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Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium

As the heart transitions from one exercise intensity to another, changes in cardiac output occur, which are modulated by alterations in force development and calcium handling. Although the steady-state force-calcium relationship at various heart rates is well investigated, regulation of these proces...

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Autores principales: Haizlip, Kaylan M., Milani-Nejad, Nima, Brunello, Lucia, Varian, Kenneth D., Slabaugh, Jessica L., Walton, Shane D., Gyorke, Sandor, Davis, Jonathan P., Biesiadecki, Brandon J., Janssen, Paul M. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413957/
https://www.ncbi.nlm.nih.gov/pubmed/25961020
http://dx.doi.org/10.1155/2015/468548
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author Haizlip, Kaylan M.
Milani-Nejad, Nima
Brunello, Lucia
Varian, Kenneth D.
Slabaugh, Jessica L.
Walton, Shane D.
Gyorke, Sandor
Davis, Jonathan P.
Biesiadecki, Brandon J.
Janssen, Paul M. L.
author_facet Haizlip, Kaylan M.
Milani-Nejad, Nima
Brunello, Lucia
Varian, Kenneth D.
Slabaugh, Jessica L.
Walton, Shane D.
Gyorke, Sandor
Davis, Jonathan P.
Biesiadecki, Brandon J.
Janssen, Paul M. L.
author_sort Haizlip, Kaylan M.
collection PubMed
description As the heart transitions from one exercise intensity to another, changes in cardiac output occur, which are modulated by alterations in force development and calcium handling. Although the steady-state force-calcium relationship at various heart rates is well investigated, regulation of these processes during transitions in heart rate is poorly understood. In isolated right ventricular muscle preparations from the rabbit, we investigated the beat-to-beat alterations in force and calcium during the transition from one stimulation frequency to another, using contractile assessments and confocal microscopy. We show that a change in steady-state conditions occurs in multiple phases: a rapid phase, which is characterized by a fast change in force production mirrored by a change in calcium transient amplitude, and a slow phase, which follows the rapid phase and occurs as the muscle proceeds to stabilize at the new frequency. This second/late phase is characterized by a quantitative dissociation between the calcium transient amplitude and developed force. Twitch timing kinetics, such as time to peak tension and 50% relaxation rate, reached steady-state well before force development and calcium transient amplitude. The dynamic relationship between force and calcium upon a switch in stimulation frequency unveils the dynamic involvement of myofilament-based properties in frequency-dependent activation.
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spelling pubmed-44139572015-05-10 Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium Haizlip, Kaylan M. Milani-Nejad, Nima Brunello, Lucia Varian, Kenneth D. Slabaugh, Jessica L. Walton, Shane D. Gyorke, Sandor Davis, Jonathan P. Biesiadecki, Brandon J. Janssen, Paul M. L. Biomed Res Int Research Article As the heart transitions from one exercise intensity to another, changes in cardiac output occur, which are modulated by alterations in force development and calcium handling. Although the steady-state force-calcium relationship at various heart rates is well investigated, regulation of these processes during transitions in heart rate is poorly understood. In isolated right ventricular muscle preparations from the rabbit, we investigated the beat-to-beat alterations in force and calcium during the transition from one stimulation frequency to another, using contractile assessments and confocal microscopy. We show that a change in steady-state conditions occurs in multiple phases: a rapid phase, which is characterized by a fast change in force production mirrored by a change in calcium transient amplitude, and a slow phase, which follows the rapid phase and occurs as the muscle proceeds to stabilize at the new frequency. This second/late phase is characterized by a quantitative dissociation between the calcium transient amplitude and developed force. Twitch timing kinetics, such as time to peak tension and 50% relaxation rate, reached steady-state well before force development and calcium transient amplitude. The dynamic relationship between force and calcium upon a switch in stimulation frequency unveils the dynamic involvement of myofilament-based properties in frequency-dependent activation. Hindawi Publishing Corporation 2015 2015-04-15 /pmc/articles/PMC4413957/ /pubmed/25961020 http://dx.doi.org/10.1155/2015/468548 Text en Copyright © 2015 Kaylan M. Haizlip et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Haizlip, Kaylan M.
Milani-Nejad, Nima
Brunello, Lucia
Varian, Kenneth D.
Slabaugh, Jessica L.
Walton, Shane D.
Gyorke, Sandor
Davis, Jonathan P.
Biesiadecki, Brandon J.
Janssen, Paul M. L.
Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium
title Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium
title_full Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium
title_fullStr Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium
title_full_unstemmed Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium
title_short Dissociation of Calcium Transients and Force Development following a Change in Stimulation Frequency in Isolated Rabbit Myocardium
title_sort dissociation of calcium transients and force development following a change in stimulation frequency in isolated rabbit myocardium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413957/
https://www.ncbi.nlm.nih.gov/pubmed/25961020
http://dx.doi.org/10.1155/2015/468548
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