Cardioprotective properties of Crataegus oxycantha extract against ischemia-reperfusion injury

被引:40
|
作者
Swaminathan, J. K. [1 ,2 ]
Khan, M. [1 ]
Mohan, I. K. [1 ]
Selvendiran, K. [1 ]
Devaraj, S. Niranjali [2 ]
Rivera, B. K. [1 ]
Kuppusamy, P. [1 ]
机构
[1] Ohio State Univ, Dept Internal Med, Ctr Biomed EPR Spect & Imaging, Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
[2] Univ Madras, Dept Biochem, Madras 600025, Tamil Nadu, India
关键词
Oxidative stress; Infarction; Ischemia-reperfusion injury; Rat heart; Crataegus oxycantha; Apoptosis; INDUCED MYOCARDIAL-INFARCTION; OXIDATIVE STRESS; GENE-EXPRESSION; RAT MYOCARDIUM; CELL-DEATH; HAWTHORN EXTRACT; HEART-FAILURE; APOPTOSIS; ACTIVATION; CARDIOMYOCYTES;
D O I
10.1016/j.phymed.2010.01.009
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The aim of the study was to investigate the cardioprotective effect and mechanism of Crataegus oxycantha (COC) extract, a well-known natural antioxidant-based cardiotonic, against ischemia/reperfusion (I/R) injury. Electron paramagnetic resonance studies showed that COC extract was capable of scavenging superoxide, hydroxyl, and peroxyl radicals, in vitro. The cardioprotective efficacy of the extract was studied in a crystalloid perfused heart model of I/R injury. Hearts were subjected to 30 min of global ischemia followed by 45 min of reperfusion. During reperfusion, COC extract was infused at a dose rate of 1 mg/ml/min for 10 min. Hearts treated with COC extract showed a significant recovery in cardiac contractile function, reduction in infarct size, and decrease in creatine kinase and lactate dehydrogenase activities. The expressions of xanthine oxidase and NADPH oxidase were significantly reduced in the treated group. A significant upregulation of the anti-apoptotic proteins Bcl-2 and Hsp70 with simultaneous downregulation of the pro-apoptotic proteins cytochrome c and cleaved caspase-3 was observed. The molecular signaling cascade including phospho-Akt (ser-473) and HIF-1 alpha that lead to the activation or suppression of apoptotic pathway also showed a significant protective role in the treatment group. No significant change in phospho-p38 levels was observed. The results suggested that the COC extract may reduce the oxidative stress in the reperfused myocardium, and play a significant role in the inhibition of apoptotic pathways leading to cardioprotection. (C) 2010 Elsevier GmbH. All rights reserved.
引用
收藏
页码:744 / 752
页数:9
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