Li Wenli, Chen Yuansen, Li Duo, Wang Haiwang, Liu Yanqing, Li Yongnan, Fan Haojun
Institute of Disaster and Emergency Medicine, Tianjin University, Tianjin, China.
Wenzhou Safety (Emergency) Institute, Tianjin University, Wenzhou, China.
Int J Artif Organs. 2025 Jan;48(1):32-39. doi: 10.1177/03913988241305085. Epub 2024 Dec 11.
The major concerns for patients who have acute lung injury (ALI) or acute respiratory distress syndrome (ARDS) associated with coronavirus disease 2019 or sepsis and undergone successful venovenous extracorporeal membrane oxygenation (VV ECMO) include a low survival rate and an uncontrollable inflammatory response. This study aimed to introduce an inflammation-related ALI/ARDS rat model supported by VV ECMO that is more suitable for clinical application to assess the immune response and thereby further improve survival after VV ECMO.
Rats were randomly divided into three groups: the sham group, the lipopolysaccharide (LPS) group, and the LPS + ECMO group. ALI/ARDS was induced via intratracheal instillation of LPS in rats. A 5.5 F specially designed bicaval cannulation was placed in the external jugular vein for drainage and reflux. Femoral artery cannulation was used to monitor blood pressure during surgery. Arterial blood gas was measured at baseline and 3 h after VV ECMO support. Finally, lung tissue, bronchoalveolar lavage fluid (BALF) and blood samples were harvested for further evaluation.
All LPS-induced ALI/ARDS rats were successfully supported by VV ECMO. The rats survived during the supporting process and maintained effective blood pressure and electrocardiogram (ECG) activity. Compared with the LPS group, VV ECMO support provided oxygen supply to restore lung function and reduced lung injury.
We successfully established an inflammation-related ALI/ARDS rat model supported by VV ECMO, in which VV ECMO support alleviated lung injury. Our rat model provides a new tool for immunological research on inflammation-related ALI/ARDS during VV ECMO.
对于患有与2019冠状病毒病或脓毒症相关的急性肺损伤(ALI)或急性呼吸窘迫综合征(ARDS)且已成功接受静脉-静脉体外膜肺氧合(VV ECMO)治疗的患者,主要担忧包括生存率低和炎症反应无法控制。本研究旨在引入一种由VV ECMO支持的、更适合临床应用的炎症相关ALI/ARDS大鼠模型,以评估免疫反应,从而进一步提高VV ECMO后的生存率。
将大鼠随机分为三组:假手术组、脂多糖(LPS)组和LPS + ECMO组。通过气管内滴注LPS诱导大鼠发生ALI/ARDS。将一根5.5F特制的双腔插管置于颈外静脉用于引流和回流。手术期间使用股动脉插管监测血压。在基线和VV ECMO支持3小时后测量动脉血气。最后,采集肺组织、支气管肺泡灌洗液(BALF)和血液样本进行进一步评估。
所有LPS诱导的ALI/ARDS大鼠均成功接受了VV ECMO支持。大鼠在支持过程中存活,并维持了有效的血压和心电图(ECG)活动。与LPS组相比,VV ECMO支持提供了氧气供应以恢复肺功能并减轻了肺损伤。
我们成功建立了一种由VV ECMO支持的炎症相关ALI/ARDS大鼠模型,其中VV ECMO支持减轻了肺损伤。我们的大鼠模型为VV ECMO期间炎症相关ALI/ARDS的免疫学研究提供了一种新工具。