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. 2017 Jun 29;8(38):63528–63550. doi: 10.18632/oncotarget.18846

Figure 5. Effects of CHMs (HQin, GG, YHS, DS, JG, and NX) on H2O2-treated ARPE-19 cells.

Figure 5

Cells treated with insulin (200 nM) were used as controls. The insulin- and CHM-treated cells were then incubated with an H2O2 (300 μM) solution. Western blot analysis was performed by staining membranes with anti-phospho-p38 MAPK, anti-p38 MAPK, anti-phospho-p44/42 MAPK, anti-p44/42 MAPK, and anti-GAPDH antibodies. (A) Western blot analysis of phospho-p38 MAPK, p38 MAPK, phospho-p44/42 MAPK, p44/42 MAPK, and GAPDH protein expression. (B) The ratio of phospho-p38 MAPK to p38 MAPK in various treatment groups versus that in untreated cells. *P < 0.05. (C) The ratio of phospho-p44/42 MAPKs to p44/42 MAPKs in various treatment groups versus that in untreated cells. *P < 0.05.