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. 2014 Dec 17;3(6):e001286. doi: 10.1161/JAHA.114.001286

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© 2014 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell.

This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

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Figure 9. — Phosphorylation of Akt and GSK‐3β. Total LV lysates, prepared from sham, non‐infarct (Non) and infarct (Inf) LV regions 1 day post‐MI, were analyzed by Western blot using phospho‐specific antibodies for Akt (ser‐473) and GSK‐3β (ser‐9). The upper panels depict autoradiograms indicating immunostaining for p‐Akt, p‐GSK‐3β and GAPDH. The lower panels exhibit quantitative analyses of p‐Akt (A) and p‐GSK‐3β (B) normalized to GAPDH. ^#P<0.05 vs Sham; *P<0.05 vs WT‐Inf; n=6. GSK, glycogen synthase kinase; hKO indicates heterozygous knockout; LV, left ventricle; MI, myocardial infarction; WT, wild‐type.