Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1981 Jan;310:97–115. doi: 10.1113/jphysiol.1981.sp013539

The tension-depolarization relationship of frog atrial trabeculae as determined by potassium contractures.

R A Chapman, J Tunstall
PMCID: PMC1274730  PMID: 6971932

Abstract

1. In the presence of extracellular Na ions K contractures evoked from isolated frog atrial trabeculae show an initial phasic and a subsequent tonic contractile response. 2. The phasic response shows a steep dependence on membrane potential, persists in Na-free fluid, but is blocked by Mn ions, D600 and tetracaine. It has an indirect dependence on the [Ca]0 and would seem to be associated with both the secondary inward current and the release of Ca2+ from intracellular stores. 3. The tonic component of the K contracture is unaffected by D600 or tetracaine, shows a shallow dependence on membrane potential but is absent in Na-free fluid. Its tension-depolarization curve is immediately affected by alteration of either the [Ca]0 or the [Na]0. The form of the tension-depolarization relationship and the effects of [Ca]0 and [Na]0 are consistent with the strength of the tonic tension being determined by a 3Na+ for 1Ca2+ exchange across the cell membrane. 4. The results agree well with those obtained previously with voltage-clamp experiments on the same tissue, and may also help with the interpretation of Ca-flux experiments.

Full text

PDF
101

Selected References

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

  1. Almers W., Best P. M. Effects of tetracaine on displacement currents and contraction of frog skeletal muscle. J Physiol. 1976 Nov;262(3):583–611. doi: 10.1113/jphysiol.1976.sp011611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Anderson T. W., Hirsch C., Kavaler F. Mechanism of activation of contraction in frog ventricular muscle. Circ Res. 1977 Oct;41(4):472–480. doi: 10.1161/01.res.41.4.472. [DOI] [PubMed] [Google Scholar]
  3. Beeler G. W., 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. doi: 10.1113/jphysiol.1970.sp009057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Benninger C., Einwächter H. M., Haas H. G., Kern R. Calcium-sodium antagonism on the frog's heart: a voltage-clamp study. J Physiol. 1976 Aug;259(3):617–645. doi: 10.1113/jphysiol.1976.sp011486. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Blaustein M. P., Hodgkin A. L. The effect of cyanide on the efflux of calcium from squid axons. J Physiol. 1969 Feb;200(2):497–527. doi: 10.1113/jphysiol.1969.sp008704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Blaustein M. P. The interrelationship between sodium and calcium fluxes across cell membranes. Rev Physiol Biochem Pharmacol. 1974;70:33–82. doi: 10.1007/BFb0034293. [DOI] [PubMed] [Google Scholar]
  7. Chapman R. A., Ellis D. Synergistic effects of cooling and caffeine on the contraction of the frog's heart. J Physiol. 1973 Jul;232(2):101P–102P. [PubMed] [Google Scholar]
  8. Chapman R. A., Ellis D. The effects of manganese ions on the contraction of the frog's heart. J Physiol. 1977 Nov;272(2):331–354. doi: 10.1113/jphysiol.1977.sp012047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Chapman R. A. Excitation-contraction coupling in cardiac muscle. Prog Biophys Mol Biol. 1979;35(1):1–52. doi: 10.1016/0079-6107(80)90002-4. [DOI] [PubMed] [Google Scholar]
  10. Chapman R. A. Experimental alteration of the relationship between the external calcium concentration and the contractile force generated by auricular trabeculae isolated from the heart of the frog, Rana pipiens. J Physiol. 1971 Oct;218(1):147–161. doi: 10.1113/jphysiol.1971.sp009608. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Chapman R. A., Miller D. J. The effects of caffeine on the contraction of the frog heart. J Physiol. 1974 Nov;242(3):589–613. doi: 10.1113/jphysiol.1974.sp010725. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Chapman R. A., Niedergerke R. Effects of calcium on the contraction of the hypodynamic frog heart. J Physiol. 1970 Dec;211(2):389–421. doi: 10.1113/jphysiol.1970.sp009284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Chapman R. A. The effects of temperature and metabolic inhibitors on the spontaneous relaxation of the potassium contracture of the heart of the frog Rana pipiens. J Physiol. 1973 Jun;231(2):233–249. doi: 10.1113/jphysiol.1973.sp010230. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Chapman R. A., Tunstall J. The dependence of the contractile force generated by frog auricular trabeculae upon the external calcium concentration. J Physiol. 1971 May;215(1):139–162. doi: 10.1113/jphysiol.1971.sp009462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Costantin L. L. Biphasic potassium contractures in frog muscle fibers. J Gen Physiol. 1971 Aug;58(2):117–130. doi: 10.1085/jgp.58.2.117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Einwächter H. M., Brommundt G. Transient tension responses of voltage-clamped frog atrial muscle related to sudden changes in external Ca or Na. Pflugers Arch. 1978 Jun 21;375(1):69–73. doi: 10.1007/BF00584150. [DOI] [PubMed] [Google Scholar]
  17. Einwächter H. M., Haas H. G., Kern R. Membrane current and contraction in frog atrial fibres. J Physiol. 1972 Dec;227(1):141–171. doi: 10.1113/jphysiol.1972.sp010024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Eisner D. A., Lederer W. J., Noble D. Caffeine and tetracaine abolish the slow inward calcium current in sheep cardiac Purkinje fibres [proceedings]. J Physiol. 1979 Aug;293:76P–77P. [PubMed] [Google Scholar]
  19. Endo M. Calcium release from the sarcoplasmic reticulum. Physiol Rev. 1977 Jan;57(1):71–108. doi: 10.1152/physrev.1977.57.1.71. [DOI] [PubMed] [Google Scholar]
  20. Gibbons W. R., Fozzard H. A. High potassium and low sodium contractures in sheep cardiac muscle. J Gen Physiol. 1971 Nov;58(5):483–510. doi: 10.1085/jgp.58.5.483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Goto M., Kimoto Y., Kato Y. A study on the excitation-contraction coupling of the bullfrog ventricle with voltage clamp technique. Jpn J Physiol. 1971 Apr;21(2):159–173. doi: 10.2170/jjphysiol.21.159. [DOI] [PubMed] [Google Scholar]
  22. Goto M., Kimoto Y., Saito M., Wada Y. Tension fall after contraction of bullfrog atrial muscle examined with the voltage clamp technique. Jpn J Physiol. 1972 Dec;22(6):637–650. doi: 10.2170/jjphysiol.22.637. [DOI] [PubMed] [Google Scholar]
  23. 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]
  24. Léoty C., Raymond G. Mechanical activity and ionic currents in frog atrial trabeculae. Pflugers Arch. 1972;334(2):114–128. doi: 10.1007/BF00586785. [DOI] [PubMed] [Google Scholar]
  25. Morad M., Orkand R. K. Excitation-concentration coupling in frog ventricle: evidence from voltage clamp studies. J Physiol. 1971 Dec;219(1):167–189. doi: 10.1113/jphysiol.1971.sp009656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Morad M., Trautwein W. The effect of the duration of the action potential on contraction in the mammalian heart muscle. Pflugers Arch Gesamte Physiol Menschen Tiere. 1968;299(1):66–82. doi: 10.1007/BF00362542. [DOI] [PubMed] [Google Scholar]
  27. NIEDERGERKE R. MOVEMENTS OF CA IN FROG HEART VENTRICLES AT REST AND DURING CONTRACTURES. J Physiol. 1963 Jul;167:515–550. doi: 10.1113/jphysiol.1963.sp007166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. NIEDERGERKE R. The potassium chloride contracture of the heart and its modification by calcium. J Physiol. 1956 Dec 28;134(3):584–599. doi: 10.1113/jphysiol.1956.sp005667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. New W., Trautwein W. The ionic nature of slow inward current and its relation to contraction. Pflugers Arch. 1972;334(1):24–38. doi: 10.1007/BF00585998. [DOI] [PubMed] [Google Scholar]
  30. Ochi R., Trautwein W. The dependence of cardiac contraction on depolarization and slow inward current. Pflugers Arch. 1971;323(3):187–203. doi: 10.1007/BF00586383. [DOI] [PubMed] [Google Scholar]
  31. Page S. G., Niedergerke R. Structures of physiological interest in the frog heart ventricle. J Cell Sci. 1972 Jul;11(1):179–203. doi: 10.1242/jcs.11.1.179. [DOI] [PubMed] [Google Scholar]
  32. Reuter H., Beeler G. W., Jr Calcium current and activation of contraction in ventricular myocardial fibers. Science. 1969 Jan 24;163(3865):399–401. doi: 10.1126/science.163.3865.399. [DOI] [PubMed] [Google Scholar]
  33. 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]
  34. Sommer J. R., Johnson E. A. Cardiac muscle. A comparative ultrastructural study with special reference to frog and chicken hearts. Z Zellforsch Mikrosk Anat. 1969;98(3):437–468. [PubMed] [Google Scholar]
  35. Vassort G. Influence of sodium ions on the regulation of frog myocardial contractility. Pflugers Arch. 1973 Mar 30;339(3):224–240. doi: 10.1007/BF00587374. [DOI] [PubMed] [Google Scholar]
  36. Vassort G., Rougier O. Membrane potential and slow inward current dependence of frog cardiac mechanical activity. Pflugers Arch. 1972;331(3):191–203. doi: 10.1007/BF00589126. [DOI] [PubMed] [Google Scholar]
  37. Wiggins J. R., Bassett A. L. Sodium-dependence of sustained force in potassium contracture of cat ventricle. Experientia. 1978 Dec 15;34(12):1591–1592. doi: 10.1007/BF02034693. [DOI] [PubMed] [Google Scholar]
  38. Wood E. H., Heppner R. L., Weidmann S. Inotropic effects of electric currents. I. Positive and negative effects of constant electric currents or current pulses applied during cardiac action potentials. II. Hypotheses: calcium movements, excitation-contraction coupling and inotropic effects. Circ Res. 1969 Mar;24(3):409–445. doi: 10.1161/01.res.24.3.409. [DOI] [PubMed] [Google Scholar]

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

RESOURCES