Curcumin Protects Against Regional Myocardial Ischemia/Reperfusion Injury Through Activation of RISK/GSK-3β and Inhibition of p38 MAPK and JNK

被引:78
作者
Jeong, Cheol-Won [1 ]
Yoo, Kyung Yeon [1 ]
Lee, Seong Heon [1 ]
Jeong, Hye Jin [1 ]
Lee, Cha Sup [1 ]
Kim, Seok Jai [1 ]
机构
[1] Chonnam Natl Univ Hosp, Dept Anesthesiol & Pain Med, Kwangju 501757, South Korea
关键词
curcumin; ischemia-reperfusion injury; kinase; rat; MITOCHONDRIAL PERMEABILITY TRANSITION; ISCHEMIA-REPERFUSION INJURY; NF-KAPPA-B; SIGNAL-TRANSDUCTION; HEART; RATS; PORE; TETRAHYDROCURCUMIN; CARDIOPROTECTION; INFARCTION;
D O I
10.1177/1074248412438102
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Curcumin, the active ingredient of turmeric (Curcuma longa), is known to have anti-inflammatory and antioxidative properties. The present study was aimed to determine the effect of curcumin in regional myocardial ischemia/reperfusion (I/R) injury and its underlying mechanisms involving the role of prosurvival kinases and apoptotic kinases. Methods: Sprague-Dawley rats (n=109) subjected to a 30-minute left anterior descending coronary artery (LAD) occlusion followed by reperfusion were assigned to receive saline (control), curcumin (100 mg/kg), wortmannin (inhibitor of phosphatidylinositol-3-OH kinase [PI3K]-Akt), wortmannin + curcumin, U0126 (inhibitor of extracellular signal-regulated kinase [ERK1/2]), U0126 + curcumin, SB216763 (inhibitor of glycogen synthase kinase [GSK-3 beta]), and SB216763 + curcumin 20 minutes before LAD occlusion. Infarct size was measured after 2 hours of reperfusion by triphenyl tetrazolium chloride staining. The phosphorylation of Akt, ERK1/2, GSK-3 beta, p38, and c-Jun N-terminal kinases (JNK) was determined by immunoblotting after 10 minutes of reperfusion. Results: Curcumin significantly reduced the infarct size compared with the control (33.1% +/- 6.2% vs 50.1% +/- 3.9%; P<.05). Wortmannin or U0126 alone did not affect the infarct size but abolished the curcumin-induced cardioprotective effect. Curcumin significantly enhanced the phosphorylation of Akt, ERK1/2, and GSK-3 beta, while it reduced that of p38 and JNK. Wortmannin or U0126 abolished enhanced phosphorylation of GSK-3 beta induced by curcumin. SB216763 alone or combined with curcumin reduced the infarct size and enhanced phosphorylation of GSK-3 beta compared with the control. Conclusions: Preconditioning by curcumin effectively protects against regional myocardial I/R injury through the activation of prosurvival kinases involving PI3K-Akt, ERK1/2, and GSK-3 beta, and attenuation of p38 and JNK.
引用
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页码:387 / 394
页数:8
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