Kitzerow Oliver, Zucker Irving H, Lisco Steven J, Wang Han-Jun
Department of Genetics Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, United States.
Deptrtment of Anesthesiology, University of Nebraska Medical Center, Omaha, NE, United States.
Front Physiol. 2022 Jan 31;13:777072. doi: 10.3389/fphys.2022.777072. eCollection 2022.
Acute lung injury (ALI) is characterized by the abrupt onset of clinically significant hypoxemia in the context of non-hydrostatic pulmonary edema. Acute lung injury is associated with cytokine release and plasma extravasation (PEx) that can cause pulmonary edema and subsequently acute respiratory distress syndrome (ARDS). Therefore, it is critical we understand the relationship between ALI and lung PEx. In addition, it is also important to assess PEx in the lungs and other organs post-ALI since ALI/ARDS often causes multi-organ failure. We hypothesized that ALI induces time-dependent lung PEx, which promotes extravasation in the heart, liver, kidney, spleen, pancreas, and gastrointestinal (GI) tract, in a time-dependent manner. To test our hypothesis, we administered bleomycin or saline via tracheal intubation in 8-week-old Sprague Dawley rats. At the terminal experiments, Evans Blue was injected (IV) through the femoral vein to allow for the visualization of PEx. Plasma extravasation of desired organs was evaluated at 3-, 7-, 14-, 21-, and 28-days after bleomycin or saline treatment by evaluating Evans Blue concentrations calorimetrically at fluorescence excitation wavelength of 620 nm (bandwidth 10 nm) and an emission wavelength of 680 nm (bandwidth 40 nm). Data show that ALI induces lung PEx beginning at day 3 and peaking between 7 and 21 days. Extravasation was also seen in all organs at varying degrees beginning at day 3 and peaking between days 7 and 14. Resolution appears to start after day 21 and continues past day 28. We conclude that ALI caused by bleomycin incites a time-dependent PEx of the lungs and multiple other organs.
急性肺损伤(ALI)的特征是在非静水压性肺水肿的情况下突然出现具有临床意义的低氧血症。急性肺损伤与细胞因子释放和血浆外渗(PEx)有关,后者可导致肺水肿,进而引发急性呼吸窘迫综合征(ARDS)。因此,了解ALI与肺PEx之间的关系至关重要。此外,评估ALI后肺及其他器官的PEx也很重要,因为ALI/ARDS常导致多器官功能衰竭。我们假设ALI会诱导时间依赖性的肺PEx,进而以时间依赖性方式促进心脏、肝脏、肾脏、脾脏、胰腺和胃肠道的外渗。为了验证我们的假设,我们通过气管插管给8周龄的Sprague Dawley大鼠注射博来霉素或生理盐水。在终末实验中,通过股静脉注射伊文思蓝以观察PEx。在博来霉素或生理盐水处理后的第3、7、14、21和28天,通过在荧光激发波长620 nm(带宽10 nm)和发射波长680 nm(带宽40 nm)下比色法评估伊文思蓝浓度,来评估目标器官的血浆外渗情况。数据显示,ALI在第3天开始诱导肺PEx,并在7至21天达到峰值。从第3天开始,所有器官也均出现不同程度的外渗,并在第7至14天达到峰值。消退似乎在第21天后开始,并持续至第28天以后。我们得出结论,博来霉素所致的ALI会引发肺和其他多个器官的时间依赖性PEx。