Balogh Johanna, Wihlborg Anna-Karin, Isackson Henrik, Joshi Bhalchandra V, Jacobson Kenneth A, Arner Anders, Erlinge David
Department of Physiological Sciences, Lund University, Lund, Sweden.
J Mol Cell Cardiol. 2005 Aug;39(2):223-30. doi: 10.1016/j.yjmcc.2005.03.007.
ATP is released as a cotransmitter together with catecholamines from sympathetic nerves. In the heart ATP has been shown to cause a pronounced positive inotropic effect and may also act in synergy with beta-adrenergic agonists to augment cardiomyocyte contractility. The aim of the present study was to investigate the inotropic effects mediated by purinergic P2 receptors using isolated mouse cardiomyocytes. Stable adenine nucleotide analogs were used and the agonist rank order for adenine nucleotide stimulation of the mouse cardiomyocytes was AR-C67085>ATPgammaS>2-MeSATP>>>2-MeSADP=0, that fits the agonist profile of the P2Y11 receptor. ATPgammaS induced a positive inotropic response in single mouse cardiomyocytes. The response was similar to that for the beta1 receptor agonist isoproterenol. The most potent response was obtained using AR-C67085, a P2Y11 receptor agonist. This agonist also potentiated contractions in isolated trabecular preparations. The adenylyl cyclase blocker (SQ22563) and phospholipase C (PLC) blocker (U73122) demonstrated that both pathways were required for the inotropic response of AR-C67085. A cAMP enzyme immunoassay confirmed that AR-C67085 increased cAMP in the cardiomyocytes. These findings are in agreement with the P2Y11 receptor, coupled both to activation of IP3 and cAMP, being a major receptor for ATP induced inotropy. Analyzing cardiomyocytes from desmin deficient mice, Des-/-, with a congenital cardiomyopathy, we found a lower sensitivity to AR-C67085, suggesting a down-regulation of P2Y11 receptor function in heart failure. The prominent action of the P2Y11 receptor in controling cardiomyocyte contractility and possible alterations in its function during cardiomyopathy may suggest this receptor as a potential therapeutic target. It is possible that agonists for the P2Y11 receptor could be used to improve cardiac output in patients with circulatory shock and that P2Y11 receptor antagonist could be beneficial in patients with congestive heart failure (CHF).
三磷酸腺苷(ATP)作为一种共递质,与儿茶酚胺一同从交感神经释放。在心脏中,ATP已被证明可引起明显的正性肌力作用,并且还可能与β-肾上腺素能激动剂协同作用,增强心肌细胞的收缩力。本研究的目的是使用分离的小鼠心肌细胞,研究嘌呤能P2受体介导的肌力作用。使用了稳定的腺苷酸类似物,并且腺苷酸刺激小鼠心肌细胞的激动剂排序为AR-C67085>ATPγS>2-甲硫基三磷酸腺苷(2-MeSATP)>>>2-甲硫基二磷酸腺苷(2-MeSADP)=0,这与P2Y11受体的激动剂特征相符。ATPγS在单个小鼠心肌细胞中诱导出正性肌力反应。该反应与β1受体激动剂异丙肾上腺素的反应相似。使用P2Y11受体激动剂AR-C67085获得了最有效的反应。该激动剂还增强了分离的小梁标本的收缩。腺苷酸环化酶阻断剂(SQ22563)和磷脂酶C(PLC)阻断剂(U73122)表明,AR-C67085的肌力反应需要这两条途径。一项环磷酸腺苷(cAMP)酶免疫测定证实,AR-C67085增加了心肌细胞中的cAMP。这些发现与P2Y11受体一致,该受体与肌醇三磷酸(IP3)和cAMP的激活均相关,是ATP诱导的肌力作用的主要受体。分析患有先天性心肌病的结蛋白缺陷小鼠(Des-/-)的心肌细胞,我们发现对AR-C67085的敏感性较低,这表明心力衰竭时P2Y11受体功能下调。P2Y11受体在控制心肌细胞收缩力方面的突出作用以及心肌病期间其功能可能的改变,可能表明该受体是一个潜在的治疗靶点。P2Y11受体激动剂有可能用于改善循环性休克患者的心输出量,而P2Y11受体拮抗剂可能对充血性心力衰竭(CHF)患者有益。