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Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder

The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80–100-Hz calls lasting ∼500 ms interleaved with silent periods (intercall interv...

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Detalles Bibliográficos
Autores principales: Nelson, Frank E., Hollingworth, Stephen, Rome, Lawrence C., Baylor, Stephen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003191/
https://www.ncbi.nlm.nih.gov/pubmed/24733838
http://dx.doi.org/10.1085/jgp.201411160
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author Nelson, Frank E.
Hollingworth, Stephen
Rome, Lawrence C.
Baylor, Stephen M.
author_facet Nelson, Frank E.
Hollingworth, Stephen
Rome, Lawrence C.
Baylor, Stephen M.
author_sort Nelson, Frank E.
collection PubMed
description The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80–100-Hz calls lasting ∼500 ms interleaved with silent periods (intercall intervals) lasting ∼10 s. To understand the intracellular movements of Ca(2+) during the intercall intervals, superfast fibers were microinjected with fluo-4, a high-affinity fluorescent Ca(2+) indicator, and stimulated by trains of 40 action potentials at 83 Hz, which mimics fiber activity during calling. The fluo-4 fluorescence signal was measured during and after the stimulus trains; the signal was also simulated with a kinetic model of the underlying myoplasmic Ca(2+) movements, including the binding and transport of Ca(2+) by the sarcoplasmic reticulum (SR) Ca(2+) pumps. The estimated total amount of Ca(2+) released from the SR during a first stimulus train is ∼6.5 mM (concentration referred to the myoplasmic water volume). At 40 ms after cessation of stimulation, the myoplasmic free Ca(2+) concentration ([Ca(2+)]) is below the threshold for force generation (∼3 µM), yet the estimated concentration of released Ca(2+) remaining in the myoplasm (Δ[Ca(M)]) is large, ∼5 mM, with ∼80% bound to parvalbumin. At 10 s after stimulation, [Ca(2+)] is ∼90 nM (three times the assumed resting level) and Δ[Ca(M)] is ∼1.3 mM, with 97% bound to parvalbumin. Ca(2+) movements during the intercall interval thus appear to be strongly influenced by (a) the accumulation of Ca(2+) on parvalbumin and (b) the slow rate of Ca(2+) pumping that ensues when parvalbumin lowers [Ca(2+)] near the resting level. With repetitive stimulus trains initiated at 10-s intervals, Ca(2+) release and pumping come quickly into balance as a result of the stability (negative feedback) supplied by the increased rate of Ca(2+) pumping at higher [Ca(2+)].
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spelling pubmed-40031912014-11-01 Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder Nelson, Frank E. Hollingworth, Stephen Rome, Lawrence C. Baylor, Stephen M. J Gen Physiol Research Articles The mating call of the Atlantic toadfish is generated by bursts of high-frequency twitches of the superfast twitch fibers that surround the swimbladder. At 16°C, a calling period can last several hours, with individual 80–100-Hz calls lasting ∼500 ms interleaved with silent periods (intercall intervals) lasting ∼10 s. To understand the intracellular movements of Ca(2+) during the intercall intervals, superfast fibers were microinjected with fluo-4, a high-affinity fluorescent Ca(2+) indicator, and stimulated by trains of 40 action potentials at 83 Hz, which mimics fiber activity during calling. The fluo-4 fluorescence signal was measured during and after the stimulus trains; the signal was also simulated with a kinetic model of the underlying myoplasmic Ca(2+) movements, including the binding and transport of Ca(2+) by the sarcoplasmic reticulum (SR) Ca(2+) pumps. The estimated total amount of Ca(2+) released from the SR during a first stimulus train is ∼6.5 mM (concentration referred to the myoplasmic water volume). At 40 ms after cessation of stimulation, the myoplasmic free Ca(2+) concentration ([Ca(2+)]) is below the threshold for force generation (∼3 µM), yet the estimated concentration of released Ca(2+) remaining in the myoplasm (Δ[Ca(M)]) is large, ∼5 mM, with ∼80% bound to parvalbumin. At 10 s after stimulation, [Ca(2+)] is ∼90 nM (three times the assumed resting level) and Δ[Ca(M)] is ∼1.3 mM, with 97% bound to parvalbumin. Ca(2+) movements during the intercall interval thus appear to be strongly influenced by (a) the accumulation of Ca(2+) on parvalbumin and (b) the slow rate of Ca(2+) pumping that ensues when parvalbumin lowers [Ca(2+)] near the resting level. With repetitive stimulus trains initiated at 10-s intervals, Ca(2+) release and pumping come quickly into balance as a result of the stability (negative feedback) supplied by the increased rate of Ca(2+) pumping at higher [Ca(2+)]. The Rockefeller University Press 2014-05 /pmc/articles/PMC4003191/ /pubmed/24733838 http://dx.doi.org/10.1085/jgp.201411160 Text en © 2014 Nelson et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Nelson, Frank E.
Hollingworth, Stephen
Rome, Lawrence C.
Baylor, Stephen M.
Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
title Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
title_full Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
title_fullStr Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
title_full_unstemmed Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
title_short Intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
title_sort intracellular calcium movements during relaxation and recovery of superfast muscle fibers of the toadfish swimbladder
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003191/
https://www.ncbi.nlm.nih.gov/pubmed/24733838
http://dx.doi.org/10.1085/jgp.201411160
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