Fig. 4From: Antioxidative effects of caffeine in a hyperoxia-based rat model of bronchopulmonary dysplasiaAcute hyperoxia resulted in an adequate oxidative stress response and caffeine reduced the response. Quantitation of lung homogenates by ELISA of a) total glutathione, b) H2O2, c) HO-1, and d) MDA/ lipid peroxidation with 3 days’ postnatal oxygen exposure (P3) and recovery (P3_P15) and 5 days’ postnatal oxygen exposure (P5) and recovery (P5_P15), respectively. Data are expressed relative to the normoxia-exposed control group (100%) and the 100% values are a) 19.2 μM/mg, 13.4 μM/mg, 17.8 μM/mg, and 13.7 μM/mg protein, b) 1.8 μM/mg, 3.1 μM/mg, 1.0 μM/mg, and 3.0 μM/mg protein, c) 17.2 ng/mg, 5.9 ng/mg, 20.0 ng/mg, and 5.2 ng/mg protein, and d) 3.3 μM/mg, 3.7 μM/mg, 1.3 μM/mg, and 3.3 μM/mg protein for P3 and P3_P15 or P5 and P5_P15 groups, respectively. Error bars represent SEM, n = 5/group. *p < 0.05 and **p < 0.01 versus control (NO); #p < 0.05 and ##p < 0.01 versus hyperoxia group (HY) with Mann Whitney testBack to article page