Membrane calcium current in ventricular myocardial fibres.
Journal: 1971/April - Journal of Physiology
ISSN: 0022-3751
PUBMED: 5503869
Abstract:
1. A slow inward current in ventricular preparations of the dog heart can be measured by the voltage clamp method without interference from the initial rapid sodium current if the sodium system is inactivated by conditioning depolarization.2. The slow inward current is very sensitive to variation in [Ca](o). It occurs above the equilibrium potential of I(Na) immediately after changing the bathing fluid to a sodium-free solution and persists under this condition for a long time without much alteration, while I(Na) is rapidly abolished. Tetrodotoxin and [Mg](o) have no effect on this current component. These results strongly support the view that the slow inward current in cardiac tissue is carried by calcium ions.3. The threshold for initiation of the calcium current is around -35 mV in Tyrode solution and is shifted to more negative potentials by either increasing [Ca](o) or reducing [Na](o).4. Calcium sensitive inward current tails associated with repolarization are assumed to represent a proportional measure of calcium conductance activated during the preceding depolarization. Calcium conductance declines rapidly with time in the inside negative potential range and slowly at positive potentials. The time constants for this ;inactivation' process vary between 40 and 700 msec in the potential range -35 to +50 mV.5. By using instantaneous current-voltage relations the reversal potential of calcium current was estimated to be about +60 mV in normal Tyrode solution. As shown in the Appendix, however, the calcium equilibrium potential cannot be considered to be constant.6. The importance of the calcium current for the plateau of the cardiac action potential is discussed.
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J Physiol 207(1): 191-209

Membrane calcium current in ventricular myocardial fibres

Abstract

1. A slow inward current in ventricular preparations of the dog heart can be measured by the voltage clamp method without interference from the initial rapid sodium current if the sodium system is inactivated by conditioning depolarization.

2. The slow inward current is very sensitive to variation in [Ca]o. It occurs above the equilibrium potential of INa immediately after changing the bathing fluid to a sodium-free solution and persists under this condition for a long time without much alteration, while INa is rapidly abolished. Tetrodotoxin and [Mg]o have no effect on this current component. These results strongly support the view that the slow inward current in cardiac tissue is carried by calcium ions.

3. The threshold for initiation of the calcium current is around -35 mV in Tyrode solution and is shifted to more negative potentials by either increasing [Ca]o or reducing [Na]o.

4. Calcium sensitive inward current tails associated with repolarization are assumed to represent a proportional measure of calcium conductance activated during the preceding depolarization. Calcium conductance declines rapidly with time in the inside negative potential range and slowly at positive potentials. The time constants for this `inactivation' process vary between 40 and 700 msec in the potential range -35 to +50 mV.

5. By using instantaneous current—voltage relations the reversal potential of calcium current was estimated to be about +60 mV in normal Tyrode solution. As shown in the Appendix, however, the calcium equilibrium potential cannot be considered to be constant.

6. The importance of the calcium current for the plateau of the cardiac action potential is discussed.

Full text

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Selected References

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  • Ashley CC, Ridgway EB. Simultaneous recording of membrane potential, calcium transient and tension in single muscle fibers. Nature. 1968 Sep 14;219(5159):1168–1169. [PubMed] [Google Scholar]
  • Beeler GW, Jr, Reuter H. Voltage clamp experiments on ventricular myocarial fibres. J Physiol. 1970 Mar;207(1):165–190.[PMC free article] [PubMed] [Google Scholar]
  • Beeler GW, Jr, Reuter H. The relation between membrane potential, membrane currents and activation of contraction in ventricular myocardial fibres. J Physiol. 1970 Mar;207(1):211–229.[PMC free article] [PubMed] [Google Scholar]
  • Carmeliet E, Van Bogaert PP. Strontium action potentials in cardiac Purkyne fibers. Arch Int Physiol Biochim. 1969 Feb;77(1):134–135. [PubMed] [Google Scholar]
  • FRANKENHAEUSER B, HODGKIN AL. The action of calcium on the electrical properties of squid axons. J Physiol. 1957 Jul 11;137(2):218–244.[PMC free article] [PubMed] [Google Scholar]
  • Hauswirth O, Noble D, Tsien RW. The mechanism of oscillatory activity at low membrane potentials in cardiac Purkinje fibres. J Physiol. 1969 Jan;200(1):255–265.[PMC free article] [PubMed] [Google Scholar]
  • HODGKIN AL, HUXLEY AF. Currents carried by sodium and potassium ions through the membrane of the giant axon of Loligo. J Physiol. 1952 Apr;116(4):449–472.[PMC free article] [PubMed] [Google Scholar]
  • HODGKIN AL, HUXLEY AF. The components of membrane conductance in the giant axon of Loligo. J Physiol. 1952 Apr;116(4):473–496.[PMC free article] [PubMed] [Google Scholar]
  • HODGKIN AL, HUXLEY AF. The dual effect of membrane potential on sodium conductance in the giant axon of Loligo. J Physiol. 1952 Apr;116(4):497–506.[PMC free article] [PubMed] [Google Scholar]
  • HODGKIN AL, HUXLEY AF. A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol. 1952 Aug;117(4):500–544.[PMC free article] [PubMed] [Google Scholar]
  • Katz AM, Repke DI. Control of myocardial contraction: the sensitivity of cardiac actomyosin to calcium ion. Science. 1966 May 27;152(3726):1242–1243. [PubMed] [Google Scholar]
  • Mascher D, Peper K. Two components of inward current in myocardial muscle fibers. Pflugers Arch. 1969;307(3):190–203. [PubMed] [Google Scholar]
  • Niedergerke R, Orkand RK. The dual effect of calcium on the action potential of the frog's heart. J Physiol. 1966 May;184(2):291–311.[PMC free article] [PubMed] [Google Scholar]
  • Noble D, Tsien RW. Outward membrane currents activated in the plateau range of potentials in cardiac Purkinje fibres. J Physiol. 1969 Jan;200(1):205–231.[PMC free article] [PubMed] [Google Scholar]
  • Noble D, Tsien RW. Reconstruction of the repolarization process in cardiac Purkinje fibres based on voltage clamp measurements of membrane current. J Physiol. 1969 Jan;200(1):233–254.[PMC free article] [PubMed] [Google Scholar]
  • Peper K, Trautwein W. A membrane current related to the plateau of the action potential of Purkinje fibers. Pflugers Arch. 1968;303(2):108–123. [PubMed] [Google Scholar]
  • Reuter H. Strom-Spannungsbeziehungen von Purkinje-Fasern bei verschiedenen extracellulären Calcium-Konzentrationen und unter Adrenalineinwirkung. Pflugers Arch Gesamte Physiol Menschen Tiere. 1966;287(4):357–367. [PubMed] [Google Scholar]
  • Reuter H. The dependence of slow inward current in Purkinje fibres on the extracellular calcium-concentration. J Physiol. 1967 Sep;192(2):479–492.[PMC free article] [PubMed] [Google Scholar]
  • Reuter H. Slow inactivation of currents in cardiac Purkinje fibres. J Physiol. 1968 Jul;197(1):233–253.[PMC free article] [PubMed] [Google Scholar]
  • Reuter H, Beeler GW., Jr Sodium current in ventricular myocardial fibers. Science. 1969 Jan 24;163(3865):397–399. [PubMed] [Google Scholar]
  • Reuter H, Beeler GW., Jr Calcium current and activation of contraction in ventricular myocardial fibers. Science. 1969 Jan 24;163(3865):399–401. [PubMed] [Google Scholar]
  • Reuter H, Scholz H. Uber den Einfluss der extracellulären Ca-Konzentration auf Membranpotential und Kontraktion isolierter Herzpräparate bei graduierter Depolarisation. Pflugers Arch Gesamte Physiol Menschen Tiere. 1968;300(2):87–107. [PubMed] [Google Scholar]
  • Reuter H, Seitz N. The dependence of calcium efflux from cardiac muscle on temperature and external ion composition. J Physiol. 1968 Mar;195(2):451–470.[PMC free article] [PubMed] [Google Scholar]
  • Rougier O, Vassort G, Garnier D, Gargouil YM, Coraboeuf E. Existence and role of a slow inward current during the frog atrial action potential. Pflugers Arch. 1969;308(2):91–110. [PubMed] [Google Scholar]
  • WEIDMANN S. Effects of calcium ions and local anesthetics on electrical properties of Purkinje fibres. J Physiol. 1955 Sep 28;129(3):568–582.[PMC free article] [PubMed] [Google Scholar]
Abstract
1. A slow inward current in ventricular preparations of the dog heart can be measured by the voltage clamp method without interference from the initial rapid sodium current if the sodium system is inactivated by conditioning depolarization.
2. The slow inward current is very sensitive to variation in [Ca]o. It occurs above the equilibrium potential of INa immediately after changing the bathing fluid to a sodium-free solution and persists under this condition for a long time without much alteration, while INa is rapidly abolished. Tetrodotoxin and [Mg]o have no effect on this current component. These results strongly support the view that the slow inward current in cardiac tissue is carried by calcium ions.3. The threshold for initiation of the calcium current is around -35 mV in Tyrode solution and is shifted to more negative potentials by either increasing [Ca]o or reducing [Na]o.
4. Calcium sensitive inward current tails associated with repolarization are assumed to represent a proportional measure of calcium conductance activated during the preceding depolarization. Calcium conductance declines rapidly with time in the inside negative potential range and slowly at positive potentials. The time constants for this `inactivation' process vary between 40 and 700 msec in the potential range -35 to +50 mV.
5. By using instantaneous current—voltage relations the reversal potential of calcium current was estimated to be about +60 mV in normal Tyrode solution. As shown in the Appendix, however, the calcium equilibrium potential cannot be considered to be constant.
6. The importance of the calcium current for the plateau of the cardiac action potential is discussed.
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