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心房利钠肽与哇巴因在心肌中的相互作用。

Interaction of atrial natriuretic peptide and ouabain in the myocardium.

机构信息

Department of Medical Neurobiology, Institute for Medical Research Israel-Canada, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Can J Physiol Pharmacol. 2012 Oct;90(10):1386-93. doi: 10.1139/y2012-112. Epub 2012 Sep 11.

DOI:10.1139/y2012-112
PMID:22966876
Abstract

Natriuretic peptides and digitalis-like compounds serve as regulators of homeostasis, including control of volume expansion and blood pressure. The aim of the present study was to explore possible interactions between atrial natriuretic peptide (ANP) and ouabain in the heart. ANP (1 nmol/L) had no effect in papillary muscle preparations from guinea pigs. Ouabain (1 µmol/L) induced positive inotropic effect. The addition of ANP prior to ouabain resulted in a significant decrease in the ouabain-induced positive inotropic effect, manifested as an attenuated increase in twitch maximal upward force slope and resting muscular tension. In addition, ANP caused an increase in Na⁺-K⁺-ATPase activity in heart microsomal preparations. The effect of ouabain on Na⁺-K⁺-ATPase activity was shown in a biphasic manner. Ouabain (0.01-1 nmol/L) had a small but significant increase on pump activity, but higher doses of ouabain inhibited activity. ANP attenuated ouabain-induced Na⁺-K⁺-ATPase activity. Furthermore, ouabain (50 nmol/L) or ANP (10 nmol/L) alone induced Akt activation in cardiomyocytes. However, ANP blocked ouabain-induced Akt activation. These results point to the existence of interactions between ANP and ouabain on Na⁺-K⁺-ATPase signaling and function in the heart, which may be mediated by regulation of Na⁺-K⁺-ATPase activity and (or) signal transduction mechanisms.

摘要

利钠肽和洋地黄样化合物作为体内平衡的调节剂,包括对容量扩张和血压的控制。本研究旨在探讨心钠肽(ANP)和哇巴因之间可能存在的相互作用。ANP(1 毫摩尔/升)对豚鼠乳头肌无作用。哇巴因(1 微摩尔/升)诱导正性变力作用。哇巴因前加入 ANP 导致哇巴因诱导的正性变力作用显著降低,表现为收缩最大向上力斜率和静息肌张力的增加减弱。此外,ANP 导致心脏微粒体制剂中 Na⁺-K⁺-ATP 酶活性增加。哇巴因对 Na⁺-K⁺-ATP 酶活性的影响呈双相方式。哇巴因(0.01-1 毫摩尔/升)对泵活性有小但显著的增加,但较高剂量的哇巴因抑制活性。ANP 减弱了哇巴因诱导的 Na⁺-K⁺-ATP 酶活性。此外,哇巴因(50 毫摩尔/升)或 ANP(10 毫摩尔/升)单独诱导心肌细胞中 Akt 激活。然而,ANP 阻断了哇巴因诱导的 Akt 激活。这些结果表明,ANP 和哇巴因在心钠肽信号和功能之间存在相互作用,这可能是通过调节 Na⁺-K⁺-ATP 酶活性和(或)信号转导机制介导的。

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