Activation of mitogen-activated protein kinases in human heart during cardiopulmonary bypass

被引:61
作者
Talmor, D
Applebaum, A
Rudich, A
Shapira, Y
Tirosh, A [1 ]
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Clin Biochem, Soroka Med Ctr, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Fac Hlth Sci, S Daniel Abraham Ctr Hlth & Nutr, Soroka Med Ctr, IL-84105 Beer Sheva, Israel
[3] Ben Gurion Univ Negev, Fac Hlth Sci, Div Anesthesiol, Soroka Med Ctr, IL-84105 Beer Sheva, Israel
[4] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Cardiothorac Surg, Soroka Med Ctr, IL-84105 Beer Sheva, Israel
关键词
myocardium; ischemia/reperfusion; stress-activated protein kinases;
D O I
10.1161/01.RES.86.9.1004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mitogen-activated protein kinases (MAPKs) have been shown to be activated in both in vitro and in vivo models of cardiac tissue in response to ischemia/reperfusion injury. We investigated whether MAPKs are activated in human heart during coronary artery bypass grafting (CABG) surgery. During elective CABG surgery of 8 patients, 3 right atrial appendage biopsies were obtained at baseline, at the end of cross-clamping, and after coronary reperfusion. The expression of the p38-MAPK, c-Jun N-terminal kinase (JNK), and extracellular signal-regulated kinases (ERK1/2) MAPKs was not altered during CABG, The phosphorylation and activation of both ERK1/2 and p38-MAPK were increased approximate to 2-fold by ischemia and even more (8- and 4-fold, respectively) by reperfusion, Although the ischemic period did not result in a significant activation of JNK, an approximate to 6-fold increase in JNK activity could be observed after reperfusion. In conclusion, distinct activation patterns of ERK1/2, p38, and JNK MAPKs can be observed in human heart during CABG.
引用
收藏
页码:1004 / 1007
页数:4
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