Bkaily Ghassan, El-Bizri Nesrine, Nader Moni, Hazzouri Khaled M, Riopel Julie, Jacques Danielle, Regoli Domenico, D'Orleans-Juste Pedro, Gobeil Fernand, Avedanian Levon
Department of Anatomy & Cell Biology, Faculty of Medicine, Université de Sherbrooke, 3001-12th Avenue North, Sherbrooke, Que., Canada J1H 5N4.
Peptides. 2005 Aug;26(8):1418-26. doi: 10.1016/j.peptides.2005.03.051.
The aim of this work is to verify if Angiotensin II (Ang II) affects the frequency of spontaneous cytosolic and nuclear Ca2+ waves in chick embryonic cardiomyocytes and if this effect is mediated via the activation of AT1 and/or AT2 receptors. Using the rapid scan technique of confocal microscopy, we observed that Ang II (10(-8)M) increases the frequency of cytosolic and nuclear Ca2+ waves. This effect was accompanied by a decrease in the amplitude of nuclear Ca2+ waves and an absence of effect on the amplitude of cytosolic Ca2+ waves. The effect of the octapeptide on both frequency and amplitude of the nuclear waves was prevented by the AT1 receptor antagonist L158809. However, blockade of the AT2 receptor using the antagonist PD123319 (10(-7)M) only prevented the effect of Ang II on the frequency of Ca2+ waves. Furthermore, the effect was prevented by both a PKC inhibitor (bisindolylmaleimide) and a PKC activator (phorbol 12,13-dibutyrate). In addition, the Ang II effect was not prevented by the blocker of the pacemaker current If. These results demonstrate that Ang II, via the activation of its receptors AT1 and AT2, affects the frequency of spontaneous Ca2+ waves and this effect seems to be mediated by the PKC pathway.
本研究的目的是验证血管紧张素II(Ang II)是否影响鸡胚心肌细胞中自发的胞质和核Ca2+波频率,以及这种效应是否通过激活AT1和/或AT2受体介导。使用共聚焦显微镜的快速扫描技术,我们观察到Ang II(10(-8)M)增加了胞质和核Ca2+波的频率。这种效应伴随着核Ca2+波振幅的降低,而对胞质Ca2+波振幅没有影响。AT1受体拮抗剂L158809可阻止八肽对核波频率和振幅的影响。然而,使用拮抗剂PD123319(10(-7)M)阻断AT2受体仅能阻止Ang II对Ca2+波频率的影响。此外,PKC抑制剂(双吲哚马来酰胺)和PKC激活剂(佛波醇12,13-二丁酸酯)均可阻止这种效应。另外,起搏电流If的阻滞剂不能阻止Ang II的效应。这些结果表明,Ang II通过激活其受体AT1和AT2,影响自发Ca2+波的频率,且这种效应似乎由PKC途径介导。