Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1977 Jan;264(2):341–365. doi: 10.1113/jphysiol.1977.sp011672

The actions of ouabain on intercellular coupling and conduction velocity in mammalian ventricular muscle.

R Weingart
PMCID: PMC1307766  PMID: 839458

Abstract

1. The effects of ouabain on the electrical coupling between cells and the conduction velocity, theta, were studied in ventricular muscle preparations from calf and cow hearts using a silicon-oil-chamber. 2. After 90 min of exposure to 2 X 10(-6) M ouabain, an increase of the inside longitudinal resistance, Ri, from 420 omega cm to 1032 omega CM was observed. Assuming a constant myoplasmic resistivity this presumably reflects a reduced electrical coupling between myocardial cells. 3. Concomitantly, theta was decreased from 50-3 to 29-4 cm/sec. This change could be explained by the observed alterations in the maximal rate of rise of the action potential, (dV/dt)max, the amplitude of the action potential Vp, the membrane capacity Cf, and the sum, respectively, of the inside and outside longitudinal resistance per unit distance (ri + ro). Quantitatively, about 60% of the decrease of theta could be accounted for by the experimentally determined increase of Ri. 4. Time course studies revealed a biphasic action of ouabain on Ri. An early dose-dependent drop in Ri, equivalent to an improvement of the intercellular coupling, was followed by a delayed massive increase in Ri, whose onset and magnitude were also concentration-dependent. 5. The delayed increase in Ri was associated with an increase of the diastolic tension. Toxic ouabain doses (2 X 10(-6) M) produced irreversible changes on both parameters, whereas thereapeutic doses (less than 5 X 10(-7) M) affected neither of them. Reversible effects on both parameters were observed at an intermediate drug concentration (10(-6) M). 6. The strong correlation between decoupling and contracture is consistent with the idea that the intracellular Ca concentration, [Ca]i, is involved in the control of the nexal conductance. This is supported by the finding that increasing the extracellular Ca concentration, [Ca]o, accelerated the ouabain-induced decoupling, whereas reducing [Ca]o retarded it. 7. If anything, the contracture slightly preceded the increase in Ri. From this it is concluded that the threshold [Ca]i for the electrical decoupling between cells must be somewhat larger than the threshold level for the tension activation. 8. The delayed increase in Ri is compatible with an inhibition of the Na pump which according to the Na-lag hypothesis predicts an increase of [Ca]i secondary to a Na-accumulation. The early drop in Ri can either be explained by a stimulation of the Na pump, or by a non-monotonic relationship between Ri and [Ca]i.

Full text

PDF
341

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baker P. F., Blaustein M. P., Hodgkin A. L., Steinhardt R. A. The influence of calcium on sodium efflux in squid axons. J Physiol. 1969 Feb;200(2):431–458. doi: 10.1113/jphysiol.1969.sp008702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Carafoli E., Tiozzo R., Lugli G., Crovetti F., Kratzing C. The release of calcium from heart mitochondria by sodium. J Mol Cell Cardiol. 1974 Aug;6(4):361–371. doi: 10.1016/0022-2828(74)90077-7. [DOI] [PubMed] [Google Scholar]
  3. Clerc L. Directional differences of impulse spread in trabecular muscle from mammalian heart. J Physiol. 1976 Feb;255(2):335–346. doi: 10.1113/jphysiol.1976.sp011283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cohen I., Daut J., Noble D. An analysis of the actions of low concentrations of ouabain on membrane currents in Purkinje fibres. J Physiol. 1976 Aug;260(1):75–103. doi: 10.1113/jphysiol.1976.sp011505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DUDEL J., TRAUTWEIN W. Elektrophysiologiche Messungen zur Strophanthinwirkung am Herzmuskel. Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1958;232(2):393–407. [PubMed] [Google Scholar]
  6. De Mello W. C. Effect of intracellular injection of calcium and strontium on cell communication in heart. J Physiol. 1975 Sep;250(2):231–245. doi: 10.1113/jphysiol.1975.sp011051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Fabiato A., Fabiato F. Effects of magnesium on contractile activation of skinned cardiac cells. J Physiol. 1975 Aug;249(3):497–517. doi: 10.1113/jphysiol.1975.sp011027. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ghysel-Burton J., Godfraind T. Proceedings: Stimulation and inhibition by ouabain of the sodium pump in guinea-pig atria. Br J Pharmacol. 1975 Oct;55(2):249P–249P. [PMC free article] [PubMed] [Google Scholar]
  9. Greenspan A. M., Morad M. Electromechanical studies on the inotropic effects of acetylstrophanthidin in ventricular muscle. J Physiol. 1975 Dec;253(2):357–384. doi: 10.1113/jphysiol.1975.sp011194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. KASSEBAUM D. G. Electrophysiological effects of strophanthin in the heart. J Pharmacol Exp Ther. 1963 Jun;140:329–338. [PubMed] [Google Scholar]
  11. Koch-Weser J. Myocardial contraction frequency and onset of cardiac glycoside action. Circ Res. 1971 Jan;28(1):34–48. doi: 10.1161/01.res.28.1.34. [DOI] [PubMed] [Google Scholar]
  12. Kushmerick M. J., Podolsky R. J. Ionic mobility in muscle cells. Science. 1969 Dec 5;166(3910):1297–1298. doi: 10.1126/science.166.3910.1297. [DOI] [PubMed] [Google Scholar]
  13. Langer G. A., Serena S. D. Effects of strophanthidin upon contraction and ionic exchange in rabbit ventricular myocardium: relation to control of active state. J Mol Cell Cardiol. 1970 Mar;1(1):65–90. doi: 10.1016/0022-2828(70)90029-5. [DOI] [PubMed] [Google Scholar]
  14. Lee K. S., Klaus W. The subcellular basis for the mechanism of inotropic action of cardiac glycosides. Pharmacol Rev. 1971 Sep;23(3):193–261. [PubMed] [Google Scholar]
  15. MCCLANE T. K. A BIPHASIC ACTION OF OUABAIN ON SODIUM TRANSPORT IN THE TOAD BLADDER. J Pharmacol Exp Ther. 1965 Apr;148:106–110. [PubMed] [Google Scholar]
  16. MENDEZ C., MENDEZ R. The action of cardiac glycosides on the excitability and conduction velocity of the mammalian atrium. J Pharmacol Exp Ther. 1957 Dec;121(4):402–413. [PubMed] [Google Scholar]
  17. MOE G. K., MENDEZ R. The action of several cardiac glycosides on conduction velocity and ventricular excitability in the dog heart. Circulation. 1951 Nov;4(5):729–734. doi: 10.1161/01.cir.4.5.729. [DOI] [PubMed] [Google Scholar]
  18. MUELLER P. OUABAIN EFFECTS ON CARDIAC CONTRACTION, ACTION POTENTIAL, AND CELLULAR POTASSIUM. Circ Res. 1965 Jul;17:46–56. doi: 10.1161/01.res.17.1.46. [DOI] [PubMed] [Google Scholar]
  19. Page E., Polimeni P. I. Magnesium exchange in rat ventricle. J Physiol. 1972 Jul;224(1):121–139. doi: 10.1113/jphysiol.1972.sp009884. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. 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. doi: 10.1113/jphysiol.1968.sp008467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Rose B., Loewenstein W. R. Calcium ion distribution in cytoplasm visualised by aequorin: diffusion in cytosol restricted by energized sequestering. Science. 1975 Dec 19;190(4220):1204–1206. doi: 10.1126/science.1198106. [DOI] [PubMed] [Google Scholar]
  22. Rose B., Loewenstein W. R. Permeability of cell junction depends on local cytoplasmic calcium activity. Nature. 1975 Mar 20;254(5497):250–252. doi: 10.1038/254250a0. [DOI] [PubMed] [Google Scholar]
  23. Rüdel R., Taylor S. R. Aequorin luminescence during contraction of amphibian skeletal muscle. J Physiol. 1973 Aug;233(1):5P–6P. [PubMed] [Google Scholar]
  24. VASSALLE M., KARIS J., HOFFMAN B. F. Toxic effects of ouabain on Purkinje fibers and ventricular muscle fibers. Am J Physiol. 1962 Sep;203:433–439. doi: 10.1152/ajplegacy.1962.203.3.433. [DOI] [PubMed] [Google Scholar]
  25. WILBRANDT W., WEISS E. M. [Antagonism between cardiac glycosides and corticosteroids in the frog's skin potential]. Arzneimittelforschung. 1960 May;10:409–412. [PubMed] [Google Scholar]
  26. Watanabe Y., Dreifus L. S. Electrophysiologic effects of digitalis on A-V transmission. Am J Physiol. 1966 Dec;211(6):1461–1466. doi: 10.1152/ajplegacy.1966.211.6.1461. [DOI] [PubMed] [Google Scholar]
  27. Weidmann S. Electrical constants of trabecular muscle from mammalian heart. J Physiol. 1970 Nov;210(4):1041–1054. doi: 10.1113/jphysiol.1970.sp009256. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. de Mello W. C. Uncoupling of heart cells produced by intracellular sodium injection. Experientia. 1975 Apr 15;31(4):460–462. doi: 10.1007/BF02026379. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES