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烟雾吸入和肺炎引起的急性肺损伤中的肺微血管通透性和血管内皮生长因子的表达。

Pulmonary microvascular hyperpermeability and expression of vascular endothelial growth factor in smoke inhalation- and pneumonia-induced acute lung injury.

机构信息

Department of Anesthesiology, Investigational Intensive Care Unit, The University of Texas Medical Branch, Galveston, TX 77550, USA.

出版信息

Burns. 2012 Nov;38(7):1072-8. doi: 10.1016/j.burns.2012.02.019. Epub 2012 May 29.

DOI:10.1016/j.burns.2012.02.019
PMID:22647495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3893691/
Abstract

INTRODUCTION

Acute lung injury (ALI) and sepsis are major contributors to the morbidity and mortality of critically ill patients. The current study was designed further evaluate the mechanism of pulmonary vascular hyperpermeability in sheep with these injuries.

METHODS

Sheep were randomized to a sham-injured control group (n=6) or ALI/sepsis group (n=7). The sheep in the ALI/sepsis group received inhalation injury followed by instillation of Pseudomonas aeruginosa into the lungs. These groups were monitored for 24 h. Additional sheep (n=16) received the injury and lung tissue was harvested at different time points to measure lung wet/dry weight ratio, vascular endothelial growth factor (VEGF) mRNA and protein expression as well as 3-nitrotyrosine protein expression in lung homogenates.

RESULTS

The injury induced severe deterioration in pulmonary gas exchange, increases in lung lymph flow and protein content, and lung water content (P<0.01 each). These alterations were associated with elevated lung and plasma nitrite/nitrate concentrations, increased tracheal blood flow, and enhanced VEGF mRNA and protein expression in lung tissue as well as enhanced 3-nitrotyrosine protein expression (P<0.05 each).

CONCLUSIONS

This study describes the time course of pulmonary microvascular hyperpermeability in a clinical relevant large animal model and may improve the experimental design of future studies.

摘要

简介

急性肺损伤(ALI)和败血症是导致重症患者发病率和死亡率的主要原因。本研究旨在进一步评估患有这些疾病的绵羊肺血管通透性增加的机制。

方法

将绵羊随机分为假损伤对照组(n=6)或 ALI/败血症组(n=7)。ALI/败血症组绵羊接受吸入性损伤,然后将铜绿假单胞菌注入肺部。监测这两组绵羊 24 小时。另外 16 只绵羊(n=16)接受损伤,并在不同时间点采集肺组织,以测量肺湿/干重比、血管内皮生长因子(VEGF)mRNA 和蛋白表达以及肺匀浆中 3-硝基酪氨酸蛋白表达。

结果

损伤导致肺气体交换严重恶化,肺淋巴流量和蛋白含量增加,肺含水量增加(P<0.01)。这些改变与肺和血浆中亚硝酸盐/硝酸盐浓度升高、气管血流增加以及肺组织中 VEGF mRNA 和蛋白表达增强以及 3-硝基酪氨酸蛋白表达增强有关(P<0.05)。

结论

本研究描述了临床相关大动物模型中肺微血管通透性的时间过程,可能改善未来研究的实验设计。

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