动脉血氧过多,伴有严重的炎症和肺表面活性物质系统的改变。已发表的数据表明基质金属蛋白酶3(Mmp3)缺乏对与ARDS相关的炎症反应具有保护作用。但是,以前尚未研究过Mmp3对生理参数和表面活性剂改变的影响。假设缺少Mmp3的小鼠(Mmp3(-/-))可以预防与ARDS相关的肺功能障碍,并维持功能性的肺表面活性剂系统。对野生型(WT)和Mmp3(-/-)小鼠进行酸抽吸,然后进行机械通气。在通气完成时,与WT小鼠相比,Mmp3(-/-)小鼠保持较高的动脉氧合。与WT小鼠相比,在Mmp3(-/-)小鼠中观察到功能性大聚集体表面活性剂形式的显着增加。这些发现进一步支持了Mmp3作为ARDS背景下药物开发的有吸引力的治疗靶标的作用。

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