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. 1990 Sep;428:653–671. doi: 10.1113/jphysiol.1990.sp018233

Stimulation-dependent facilitation of the high threshold calcium current in guinea-pig ventricular myocytes.

A C Zygmunt 1, J Maylie 1
PMCID: PMC1181668  PMID: 2172526

Abstract

1. Stimulation-dependent modulation of Ca currents was examined in guinea-pig ventricular myocytes at room temperature. Whole-cell recordings of Ca currents were made under conditions which minimized ionic fluxes through other channels. 2. Stimulation from rest at a rate of 2 Hz resulted in a decrease of the low threshold Ca current within one pulse and facilitation of the high threshold Ca current within five pulses. Facilitation was associated with a reduction in the rate of inactivation. 3. Pulse durations as short as 10 ms facilitated the high threshold Ca current in subsequent pulses. Facilitation produced by a single pulse decayed with a half-time of several seconds. 4. Substitution of Ba2+ or Sr2+ for external Ca2+ reduced the rate of inactivation of the high threshold Ca current and abolished facilitation of the current. 5. Facilitation persisted with 40 microM-Ruthenium Red added to the internal solution or 0.2-2 microM-ryanodine added to the bath solution to reduce Ca2+ release from the sarcoplasmic reticulum. 6. Facilitation was modulated by isoprenaline. Low concentrations of isoprenaline (5-10 nM) increased the amount of facilitation. Isoprenaline (1 microM) increased the Ca current approximately 3-fold, however, facilitation was nearly abolished. 7. Caffeine (0.5 and 1 mM) affected the Ca current and facilitation in a manner similar to 1 microM-isoprenaline. It increased the Ca currents approximately 2.5-fold and facilitation was not observed. 8. We conclude that stimulation-dependent facilitation of the high threshold Ca current is mediated by calcium and hypothesize that calcium affects a site near the Ca channel that modifies the rate of inactivation. The common actions of caffeine and high concentrations of isoprenaline suggest that calcium modulates a phosphorylation step.

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Selected References

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

  1. Argibay J. A., Fischmeister R., Hartzell H. C. Inactivation, reactivation and pacing dependence of calcium current in frog cardiocytes: correlation with current density. J Physiol. 1988 Jul;401:201–226. doi: 10.1113/jphysiol.1988.sp017158. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baylor S. M., Hollingworth S., Marshall M. W. Effects of intracellular ruthenium red on excitation-contraction coupling in intact frog skeletal muscle fibres. J Physiol. 1989 Jan;408:617–635. doi: 10.1113/jphysiol.1989.sp017480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bean B. P., Nowycky M. C., Tsien R. W. Beta-adrenergic modulation of calcium channels in frog ventricular heart cells. 1984 Jan 26-Feb 1Nature. 307(5949):371–375. doi: 10.1038/307371a0. [DOI] [PubMed] [Google Scholar]
  4. Bean B. P. Two kinds of calcium channels in canine atrial cells. Differences in kinetics, selectivity, and pharmacology. J Gen Physiol. 1985 Jul;86(1):1–30. doi: 10.1085/jgp.86.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cohen N. M., Lederer W. J. Changes in the calcium current of rat heart ventricular myocytes during development. J Physiol. 1988 Dec;406:115–146. doi: 10.1113/jphysiol.1988.sp017372. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fabiato A., Fabiato F. Calculator programs for computing the composition of the solutions containing multiple metals and ligands used for experiments in skinned muscle cells. J Physiol (Paris) 1979;75(5):463–505. [PubMed] [Google Scholar]
  7. Fedida D., Noble D., Spindler A. J. Mechanism of the use dependence of Ca2+ current in guinea-pig myocytes. J Physiol. 1988 Nov;405:461–475. doi: 10.1113/jphysiol.1988.sp017342. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Fedida D., Noble D., Spindler A. J. Use-dependent reduction and facilitation of Ca2+ current in guinea-pig myocytes. J Physiol. 1988 Nov;405:439–460. doi: 10.1113/jphysiol.1988.sp017341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. Field A. C., Hill C., Lamb G. D. Asymmetric charge movement and calcium currents in ventricular myocytes of neonatal rat. J Physiol. 1988 Dec;406:277–297. doi: 10.1113/jphysiol.1988.sp017380. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gurney A. M., Charnet P., Pye J. M., Nargeot J. Augmentation of cardiac calcium current by flash photolysis of intracellular caged-Ca2+ molecules. Nature. 1989 Sep 7;341(6237):65–68. doi: 10.1038/341065a0. [DOI] [PubMed] [Google Scholar]
  12. 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]
  13. Hansford R. G., Lakatta E. G. Ryanodine releases calcium from sarcoplasmic reticulum in calcium-tolerant rat cardiac myocytes. J Physiol. 1987 Sep;390:453–467. doi: 10.1113/jphysiol.1987.sp016711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hiraoka M., Kawano S. Mechanism of increased amplitude and duration of the plateau with sudden shortening of diastolic intervals in rabbit ventricular cells. Circ Res. 1987 Jan;60(1):14–26. doi: 10.1161/01.res.60.1.14. [DOI] [PubMed] [Google Scholar]
  15. Horne P., Triggle D. J., Venter J. C. Nitrendipine and isoproterenol induce phosphorylation of a 42,000 dalton protein that co-migrates with the affinity labeled calcium channel regulatory subunit. Biochem Biophys Res Commun. 1984 Jun 29;121(3):890–898. doi: 10.1016/0006-291x(84)90761-7. [DOI] [PubMed] [Google Scholar]
  16. Hosey M. M., Borsotto M., Lazdunski M. Phosphorylation and dephosphorylation of dihydropyridine-sensitive voltage-dependent Ca2+ channel in skeletal muscle membranes by cAMP- and Ca2+-dependent processes. Proc Natl Acad Sci U S A. 1986 Jun;83(11):3733–3737. doi: 10.1073/pnas.83.11.3733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hoshi T., Rothlein J., Smith S. J. Facilitation of Ca2+-channel currents in bovine adrenal chromaffin cells. Proc Natl Acad Sci U S A. 1984 Sep;81(18):5871–5875. doi: 10.1073/pnas.81.18.5871. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Imoto Y., Yatani A., Reeves J. P., Codina J., Birnbaumer L., Brown A. M. Alpha-subunit of Gs directly activates cardiac calcium channels in lipid bilayers. Am J Physiol. 1988 Oct;255(4 Pt 2):H722–H728. doi: 10.1152/ajpheart.1988.255.4.H722. [DOI] [PubMed] [Google Scholar]
  19. Kaibara M., Kameyama M. Inhibition of the calcium channel by intracellular protons in single ventricular myocytes of the guinea-pig. J Physiol. 1988 Sep;403:621–640. doi: 10.1113/jphysiol.1988.sp017268. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kass R. S., Sanguinetti M. C. Inactivation of calcium channel current in the calf cardiac Purkinje fiber. Evidence for voltage- and calcium-mediated mechanisms. J Gen Physiol. 1984 Nov;84(5):705–726. doi: 10.1085/jgp.84.5.705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kimura J., Miyamae S., Noma A. Identification of sodium-calcium exchange current in single ventricular cells of guinea-pig. J Physiol. 1987 Mar;384:199–222. doi: 10.1113/jphysiol.1987.sp016450. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Lee K. S., Marban E., Tsien R. W. Inactivation of calcium channels in mammalian heart cells: joint dependence on membrane potential and intracellular calcium. J Physiol. 1985 Jul;364:395–411. doi: 10.1113/jphysiol.1985.sp015752. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Ma J., Fill M., Knudson C. M., Campbell K. P., Coronado R. Ryanodine receptor of skeletal muscle is a gap junction-type channel. Science. 1988 Oct 7;242(4875):99–102. doi: 10.1126/science.2459777. [DOI] [PubMed] [Google Scholar]
  24. Maylie J., Morad M. A transient outward current related to calcium release and development of tension in elephant seal atrial fibres. J Physiol. 1984 Dec;357:267–292. doi: 10.1113/jphysiol.1984.sp015500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Mitra R., Morad M. A uniform enzymatic method for dissociation of myocytes from hearts and stomachs of vertebrates. Am J Physiol. 1985 Nov;249(5 Pt 2):H1056–H1060. doi: 10.1152/ajpheart.1985.249.5.H1056. [DOI] [PubMed] [Google Scholar]
  26. Mitra R., Morad M. Two types of calcium channels in guinea pig ventricular myocytes. Proc Natl Acad Sci U S A. 1986 Jul;83(14):5340–5344. doi: 10.1073/pnas.83.14.5340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Pessah I. N., Francini A. O., Scales D. J., Waterhouse A. L., Casida J. E. Calcium-ryanodine receptor complex. Solubilization and partial characterization from skeletal muscle junctional sarcoplasmic reticulum vesicles. J Biol Chem. 1986 Jul 5;261(19):8643–8648. [PubMed] [Google Scholar]
  28. Reichardt L. F., Kelly R. B. A molecular description of nerve terminal function. Annu Rev Biochem. 1983;52:871–926. doi: 10.1146/annurev.bi.52.070183.004255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Richardt G., Waas W., Kranzhöfer R., Mayer E., Schömig A. Adenosine inhibits exocytotic release of endogenous noradrenaline in rat heart: a protective mechanism in early myocardial ischemia. Circ Res. 1987 Jul;61(1):117–123. doi: 10.1161/01.res.61.1.117. [DOI] [PubMed] [Google Scholar]
  30. Schouten V. J., Morad M. Regulation of Ca2+ current in frog ventricular myocytes by the holding potential, c-AMP and frequency. Pflugers Arch. 1989 Oct;415(1):1–11. doi: 10.1007/BF00373135. [DOI] [PubMed] [Google Scholar]
  31. Tseng G. N. Calcium current restitution in mammalian ventricular myocytes is modulated by intracellular calcium. Circ Res. 1988 Aug;63(2):468–482. doi: 10.1161/01.res.63.2.468. [DOI] [PubMed] [Google Scholar]
  32. Tseng G. N., Hoffman B. F. Two components of transient outward current in canine ventricular myocytes. Circ Res. 1989 Apr;64(4):633–647. doi: 10.1161/01.res.64.4.633. [DOI] [PubMed] [Google Scholar]
  33. Tsien R. W., Bean B. P., Hess P., Lansman J. B., Nilius B., Nowycky M. C. Mechanisms of calcium channel modulation by beta-adrenergic agents and dihydropyridine calcium agonists. J Mol Cell Cardiol. 1986 Jul;18(7):691–710. doi: 10.1016/s0022-2828(86)80941-5. [DOI] [PubMed] [Google Scholar]
  34. Tsien R. Y. New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures. Biochemistry. 1980 May 27;19(11):2396–2404. doi: 10.1021/bi00552a018. [DOI] [PubMed] [Google Scholar]

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