Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1991 Jun;437:27–48. doi: 10.1113/jphysiol.1991.sp018581

Inactivation kinetics of calcium current of acutely dissociated CA1 pyramidal cells of the mature guinea-pig hippocampus.

A R Kay 1
PMCID: PMC1180033  PMID: 1653853

Abstract

1. The process of inactivation of the Ca2+ current of acutely dissociated pyramidal cells from the CA1 subfield of mature guinea-pig hippocampus was characterized. The decline of the current after rapid activation could be approximated well by the sum of two exponentials (time constants approximately 200 ms and 2 s) and a constant offset. 2. The time constants of inactivation exhibited a voltage dependence consistent with a voltage-dependent mechanism. However, under conditions which normally counteract Ca(2+)-dependent inactivation (viz. intracellular bis(O-aminophenoxy)-ethane-N,N,N',N'-tetraacetic acid (BAPTA) and external Ba2+) all three showed a U-shaped inactivation curve, characteristic of Ca(2+)-dependent inactivation. 3. The rate of inactivation was found to increase with current at a given voltage; however, increasing external divalent ion concentrations did not accelerate inactivation. 4. Calcium imaging experiments, using the Ca(2+)-sensitive probe, Fura-2, were performed to estimate the accumulation of Ca2+ in the presence of 10 mM-intracellular BAPTA. Under these conditions voltage steps which induced maximal Ca2+ currents lead to free Ca2+ concentrations of less than 500 nM in the bulk of the cytoplasm. 5. Elevation of the intracellular free Ca2+ concentration to above 1 microM suppressed all the components of the Ca2+ current. However, even at a concentration of 3 microM-Ca2+ the U-shaped inactivation curve persisted. 6. Substitution of Ca2+ for Ba2+ led to an acceleration of inactivation through an increase in the proportion of the fast process of inactivation and an acceleration of both the fast and slow rates of inactivation. 7. During the slow decline of Ca2+ current ('run-down') the proportion of all three components remained approximately constant and there was little change in the rate of inactivation. 8. On the basis of the results I suggest that inactivation results fro a dual process of voltage- and Ca(2+)-dependent inactivation. Ca(2+)-dependent inactivation seems to result from the accumulation of Ca2+ close to the channel mouth. 9. The macroscopic properties of the Ca2+ channel are consistent with the existence of one channel type in the CA1 pyramidal cells.

Full text

PDF

Images in this article

Selected References

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

  1. Almers W., McCleskey E. W., Palade P. T. A non-selective cation conductance in frog muscle membrane blocked by micromolar external calcium ions. J Physiol. 1984 Aug;353:565–583. doi: 10.1113/jphysiol.1984.sp015351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Armstrong C. M., Lopez-Barneo J. External calcium ions are required for potassium channel gating in squid neurons. Science. 1987 May 8;236(4802):712–714. doi: 10.1126/science.2437654. [DOI] [PubMed] [Google Scholar]
  3. Ashcroft F. M., Stanfield P. R. Calcium inactivation in skeletal muscle fibres of the stick insect, Carausius morosus. J Physiol. 1982 Sep;330:349–372. doi: 10.1113/jphysiol.1982.sp014345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brown A. M., Morimoto K., Tsuda Y., wilson D. L. Calcium current-dependent and voltage-dependent inactivation of calcium channels in Helix aspersa. J Physiol. 1981 Nov;320:193–218. doi: 10.1113/jphysiol.1981.sp013944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Byerly L., Yazejian B. Intracellular factors for the maintenance of calcium currents in perfused neurones from the snail, Lymnaea stagnalis. J Physiol. 1986 Jan;370:631–650. doi: 10.1113/jphysiol.1986.sp015955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Campbell D. L., Giles W. R., Hume J. R., Shibata E. F. Inactivation of calcium current in bull-frog atrial myocytes. J Physiol. 1988 Sep;403:287–315. doi: 10.1113/jphysiol.1988.sp017250. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Carbone E., Lux H. D. A low voltage-activated, fully inactivating Ca channel in vertebrate sensory neurones. Nature. 1984 Aug 9;310(5977):501–502. doi: 10.1038/310501a0. [DOI] [PubMed] [Google Scholar]
  8. Chad J. E., Eckert R. An enzymatic mechanism for calcium current inactivation in dialysed Helix neurones. J Physiol. 1986 Sep;378:31–51. doi: 10.1113/jphysiol.1986.sp016206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Chad J. E., Eckert R. Calcium domains associated with individual channels can account for anomalous voltage relations of CA-dependent responses. Biophys J. 1984 May;45(5):993–999. doi: 10.1016/S0006-3495(84)84244-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Chandler W. K., Meves H. Evidence for two types of sodium conductance in axons perfused with sodium fluoride solution. J Physiol. 1970 Dec;211(3):653–678. doi: 10.1113/jphysiol.1970.sp009298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Choi D. W. Calcium-mediated neurotoxicity: relationship to specific channel types and role in ischemic damage. Trends Neurosci. 1988 Oct;11(10):465–469. doi: 10.1016/0166-2236(88)90200-7. [DOI] [PubMed] [Google Scholar]
  12. Connor J. A. Digital imaging of free calcium changes and of spatial gradients in growing processes in single, mammalian central nervous system cells. Proc Natl Acad Sci U S A. 1986 Aug;83(16):6179–6183. doi: 10.1073/pnas.83.16.6179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Eckert R., Chad J. E. Inactivation of Ca channels. Prog Biophys Mol Biol. 1984;44(3):215–267. doi: 10.1016/0079-6107(84)90009-9. [DOI] [PubMed] [Google Scholar]
  14. Fox A. P. Voltage-dependent inactivation of a calcium channel. Proc Natl Acad Sci U S A. 1981 Feb;78(2):953–956. doi: 10.1073/pnas.78.2.953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
  16. Gutnick M. J., Lux H. D., Swandulla D., Zucker H. Voltage-dependent and calcium-dependent inactivation of calcium channel current in identified snail neurones. J Physiol. 1989 May;412:197–220. doi: 10.1113/jphysiol.1989.sp017611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Gähwiler B. H., Brown D. A. Effects of dihydropyridines on calcium currents in CA3 pyramidal cells in slice cultures of rat hippocampus. Neuroscience. 1987 Mar;20(3):731–738. doi: 10.1016/0306-4522(87)90236-3. [DOI] [PubMed] [Google Scholar]
  18. HODGKIN A. L., KATZ B. The effect of sodium ions on the electrical activity of giant axon of the squid. J Physiol. 1949 Mar 1;108(1):37–77. doi: 10.1113/jphysiol.1949.sp004310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. 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]
  20. Kay A. R., Wong R. K. Calcium current activation kinetics in isolated pyramidal neurones of the Ca1 region of the mature guinea-pig hippocampus. J Physiol. 1987 Nov;392:603–616. doi: 10.1113/jphysiol.1987.sp016799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Kay A. R., Wong R. K. Isolation of neurons suitable for patch-clamping from adult mammalian central nervous systems. J Neurosci Methods. 1986 May;16(3):227–238. doi: 10.1016/0165-0270(86)90040-3. [DOI] [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. Lux H. D., Brown A. M. Single channel studies on inactivation of calcium currents. Science. 1984 Jul 27;225(4660):432–434. doi: 10.1126/science.6330896. [DOI] [PubMed] [Google Scholar]
  24. Matteson D. R., Armstrong C. M. Properties of two types of calcium channels in clonal pituitary cells. J Gen Physiol. 1986 Jan;87(1):161–182. doi: 10.1085/jgp.87.1.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Nowycky M. C., Fox A. P., Tsien R. W. Three types of neuronal calcium channel with different calcium agonist sensitivity. Nature. 1985 Aug 1;316(6027):440–443. doi: 10.1038/316440a0. [DOI] [PubMed] [Google Scholar]
  26. Pitler T. A., Landfield P. W. Probable Ca2+-mediated inactivation of Ca2+ currents in mammalian brain neurons. Brain Res. 1987 Apr 28;410(1):147–153. doi: 10.1016/s0006-8993(87)80037-9. [DOI] [PubMed] [Google Scholar]
  27. Plant T. D., Standen N. B., Ward T. A. The effects of injection of calcium ions and calcium chelators on calcium channel inactivation in Helix neurones. J Physiol. 1983 Jan;334:189–212. doi: 10.1113/jphysiol.1983.sp014489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Regehr W. G., Connor J. A., Tank D. W. Optical imaging of calcium accumulation in hippocampal pyramidal cells during synaptic activation. Nature. 1989 Oct 12;341(6242):533–536. doi: 10.1038/341533a0. [DOI] [PubMed] [Google Scholar]
  29. Sherman A., Keizer J., Rinzel J. Domain model for Ca2(+)-inactivation of Ca2+ channels at low channel density. Biophys J. 1990 Oct;58(4):985–995. doi: 10.1016/S0006-3495(90)82443-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Simon S. M., Llinás R. R. Compartmentalization of the submembrane calcium activity during calcium influx and its significance in transmitter release. Biophys J. 1985 Sep;48(3):485–498. doi: 10.1016/S0006-3495(85)83804-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Swandulla D., Armstrong C. M. Fast-deactivating calcium channels in chick sensory neurons. J Gen Physiol. 1988 Aug;92(2):197–218. doi: 10.1085/jgp.92.2.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Tillotson D. Inactivation of Ca conductance dependent on entry of Ca ions in molluscan neurons. Proc Natl Acad Sci U S A. 1979 Mar;76(3):1497–1500. doi: 10.1073/pnas.76.3.1497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Tsien R. W., Hess P., McCleskey E. W., Rosenberg R. L. Calcium channels: mechanisms of selectivity, permeation, and block. Annu Rev Biophys Biophys Chem. 1987;16:265–290. doi: 10.1146/annurev.bb.16.060187.001405. [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]
  35. Yaari Y., Hamon B., Lux H. D. Development of two types of calcium channels in cultured mammalian hippocampal neurons. Science. 1987 Feb 6;235(4789):680–682. doi: 10.1126/science.2433765. [DOI] [PubMed] [Google Scholar]

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

RESOURCES