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Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients

Rationale: Discordant alternans, a phenomenon in which the action potential duration (APDs) and/or intracellular calcium transient durations (CaDs) in different spatial regions of cardiac tissue are out of phase, present a dynamical instability for complex spatial dispersion that can be associated w...

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Autores principales: Uzelac, Ilija, Ji, Yanyan C., Hornung, Daniel, Schröder-Scheteling, Johannes, Luther, Stefan, Gray, Richard A., Cherry, Elizabeth M., Fenton, Flavio H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655020/
https://www.ncbi.nlm.nih.gov/pubmed/29104543
http://dx.doi.org/10.3389/fphys.2017.00819
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author Uzelac, Ilija
Ji, Yanyan C.
Hornung, Daniel
Schröder-Scheteling, Johannes
Luther, Stefan
Gray, Richard A.
Cherry, Elizabeth M.
Fenton, Flavio H.
author_facet Uzelac, Ilija
Ji, Yanyan C.
Hornung, Daniel
Schröder-Scheteling, Johannes
Luther, Stefan
Gray, Richard A.
Cherry, Elizabeth M.
Fenton, Flavio H.
author_sort Uzelac, Ilija
collection PubMed
description Rationale: Discordant alternans, a phenomenon in which the action potential duration (APDs) and/or intracellular calcium transient durations (CaDs) in different spatial regions of cardiac tissue are out of phase, present a dynamical instability for complex spatial dispersion that can be associated with long-QT syndrome (LQTS) and the initiation of reentrant arrhythmias. Because the use of numerical simulations to investigate arrhythmic effects, such as acquired LQTS by drugs is beginning to be studied by the FDA, it is crucial to validate mathematical models that may be used during this process. Objective: In this study, we characterized with high spatio-temporal resolution the development of discordant alternans patterns in transmembrane voltage (V(m)) and intracellular calcium concentration ([Ca(i)](+2)) as a function of pacing period in rabbit hearts. Then we compared the dynamics to that of the latest state-of-the-art model for ventricular action potentials and calcium transients to better understand the underlying mechanisms of discordant alternans and compared the experimental data to the mathematical models representing V(m) and [Ca(i)](+2) dynamics. Methods and Results: We performed simultaneous dual optical mapping imaging of V(m) and [Ca(i)](+2) in Langendorff-perfused rabbit hearts with higher spatial resolutions compared with previous studies. The rabbit hearts developed discordant alternans through decreased pacing period protocols and we quantified the presence of multiple nodal points along the direction of wave propagation, both in APD and CaD, and compared these findings with results from theoretical models. In experiments, the nodal lines of CaD alternans have a steeper slope than those of APD alternans, but not as steep as predicted by numerical simulations in rabbit models. We further quantified several additional discrepancies between models and experiments. Conclusions: Alternans in CaD have nodal lines that are about an order of magnitude steeper compared to those of APD alternans. Current action potential models lack the necessary coupling between voltage and calcium compared to experiments and fail to reproduce some key dynamics such as, voltage amplitude alternans, smooth development of calcium alternans in time, conduction velocity and the steepness of the nodal lines of APD and CaD.
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spelling pubmed-56550202017-11-03 Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients Uzelac, Ilija Ji, Yanyan C. Hornung, Daniel Schröder-Scheteling, Johannes Luther, Stefan Gray, Richard A. Cherry, Elizabeth M. Fenton, Flavio H. Front Physiol Physiology Rationale: Discordant alternans, a phenomenon in which the action potential duration (APDs) and/or intracellular calcium transient durations (CaDs) in different spatial regions of cardiac tissue are out of phase, present a dynamical instability for complex spatial dispersion that can be associated with long-QT syndrome (LQTS) and the initiation of reentrant arrhythmias. Because the use of numerical simulations to investigate arrhythmic effects, such as acquired LQTS by drugs is beginning to be studied by the FDA, it is crucial to validate mathematical models that may be used during this process. Objective: In this study, we characterized with high spatio-temporal resolution the development of discordant alternans patterns in transmembrane voltage (V(m)) and intracellular calcium concentration ([Ca(i)](+2)) as a function of pacing period in rabbit hearts. Then we compared the dynamics to that of the latest state-of-the-art model for ventricular action potentials and calcium transients to better understand the underlying mechanisms of discordant alternans and compared the experimental data to the mathematical models representing V(m) and [Ca(i)](+2) dynamics. Methods and Results: We performed simultaneous dual optical mapping imaging of V(m) and [Ca(i)](+2) in Langendorff-perfused rabbit hearts with higher spatial resolutions compared with previous studies. The rabbit hearts developed discordant alternans through decreased pacing period protocols and we quantified the presence of multiple nodal points along the direction of wave propagation, both in APD and CaD, and compared these findings with results from theoretical models. In experiments, the nodal lines of CaD alternans have a steeper slope than those of APD alternans, but not as steep as predicted by numerical simulations in rabbit models. We further quantified several additional discrepancies between models and experiments. Conclusions: Alternans in CaD have nodal lines that are about an order of magnitude steeper compared to those of APD alternans. Current action potential models lack the necessary coupling between voltage and calcium compared to experiments and fail to reproduce some key dynamics such as, voltage amplitude alternans, smooth development of calcium alternans in time, conduction velocity and the steepness of the nodal lines of APD and CaD. Frontiers Media S.A. 2017-10-20 /pmc/articles/PMC5655020/ /pubmed/29104543 http://dx.doi.org/10.3389/fphys.2017.00819 Text en Copyright © 2017 Uzelac, Ji, Hornung, Schröder-Scheteling, Luther, Gray, Cherry and Fenton. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Uzelac, Ilija
Ji, Yanyan C.
Hornung, Daniel
Schröder-Scheteling, Johannes
Luther, Stefan
Gray, Richard A.
Cherry, Elizabeth M.
Fenton, Flavio H.
Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients
title Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients
title_full Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients
title_fullStr Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients
title_full_unstemmed Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients
title_short Simultaneous Quantification of Spatially Discordant Alternans in Voltage and Intracellular Calcium in Langendorff-Perfused Rabbit Hearts and Inconsistencies with Models of Cardiac Action Potentials and Ca Transients
title_sort simultaneous quantification of spatially discordant alternans in voltage and intracellular calcium in langendorff-perfused rabbit hearts and inconsistencies with models of cardiac action potentials and ca transients
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655020/
https://www.ncbi.nlm.nih.gov/pubmed/29104543
http://dx.doi.org/10.3389/fphys.2017.00819
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