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Intermittent hypoxia attenuates ischemia/reperfusion induced apoptosis in cardiac myocytes via regulating Bcl-2/Bax expression 被引量:47

Intermittent hypoxia attenuates ischemia/reperfusion induced apoptosis in cardiac myocytes via regulating Bcl-2/Bax expression
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摘要 Intermittent hypoxia has been shown to provide myocardial protection against ishemia/reperfusion-induced injury.Cardiac myocyte loss through apoptosis has been reported in ischemia/reperfusion injury. Our aim was to investigate whether intermittent hypoxia could attenuate ischemia/reperfusion-induced apoptosis in cardiac myocytes and its potential mechanisms. Adult male Sprague-Dawley rats were exposed to hypoxia simulated 5000 m in a hypobaric chamber for 6 h/day, lasting 42 days. Normoxia group rats were kept under normoxic conditions. Isolated perfused hearts from both groups were subjected to 30 min of global ischemia followed by 60 min reperfusion.Incidence of apoptosis in cardiac myocytes was determined by terminal deoxynucleotidyl transferase mediated dUTP nick end labeling (TUNEL) and DNA agarose gel electrophoresis. Expressions of apoptosis related proteins,Bax and Bcl-2, in cytosolic and membrane fraction were detected by Western Blotting. After ischemia/reperfusion,enhanced recovery of cardiac function was observed in intermittent hypoxia hearts compared with normoxia group.Ischemia/reperfusion-induced apoptosis, as evidenced by TUNEL-positive nuclei and DNA fragmentation, was significantly reduced in intermittent hypoxia group compared with normoxia group. After ischemia/reperfusion,expression of Bax in both cytosolic and membrane fractions was decreased in intermittent hypoxia hearts compared with normoxia group. Although ischemia/reperfusion did not induce changes in the level of Bcl-2 expression in cytosolic fraction between intermittent hypoxia and normoxia groups, the expression of Bcl-2 in membrane fraction was upregulated in intermittent hypoxia group compared with normoxia group. These results indicated that the cardioprotection of intermittent hypoxia against ischemia/reperfusion injury appears to be in part due to reduce myocardial apoptosis. Intermittent hypoxia attenuated ischemia/reperfusion-induced apoptosis via increasing the ratio of Bcl-2/Bax, especially in membrane fraction.
出处 《Cell Research》 SCIE CAS CSCD 2003年第5期385-391,共7页 细胞研究(英文版)
基金 The study was supported by grants from National Natural Science Foundation of China the Science and Technology committee of Shanghai Municipality(02JC14038).
关键词 intermittent hypoxia APOPTOSIS cardiac myocytes BAX Bcl-2. 心肌细胞 组织缺氧 表达 转移酶
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  • 1Zhuang J G,Biol Signals Recept,1999年,8卷,316页 被引量:1
  • 2Tan D X,J Pineal Res,1998年,25卷,184页 被引量:1
  • 3Chen M,Exp Clin Cardiol,1997年,2卷,179页 被引量:1
  • 4Wang X L,Progress of Cardiovascular Pharmacology (1994~1995),1995年,77页 被引量:1
  • 5Pei S X,Quart J Med,1989年,71卷,266期,555页 被引量:1
  • 6Han Z,Cell Death Differ,2000年,7卷,6期,521页 被引量:1
  • 7Chang Y C,Cell Res,2000年,10卷,233页 被引量:1
  • 8Luo X,Cell,1998年,94卷,481页 被引量:1
  • 9Fang M,Cancer Lett,1998年,127卷,1/2期,113页 被引量:1
  • 10Kruman I,J Neurosci Res,1998年,51卷,3期,293页 被引量:1

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