Abstract:Objective To explore the effects of Edaravone in hyperoxic lung injury in neonatal mice so as to provide experimental and theoretical evidences for controlling hyperoxic lung injury in neonate. Methods Neonatal mice were randomly divided into air + normal saline, air + Edaravone, hyperoxia + normal saline, hyperoxia + Edaravone groups. At the end of exposure (on the 3rd, 7th, 10th, 14th and 21st day), IL-4 and IFN-γ in lung homogenate were evaluated by ELISA, and TGF-β1 and optical density (OD) in lung slices were determined using immunohistochemical stain and computerized graphic analysis techniques. Results With the increasing time of exposure, IL-4, IFN-γ and TGF-β1 of the hyperoxic group were increasing and higher than those in the air group, lung injury also aggravated. Compared to the hyperoxic group, the treatment group showed increased IFN-γ and decreased IL-4 and TGF-β1; histopathological changes were alleviated as well. Conclusions Hyperoxia can result in acute lung injury in neonatal mice. Edaravone can regulate the content and ratio of IFN-γ and IL-4, decrease the expression of TGF-β1, thus play a role in prevention and treatment of hyperoxic lung injury.