Fig. 4From: Effect of Moringa oleifera stem extract on hydrogen peroxide-induced opacity of cultured mouse lensEffects of MOSE and luteolin on expressions of SOD, CAT and PPARα. Lenses were pretreated with MOSE (0.5 and 1.0 mg/mL) or luteolin (0.05 mg/ mL) for 24 h, followed by incubation with H2O2 (1 mM) for another 24 h, and then recovered in fresh medium for 48 h. Then, protein expressions were determined by western blot (a). Quantification of western blot for SOD (b), CAT (c), and PPARα (d). Data are expressed as the mean ± SEM (n = 3); #P < 0.05 and ##P < 0.01, compared with the normal control group; *P < 0.05 and **P < 0.01, compared with the H2O2 treatment groupBack to article page