Neurophysiology

, Volume 20, Issue 6, pp 559–564 | Cite as

Effects of microiontophoretically injected AMP and cAMP on calcium current in dialyzed Helix pomatia neurons

  • N. I. Kononenko
  • A. D. Shcherbatko
Article
  • 16 Downloads

Abstract

The effects of injecting cells with adenosine monophosphate (AMP) and cyclic adenosine monophosphate (cAMP) on calcium current were investigated during intracellular dialysis ofHelixpomatia neurons. Microiontophoretically injected AMP was found to lead to reinstatement of calcium current following dialysis-induced “wash-out,” as well as considerable stabilization of this current with the extracellular medium at normal pH. Current-voltage relationship of the current would then undergo a 10 mV shift towards depolarization values. Perfusing the cell with a solution containing 10 mM AMP then produced a qualitatively identical effect. Injecting the neuron iontophoretically with cAMP led to a decline in the amplitude of calcium current under the same conditions. Neither raising the pH of the intracellular solution to 8.1 nor adding 4-aminopyridine in order to depress the hydrogen ion current produced a qualitative alteration in the effects of injecting AMP and cAMP on calcium current.

Keywords

Hydrogen Calcium Adenosine Adenosine Monophosphate Calcium Current 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature Cited

  1. 1.
    P. A. Doroshenko and A. E. Martynyuk, “Hydrogen ions and nonspecific outward current at the membrane of intracellularly perfused nerve cells inHelix pomatia” Biol. Membr.,2, No. 1, 42–49 (1985).Google Scholar
  2. 2.
    N. I. Kononenko and A. D. Shcherbatko, “Effects of synaptic activation and serotonin application on potassium current inHelix pomatia neurons,” Neirofiziologiya,18, No. 1, 77–85 (1986).Google Scholar
  3. 3.
    J. B. Aldenhoff, G. Hofmeier, H. D. Lux, and D. Swandulla, “Stimulation of a sodium influx by cAMP inHelix neurons,” Brain Res.,276, No. 2, 289–296 (1983).Google Scholar
  4. 4.
    L. Byerly and B. Yazejian, “Intracellular factors for the maintenance of calcium currents in perfused neurones from the snailLymnaea stagnalis,” J. Physiol.,370, 631–650 (1986).Google Scholar
  5. 5.
    E. Cherubini and R. A. North, “Inhibition of calcium spikes and transmitter release by γ-aminobutyric acid in the guinea-pig myenteric plexus,” Br. J. Pharmacol.,82, No. 1, 101–105 (1984).Google Scholar
  6. 6.
    J. A. Connor and P. Hockberger, “A novel membrane sodium current induced by injection of cyclic nucleotides into gastropod neurones,” J. Physiol.,354, 139–162 (1984).Google Scholar
  7. 7.
    P. A. Doroshenko, P. G. Kostyuk, and A. E. Martynyuk, “Intracellular metabolism of adenosine 3′, 5′-cyclic monophosphate and calcium inward current in perfused neurones ofHelix pomatia,” Neuroscience,7, No. 9, 2125–2134 (1982).Google Scholar
  8. 8.
    P. A. Doroshenko, P. G. Kostyuk, A. E. Martynyuk, et al., “Intracellular protein kinase and calcium inward currents in perfused neurones of the snailHelix pomatia,” Neuroscience,11, No. 1, 263–267 (1984).Google Scholar
  9. 9.
    K. Dunlap and G. D. Fischabach, “Neutrotransmitters decrease the calcium conductance activated by depolarization of embryonic chick sensory neurones,” J. Physiol.,317, 519–535 (1981).Google Scholar
  10. 10.
    S. A. Fedulova, P. G. Kostyuk, and N. S. Veselovsky, “Calcium channels in the somatic membrane of the rat dorsal root ganglion neurons. Effect of cAMP,” Brain Res.,214, No. 2, 210–214 (1981).Google Scholar
  11. 11.
    N. Hara, M. Sawada, and T. Maeno, “Influences of pressure-injected cyclic AMP on membrane current and characteristics of an identified neuron ofAplysia kurodai,” Jpn. J. Physiol.,35, No. 2, 985–1012 (1985).Google Scholar
  12. 12.
    N. I. Kononenko, P. G. Kostyuk, and A. D. Shcherbatko, “The effect of intracellular cAMP injections on stationary membrane conductance and voltage and time-dependent ionic currents in identified snail neurons,” Brain Res.,268, No. 2, 321–338 (1983).Google Scholar
  13. 13.
    N. I. Kononenko, P. G. Kostyuk, and A. D. Scherbatko, “Properties of cAMP-induced transmembrane current in mollusc neurons,” Brain Res.,376, No. 2, 239–245 (1986).Google Scholar
  14. 14.
    P. G. Kostyuk, O. A. Krishtal, and V. I. Pidoplichko, “Effect of internal fluoride and phosphate on membrane currents during intracellular dialysis of nerve cells,” Nature,257, No. 7, 691–693 (1975).Google Scholar
  15. 15.
    N. Mo, R. Ammari, and N. J. Dun, “Prostaglandin E1 inhibits calcium-dependent potentials in mammalian sympathetic neurons,” Brain Res.,334, No. 2, 325–329 (1985).Google Scholar
  16. 16.
    H. Reuter, “Localization of beta adrenergic receptors and effects of adrenaline and cyclic nucleotides on action potentials, ionic currents and tension in mammalian cardiac muscle,” J. Physiol.,242, No. 10, 429–451 (1974).Google Scholar
  17. 17.
    H. Reuter, “Properties of two inward membrane currents in the heart,” Ann. Rev. Physiol.,41, No. 3, 413–424 (1979).Google Scholar
  18. 18.
    H. Reuter, “Calcium channel modulation by neurotransmitters, enzymes and drugs,” Nature,301, 569–574 (1983).Google Scholar

Copyright information

© Plenum Publishing Corporation 1989

Authors and Affiliations

  • N. I. Kononenko
  • A. D. Shcherbatko

There are no affiliations available

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