Figure 4. Mitochondrial functions in aged astrocytes were found declined and berberine may have relieved effect. (A) Cell viability assay of astrocytes by using different concentration of H2O2. (B) Representative immunoblots and (C) Quantitation of P53, P21, P16 and β-actin, in astrocytes treated with H2O2 and berberine. β-actin was a loading control and data are expressed relative to control, n = 3. (D) Cytokine ELISA of IL-6 in culture medium of astrocytes treated with or without H2O2. (E) JC-1 staining. The red and green fluorescence reflects changes in the mitochondrial membrane potential of astrocytes treated with or without H2O2 and berberine, the group of CCCP is used as a positive control. n = 3. ×200 magnification. (F) ATP content was detected by the ATP Assess Kit. (G) Representative immunoblots and (H) Quantitation of Drp1, Mfn2, Opa-1 and β-actin, in astrocytes treated with H2O2 and berberine. β-actin was a loading control and data are expressed relative to control, n = 3. All experiments were expressed as the mean +/−S.D, analyzed by ANOVA followed by Tukey’s test, *P < 0.05, **P < 0.01, ***P < 0.001, ns represents no significance.