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NGR1 blocked JNK signalling pathway activated by H2O2. (A) MC3T3‐E1 cells were incubated with 25 μM NGR1 for 24 h before treating with 0.75 mM H2O2 for 6 h. Representative Western blotting and the quantification of phosphorylated JNK (pJNK) relative to JNK. (B) Representative Western blotting and the quantification of pJNK relative to JNK in SP600125 or Anisomycin pretreating for 1 h groups. Data are shown as mean ± SD. ***p < 0.001, ****p < 0.0001
