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. 2019 Sep 18;10:1051. doi: 10.3389/fphar.2019.01051

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Copyright © 2019 Boknik, Drzewiecki, Eskandar, Gergs, Hofmann, Treede, Grote-Wessels, Fabritz, Kirchhof, Fortmüller, Müller, Schmitz, Zimmermann, Kirchhefer and Neumann

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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A_2A-AR exhibited increased the phosphorylation state of proteins in the reperfusion injury salvage kinase (= RISK) pathway. After 20 min ischemia and 40 min reperfusion, isolated perfused hearts (WT and A_2A-TG) were freeze-clamped. Tissue was homogenized and subjected to electrophoresis and Western blotting. Insets indicate the expression of total ERK and total AKT as well as phosphorylated AKT (pAKT) and phosphorylated ERK (pERK), indicated by arrows and molecular weight in kDa. Ordinates represent the ratio of pAKT to AKT or pERK to ERK. Numbers in brackets indicate the number of hearts studied. ^★p < 0.05 vs. WT.