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Time profile of oxidative stress and neutrophil activation in ovine acute lung injury and sepsis

机译:时间的氧化应激和嗜中性粒细胞激活在绵羊的急性肺损伤和败血症

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摘要

The formation of oxidative stress in the lung and activation of neutrophils are major determinants in the development of respiratory failure after acute lung injury and sepsis. However, the time changes of these pathogenic factors have not been sufficiently described. Twenty-four chronically instrumented sheep were subjected to cotton smoke inhalation injury and instillation of live Pseudomonas aeruginosa into both lungs. The sheep were euthanized at 4, 8, 12, 18, and 24 h after injury. Additional sheep received sham injury and were euthanized after 24 h. Pulmonary function was assessed by determination of oxygenation index and pulmonary shunt fraction. In addition, lung tissue was harvested at the respective time points for the measurement of malondialdehyde, interleukin 6, poly(ADP ribose), myeloperoxidase, and alveolar polymorphonuclear neutrophil score. The injury induced severe respiratory failure that was associated with an early increase in lipid peroxidation and interleukin 6 expression. The injury further led to an increase in poly(ADP ribose) activity that reached its peak at 12 h after injury and declined afterward. In addition, progressive increases in markers of neutrophil accumulation in the lung were observed. The peak of neutrophil accumulation in the lung was associated with a severe depletion of circulating neutrophils. The results from our model may enhance the understanding of the pathophysiological alterations after acute lung injury and sepsis and thus be useful in exploring therapeutic interventions directed at modifying the expression or activation of inflammatory mediators.
机译:在肺癌和氧化应激的形成活化的中性粒细胞是主要决定因素在呼吸衰竭后的发展急性肺损伤和败血症。这些致病因素没有变化充分描述。检测羊受到棉花烟吸入损伤和滴剂的生活铜绿假单胞菌为两肺。安乐死在4、8、12、18、24 h后受伤。24小时后被安乐死,肺功能被氧化测定评估指数和肺分流分数。肺组织在各自的收获丙二醛的测定,白介素6、保利(ADP核糖)、髓过氧化物酶,多形核中性粒细胞和肺泡得分。受伤引起的严重的呼吸衰竭这是与早期增加有关脂质过氧化和白介素6表达式。损伤进一步导致增加聚ADP核糖)活动达到顶峰在12 h受伤后,拒绝之后。逐步增加中性粒细胞的标志肺观察积累。中性粒细胞积聚在肺部与循环的严重损耗中性粒细胞。增强的理解急性肺后病理生理改变损伤和败血症,因此是有益的探索治疗性干预措施针对修改表达或激活的炎症介质。

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