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. 2011 Dec 15;6(12):e29226. doi: 10.1371/journal.pone.0029226

Figure 3. The role of antioxidants and ALDH in the stress resistance of murine ALDHhi myoblasts.

Figure 3

(a) When the antioxidant levels of ALDHhi myoblasts were decreased by treatment with diethyl maleate (DEM), their proliferation rate was decreased to that of ALDHlo myoblasts (n = 5). (* indicates p<0.05 at a given timepoint.) (b) By increasing the antioxidant levels of ALDHlo cells with XJB prior to oxidative stress (H2O2, 250 µM) exposure, the proliferation rate in oxidative stress was increased to the levels observed in ALDHhi myoblasts. (c) DEAB (50 µM) treatment of ALDHhi murine myoblasts significantly decreased their proliferative rate in the absence of oxidative stress compared to untreated ALDHhi myoblasts. (d) However, DEAB treatment had no statistically significant effect on the oxidative stress (H2O2, 250 µM) resistance of ALDHhi myoblasts in terms of proliferation with the exception of an isolated data point at 24 hrs (p = 0.034).