Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1977 Apr 1;69(4):463–474. doi: 10.1085/jgp.69.4.463

The effect of extracellular potassium on the intracellular potassium ion activity and transmembrane potentials of beating canine cardiac Purkinje fibers

PMCID: PMC2215048  PMID: 853287

Abstract

We used open tip microelectrodes containing a K+-sensitive liquid ion exchanger to determine directly the intracellular K+ activity in beating canine cardiac Purkinje fibers. For preparations superfused with Tyrode's solution in which the K+ concentration was 4.0 mM, intracellular K+ activity (ak) was 130.0+/-2.3 mM (mean+/-SE) at 37 degrees C. The calculated K+ equilibrium potential (EK) was -100.6+/- 0.5 mV. Maximum diastolic potential (ED) and resting transmembrane potential (EM) were measured with conventional microelectrodes filled with 3 M KCl and were -90.6+/-0.3 and -84.4+/-0.4 mV, respectively. When [K+]o was decreased to 2.0 mM or increased to 6.0, 10.0, and 16.0 mM, ak remained the same. At [K+]o=2.0, ED was -97.3+/-0.4 and Em - 86.0+/-0.7 mV; at [K+]o=16.0, ED fell to -53.8+/-0.4 mV and Em to the same value. Over this range of values for [K+]o, EK changed from - 119.0+/-0.3 to -63.6+/-0.2 mV. These values for EK are consistent with those previously estimated indirectly by other techniques.

Full Text

The Full Text of this article is available as a PDF (700.4 KB).

Selected References

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

  1. ADRIAN R. H. The effect of internal and external potassium concentration on the membrane potential of frog muscle. J Physiol. 1956 Sep 27;133(3):631–658. doi: 10.1113/jphysiol.1956.sp005615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Armstrong W. M., Lee C. O. Sodium and potassium activities in normal and "sodium-rich" frog skeletal muscle. Science. 1971 Jan 29;171(3969):413–415. doi: 10.1126/science.171.3969.413. [DOI] [PubMed] [Google Scholar]
  3. Aronson R. S., Gelles J. M., Hoffman B. F. A new method for producing short cardiac Purkinje fibers suitable for voltage clamp. J Appl Physiol. 1973 Apr;34(4):527–530. doi: 10.1152/jappl.1973.34.4.527. [DOI] [PubMed] [Google Scholar]
  4. Brown A. M., Sutton R. B., Walker J. L., Jr Increased chloride conductance as the proximate cause of hydrogen ion concentration effects in Aplysia neurons. J Gen Physiol. 1970 Nov;56(5):559–582. doi: 10.1085/jgp.56.5.559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. CARMELIET E. E. Chloride ions and the membrane potential of Purkinje fibres. J Physiol. 1961 Apr;156:375–388. doi: 10.1113/jphysiol.1961.sp006682. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. CONWAY E. J. Nature and significance of concentration relations of potassium and sodium ions in skeletal muscle. Physiol Rev. 1957 Jan;37(1):84–132. doi: 10.1152/physrev.1957.37.1.84. [DOI] [PubMed] [Google Scholar]
  7. Cope F. W. Nuclear magnetic resonance evidence using D2O for structured water in muscle and brain. Biophys J. 1969 Mar;9(3):303–319. doi: 10.1016/S0006-3495(69)86388-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cornwall M. C., Peterson D. F., Kunze D. L., Walker J. L., Brown A. M. Intracellular potassium and chloride activities measured with liquid ion exchanger microelectrodes. Brain Res. 1970 Oct 28;23(3):433–436. doi: 10.1016/0006-8993(70)90070-3. [DOI] [PubMed] [Google Scholar]
  9. HINKE J. A. Glass micro-electrodes for measuring intracellular activities of sodium and potassium. Nature. 1959 Oct 17;184(Suppl 16):1257–1258. doi: 10.1038/1841257a0. [DOI] [PubMed] [Google Scholar]
  10. HINKE J. A. The measurement of sodium and potassium activities in the squid axon by means of cation-selective glass micro-electrodes. J Physiol. 1961 Apr;156:314–335. doi: 10.1113/jphysiol.1961.sp006678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. HODGKIN A. L., HOROWICZ P. The influence of potassium and chloride ions on the membrane potential of single muscle fibres. J Physiol. 1959 Oct;148:127–160. doi: 10.1113/jphysiol.1959.sp006278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hazlewood C. F., Nichols B. L., Chamberlain N. F. Evidence for the existence of a minimum of two phases of ordered water in skeletal muscle. Nature. 1969 May 24;222(5195):747–750. doi: 10.1038/222747a0. [DOI] [PubMed] [Google Scholar]
  13. Kline R., Morad M. Potassium efflux and accumulation in heart muscle. Evidence from K +/- electrode experiments. Biophys J. 1976 Apr;16(4):367–372. doi: 10.1016/S0006-3495(76)85694-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kunze D. L., Brown A. M. Internal potassium and chloride activities and the effects of acetylcholine on identifiable Aplysia neurones. Nat New Biol. 1971 Feb 24;229(8):229–231. doi: 10.1038/newbio229229a0. [DOI] [PubMed] [Google Scholar]
  15. LEV A. A. DETERMINATION OF ACTIVITY AND ACTIVITY COEFFICIENTS OF POTASSIUM AND SODIUM IONS IN FROG MUSCLE FIBRES. Nature. 1964 Mar 14;201:1132–1134. doi: 10.1038/2011132a0. [DOI] [PubMed] [Google Scholar]
  16. LING G., GERARD R. W. The normal membrane potential of frog sartorius fibers. J Cell Physiol. 1949 Dec;34(3):383–396. doi: 10.1002/jcp.1030340304. [DOI] [PubMed] [Google Scholar]
  17. Lee C. O., Armstrong W. M. State and distribution of potassium and sodium ions in frog skeletal muscle. J Membr Biol. 1974;15(4):331–362. doi: 10.1007/BF01870094. [DOI] [PubMed] [Google Scholar]
  18. Lee C. O., Fozzard H. A. Activities of potassium and sodium ions in rabbit heart muscle. J Gen Physiol. 1975 Jun;65(6):695–708. doi: 10.1085/jgp.65.6.695. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ling G. N., Miller C., Ochsenfeld M. M. The physical state of solutes and water in living cells according to the association-induction hypothesis. Ann N Y Acad Sci. 1973 Mar 30;204:6–50. doi: 10.1111/j.1749-6632.1973.tb30770.x. [DOI] [PubMed] [Google Scholar]
  20. Noble D., Tsien R. W. The kinetics and rectifier properties of the slow potassium current in cardiac Purkinje fibres. J Physiol. 1968 Mar;195(1):185–214. doi: 10.1113/jphysiol.1968.sp008454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. PAGE E., SOLOMON A. K. Cat heart muscle in vitro. I. Cell volumes and intracellular concentrations in papillary muscle. J Gen Physiol. 1960 Nov;44:327–344. doi: 10.1085/jgp.44.2.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Page E., McCallister L. P., Power B. Sterological measurements of cardiac ultrastructures implicated in excitation-contraction coupling. Proc Natl Acad Sci U S A. 1971 Jul;68(7):1465–1466. doi: 10.1073/pnas.68.7.1465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Russell J. M., Brown A. M. Active transport of potassium by the giant neuron of the aplysia abdominal ganglion. J Gen Physiol. 1972 Nov;60(5):519–533. doi: 10.1085/jgp.60.5.519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Sommer J. R., Johnson E. A. Cardiac muscle. A comparative study of Purkinje fibers and ventricular fibers. J Cell Biol. 1968 Mar;36(3):497–526. doi: 10.1083/jcb.36.3.497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. VASSALLE M. CARDIAC PACEMAKER POTENTIALS AT DIFFERENT EXTRA-AND INTRACELLULAR K CONCENTRATIONS. Am J Physiol. 1965 Apr;208:770–775. doi: 10.1152/ajplegacy.1965.208.4.770. [DOI] [PubMed] [Google Scholar]
  26. Walker J. L., Ladle R. O. Frog heart intracellular potassium activities measured with potassium microelectrodes. Am J Physiol. 1973 Jul;225(1):263–267. doi: 10.1152/ajplegacy.1973.225.1.263. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES