医学
炎症
肺
支气管肺泡灌洗
潮气量
通风(建筑)
机械通风
嘌呤能受体
胸膜腔
细胞因子
病理
免疫学
麻醉
呼吸系统
内科学
受体
外科
机械工程
工程类
作者
R.F. Baldi,Marissa W. Koh,Colleen J. Thomas,Tomasz Sabbat,Fang Jiang,Stefania Tsatsari,Kieron Young,Alexander Wilson-Slomkowski,Sanooj Soni,Kieran P. O’Dea,Brijesh Patel,Masao Takata,Michael R. Wilson
标识
DOI:10.1165/rcmb.2023-0332oc
摘要
Mechanical ventilation contributes to the morbidity and mortality of patients in intensive care, likely through the exacerbation and dissemination of inflammation. Despite the proximity of the pleural cavity to the lungs and exposure to physical forces, little attention has been paid to its potential as an inflammatory source during ventilation. Here, we investigate the pleural cavity as a novel site of inflammation during ventilator-induced lung injury. Mice were subjected to low or high tidal volume ventilation strategies for up to 3 hours. Ventilation with a high tidal volume significantly increased cytokine and total protein levels in BAL and pleural lavage fluid. In contrast, acid aspiration, explored as an alternative model of injury, only promoted intraalveolar inflammation, with no effect on the pleural space. Resident pleural macrophages demonstrated enhanced activation after injurious ventilation, including upregulated ICAM-1 and IL-1β expression, and the release of extracellular vesicles.
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