Skip to main content

Neuromodulatory Roles of Adenosine Receptors Coupling to the Calcium Channel and Adenylate Cyclase

  • Chapter
  • First Online:
Neurotransmitter Receptors

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 175))

Abstract

It has been shown that ATP is stored together with acetylcholine or catecholamines in synaptic vesicles and released from nerve terminals by electrical stimulation. The released ATP is degraded to adenosine extracellularly. Adenosine derivatives also might be released from excited postsynaptic neurons. Therefore, during and after stimulation, adenosine derivatives are accumulated in the synaptic cleft. Physiological functions of ATP and adenosine have been reported. In the peripheral nervous system, adenosine reduces the quantum content and frequency of miniature end-plate potentials in the rat phrenic nerve-diaphragm preparation (1). In the central nervous system, we found that extracellular addition of adenosine derivatives caused two effects on the post-synaptic potentials (PSP) evoked by electrical stimulation of lateral olfactory tract (LOT) and recorded from the surface of olfactory cortex slices: one is the direct inhibition of PSP (2,3) and the other is indirect facilitation via cyclic AMP which appears after the removal of adenosine (4). By iontophoretic studies, it has been shown that adenosine derivatives have a depressant action on the firing of neurons in several regions of the rat brain (5). These effects are suggested to be presynaptic and mediated by two different types of adenosine receptor on the presynaptic membrane, which regulate transmitter release by changing the intracellular concentration of Ca2+ or cyclic AMP in the nerve terminals. The physiological significance of adenosine derivatives on neurotransmission in the mammalian central nervous system is discussed especially in relation to facilitation as a possible mechanism of post-tetanic potentiation (PTP) and heterosynaptic facilitation (HSF) which are considered to be basic electrophysiological models of learning and memory (6).

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. B. L. Ginsborg and G. D. S. Hirst, The effect of adenosine on the release of the transmitter from the phrenic nerve of the rat, J. Physiol. (London), 224: 629 (1972).

    Article  CAS  Google Scholar 

  2. Y. Okada and Y. Kuroda, Inhibitory action of adenosine and adenosine analogs on neurotransmission in the olfactory cortex slice of guinea pig, Eur. J. Pharmacol. 61: 137 (1980).

    Article  CAS  Google Scholar 

  3. Y. Kuroda, M. Saito, and K. Kobayashi, Concomitant changes in cyclic AMP level and postsynaptic potentials of olfactory cortex slices induced by adenosine derivatives, Brain Res. 109: 196 (1976).

    Article  CAS  Google Scholar 

  4. Y. Kuroda, Physiological roles of adenosine derivatives which are released during neurotransmission in mammalian brain, J. Physiol. (Paris) 74: 463 (1978).

    CAS  Google Scholar 

  5. J. W. Phillis, G. K. Kostopoulos and J. J. Limacher, A potent depressant action of adenine derivatives on cerebral cortical neurons, Eur. J. Pharmacol. 30: 125 (1975).

    Article  CAS  Google Scholar 

  6. Y. Kuroda, Neuronal plasticity and adenosine derivatives in mammalian brain, in: “Physiology and Pharmacology of Adenosine Derivatives,” J. W. Daly, Y. Kuroda, J. W. Phillis, H. Shimizu, and M. Ui, eds., Raven Press, New York, (1983).

    Google Scholar 

  7. Y. Kuroda and H. Mcllwain, Uptake and release of 14C adenine derivatives at beds of mammalian cortical synaptosomes in superfusion system, J. Neurochem. 22: 691 (1974).

    Article  CAS  Google Scholar 

  8. T. D. White, Release of ATP from a synaptosomal preparation by elevated extracellular K and by veratridine, J. Neurochem. 30: 329 (1978).

    Article  CAS  Google Scholar 

  9. I. H. Heller and H. Mcllwain, Release of 14C adenine derivatives from isolated subsystems of the guinea pig brain: Actions of electrical stimulation and of papaverine, Brain Res. 53: 105 (1973).

    Article  CAS  Google Scholar 

  10. C. Yamamoto and H. Mcllwain, Electrical activities in thin sections from the mammalian brain maintained in chemically defined media in vitro, J. Neurochem. 13: 1333 (1966).

    Article  CAS  Google Scholar 

  11. Y. Kuroda, Brain slices: Assay systems for the neurotoxicity of environmental pollutants and drugs on mammalian central nervous system, in: “Mechanisms of Toxicity and Hazard Evaluation,” H. Holmstedt, R. Lauwerys, M. Mercier, and M. Roberfroid, eds., Elsevier/North-Holland Biomedical Press, Amsterdam, p. 59 (1980).

    Google Scholar 

  12. Y. Kuroda and K. Kobayashi, Physiological role of presynaptic “adenosine receptors” in mammalian brain, Jpn. J. Pharmacol. 29: 45 (1979).

    Google Scholar 

  13. C. N. Scholfield, Depression of evoked potentials in brain slices by adenosine compounds, Brit. J. Pharmacol. 63: 239 (1978).

    CAS  Google Scholar 

  14. Y. Kuroda and K. Kobayashi, Feed-back regulation of synaptic transmission by adenosine derivatives in mammalian brain, Neurosci. Lett. [Suppl.] 2: 2 (1979).

    Google Scholar 

  15. C. D. Richards and R. Sercombe, Calcium, magnesium and the electrical activity of guinea pig olfactory cortex in vitro, J. Physiol. (London) 211: 571 (1970).

    Article  CAS  Google Scholar 

  16. Y. Kuroda, M. Saito, and K. Kobayashi, High concentration of calcium prevents the inhibition of postsynaptic potentials and the accumulation of cyclic AMP induced by adenosine in brain slices, Proc. Jpn. Acad. 52: 86 (1976).

    Article  CAS  Google Scholar 

  17. Y. Kuroda and K. Kobayashi, Post-tetanic potentiation can be mediated by adenosine-induced increase of cyclic AMP in the presynaptic terminal, Proc. Intern. Union Physiol. Soc. 14: 534 (1980).

    Google Scholar 

  18. A. Sattin and T. W. Rall, The effect of adenosine and adenine nucleotides on the cyclic adenosine 3’,5’-phosphate content of guinea pig cerebral cortex slices, Mol. Pharmacol. 6: 13 (1970).

    CAS  Google Scholar 

  19. T. Shimahara and L. Tauc, Cyclic AMP induced by serotonin modulates the activity of an identified synapse in Aplysia by facilitating the active permeability to calcium, Brain Res. 127: 168 (1977).

    Article  CAS  Google Scholar 

  20. G. F. Wooten, N. B Thoa, I. J. Kopin and J. Axelrod, Enhanced release of dopamine-ß-hydroxylase and norepinephrine from sympathetic nerves by dibutyryl cyclic adenosine monophosphate and theophylline, Mol. Pharmacol. 9: 178 (1973).

    CAS  Google Scholar 

  21. L. Cubeddu, E. Barnes, and N. Weiner, Release of norepinephrine and dopamine hydroxylase by nerve stimulation. IV. An evaluation of a role for cyclic AMP, J. Pharmacol. Exp. Ther. 193: 105 (1975).

    CAS  PubMed  Google Scholar 

  22. K. Kobayashi, Y. Kuroda, and M. Yoshioka, Change of cyclic AMP level in synaptosomes from cerebral cortex: Increase by adenosine derivatives, J. Neurochem. 36: 86 (1981).

    Article  CAS  Google Scholar 

  23. D. Van Calker, M. Muller, and B. Hamprecht, Adenosine regulates via two different types of receptors: The accumulation of cyclic AMP in cultured brain cells, J. Neurochem. 33: 999 (1979).

    Article  Google Scholar 

  24. J. C. Eccles, “The Understanding of the Brain,” 2nd edition, McGraw-Hill, New York (1977).

    Google Scholar 

  25. M. Klein and E. Kandel, Presynaptic modulation of voltage-dependent Ca 2+-current: Mechanism for behavioral sensitization in Aplysia californica, Proc. Natl. Acad. Sci. USA 75: 3512 (1978).

    Article  ADS  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1984 Plenum Press, New York

About this chapter

Cite this chapter

Kuroda, Y. (1984). Neuromodulatory Roles of Adenosine Receptors Coupling to the Calcium Channel and Adenylate Cyclase. In: Kito, S., Segawa, T., Kuriyama, K., Yamamura, H.I., Olsen, R.W. (eds) Neurotransmitter Receptors. Advances in Experimental Medicine and Biology, vol 175. Springer, New York, NY. https://doi.org/10.1007/978-1-4684-4805-4_12

Download citation

  • DOI: https://doi.org/10.1007/978-1-4684-4805-4_12

  • Published:

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4684-4807-8

  • Online ISBN: 978-1-4684-4805-4

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics