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. 1986 Aug;377:61–88. doi: 10.1113/jphysiol.1986.sp016177

Properties of the hyperpolarizing-activated current (if) in cells isolated from the rabbit sino-atrial node.

D DiFrancesco, A Ferroni, M Mazzanti, C Tromba
PMCID: PMC1182823  PMID: 2432247

Abstract

Individual cells were isolated from the sino-atrial node area of the rabbit heart using an enzyme medium containing collagenase and elastase. After enzymatic treatment the cells were placed in normal Tyrode solution, where beating resumed in a fraction of them. Isolated cells were studied in the whole cell configuration. Action potentials as well as membrane currents under voltage-clamp conditions were similar to those in multicellular preparations. Pulses to voltages more negative than about -50 mV caused activation of the hyperpolarizing-activated current, if. Investigation of the properties of this current was carried out under conditions that limited the influence of other current systems during voltage clamp. The if current activation range usually extended approximately from -50 to -100 mV, but varied from cell to cell. In several cases, pulsing to the region of -40 mV elicited a sizeable if. Both current activation and deactivation during voltage steps had S-shaped time courses. A high variability was however observed in the sigmoidal behaviour of if kinetics. Plots of the fully-activated current-voltage (I-V) relation in different extracellular Na and K concentrations showed that both ions carry the current if. While changes in the external Na concentration caused the current I-V relation to undergo simple shifts along the voltage axis, changes in extracellular K concentration were also associated with changes in its slope. Again, a large variability was observed in the increase of I-V slope on raising the external K concentration. The current if was strongly depressed by Cs, and the block induced by 5 mM-Cs was markedly voltage dependent. Adrenaline (1-5 microM) and noradrenaline (1 microM) increased the current if around the half-activation voltage range and accelerated its activation at more negative voltages. Often, however, drug application failed to elicit any modification of if. Current run-down was observed in nearly all cells, although at a highly variable rate. It was accelerated by raising the extracellular K concentration but did not show a marked use dependence. Both the if activation curve and the fully activated I-V relation were affected by run-down, the former being shifted to more negative values along the voltage axis and the latter being depressed with no apparent change of the if reversal potential.(ABSTRACT TRUNCATED AT 400 WORDS)

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Selected References

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  1. Bader C. R., Bertrand D. Effect of changes in intra- and extracellular sodium on the inward (anomalous) rectification in salamander photoreceptors. J Physiol. 1984 Feb;347:611–631. doi: 10.1113/jphysiol.1984.sp015086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brown H. F., DiFrancesco D., Noble S. J. How does adrenaline accelerate the heart? Nature. 1979 Jul 19;280(5719):235–236. doi: 10.1038/280235a0. [DOI] [PubMed] [Google Scholar]
  3. Brown H., Difrancesco D., Noble S. Cardiac pacemaker oscillation and its modulation by autonomic transmitters. J Exp Biol. 1979 Aug;81:175–204. doi: 10.1242/jeb.81.1.175. [DOI] [PubMed] [Google Scholar]
  4. Brown H., Difrancesco D. Voltage-clamp investigations of membrane currents underlying pace-maker activity in rabbit sino-atrial node. J Physiol. 1980 Nov;308:331–351. doi: 10.1113/jphysiol.1980.sp013474. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Byerly L., Hagiwara S. Calcium currents in internally perfused nerve cell bodies of Limnea stagnalis. J Physiol. 1982 Jan;322:503–528. doi: 10.1113/jphysiol.1982.sp014052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Callewaert G., Carmeliet E., Vereecke J. Single cardiac Purkinje cells: general electrophysiology and voltage-clamp analysis of the pace-maker current. J Physiol. 1984 Apr;349:643–661. doi: 10.1113/jphysiol.1984.sp015179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cohen I. S., Falk R. T., Mulrine N. K. Actions of barium and rubidium on membrane currents in canine Purkinje fibres. J Physiol. 1983 May;338:589–612. doi: 10.1113/jphysiol.1983.sp014691. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Datyner N. B., Gintant G. A., Cohen I. S. Microprocessor controlled trituration device for the dissociation of cardiac and other tissues. Pflugers Arch. 1985 Jan;403(1):105–108. doi: 10.1007/BF00583289. [DOI] [PubMed] [Google Scholar]
  9. DiFrancesco D. A new interpretation of the pace-maker current in calf Purkinje fibres. J Physiol. 1981 May;314:359–376. doi: 10.1113/jphysiol.1981.sp013713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. DiFrancesco D. A study of the ionic nature of the pace-maker current in calf Purkinje fibres. J Physiol. 1981 May;314:377–393. doi: 10.1113/jphysiol.1981.sp013714. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. DiFrancesco D. 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. doi: 10.1113/jphysiol.1982.sp014315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. DiFrancesco D. Characterization of the pace-maker current kinetics in calf Purkinje fibres. J Physiol. 1984 Mar;348:341–367. doi: 10.1113/jphysiol.1984.sp015114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. DiFrancesco D., Ferroni A. Delayed activation of the cardiac pacemaker current and its dependence on conditioning pre-hyperpolarizations. Pflugers Arch. 1983 Mar 1;396(3):265–267. doi: 10.1007/BF00587866. [DOI] [PubMed] [Google Scholar]
  14. DiFrancesco D., Noma A., Trautwein W. Kinetics and magnitude of the time-dependent potassium current in the rabbit sinoatrial node: effect of external potassium. Pflugers Arch. 1979 Sep;381(3):271–279. doi: 10.1007/BF00583259. [DOI] [PubMed] [Google Scholar]
  15. DiFrancesco D., Ojeda C. Properties of the current if in the sino-atrial node of the rabbit compared with those of the current iK, in Purkinje fibres. J Physiol. 1980 Nov;308:353–367. doi: 10.1113/jphysiol.1980.sp013475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. DiFrancesco D. The cardiac hyperpolarizing-activated current, if. Origins and developments. Prog Biophys Mol Biol. 1985;46(3):163–183. doi: 10.1016/0079-6107(85)90008-2. [DOI] [PubMed] [Google Scholar]
  17. Earm Y. E., Shimoni Y., Spindler A. J. A pace-maker-like current in the sheep atrium and its modulation by catecholamines. J Physiol. 1983 Sep;342:569–590. doi: 10.1113/jphysiol.1983.sp014869. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Fenwick E. M., Marty A., Neher E. Sodium and calcium channels in bovine chromaffin cells. J Physiol. 1982 Oct;331:599–635. doi: 10.1113/jphysiol.1982.sp014394. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Halliwell J. V., Adams P. R. Voltage-clamp analysis of muscarinic excitation in hippocampal neurons. Brain Res. 1982 Oct 28;250(1):71–92. doi: 10.1016/0006-8993(82)90954-4. [DOI] [PubMed] [Google Scholar]
  20. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  21. Hauswirth O., Noble D., Tsien R. W. Adrenaline: mechanism of action on the pacemaker potential in cardiac Purkinje fibers. Science. 1968 Nov 22;162(3856):916–917. doi: 10.1126/science.162.3856.916. [DOI] [PubMed] [Google Scholar]
  22. Isenberg G., Klockner U. Calcium tolerant ventricular myocytes prepared by preincubation in a "KB medium". Pflugers Arch. 1982 Oct;395(1):6–18. doi: 10.1007/BF00584963. [DOI] [PubMed] [Google Scholar]
  23. Loffelholz K., Scholz H. Inhibition of Mn plus plus-catalyzed autoxidation of adrenaline by ascorbic acid. Experientia. 1970 Jun 15;26(6):637–638. doi: 10.1007/BF01898734. [DOI] [PubMed] [Google Scholar]
  24. Mayer M. L., Westbrook G. L. A voltage-clamp analysis of inward (anomalous) rectification in mouse spinal sensory ganglion neurones. J Physiol. 1983 Jul;340:19–45. doi: 10.1113/jphysiol.1983.sp014747. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Maylie J., Morad M. Ionic currents responsible for the generation of pace-maker current in the rabbit sino-atrial node. J Physiol. 1984 Oct;355:215–235. doi: 10.1113/jphysiol.1984.sp015415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Nakayama T., Kurachi Y., Noma A., Irisawa H. Action potential and membrane currents of single pacemaker cells of the rabbit heart. Pflugers Arch. 1984 Nov;402(3):248–257. doi: 10.1007/BF00585507. [DOI] [PubMed] [Google Scholar]
  27. 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]
  28. Noma A., Irisawa H. Membrane currents in the rabbit sinoatrial node cell as studied by the double microelectrode method. Pflugers Arch. 1976 Jun 29;364(1):45–52. doi: 10.1007/BF01062910. [DOI] [PubMed] [Google Scholar]
  29. Noma A., Kotake H., Irisawa H. Slow inward current and its role mediating the chronotropic effect of epinephrine in the rabbit sinoatrial node. Pflugers Arch. 1980 Oct;388(1):1–9. doi: 10.1007/BF00582621. [DOI] [PubMed] [Google Scholar]
  30. Noma A., Morad M., Irisawa H. Does the "pacemaker current" generate the diastolic depolarization in the rabbit SA node cells? Pflugers Arch. 1983 May;397(3):190–194. doi: 10.1007/BF00584356. [DOI] [PubMed] [Google Scholar]
  31. Noma A., Yanagihara K., Irisawa H. Inward current of the rabbit sinoatrial node cell. Pflugers Arch. 1977 Nov 25;372(1):43–51. doi: 10.1007/BF00582205. [DOI] [PubMed] [Google Scholar]
  32. Peper K., Trautwein W. A note on the pacemaker current in Purkinje fibers. Pflugers Arch. 1969 Jun 19;309(4):356–361. doi: 10.1007/BF00587758. [DOI] [PubMed] [Google Scholar]
  33. Powell T., Terrar D. A., Twist V. W. Electrical properties of individual cells isolated from adult rat ventricular myocardium. J Physiol. 1980 May;302:131–153. doi: 10.1113/jphysiol.1980.sp013234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Powell T., Twist V. W. A rapid technique for the isolation and purification of adult cardiac muscle cells having respiratory control and a tolerance to calcium. Biochem Biophys Res Commun. 1976 Sep 7;72(1):327–333. doi: 10.1016/0006-291x(76)90997-9. [DOI] [PubMed] [Google Scholar]
  35. Taniguchi J., Kokubun S., Noma A., Irisawa H. Spontaneously active cells isolated from the sino-atrial and atrio-ventricular nodes of the rabbit heart. Jpn J Physiol. 1981;31(4):547–558. doi: 10.2170/jjphysiol.31.547. [DOI] [PubMed] [Google Scholar]
  36. Tsien R. W. Effects of epinephrine on the pacemaker potassium current of cardiac Purkinje fibers. J Gen Physiol. 1974 Sep;64(3):293–319. doi: 10.1085/jgp.64.3.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Tsien R. W., Giles W., Greengard P. Cyclic AMP mediates the effects of adrenaline on cardiac purkinje fibres. Nat New Biol. 1972 Dec 6;240(101):181–183. doi: 10.1038/newbio240181a0. [DOI] [PubMed] [Google Scholar]
  38. Tsien R. W. Mode of action of chronotropic agents in cardiac Purkinje fibers. Does epinephrine act by directly modifying the external surface charge? J Gen Physiol. 1974 Sep;64(3):320–342. doi: 10.1085/jgp.64.3.320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Yanagihara K., Irisawa H. Inward current activated during hyperpolarization in the rabbit sinoatrial node cell. Pflugers Arch. 1980 May;385(1):11–19. doi: 10.1007/BF00583909. [DOI] [PubMed] [Google Scholar]

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