Lukkarinen Heikki, Laine Jukka, Lehtonen Jani, Zagariya Alexander, Vidyasagar Dharmapuri, Aho Heikki, Kääpä Peka
Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, FIN-20014 Turku, Finland.
Pediatr Res. 2004 Feb;55(2):326-33. doi: 10.1203/01.PDR.0000100901.88697.66. Epub 2003 Nov 6.
Lung tissue inflammation and apoptosis are implicated in the pathogenesis of meconium aspiration-induced lung injury in the newborn, but the mechanisms of these reactions are still poorly known. We investigated the time-dependent leukocyte influx and appearance of apoptosis, as well as the contribution of angiotensin (ANG) II receptor action on these processes in the meconium-induced lung injury. Experimental meconium aspiration was induced by intratracheal instillation of human meconium in 18 rats, and eight rats were further pretreated with an unspecific ANG II receptor inhibitor saralasin. Rats were ventilated with 60% oxygen for 1, 3, or 5 h, and the lungs were then studied histologically for tissue injury and with DNA nick-end labeling and electron microscopy for apoptotic cell death. Lung tissue myeloperoxidase activity and expression of angiotensinogen mRNA and endothelial monocyte-activating polypeptide (EMAP) II protein were also analyzed. The meconium-instilled lungs showed increasing neutrophil migration and histologic injury after the first hour, whereas the number of epithelial apoptotic cells was elevated from the control level throughout the study. Myeloperoxidase activity was high, and the angiotensinogen mRNA and EMAP II protein was up-regulated at 5 h after the meconium insult. Pretreatment with saralasin significantly prevented the increase in lung tissue myeloperoxidase activity, EMAP II, and lung epithelial apoptosis. The results suggest that pulmonary meconium insult rapidly results in epithelial apoptosis, before significant neutrophil sequestration into the lungs. Apoptotic cell death is further connected with ANG II receptor action in the meconium-contaminated lung tissue.
肺组织炎症和细胞凋亡与新生儿胎粪吸入性肺损伤的发病机制有关,但这些反应的机制仍知之甚少。我们研究了胎粪诱导的肺损伤中白细胞的时间依赖性流入和凋亡的出现,以及血管紧张素(ANG)II受体作用对这些过程的影响。通过向18只大鼠气管内滴注人胎粪诱导实验性胎粪吸入,另外8只大鼠预先用非特异性ANG II受体抑制剂沙拉新进行预处理。大鼠用60%氧气通气1、3或5小时,然后对肺组织进行组织学检查以评估组织损伤,并用DNA缺口末端标记法和电子显微镜观察凋亡细胞死亡情况。还分析了肺组织髓过氧化物酶活性、血管紧张素原mRNA表达和内皮单核细胞激活多肽(EMAP)II蛋白表达。胎粪滴注后的肺在第1小时后显示中性粒细胞迁移增加和组织学损伤,而在整个研究过程中上皮凋亡细胞数量均高于对照水平。髓过氧化物酶活性较高,胎粪损伤后5小时血管紧张素原mRNA和EMAP II蛋白上调。沙拉新预处理显著阻止了肺组织髓过氧化物酶活性、EMAP II和肺上皮细胞凋亡的增加。结果表明,肺部胎粪损伤在大量中性粒细胞滞留于肺之前迅速导致上皮细胞凋亡。在受胎粪污染的肺组织中,凋亡细胞死亡与ANG II受体作用进一步相关。