Non-β-blocking carvedilol analog, VK-II-86, prevents ouabain-induced cardiotoxicity

GONANO, LUIS A.; TOTEFF, TAMARA; NEGRONI, JORGE; NEIMAN, GABRIEL; WAYNE CHEN, S.R.; GONANO, LUIS A.; TOTEFF, TAMARA; NEGRONI, JORGE; SEPÚLVEDA, MARISA; NEIMAN, GABRIEL; RACIOPPI, MARÍA FLORENCIA; WAYNE CHEN, S.R.; RUOCCO, MARÍA JULIETA FERNÁNDEZ; MIRIUKA, SANTIAGO G.; MATTIAZZI, ALICIA; MORELL, MALENA; SEPÚLVEDA, MARISA; LASCANO, ELENA; RACIOPPI, MARÍA FLORENCIA; MEDEI, EMILIANO; RUOCCO, MARÍA JULIETA FERNÁNDEZ; BACK, THOMAS G.; MIRIUKA, SANTIAGO G.; PETROFF, MARTIN VILA; MATTIAZZI, ALICIA; MORELL, MALENA; LASCANO, ELENA; MEDEI, EMILIANO; BACK, THOMAS G.; PETROFF, MARTIN VILA

CIRCULATION JOURNAL

JAPANESE CIRCULATION SOC

Año: 2018 vol. 83 p. 41 - 51

1346-9843

Background: It has been shown that carvedilol and its non β-blocking analog, VK-II-86, inhibit spontaneous Ca2+ release from the sarcoplasmic reticulum (SR). The aim of this study is to determine whether carvedilol and VK-II-86 suppress ouabain-induced arrhythmogenic Ca2+ waves and apoptosis in cardiac myocytes. Methods and Results: Rat cardiac myocytes were exposed to toxic doses of ouabain (50 µmol/L). Cell length (contraction) was monitored in electrically stimulated and non-stimulated conditions. Ouabain treatment increased contractility, frequency of spontaneous contractions and apoptosis compared to control cells. Carvedilol (1 µmol/L) or VK-II-86 (1 µmol/L) did not affect ouabain-induced inotropy, but significantly reduced the frequency of Ca2+ waves, spontaneous contractions and cell death evoked by ouabain treatment. This antiarrhythmic effect was not associated with a reduction in Ca2+ calmodulin-dependent protein kinase II (CaMKII) activity, phospholamban and ryanodine receptor phosphorylation or SR Ca2+ load. Similar results could be replicated in human cardiomyocytes derived from stem cells and in a mathematical model of human myocytes. Conclusions: Carvedilol and VK-II-86 are effective to prevent ouabain-induced apoptosis and spontaneous contractions indicative of arrhythmogenic activity without affecting inotropy and demonstrated to be effective in human models, thus emerging as a therapeutic tool for the prevention of digitalis-induced arrhythmias and cardiac toxicity.