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Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors

Cardiomyocyte Na(+) and Ca(2+) mishandling, upregulated Ca(2+)/calmodulin-dependent kinase II (CaMKII), and increased reactive oxygen species (ROS) are characteristics of various heart diseases, including heart failure (HF), long QT (LQT) syndrome, and catecholaminergic polymorphic ventricular tachy...

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Autores principales: Hegyi, Bence, Pölönen, Risto-Pekka, Hellgren, Kim T., Ko, Christopher Y., Ginsburg, Kenneth S., Bossuyt, Julie, Mercola, Mark, Bers, Donald M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516771/
https://www.ncbi.nlm.nih.gov/pubmed/34648073
http://dx.doi.org/10.1007/s00395-021-00900-9
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author Hegyi, Bence
Pölönen, Risto-Pekka
Hellgren, Kim T.
Ko, Christopher Y.
Ginsburg, Kenneth S.
Bossuyt, Julie
Mercola, Mark
Bers, Donald M.
author_facet Hegyi, Bence
Pölönen, Risto-Pekka
Hellgren, Kim T.
Ko, Christopher Y.
Ginsburg, Kenneth S.
Bossuyt, Julie
Mercola, Mark
Bers, Donald M.
author_sort Hegyi, Bence
collection PubMed
description Cardiomyocyte Na(+) and Ca(2+) mishandling, upregulated Ca(2+)/calmodulin-dependent kinase II (CaMKII), and increased reactive oxygen species (ROS) are characteristics of various heart diseases, including heart failure (HF), long QT (LQT) syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT). These changes may form a vicious cycle of positive feedback to promote cardiac dysfunction and arrhythmias. In HF rabbit cardiomyocytes investigated in this study, the inhibition of CaMKII, late Na(+) current (I(NaL)), and leaky ryanodine receptors (RyRs) all attenuated the prolongation and increased short-term variability (STV) of action potential duration (APD), but in age-matched controls these inhibitors had no or minimal effects. In control cardiomyocytes, we enhanced RyR leak (by low [caffeine] plus isoproterenol mimicking CPVT) which markedly increased STV and delayed afterdepolarizations (DADs). These proarrhythmic changes were significantly attenuated by both CaMKII inhibition and mitochondrial ROS scavenging, with a slight synergy with I(NaL) inhibition. Inducing LQT by elevating I(NaL) (by Anemone toxin II, ATX-II) caused markedly prolonged APD, increased STV, and early afterdepolarizations (EADs). Those proarrhythmic ATX-II effects were largely attenuated by mitochondrial ROS scavenging, and partially reduced by inhibition of CaMKII and pathological leaky RyRs using dantrolene. In human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) bearing LQT3 mutation SCN5A N406K, dantrolene significantly attenuated cell arrhythmias and APD prolongation. Targeting critical components of the Na(+)–Ca(2+)–CaMKII–ROS–I(NaL) arrhythmogenic vicious cycle may exhibit important on-target and also trans-target effects (e.g., I(NaL) and RyR inhibition can alter I(NaL)-mediated LQT3 effects). Incorporating this vicious cycle into therapeutic strategies provides novel integrated insight for treating cardiac arrhythmias and diseases.
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spelling pubmed-85167712021-10-29 Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors Hegyi, Bence Pölönen, Risto-Pekka Hellgren, Kim T. Ko, Christopher Y. Ginsburg, Kenneth S. Bossuyt, Julie Mercola, Mark Bers, Donald M. Basic Res Cardiol Original Contribution Cardiomyocyte Na(+) and Ca(2+) mishandling, upregulated Ca(2+)/calmodulin-dependent kinase II (CaMKII), and increased reactive oxygen species (ROS) are characteristics of various heart diseases, including heart failure (HF), long QT (LQT) syndrome, and catecholaminergic polymorphic ventricular tachycardia (CPVT). These changes may form a vicious cycle of positive feedback to promote cardiac dysfunction and arrhythmias. In HF rabbit cardiomyocytes investigated in this study, the inhibition of CaMKII, late Na(+) current (I(NaL)), and leaky ryanodine receptors (RyRs) all attenuated the prolongation and increased short-term variability (STV) of action potential duration (APD), but in age-matched controls these inhibitors had no or minimal effects. In control cardiomyocytes, we enhanced RyR leak (by low [caffeine] plus isoproterenol mimicking CPVT) which markedly increased STV and delayed afterdepolarizations (DADs). These proarrhythmic changes were significantly attenuated by both CaMKII inhibition and mitochondrial ROS scavenging, with a slight synergy with I(NaL) inhibition. Inducing LQT by elevating I(NaL) (by Anemone toxin II, ATX-II) caused markedly prolonged APD, increased STV, and early afterdepolarizations (EADs). Those proarrhythmic ATX-II effects were largely attenuated by mitochondrial ROS scavenging, and partially reduced by inhibition of CaMKII and pathological leaky RyRs using dantrolene. In human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) bearing LQT3 mutation SCN5A N406K, dantrolene significantly attenuated cell arrhythmias and APD prolongation. Targeting critical components of the Na(+)–Ca(2+)–CaMKII–ROS–I(NaL) arrhythmogenic vicious cycle may exhibit important on-target and also trans-target effects (e.g., I(NaL) and RyR inhibition can alter I(NaL)-mediated LQT3 effects). Incorporating this vicious cycle into therapeutic strategies provides novel integrated insight for treating cardiac arrhythmias and diseases. Springer Berlin Heidelberg 2021-10-14 2021 /pmc/articles/PMC8516771/ /pubmed/34648073 http://dx.doi.org/10.1007/s00395-021-00900-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Contribution
Hegyi, Bence
Pölönen, Risto-Pekka
Hellgren, Kim T.
Ko, Christopher Y.
Ginsburg, Kenneth S.
Bossuyt, Julie
Mercola, Mark
Bers, Donald M.
Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors
title Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors
title_full Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors
title_fullStr Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors
title_full_unstemmed Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors
title_short Cardiomyocyte Na(+) and Ca(2+) mishandling drives vicious cycle involving CaMKII, ROS, and ryanodine receptors
title_sort cardiomyocyte na(+) and ca(2+) mishandling drives vicious cycle involving camkii, ros, and ryanodine receptors
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516771/
https://www.ncbi.nlm.nih.gov/pubmed/34648073
http://dx.doi.org/10.1007/s00395-021-00900-9
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