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. 2015 Jul 1;290(33):20438–20447. doi: 10.1074/jbc.M115.657379

FIGURE 1.

FIGURE 1.

DHA stimulates glucose uptake through AMPK. A, cells were stimulated with DHA for the indicated times and were analyzed by Western blotting with antibodies against phospho-AMPK and phospho-ACC. AMPK and ACC served as controls. The results are representative of four independent experiments. *, p < 0.05 versus basal conditions. B, cells were stimulated with various doses of DHA, and cell lysates were analyzed by Western blotting with antibodies against phospho-AMPK and phospho-ACC. AMPK and ACC served as controls. The results are representative of four independent experiments. *, p < 0.05 versus basal conditions. C, L6 myoblasts were differentiated and stimulated with various doses of DHA for 1 h, and 2-DG uptake was assayed. *, p < 0.05 compared with control. D, L6 myoblasts were differentiated and stimulated using 50 μm DHA for 1 h in the presence of compound C, and 2-DG uptake was assayed. *, p < 0.05 compared with DHA-treated cells. E, L6 myoblasts were transiently transfected with AMPKα2 siRNA for 2 days and stimulated using 50 μm DHA for 1 h, and 2-DG uptake was assayed. *, p < 0.05 compared with control. IB, immunoblot.