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PMID: 7932232 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cation-dependent gating of the hyperpolarization-activated cation current in the rabbit sino-atrial node cells.

The Journal of physiology ·Vol. 477 ( Pt 3) ·1994-06-15 ·Pages 423-35

Maruoka F, Nakashima Y, Takano M, Ono K, Noma A

Abstract

1. The gating properties of the hyperpolarization-activated cation current (I(f) or Ih) were investigated in single pacemaker cells dissociated from the rabbit sino-atrial node. 2. The whole-cell I(f) was recorded in the presence of different external cations. The inward I(f) was increased when external Na+ was replaced with K+, and was decreased in Li+ or Rb+ solution. In Tris+ and Cs+ solutions, the inward I(f) was negligible. The outward tail current recorded upon depolarization was largest in Li+ solution and smaller in a sequence of Na+, Tris+ and K+ solutions. In Rb+ and Cs+ solutions, only a small tail current was recorded. 3. The outward tail current had a 'shoulder' in Na+ solution, which was much delayed by replacing Na+ with Li+. In K+ solution, the decay of the tail current was much faster, and no obvious shoulder was recorded. The tail current was slowest in Li(+)-rich and 0 mM K+ solution, and was progressively accelerated by adding K+ over the range from 0 to 3 mM. The tail current at 30 mM [K+]o showed only a small shoulder. A common binding site to modulate the I(f) deactivation was suggested for monovalent cations. 4. The shoulder of the I(f) tail became more evident as I(f) was activated to a larger extent either by prolonging the duration or by increasing the amplitude of the preceding hyperpolarization in both Na+ and Li+ solutions. 5. The I(f) was first activated by hyperpolarizing the membrane to -110 mV, and then deactivated by depolarization. The inward tail current at -50 mV showed a single exponential decay. At more positive potentials, the shoulder of the outward tail currents became more evident and the rate of the final decay was increased. 6. The time course of I(f) activation was well fitted with the sum of two exponential functions. Time constants of both components were not affected by the external cation (Na+, K+ or Li+) replacement. Likewise, the quasi-steady state activation was conserved when external Na+ was replaced with Li+. 7. Two closed and three open states were assumed in a sequential state model of the I(f) channel. The cation effects were well simulated by assuming that the deactivation rate was selectively modulated. The flow of I(f) during the spontaneous action potential was calculated. The activation of I(f) started on repolarization to the maximum diastolic potential and reached a maximum in the middle of the diastolic period. Its peak amplitude was 14% of the net inward current during the diastolic period.

MeSH Terms
Animals Cations/pharmacology Drug Interactions Electric Conductivity Electrophysiology Ion Channel Gating/drug effects Kinetics Lithium/pharmacology Potassium/pharmacology Rabbits Sinoatrial Node/cytology,drug effects,physiology Sodium/pharmacology Time Factors
Chemicals
Cations Lithium Sodium Potassium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Maruoka F
Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Nakashima Y
Takano M
Ono K
Noma A
References (38)
38 references, click to expand
  1. Muscarinic modulation of cardiac rate at low acetylcholine concentrations.
    Science. 1989 Feb 3;243(4891):669-71 PMID: 2916119
  2. Outward currents through the inwardly rectifying potassium channel of guinea-pig ventricular cells.
    Jpn J Physiol. 1988;38(1):77-91 PMID: 2455088
  3. Muscarinic control of the hyperpolarization-activated current (if) in rabbit sino-atrial node myocytes.
    J Physiol. 1988 Nov;405:493-510 PMID: 2475609
  4. Modulation by intracellular Ca2+ of the hyperpolarization-activated inward current in rabbit single sino-atrial node cells.
    J Physiol. 1989 Feb;409:121-41 PMID: 2479735
  5. Rubidium ions and the gating of delayed rectifier potassium channels of frog skeletal muscle.
    J Physiol. 1989 Apr;411:597-610 PMID: 2614736
  6. Regulation of cardiac pacemaker current If in excised membranes from sinoatrial node cells.
    Am J Physiol. 1990 Jun;258(6 Pt 2):H1947-51 PMID: 2163222
  7. Rabbit sino-atrial node cells: isolation and electrophysiological properties.
    J Physiol. 1990 Sep;428:405-24 PMID: 2231420
  8. Pacemaking in rabbit isolated sino-atrial node cells during Cs+ block of the hyperpolarization-activated current if.
    J Physiol. 1990 Oct;429:401-9 PMID: 2177505
  9. The contribution of the 'pacemaker' current (if) to generation of spontaneous activity in rabbit sino-atrial node myocytes.
    J Physiol. 1991 Mar;434:23-40 PMID: 2023118
  10. Voltage clamp measurements of the hyperpolarization-activated inward current I(f) in single cells from rabbit sino-atrial node.
    J Physiol. 1991 Mar;434:57-83 PMID: 1708824
  11. Block of the cardiac pacemaker current (If) in the rabbit sino-atrial node and in canine Purkinje fibres by 9-amino-1,2,3,4-tetrahydroacridine.
    Pflugers Arch. 1991 Feb;417(6):611-5 PMID: 2057325
  12. Properties of a hyperpolarization-activated cation current and its role in rhythmic oscillation in thalamic relay neurones.
    J Physiol. 1990 Dec;431:291-318 PMID: 1712843
  13. Intracellular calcium does not directly modulate cardiac pacemaker (if) channels.
    Pflugers Arch. 1991 Dec;419(6):662-4 PMID: 1724077
  14. External K+ increases Na+ conductance of the hyperpolarization-activated current in rabbit cardiac pacemaker cells.
    Pflugers Arch. 1992 Jun;421(2-3):97-9 PMID: 1326752
  15. Control of the hyperpolarization-activated cation current by external anions in rabbit sino-atrial node cells.
    J Physiol. 1992;453:307-18 PMID: 1281504
  16. Ionic selectivity of Ih channels of rod photoreceptors in tiger salamanders.
    J Gen Physiol. 1992 Nov;100(5):749-65 PMID: 1282144
  17. Cardiac pacemaking in the sinoatrial node.
    Physiol Rev. 1993 Jan;73(1):197-227 PMID: 8380502
  18. Anomalous permeabilities of the egg cell membrane of a starfish in K+-Tl+ mixtures.
    J Gen Physiol. 1977 Sep;70(3):269-81 PMID: 561161
  19. Life time and elementary conductance of the channels mediating the excitatory effects of acetylcholine in Aplysia neurones.
    J Physiol. 1978 May;278:177-206 PMID: 671284
  20. Effects of internal potassium and sodium on the anomalous rectification of the starfish egg as examined by internal perfusion.
    J Physiol. 1979 Jul;292:251-65 PMID: 573790
  21. Inward current activated during hyperpolarization in the rabbit sinoatrial node cell.
    Pflugers Arch. 1980 MAY;385(1):11-9 PMID: 7191093
  22. Sodium channel permeation in squid axons. I: Reversal potential experiments.
    J Physiol. 1980 Oct;307:217-42 PMID: 6259334
  23. K+ channels close more slowly in the presence of external K+ and Rb+.
    Nature. 1981 Jun 4;291(5814):427-9 PMID: 6264306
  24. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.
    Pflugers Arch. 1981 Aug;391(2):85-100 PMID: 6270629
  25. A new interpretation of the pace-maker current in calf Purkinje fibres.
    J Physiol. 1981 May;314:359-76 PMID: 6273533
  26. A study of the ionic nature of the pace-maker current in calf Purkinje fibres.
    J Physiol. 1981 May;314:377-93 PMID: 6273534
  27. Inward rectification in frog skeletal muscle fibres and its dependence on membrane potential and external potassium.
    J Physiol. 1981;319:295-309 PMID: 6976432
  28. Block and activation of the pace-maker channel in calf purkinje fibres: effects of potassium, caesium and rubidium.
    J Physiol. 1982 Aug;329:485-507 PMID: 6292407
  29. Calcium tolerant ventricular myocytes prepared by preincubation in a "KB medium".
    Pflugers Arch. 1982 Oct;395(1):6-18 PMID: 7177773
  30. Delayed activation of the cardiac pacemaker current and its dependence on conditioning pre-hyperpolarizations.
    Pflugers Arch. 1983 Mar 1;396(3):265-7 PMID: 6302637
  31. Does the "pacemaker current" generate the diastolic depolarization in the rabbit SA node cells?
    Pflugers Arch. 1983 May;397(3):190-4 PMID: 6878006
  32. Characterization of the pace-maker current kinetics in calf Purkinje fibres.
    J Physiol. 1984 Mar;348:341-67 PMID: 6325672
  33. Mechanism of ion permeation through calcium channels.
    Nature. 1984 May 31-Jun 6;309(5967):453-6 PMID: 6328315
  34. Inactivation of Ca channels.
    Prog Biophys Mol Biol. 1984;44(3):215-67 PMID: 6095365
  35. Characterization of single pacemaker channels in cardiac sino-atrial node cells.
    Nature. 1986 Dec 4-10;324(6096):470-3 PMID: 2431323
  36. Properties of the hyperpolarizing-activated current (if) in cells isolated from the rabbit sino-atrial node.
    J Physiol. 1986 Aug;377:61-88 PMID: 2432247
  37. The properties and function of inward rectification in rod photoreceptors of the tiger salamander.
    J Physiol. 1987 Sep;390:319-33 PMID: 2450992
  38. Inhibition of the hyperpolarization-activated current (if) induced by acetylcholine in rabbit sino-atrial node myocytes.
    J Physiol. 1988 Nov;405:477-91 PMID: 3255798
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1994-06-15
Pages
423-35
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1155607
Subset
IM
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