Ouabain worsens diastolic sarcomere length in myocytes from a cardiomyopathy mouse model

Diastolic dysfunction is a major feature of hypertrophic cardiomyopathy (HCM). Data from patient tissue and animal models associate increased Ca2+ sensitivity of myofilaments with altered Na+ and Ca2+ ion homeostasis in cardiomyocytes with diastolic dysfunction. In this study, we tested the acute effects of ouabain on ventricular myocytes of an HCM mouse model. The effects of ouabain on contractility and Ca2+ transients were tested in intact adult mouse ventricular myocytes (AMVMs) of Mybpc3-targeted knock-in (KI) and wild-type (WT) mice. Concentration-response assessment of contractile function revealed low sensitivity of AMVMs to ouabain (10 mu M) compared to literature data on human cardiomyocytes (100 nM). Three hundred mu M ouabain increased contraction amplitude (WT similar to 1.8-fold; KI similar to 1.5-fold) and diastolic intracellular Ca2+ in both WT and KI (+12-18%), but further decreased diastolic sarcomere length in KI cardiomyocytes (-5%). Western Blot analysis of whole heart protein extracts revealed 50% lower amounts of Na+/K+ ATPase (NKA) in KI than in WT. Ouabain worsened the diastolic phenotype of KI cardiomyocytes at concentrations which did not impair WT diastolic function. Ouabain led to an elevation of intracellular Ca2+, which was poorly tolerated in KI showing already high cytosolic Ca2+ at baseline due to increased myofilament Ca2+ sensitivity. Lower amounts of NKA in KI could amplify the need to exchange excessive intracellular Na+ for Ca2+ and thereby explain the general tendency to higher diastolic Ca2+ in KI.

Automated summary

Diastolic dysfunction is a major feature of hypertrophic cardiomyopathy (HCM). This study found that ouabain has acute effects on ventricular myocytes of an HCM mouse model, particularly worsening diastolic phenotype in KI cardiomyocytes. Lower amounts of Na+/K+ ATPase (NKA) in KI may amplify the impact of ouabain-induced elevation of intracellular Ca2+.