Experimental Drug Research and Production Zone, Institute of Biomedical Chemistry, 119121 Moscow, Russia.
LLC "SuperGene", 119270 Moscow, Russia.
Int J Mol Sci. 2022 Aug 18;23(16):9307. doi: 10.3390/ijms23169307.
Acute lung injury (ALI) as a model of acute respiratory distress syndrome is characterized by inflammation, complex coagulation, and hematologic abnormalities which result in the formation of fibrin-platelet microthrombi in the pulmonary vessels with the rapid development of progressive respiratory dysfunction. We hypothesize that a nebulized fibrinolytic agent, non-immunogenic staphylokinase (nSta), may be useful for ALI therapy. First, the effect of the nebulized nSta (0.2 mg/kg, 1.0 mg/kg, or 2.0 mg/kg) on the coagulogram parameters was studied in healthy rats. ALI was induced in mice by nebulized administration of lipopolysaccharide (LPS) at a dose of 10 mg/kg. nSta (0.2 mg/kg, 0.4 mg/kg or 0.6 mg/kg) was nebulized 30 min, 24 h, and 48 h after LPS administration. The level of pro-inflammatory cytokines was determined in the blood on the 8th day after LPS and nSta administration. The assessment of lung damage was based on their weighing and microscopic analysis. Fibrin/fibrinogen deposition in the lungs was determined by immunohistochemistry. After nSta nebulization in healthy rats, the fibrinogen blood level as well as activated partial thromboplastin time and prothrombin time did not change. In the nebulized ALI model, the mice showed an increase in lung weight due to their edema and rising fibrin deposition. An imbalance of proinflammatory cytokines was also found. Forty percent of mice with ALI without nSta nebulization had died. Nebulized nSta at a dose of 0.2 mg/kg reduced the severity of ALI: a decrease in interstitial edema and inflammatory infiltration was noted. At a dose of 0.4 mg/kg of nebulized nSta, the animals showed no peribronchial edema and the bronchi had an open clear lumen. At a dose of 0.6 mg/kg of nebulized nSta, the manifestations of ALI were completely eliminated. A significant dose-dependent reduction of the fibrin-positive areas in the lungs of mice with ALI was established. Nebulized nSta had a normalizing effect on the proinflammatory cytokines in blood- interleukin (IL)-1α, IL-17A, IL-6, and granulocyte-macrophage colony-stimulating factor (GM-CSF). These data showed the effectiveness of nebulized nSta and the perspectives of its clinical usage in COVID-19 patients with acute respiratory distress syndrome (ARDS).
急性肺损伤 (ALI) 作为急性呼吸窘迫综合征的模型,其特征是炎症、复杂的凝血和血液异常,导致肺血管中形成纤维蛋白-血小板微血栓,并迅速发展为进行性呼吸功能障碍。我们假设雾化纤溶剂非免疫性葡萄球菌激酶 (nSta) 可用于 ALI 治疗。首先,在健康大鼠中研究了雾化 nSta(0.2mg/kg、1.0mg/kg 或 2.0mg/kg)对凝血谱参数的影响。通过雾化给予脂多糖 (LPS) 10mg/kg 诱导小鼠 ALI。在 LPS 给药后 30min、24h 和 48h 雾化给予 nSta(0.2mg/kg、0.4mg/kg 或 0.6mg/kg)。在 LPS 和 nSta 给药后第 8 天测定血液中促炎细胞因子水平。根据其重量和显微镜分析评估肺损伤。通过免疫组织化学测定肺中纤维蛋白/纤维蛋白原的沉积。在健康大鼠雾化 nSta 后,纤维蛋白原的血液水平以及活化部分凝血活酶时间和凝血酶原时间没有改变。在雾化 ALI 模型中,由于水肿和纤维蛋白沉积增加,小鼠的肺重增加。还发现促炎细胞因子的不平衡。40%未经 nSta 雾化的 ALI 小鼠死亡。雾化 nSta (0.2mg/kg)可降低 ALI 的严重程度:观察到间质水肿和炎症浸润减少。雾化 nSta (0.4mg/kg)剂量时,动物无细支气管周围水肿,支气管腔清晰开放。雾化 nSta (0.6mg/kg)剂量时,ALI 表现完全消除。还确定了在患有 ALI 的小鼠的肺中纤维蛋白阳性区域具有显著的剂量依赖性减少。雾化 nSta 对血液中的促炎细胞因子具有正常化作用-白细胞介素 (IL)-1α、IL-17A、IL-6 和粒细胞-巨噬细胞集落刺激因子 (GM-CSF)。这些数据显示了雾化 nSta 的有效性及其在 COVID-19 伴有急性呼吸窘迫综合征(ARDS)的患者中的临床应用前景。