Li Yongnan, Huang Jian, Zhang Rongzhi, Wang Shixiong, Cheng Xingdong, Zhang Pengbin, Zhai Kerong, Wang Wei, Liu Debin, Gao Bingren
Department of Cardiac Surgery, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, China.
Laboratory of Extracorporeal Life Support, Lanzhou University Second Hospital, Lanzhou University, Lanzhou, China.
Perfusion. 2023 Jan;38(1):85-91. doi: 10.1177/02676591211031468. Epub 2021 Aug 11.
Venovenous extracorporeal membrane oxygenation (VV ECMO) is now considered a reasonable option to salvage acute respiratory distress syndrome (ARDS). However, we lack a rodent model for experimental studies. This study was undertaken to establish an animal model of VV ECMO in ARDS rats.
A total of 18 Sprague-Dawley (SD) rats (350 ± 50 g) were used in this study. Using a rat model of oleic acid (OA)-induced ARDS, VV ECMO was established through cavoatrial cannulation of the right jugular vein for venous drainage and venous reinfusion with a specially designed three-cavity catheter. Continuous arterial pressure monitoring was implemented by using a catheter through cannulation of the right femoral artery. The central temperature was monitored with a rectal probe. Arterial blood gas monitoring was implemented by a blood gas analyzer at three-time points: at baseline, 1-hour (after OA modeling), and 3.5-hour (after VV ECMO support). Lung tissue and bronchoalveolar lavage fluid were harvested respectively for protein concentration and pulmonary histologic evaluation to confirm the alleviation of lung injury during VV ECMO.
Following ARDS induced by OA, ten rats were successfully established on VV ECMO without failure and survived the ECMO procedure. VV ECMO alleviated lung injury and restored adequate circulation for the return of lung function and oxygenation. VV ECMO was associated with decreased lung injury score, wet/dry weight ratio, and fluid leakage into airspaces.
We have established a reliable, economical, and functioning ARDS rat model of VV ECMO.
静脉-静脉体外膜肺氧合(VV ECMO)目前被认为是挽救急性呼吸窘迫综合征(ARDS)的合理选择。然而,我们缺乏用于实验研究的啮齿动物模型。本研究旨在建立ARDS大鼠的VV ECMO动物模型。
本研究共使用18只体重350±50克的Sprague-Dawley(SD)大鼠。利用油酸(OA)诱导的ARDS大鼠模型,通过右颈静脉腔房插管进行静脉引流,并使用专门设计的三腔导管进行静脉再灌注,建立VV ECMO。通过右股动脉插管使用导管进行连续动脉压监测。用直肠探头监测中心温度。在三个时间点通过血气分析仪进行动脉血气监测:基线、1小时(OA建模后)和3.5小时(VV ECMO支持后)。分别采集肺组织和支气管肺泡灌洗液进行蛋白质浓度和肺组织学评估,以确认VV ECMO期间肺损伤的减轻。
在OA诱导ARDS后,10只大鼠成功建立了VV ECMO且无失败,并在ECMO过程中存活。VV ECMO减轻了肺损伤,恢复了足够的循环,使肺功能和氧合得以恢复。VV ECMO与肺损伤评分降低、湿/干重比降低以及气腔内液体渗漏减少相关。
我们建立了一种可靠、经济且有效的ARDS大鼠VV ECMO模型。