Soukka Hanna R, Ahotupa Markku, Ruutu Merja, Kääpä Pekka O
Research Centre of Applied and Preventive Cardiovascular Medicine and Department of Pediatrics, University of Turku, Finland.
Am J Perinatol. 2002 Jul;19(5):279-84. doi: 10.1055/s-2002-33089.
Acute lung injury induced by meconium aspiration is characterized by rapidly developing pulmonary inflammation with influx of activated polymorphonuclear cells. To evaluate the role of meconium in the activation of these invading cells, we described the oxidative capacity of circulating neutrophils after intratracheal administration of thick human meconium in pigs. We also examined the direct effects of varying meconium concentrations on the oxidative burst of human neutrophils in vitro. In neutrophils isolated from meconium-insufflated pigs, phorbol myristate acetate stimulation led to an average 11.7-fold increase in production of reactive oxygen species, measured by chemiluminescence, whereas the increase in control cells from saline-instilled pigs was only 3.1-fold, p =.012 between the groups. Activation of unstimulated human leukocytes by meconium resulted in a dose-dependent response. The lowest meconium concentration (0.2 mg/mL) had an inhibitory effect on neutrophil activation, whereas higher concentrations of meconium (1 and 2 mg/mL) increased neutrophil oxygen radical production progressively. These results thus indicate that moderate and high concentrations of aspirated meconium rapidly activate circulating neutrophils with a resulting oxidative burst contributing to pulmonary tissue injury, whereas low contamination of the aspirated material may in fact suppress the development of oxidative lung injury.
胎粪吸入所致急性肺损伤的特征是迅速发展的肺部炎症,伴有活化多形核细胞的流入。为了评估胎粪在这些侵入细胞激活中的作用,我们描述了猪气管内注入浓稠人胎粪后循环中性粒细胞的氧化能力。我们还在体外研究了不同浓度胎粪对人中性粒细胞氧化爆发的直接影响。在从注入胎粪的猪分离出的中性粒细胞中,佛波酯肉豆蔻酸酯刺激导致通过化学发光测量的活性氧产生平均增加11.7倍,而从注入生理盐水的猪分离出的对照细胞中的增加仅为3.1倍,两组之间p = 0.012。胎粪对未刺激的人白细胞的激活导致剂量依赖性反应。最低胎粪浓度(0.2mg/mL)对中性粒细胞激活有抑制作用,而较高浓度的胎粪(1和2mg/mL)逐渐增加中性粒细胞氧自由基的产生。因此,这些结果表明,中等和高浓度的吸入胎粪可迅速激活循环中的中性粒细胞,导致氧化爆发,从而导致肺组织损伤,而吸入物质的低污染实际上可能抑制氧化肺损伤的发展。