Tenghao Shao, Ning Chen, Shenghai Wang, Qinlong Sun, Jiaqian Wu, Kuo Wang, Zhanbiao Yu, Xigang Ma
Department of Critical Care Medicine, Affiliated Hospital of Hebei University, Baoding, Hebei 071000, China.
Department of Critical Care Medicine, General Hospital of Ningxia Medical University, Yinchuan, Ningxia 750004, China.
Evid Based Complement Alternat Med. 2020 Jun 20;2020:8350579. doi: 10.1155/2020/8350579. eCollection 2020.
Reducing inflammation can effectively relieve acute lung injury (ALI). . To test whether keratinocyte growth factor-2 (KGF-2) can reduce oleic acid-induced inflammation in ALI of rats and explore its possible mechanism. . 45 Sprague-Dawley rats were randomly divided into control group, ALI group, and ALI + KGF-2 group. The animal model of acute lung injury was established by injecting 0.1 mL/kg oleic acid into the tail vein of rats. Rats in the control group were injected with equal volume of normal saline (NS). Each group needs pretreatment 72 hours before the preparation of the acute lung injury model. The control group and ALI group were instilled with 5 ml/kg NS through the airway, and the same amount of KGF-2 was instilled in the ALI + KGF-2 group. It takes 8 hours to successfully prepare the ALI model. Observe the pathological changes of lung tissue through light microscopy, ultrastructural changes through electron microscopy, and the lung wettability/dry weight (w/d) ratio and lung permeability index (LPI). By detecting changes in inflammatory factors in lung tissue and changes in the number of BALF cells, the changes in inflammation in each group were observed. The expressions of Wnt5a, -catenin, and APC in lung tissue were detected by immunohistochemistry and Western blot. The changes of key proteins in Wnt/-catenin signaling pathway in the lung tissue of each group were observed. . Compared with the ALI group, after KGF-2 pretreatment, the degree of lung injury was reduced, the expression of inflammatory factors was reduced, and the number of red blood cells and white blood cells in BALF was reduced. It can also be observed that the expression of Wnt5a, -catenin, and APC, a key protein in the Wnt/-catenin signaling pathway, is reduced. The analysis showed that the number of inflammatory factors, red blood cells, and white blood cells in BALF was positively correlated with the expression of Wnt5a, -catenin, and APC. . KGF-2 may reduce the inflammatory response in ALI induced by oleic acid by regulating key proteins in the Wnt/-catenin signaling pathway.
减轻炎症可有效缓解急性肺损伤(ALI)。为了测试角质形成细胞生长因子-2(KGF-2)是否能减轻油酸诱导的大鼠ALI炎症,并探索其可能的机制。将45只Sprague-Dawley大鼠随机分为对照组、ALI组和ALI+KGF-2组。通过向大鼠尾静脉注射0.1 mL/kg油酸建立急性肺损伤动物模型。对照组大鼠注射等体积的生理盐水(NS)。每组在制备急性肺损伤模型前72小时需要进行预处理。对照组和ALI组通过气道滴注5 ml/kg NS,ALI+KGF-2组滴注等量的KGF-2。成功制备ALI模型需要8小时。通过光学显微镜观察肺组织的病理变化,通过电子显微镜观察超微结构变化,以及肺湿重/干重(w/d)比值和肺通透性指数(LPI)。通过检测肺组织中炎症因子的变化和BALF细胞数量的变化,观察每组炎症的变化。通过免疫组织化学和蛋白质印迹法检测肺组织中Wnt5a、β-连环蛋白和APC的表达。观察每组肺组织中Wnt/β-连环蛋白信号通路关键蛋白的变化。与ALI组相比,KGF-2预处理后,肺损伤程度减轻,炎症因子表达降低,BALF中红细胞和白细胞数量减少。还可观察到Wnt/β-连环蛋白信号通路关键蛋白Wnt5a、β-连环蛋白和APC的表达降低。分析表明,BALF中炎症因子、红细胞和白细胞数量与Wnt5a、β-连环蛋白和APC的表达呈正相关。KGF-2可能通过调节Wnt/β-连环蛋白信号通路中的关键蛋白来减轻油酸诱导的ALI炎症反应。