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一种新型的重症急性呼吸窘迫综合征兔模型:酸误吸与有害机械通气的协同作用

A novel rabbit model of severe ARDS: Synergistic effects of acid aspiration and harmful mechanical ventilation.

作者信息

Košútová Petra, Nemcová Nikollet, Kolomazník Maroš, Čalkovská Andrea, Mikolka Pavol

机构信息

Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.

Department of Physiology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovakia.

出版信息

Transl Res. 2025 Jul;281:43-54. doi: 10.1016/j.trsl.2025.05.009. Epub 2025 May 29.

Abstract

BACKGROUND

Acute respiratory distress syndrome (ARDS) is characterised by severe inflammation and pulmonary edema, often leading to respiratory failure. This study aims to develop a stable and relevant rabbit model of severe ARDS using hydrochloric acid (HCl) aspiration and ventilator-induced lung injury (VILI).

METHODS

Adult New Zealand rabbits were divided into four groups: Saline (n = 9), 1-hit 3.0 (HCl 3 ml/kg, n = 7), 1-hit 6.0 (HCl 6 ml/kg, n = 7), and 2-hit (HCl 3 ml/kg and ventilation with V 20 ml/kg, zero PEEP, RR 20-30 bpm, and FiO 1.0 to mimic VILI, n = 14). PaO/FiO ratio, oxygenation index, oxygen saturation, PaCO, ventilation efficiency index and alveolar-arterial gradient were evaluated every hour for 4 h after induction of lung injury. The post-mortem analysis included total and differential cell counts in bronchoalveolar lavage fluid (BALF), evaluation of lung edema formation, biochemical and histological examination of lung tissue.

RESULTS

In the 2-hit group, we observed a significant deterioration of all lung function parameters (P/F ratio, oxygenation index, ventilation efficiency index, and alveolar-arterial gradient) compared to the saline group. Similarly, a deterioration was observed in the 1-hit 6.0 group. When analysing the inflammatory profile, we observed significantly increased levels of chemokines and cytokines (TNFα, IL-1β, IL-6, IL-8, ET-1, MCP, H1F, MIP) and oxidative stress parameters (3NT, MDA, AOPP, catalase and GSH/GSSG) in BALF in the 2-hit group compared to the saline group. Intratracheal administration of HCl alone did not have a significant impact on inflammation as the combination of two insults. An increased wet-to-dry lung weight ratio (W/D), indicative of pulmonary edema, was observed in both the 2-hit and 1-hit 6.0 groups compared to the saline group. An increased level of protein content in BALF and total lung injury score were observed in the 2-hit group compared to the saline group, 1-hit 3.0 and 1-hit 6.0.

CONCLUSION

The combination of hydrochloric acid aspiration and ventilator-induced lung injury reliably reproduces key features of severe ARDS, offering a robust and clinically relevant model for investigating its complex pathophysiology and evaluating novel therapeutic interventions.

摘要

背景

急性呼吸窘迫综合征(ARDS)的特征是严重炎症和肺水肿,常导致呼吸衰竭。本研究旨在利用盐酸(HCl)吸入和呼吸机诱导的肺损伤(VILI)建立一种稳定且相关的重度ARDS兔模型。

方法

成年新西兰兔分为四组:生理盐水组(n = 9)、单次打击3.0组(HCl 3 ml/kg,n = 7)、单次打击6.0组(HCl 6 ml/kg,n = 7)和两次打击组(HCl 3 ml/kg并以V 20 ml/kg通气,零呼气末正压,呼吸频率20 - 30次/分钟,吸入氧浓度1.0以模拟VILI,n = 14)。在诱导肺损伤后4小时内,每小时评估动脉血氧分压/吸入氧浓度比值、氧合指数、血氧饱和度、动脉血二氧化碳分压、通气效率指数和肺泡 - 动脉氧分压差。尸检分析包括支气管肺泡灌洗液(BALF)中的总细胞计数和分类计数、肺水肿形成评估、肺组织的生化和组织学检查。

结果

与生理盐水组相比,两次打击组所有肺功能参数(P/F比值、氧合指数、通气效率指数和肺泡 - 动脉氧分压差)均显著恶化。同样,单次打击6.0组也出现了恶化。在分析炎症特征时,与生理盐水组相比,两次打击组BALF中的趋化因子和细胞因子(TNFα、IL - 1β、IL - 6、IL - 8、ET - 1、MCP、H1F、MIP)以及氧化应激参数(3NT、MDA、AOPP、过氧化氢酶和GSH/GSSG)水平显著升高。单独气管内给予HCl对炎症的影响不如两种损伤联合作用显著。与生理盐水组相比,两次打击组和单次打击6.0组均观察到肺湿重与干重比值(W/D)增加,提示肺水肿。与生理盐水组、单次打击3.0组和单次打击6.0组相比,两次打击组BALF中的蛋白质含量水平和总肺损伤评分增加。

结论

盐酸吸入和呼吸机诱导的肺损伤联合作用可靠地再现了重度ARDS的关键特征,为研究其复杂的病理生理学和评估新的治疗干预措施提供了一个强大且与临床相关的模型。

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