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Action Potential Parameters Affecting Excitation-Contraction Coupling

In quantifying type B potentiation effects, given earlier merely qualitatively, it is found that Zn(2+), 1—50 µM, causes increases in action potential duration, twitch tension, and twitch contraction period time, which are all directly proportional to the log of the concentration. Hence, the duratio...

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Detalles Bibliográficos
Autores principales: Taylor, Stuart R., Preiser, Hanna, Sandow, Alexander
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2203185/
https://www.ncbi.nlm.nih.gov/pubmed/4537382
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author Taylor, Stuart R.
Preiser, Hanna
Sandow, Alexander
author_facet Taylor, Stuart R.
Preiser, Hanna
Sandow, Alexander
author_sort Taylor, Stuart R.
collection PubMed
description In quantifying type B potentiation effects, given earlier merely qualitatively, it is found that Zn(2+), 1—50 µM, causes increases in action potential duration, twitch tension, and twitch contraction period time, which are all directly proportional to the log of the concentration. Hence, the duration of the action potential, i.e. the magnitude of its mechanically effective period, is a causal factor quantitatively determining the degree of mechanical activation in the isometric twitch. In higher concentrations of Zn(2+) up to 1000 µM, the spike duration and the contraction time continue to increase but the twitch tension is disproportionately smaller, evidently because the high zinc (500—1000 µM) raises the mechanical threshold of excitation-contraction (E—C) coupling and reduces the intrinsic strength of the contractile system. Eserine (1.5 mM) and also high Zn(2+) not only cause type B potentiation effects, but also slow the rise of the spike, thus causing retardation of the very onset of tension production, which is even greater for high Zn(2+) because of the raised mechanical threshold. This retardation is then succeeded by the faster tension output characteristic of type B potentiation resulting from spike prolongation. Thus, the changes in the consecutive, rising and falling phases of the action potential explicitly register their separate effects in the respective very earliest and directly following periods of twitch output; i.e., each phase of the action potential produces its own mechanical "transform." These transforms, and other effects, suggest that the release of activator Ca(2+) from the sarcoplasmic reticulum during E—C coupling can be graded in both the rate and the total amount of the release.
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spelling pubmed-22031852008-04-23 Action Potential Parameters Affecting Excitation-Contraction Coupling Taylor, Stuart R. Preiser, Hanna Sandow, Alexander J Gen Physiol Article In quantifying type B potentiation effects, given earlier merely qualitatively, it is found that Zn(2+), 1—50 µM, causes increases in action potential duration, twitch tension, and twitch contraction period time, which are all directly proportional to the log of the concentration. Hence, the duration of the action potential, i.e. the magnitude of its mechanically effective period, is a causal factor quantitatively determining the degree of mechanical activation in the isometric twitch. In higher concentrations of Zn(2+) up to 1000 µM, the spike duration and the contraction time continue to increase but the twitch tension is disproportionately smaller, evidently because the high zinc (500—1000 µM) raises the mechanical threshold of excitation-contraction (E—C) coupling and reduces the intrinsic strength of the contractile system. Eserine (1.5 mM) and also high Zn(2+) not only cause type B potentiation effects, but also slow the rise of the spike, thus causing retardation of the very onset of tension production, which is even greater for high Zn(2+) because of the raised mechanical threshold. This retardation is then succeeded by the faster tension output characteristic of type B potentiation resulting from spike prolongation. Thus, the changes in the consecutive, rising and falling phases of the action potential explicitly register their separate effects in the respective very earliest and directly following periods of twitch output; i.e., each phase of the action potential produces its own mechanical "transform." These transforms, and other effects, suggest that the release of activator Ca(2+) from the sarcoplasmic reticulum during E—C coupling can be graded in both the rate and the total amount of the release. The Rockefeller University Press 1972-04-01 /pmc/articles/PMC2203185/ /pubmed/4537382 Text en Copyright © 1972 by The Rockefeller University Press 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 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Taylor, Stuart R.
Preiser, Hanna
Sandow, Alexander
Action Potential Parameters Affecting Excitation-Contraction Coupling
title Action Potential Parameters Affecting Excitation-Contraction Coupling
title_full Action Potential Parameters Affecting Excitation-Contraction Coupling
title_fullStr Action Potential Parameters Affecting Excitation-Contraction Coupling
title_full_unstemmed Action Potential Parameters Affecting Excitation-Contraction Coupling
title_short Action Potential Parameters Affecting Excitation-Contraction Coupling
title_sort action potential parameters affecting excitation-contraction coupling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2203185/
https://www.ncbi.nlm.nih.gov/pubmed/4537382
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