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Effects of meconium aspiration in isolated perfused rat lungs.

机译:胎粪吸入对离体灌注大鼠肺的影响。

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Our objective was to study meconium-induced lung injury in isolated perfused rat lungs exposed to anoxia. Our working hypothesis was that meconium-induced lung injury is independent of preexisting hypoxia, and that hypoxia will increase severity of lung injury observed after meconium aspiration. We compared five different groups of animals (n = 5) for pulmonary arterial pressure (PAP), weight lung changes, and TNFalpha expression. Group I had lungs instilled with 4 ml of normal saline. Group II had lungs exposed to 5 min of anoxia. Group III had lungs instilled with 4 ml of 30% filtered human meconium. Group IV had lungs exposed to 5 min of anoxia and then instilled with 4 ml of 30% filtered human meconium. Group V had lungs instilled with 4 ml of 30% unfiltered human meconium. Our subjects were adult Sprague-Dawley rats. The isolated rat lung model was prepared according to Levey and Gast (J Appl Physiol 1966;21:313-316). Lungs were ventilated with room air. Anoxia was caused by the use of N(2). The pulmonary artery was cannulated, and pulmonary arterial pressure and lung weight were measured. Lung weight and pulmonary arterial pressure were monitored for 120 min, and TNFalpha levels were measured in effluent at 15, 30, 60, and 120 min. Experiments were done at the Michael Reese Hospital (Chicago, IL). At the end of the experiment, PAP reached its highest values in group V (10.0 +/- 1.7 mmHg). Final PAPs in groups I-IV were: 4.85 +/- 0.3, 4.99 +/- 0.4, 5.93 +/- 0.3, and 7.25 +/- 0.51 mmHg, respectively). Lung wet weight increased significantly only in groups IV and V vs. group I; at 120 min, they were: 0.96 +/- 0.3 g, P < 0.01, and 1.5 g +/- 0.2 g, P < 0.01, respectively. TNFalpha levels did not change significantly over time in group I. TNFalpha is a marker as well as proprietor of pulmonary inflammatory response. TNFalpha reached its highest levels in groups IV and V: 595 and 753 pg/ml at 120 min, respectively. In conclusion, a short episode of anoxia prior to meconium aspiration may increase lung sensitivity to meconium-induced lung injury. This effect may be moderated by the TNFalpha present in the pulmonary circulation.
机译:我们的目的是研究暴露于缺氧的孤立灌注大鼠肺中的胎粪诱导的肺损伤。我们的工作假设是,胎粪引起的肺损伤与既存的缺氧无关,并且缺氧会增加胎粪吸入后观察到的肺损伤的严重性。我们比较了五组不同的动物(n = 5)的肺动脉压(PAP),肺重量变化和TNFalpha表达。第一组肺部滴入4毫升生理盐水。第二组的肺暴露于缺氧5分钟。第三组的肺部注入了4 ml 30%过滤的人胎粪。第四组的肺暴露于缺氧5分钟,然后滴入4 ml 30%过滤的人胎粪。第五组的肺部滴入4 ml 30%未过滤的人胎粪。我们的受试者是成年的Sprague-Dawley大鼠。根据Levey和Gast(J Appl Physiol 1966; 21:313-316)制备分离的大鼠肺模型。肺用室内空气通风。厌氧症是由于使用N(2)引起的。插入肺动脉,并测量肺动脉压和肺重量。监测肺重量和肺动脉压120分钟,并在15、30、60和120分钟时测量流出物中的TNFα水平。实验是在迈克尔·里斯医院(伊利诺伊州芝加哥)进行的。实验结束时,PAP在V组达到最高值(10.0 +/- 1.7 mmHg)。 I-IV组的最终PAP分别为:4.85 +/- 0.3、4.99 +/- 0.4、5.93 +/- 0.3和7.25 +/- 0.51 mmHg。与I组相比,IV和V组仅肺湿重显着增加。在120分钟时,它们分别为:0.96 +/- 0.3 g,P <0.01和1.5 g +/- 0.2 g,P <0.01。在I组中,TNFα水平没有随时间变化显着。TNFα是肺炎性反应的标志物和所有者。 TNFalpha在第IV和V组达到最高水平:分别在120分钟时为595和753 pg / ml。总之,在胎粪吸入前短暂缺氧可增加肺对胎粪诱发的肺损伤的敏感性。肺循环中存在的TNFα可减轻这种作用。

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