Synergistic protective effect of ischemic preconditioning and allopurinol on ischemia/reperfusion injury in rat liver

被引:32
作者
Lee, Woo-Yong [1 ]
Lee, Sun-Mee [1 ]
机构
[1] Sungkyunkwan Univ, Coll Pharm, Suwon 440746, South Korea
基金
新加坡国家研究基金会;
关键词
ischemic preconditioning; allopurinol; oxidative stress; mitochondrial permeability transition; energy metabolism; MITOCHONDRIAL PERMEABILITY TRANSITION; REPERFUSION INJURY; OXIDATIVE STRESS; XANTHINE-OXIDASE; ADENOSINE; GLUTATHIONE; TISSUES; DAMAGE; PHASE;
D O I
10.1016/j.bbrc.2006.08.140
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study examined the effects of ischemic preconditioning (IPC), allopurinol (Allo) or a combination of both on the extent of mitochondrial injury caused by hepatic ischemia/reperfusion (I/R). I/R increased the serum aminotransferase activity and the level of mitochondrial lipid peroxidation, whereas it decreased the mitochondrial glutathione level. Either IPC or Allo alone attenuated these changes with Alto + IPC having a synergistic effect. Allo increased the serum nitrite and nitrate level after brief ischemia. The significant peroxide production observed after 10 min of reperfusion after sustained ischemia was markedly attenuated by Allo + IPC. The mitochondria isolated after I/R were swollen, which was reduced by Allo + IPC. At the end of ischemia, the hepatic ATP level was lower and there was significant xanthine accumulation, which was attenuated by Allo + IPC. These results suggest that IPC and Allo act synergistically to protect cells against mitochondrial injury and preserve the hepatic energy metabolism during hepatic I/R. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1087 / 1093
页数:7
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