Suppression of Excessive Histone Deacetylases Activity in Diabetic Hearts Attenuates Myocardial Ischemia/Reperfusion Injury via Mitochondria Apoptosis Pathway

<div>Expressions of p-Akt, p-Foxo3a, and Bim. Representative myocardial p-Akt, total-Akt (a), total-Foxo3a (b), Bim (c), cytoplasm p-Foxo3a (d), cytoplasm Foxo3a (e), and nuclear Foxo3a (f) Western blots images and protein levels analysis. GAPDH or Lamin b1 served as the loading control. 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Journal of Diabetes Research

fig5

Figure 5

Figure 5: Suppression of Excessive Histone Deacetylases Activity in Diabetic Hearts Attenuates Myocardial Ischemia/Reperfusion Injury via Mitochondria Apoptosis Pathway 

Figure 5 | Suppression of Excessive Histone Deacetylases Activity in Diabetic Hearts Attenuates Myocardial Ischemia/Reperfusion Injury via Mitochondria Apoptosis Pathway 