Zhao M W, Sun D J, Ma D L
Department of Respiratory Disease, 3rd Hospital, Beijing Medical University.
Zhonghua Nei Ke Za Zhi. 1994 Mar;33(3):158-61.
Thirty-six mice were divided into a control group, lung injury group by oleic acid and protected group with interleukin-1 receptor antagonist (IL-1ra). There were 12 mice in each group. Oleic acid was injected into the tail vein of the mouse with a dose of 0.2 ml/kg to produce a model of acute lung injury (ALI). The result indicates that preadministration of IL-1ra to the mouse with ALI can decrease the lung index, lung wet-to-dry weight ratio and leakage of protein from pulmonary capillary, elevate PaO2, and significantly attenuate lung histologic injury (alveoli edema, alveoli hemorrhage, lung necrosis, inflammatory cell invasion). It is suggested that IL-1ra has protective effect on oleic acid-induced lung injury and may be a potential tool for treatment of ARDS.
36只小鼠被分为对照组、油酸诱导的肺损伤组和白细胞介素-1受体拮抗剂(IL-1ra)保护组。每组12只小鼠。以0.2 ml/kg的剂量将油酸注入小鼠尾静脉以建立急性肺损伤(ALI)模型。结果表明,对ALI小鼠预先给予IL-1ra可降低肺指数、肺湿干重比和肺毛细血管蛋白渗漏,提高动脉血氧分压(PaO2),并显著减轻肺组织学损伤(肺泡水肿、肺泡出血、肺坏死、炎性细胞浸润)。提示IL-1ra对油酸诱导的肺损伤具有保护作用,可能是治疗急性呼吸窘迫综合征(ARDS)的一种潜在手段。