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Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis

The action potential duration (APD) of isolated guinea pig papillary muscle is directly related to the medium glucose concentration regardless of the gas mixture with which it is in equilibrium. The APD can be maintained at control value for many hours by a glucose concentration of 50 mM in the comp...

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Autores principales: MacLeod, Don P., Prasad, K.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1969
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2202879/
https://www.ncbi.nlm.nih.gov/pubmed/5783011
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author MacLeod, Don P.
Prasad, K.
author_facet MacLeod, Don P.
Prasad, K.
author_sort MacLeod, Don P.
collection PubMed
description The action potential duration (APD) of isolated guinea pig papillary muscle is directly related to the medium glucose concentration regardless of the gas mixture with which it is in equilibrium. The APD can be maintained at control value for many hours by a glucose concentration of 50 mM in the complete absence of oxygen. Following reduction of the APD by incubation of the muscle in medium containing 5 mM glucose, adjustment of the glucose concentration to 50 mM will cause restoration of normal APD. Phlorizin has been shown to competitively interfere with the effect of glucose on the APD and insulin to prevent or reverse the effect of phlorizin. Nonmetabolizable sugars cannot produce glucose-like effects on the APD. Adrenaline, noradrenaline, and isopropylnoradrenaline increased the reduced APD of papillary muscles incubated in the absence of oxygen in a medium containing 5 mM glucose coincident with an increase in contractile force. The effect of isopropylnoradrenaline was blocked by acetylcholine and propranolol. In the presence of iodoacetate and 2-deoxyglucose, isopropylnoradrenaline increased contractile force but not the reduced APD. Aminophylline was found to produce changes in the reduced APD similar to those caused by the sympathomimetic amines. The findings clearly support the hypothesis that anaerobic metabolism utilizing either glycogen or exogenous glucose is capable of maintaining normal transmembrane electrical activity in guinea pig papillary muscle.
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spelling pubmed-22028792008-04-23 Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis MacLeod, Don P. Prasad, K. J Gen Physiol Article The action potential duration (APD) of isolated guinea pig papillary muscle is directly related to the medium glucose concentration regardless of the gas mixture with which it is in equilibrium. The APD can be maintained at control value for many hours by a glucose concentration of 50 mM in the complete absence of oxygen. Following reduction of the APD by incubation of the muscle in medium containing 5 mM glucose, adjustment of the glucose concentration to 50 mM will cause restoration of normal APD. Phlorizin has been shown to competitively interfere with the effect of glucose on the APD and insulin to prevent or reverse the effect of phlorizin. Nonmetabolizable sugars cannot produce glucose-like effects on the APD. Adrenaline, noradrenaline, and isopropylnoradrenaline increased the reduced APD of papillary muscles incubated in the absence of oxygen in a medium containing 5 mM glucose coincident with an increase in contractile force. The effect of isopropylnoradrenaline was blocked by acetylcholine and propranolol. In the presence of iodoacetate and 2-deoxyglucose, isopropylnoradrenaline increased contractile force but not the reduced APD. Aminophylline was found to produce changes in the reduced APD similar to those caused by the sympathomimetic amines. The findings clearly support the hypothesis that anaerobic metabolism utilizing either glycogen or exogenous glucose is capable of maintaining normal transmembrane electrical activity in guinea pig papillary muscle. The Rockefeller University Press 1969-06-01 /pmc/articles/PMC2202879/ /pubmed/5783011 Text en Copyright © 1969 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
MacLeod, Don P.
Prasad, K.
Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis
title Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis
title_full Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis
title_fullStr Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis
title_full_unstemmed Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis
title_short Influence of Glucose on the Transmembrane Action Potential of Papillary Muscle : Effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis
title_sort influence of glucose on the transmembrane action potential of papillary muscle : effects of concentration, phlorizin and insulin, nonmetabolizable sugars, and stimulators of glycolysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2202879/
https://www.ncbi.nlm.nih.gov/pubmed/5783011
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