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Langer, G. A.
Klassen, M. G.
Rich, T. L.
Langer, G. A.
Klassen, M. G.
author Rich, T. L.
Langer, G. A.
Klassen, M. G.
spellingShingle Rich, T. L.
Langer, G. A.
Klassen, M. G.
American Journal of Physiology-Heart and Circulatory Physiology
Two components of coupling calcium in single ventricular cell of rabbits and rats
Physiology (medical)
Cardiology and Cardiovascular Medicine
Physiology
author_sort rich, t. l.
spelling Rich, T. L. Langer, G. A. Klassen, M. G. 0363-6135 1522-1539 American Physiological Society Physiology (medical) Cardiology and Cardiovascular Medicine Physiology http://dx.doi.org/10.1152/ajpheart.1988.254.5.h937 <jats:p> A system for rapid superfusion with simultaneous measurement of contractile amplitude of single adult rat and rabbit ventricular cells is used to measure cellular response to alterations of the superfusate achieved in less than 0.3 s. The time course of contractile response of the cells to extracellular Ca concentration [( Ca]o) depletion and repletion identifies "fast" and "slow" cellular pools of Ca that contribute to contraction. The fast pool can be totally depleted or repleted within a single diastolic period. Depletion of this pool completely eliminates contraction in both rat and rabbit cell. Experiments using dimethonium to investigate the effect of Ca in the diffuse double layer and dodecyl sulfate to specifically augment sarcolemmal fixed-negative charge indicate that sarcolemmal binding sites may represent a major fraction of the fast pool. At 1 mM [Ca]o, this pool is functionally saturated in the rat but not nearly saturated in the rabbit. After 10 min Ca depletion more than 60 s of Ca repletion are required to restore full contraction amplitude. This indicates the presence of a slow pool of Ca that contributes to contraction. This pool, at 1 mM [Ca]o, is nearly functionally saturated in the rabbit but not nearly so in the rat. The responses to Ca depletion and repletion, Na depletion and repletion, and 1 microM ryanodine indicate that the contribution of Ca to contraction from the slow pool is much greater in the rat than in the rabbit and that its cellular locus is probably the sarcoplasmic reticulum. </jats:p> Two components of coupling calcium in single ventricular cell of rabbits and rats American Journal of Physiology-Heart and Circulatory Physiology
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title Two components of coupling calcium in single ventricular cell of rabbits and rats
title_unstemmed Two components of coupling calcium in single ventricular cell of rabbits and rats
title_full Two components of coupling calcium in single ventricular cell of rabbits and rats
title_fullStr Two components of coupling calcium in single ventricular cell of rabbits and rats
title_full_unstemmed Two components of coupling calcium in single ventricular cell of rabbits and rats
title_short Two components of coupling calcium in single ventricular cell of rabbits and rats
title_sort two components of coupling calcium in single ventricular cell of rabbits and rats
topic Physiology (medical)
Cardiology and Cardiovascular Medicine
Physiology
url http://dx.doi.org/10.1152/ajpheart.1988.254.5.h937
publishDate 1988
physical H937-H946
description <jats:p> A system for rapid superfusion with simultaneous measurement of contractile amplitude of single adult rat and rabbit ventricular cells is used to measure cellular response to alterations of the superfusate achieved in less than 0.3 s. The time course of contractile response of the cells to extracellular Ca concentration [( Ca]o) depletion and repletion identifies "fast" and "slow" cellular pools of Ca that contribute to contraction. The fast pool can be totally depleted or repleted within a single diastolic period. Depletion of this pool completely eliminates contraction in both rat and rabbit cell. Experiments using dimethonium to investigate the effect of Ca in the diffuse double layer and dodecyl sulfate to specifically augment sarcolemmal fixed-negative charge indicate that sarcolemmal binding sites may represent a major fraction of the fast pool. At 1 mM [Ca]o, this pool is functionally saturated in the rat but not nearly saturated in the rabbit. After 10 min Ca depletion more than 60 s of Ca repletion are required to restore full contraction amplitude. This indicates the presence of a slow pool of Ca that contributes to contraction. This pool, at 1 mM [Ca]o, is nearly functionally saturated in the rabbit but not nearly so in the rat. The responses to Ca depletion and repletion, Na depletion and repletion, and 1 microM ryanodine indicate that the contribution of Ca to contraction from the slow pool is much greater in the rat than in the rabbit and that its cellular locus is probably the sarcoplasmic reticulum. </jats:p>
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author Rich, T. L., Langer, G. A., Klassen, M. G.
author_facet Rich, T. L., Langer, G. A., Klassen, M. G., Rich, T. L., Langer, G. A., Klassen, M. G.
author_sort rich, t. l.
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description <jats:p> A system for rapid superfusion with simultaneous measurement of contractile amplitude of single adult rat and rabbit ventricular cells is used to measure cellular response to alterations of the superfusate achieved in less than 0.3 s. The time course of contractile response of the cells to extracellular Ca concentration [( Ca]o) depletion and repletion identifies "fast" and "slow" cellular pools of Ca that contribute to contraction. The fast pool can be totally depleted or repleted within a single diastolic period. Depletion of this pool completely eliminates contraction in both rat and rabbit cell. Experiments using dimethonium to investigate the effect of Ca in the diffuse double layer and dodecyl sulfate to specifically augment sarcolemmal fixed-negative charge indicate that sarcolemmal binding sites may represent a major fraction of the fast pool. At 1 mM [Ca]o, this pool is functionally saturated in the rat but not nearly saturated in the rabbit. After 10 min Ca depletion more than 60 s of Ca repletion are required to restore full contraction amplitude. This indicates the presence of a slow pool of Ca that contributes to contraction. This pool, at 1 mM [Ca]o, is nearly functionally saturated in the rabbit but not nearly so in the rat. The responses to Ca depletion and repletion, Na depletion and repletion, and 1 microM ryanodine indicate that the contribution of Ca to contraction from the slow pool is much greater in the rat than in the rabbit and that its cellular locus is probably the sarcoplasmic reticulum. </jats:p>
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spelling Rich, T. L. Langer, G. A. Klassen, M. G. 0363-6135 1522-1539 American Physiological Society Physiology (medical) Cardiology and Cardiovascular Medicine Physiology http://dx.doi.org/10.1152/ajpheart.1988.254.5.h937 <jats:p> A system for rapid superfusion with simultaneous measurement of contractile amplitude of single adult rat and rabbit ventricular cells is used to measure cellular response to alterations of the superfusate achieved in less than 0.3 s. The time course of contractile response of the cells to extracellular Ca concentration [( Ca]o) depletion and repletion identifies "fast" and "slow" cellular pools of Ca that contribute to contraction. The fast pool can be totally depleted or repleted within a single diastolic period. Depletion of this pool completely eliminates contraction in both rat and rabbit cell. Experiments using dimethonium to investigate the effect of Ca in the diffuse double layer and dodecyl sulfate to specifically augment sarcolemmal fixed-negative charge indicate that sarcolemmal binding sites may represent a major fraction of the fast pool. At 1 mM [Ca]o, this pool is functionally saturated in the rat but not nearly saturated in the rabbit. After 10 min Ca depletion more than 60 s of Ca repletion are required to restore full contraction amplitude. This indicates the presence of a slow pool of Ca that contributes to contraction. This pool, at 1 mM [Ca]o, is nearly functionally saturated in the rabbit but not nearly so in the rat. The responses to Ca depletion and repletion, Na depletion and repletion, and 1 microM ryanodine indicate that the contribution of Ca to contraction from the slow pool is much greater in the rat than in the rabbit and that its cellular locus is probably the sarcoplasmic reticulum. </jats:p> Two components of coupling calcium in single ventricular cell of rabbits and rats American Journal of Physiology-Heart and Circulatory Physiology
spellingShingle Rich, T. L., Langer, G. A., Klassen, M. G., American Journal of Physiology-Heart and Circulatory Physiology, Two components of coupling calcium in single ventricular cell of rabbits and rats, Physiology (medical), Cardiology and Cardiovascular Medicine, Physiology
title Two components of coupling calcium in single ventricular cell of rabbits and rats
title_full Two components of coupling calcium in single ventricular cell of rabbits and rats
title_fullStr Two components of coupling calcium in single ventricular cell of rabbits and rats
title_full_unstemmed Two components of coupling calcium in single ventricular cell of rabbits and rats
title_short Two components of coupling calcium in single ventricular cell of rabbits and rats
title_sort two components of coupling calcium in single ventricular cell of rabbits and rats
title_unstemmed Two components of coupling calcium in single ventricular cell of rabbits and rats
topic Physiology (medical), Cardiology and Cardiovascular Medicine, Physiology
url http://dx.doi.org/10.1152/ajpheart.1988.254.5.h937