Adenosine protects against angiotensin II-induced apoptosis in rat cardiocyte cultures

被引:19
|
作者
Goldenberg, I
Shainberg, A [1 ]
Jacobson, KA
Shneyvays, V
Grossman, E
机构
[1] Bar Ilan Univ, Fac Life Sci, Gonda Goldschmied Med Diagnost Res Ctr, IL-52900 Ramat Gan, Israel
[2] Chaim Sheba Med Ctr, IL-52621 Tel Hashomer, Israel
[3] NIH, Mol Recognit Sect, Bioorgan Chem Lab, Bethesda, MD 20892 USA
关键词
A(1) and A(3) adenosine receptors; angiotensin II; apoptosis; cardiomyocytes; Feulgen and TUNEL stainings;
D O I
10.1023/A:1025551229566
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Adenosine has been found to be cardioprotective during episodes of cardiac ischemia/reperfusion through activation of the A(1) and possibly A(3) receptors. Therefore, we have investigated whether activation of these receptors can protect also against apoptotic death induced by angiotensin II (Ang II) in neonatal rat cardiomyocyte cultures. Exposure to Ang II (10 nM) resulted in a 3-fold increase in programmed cell death (p < 0.05). Pretreatment with the A(3) adenosine receptor agonist 2-chloro-N-6-cyclopentyladenosine (CCPA, 1 μM), abolished the effects of Ang II on programmed cardiomyocyte death. Moreover, exposure of cells to the A(1) adenosine receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (CPX) before pretreatment with CCPA, prevented the protective effect of the latter. Pretreatment with the A(3) adenosine receptor agonist N-6-(3-iodobenzyl) adenosine-5'-N-methyluronamide (IB-MECA, 0.1 μM), led to a partial decrease in apoptotic rate induced by Ang II. Exposure of myocytes to Ang II caused an immediate increase in the concentration of intracellular free Ca2+ that lasted 40-60 sec. Pretreatment of cells with CCPA or IB-MECA did not block Ang II-induced Ca2+ elevation. In conclusion, activation of adenosine A(1) receptors can protect the cardiac cells from apoptosis induced by Ang II, while activation of the adenosine A(3) receptors confers partial cardioprotection.
引用
收藏
页码:133 / 139
页数:7
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