Translational Intensive Care Unit, Department of Anesthesiology, The University of Texas Medical Branch, Galveston, TX, USA.
Department of Pharmacology and Toxicology, The University of Texas Medical Branch, Galveston, TX, USA.
Sci Rep. 2023 Dec 15;13(1):22367. doi: 10.1038/s41598-023-48720-2.
Characterization of the pathophysiology of ARDS following chlorine gas inhalation in clinically relevant translational large animal models is essential, as the opportunity for clinical trials in this type of trauma is extremely limited. To investigate Cl concentration and gender-dependent ARDS severity. Sheep (n = 54) were exposed to air or Cl premixed in air at a concentration of 50, 100, 200, and 300 ppm for 30 min under anesthesia/analgesia and monitored for an additional 48 h in a conscious state. Cardiopulmonary variables and survival endpoints were compared between male and female sheep. Overall there were no significant differences in the responses of female and male sheep except pulmonary oxygenation tended to be better in the male sheep (300 ppm group), and the pulmonary arterial pressure was lower (200 ppm group). The onset of mild ARDS (200 < PaO/FiO ≤ 300) was observed at 36 h post exposure in the 50 ppm group, whereas the 100 ppm group developed mild and moderate (100 ≤ PaO/FiO ≤ 200) ARDS by 12 and 36 h after injury, respectively. The 200 ppm and 300 ppm groups developed moderate ARDS within 6 and 3 h after injury, respectively. The 300 ppm group progressed to severe (PaO/FiO ≤ 100) ARDS at 18 h after injury. Increases in pPeak and pPlateau were noted in all injured animals. Compared to sham, inhalation of 200 ppm and 300 ppm Cl significantly increased lung extravascular water content. The thoracic cavity fluid accumulation dose-dependently increased with the severity of trauma as compared to sham. At necropsy, the lungs were red, heavy, solidified, and fluid filled; the injury severity grew with increasing Cl concentration. The severity of ARDS and mortality rate directly correlated to inhaled Cl concentrations. No significant sex-dependent differences were found in measured endpoint variables.
氯吸入致急性呼吸窘迫综合征的病理生理学特征在临床上相关的大型动物模型中进行描述至关重要,因为这种类型的创伤进行临床试验的机会极为有限。本研究旨在探讨氯浓度与性别依赖性急性呼吸窘迫综合征严重程度的关系。羊(n=54)在麻醉/镇痛下暴露于空气或空气中预混合的氯(浓度分别为 50、100、200 和 300ppm)30min,并在清醒状态下监测 48h。比较了雄性和雌性绵羊的心肺变量和生存终点。除了雄性绵羊的肺氧合作用(300ppm 组)似乎更好,肺动脉压更低(200ppm 组)外,雌性和雄性绵羊的反应没有显著差异。在 50ppm 组中,轻度急性呼吸窘迫综合征(200<PaO/FiO≤300)在暴露后 36h 出现,而 100ppm 组在损伤后 12 和 36h 分别出现轻度和中度(100≤PaO/FiO≤200)急性呼吸窘迫综合征。200ppm 和 300ppm 组在损伤后分别在 6 和 3h 内发展为中度急性呼吸窘迫综合征。300ppm 组在损伤后 18h 进展为严重(PaO/FiO≤100)急性呼吸窘迫综合征。所有受伤动物的 pPeak 和 pPlateau 均增加。与假手术组相比,吸入 200ppm 和 300ppm 氯显著增加了肺血管外水含量。与假手术组相比,胸腔积液量随创伤严重程度呈剂量依赖性增加。尸检时,肺呈红色、沉重、固化和充满液体;损伤严重程度随氯浓度的增加而增加。急性呼吸窘迫综合征的严重程度和死亡率与吸入的氯浓度直接相关。在测量的终点变量中未发现明显的性别依赖性差异。