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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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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. |
format | Online Article Text |
id | pubmed-4413957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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