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. 2011 Nov;339(2):451–463. doi: 10.1124/jpet.111.180505

Fig. 4.

Fig. 4.

Fig. 4.

11,12-EET suppression of ATO-induced p38 and JNK activation. Cells were starved overnight, preincubated with 11,12-EET or p38/JNK inhibitor for 12 h, and incubated with ATO or H2O2 for 15 min. Data are representative of three independent experiments. Results shown are mean ± S.E.M. (n = 3). A and B, p38 and JNK activation in Tca-8113 cells treated with ATO (10 μM), 11,12-EET (100 nM), and H2O2 (200 μM) as indicated. C and D, flow cytometric analysis of Tca-8113 cells treated with p38 inhibitor (20 μM) as indicated for 24 h using Annexin V-FITC and PI staining. E and F, flow cytometric analysis of Tca-8113 cells treated with JNK inhibitor (50 μM) as indicated for 24 h using Annexin V-FITC and PI staining. *, p < 0.05 versus control; **, p < 0.05 versus ATO; #, p < 0.05 versus ATO+EET or ATO+p38/JNK Inhibitor.