Skip to main content
Log in

Reaction of Neurons to Alkaloid Agonists of Opioid Receptors during Modulation of Phosphodiesterases

  • Published:
Bulletin of Experimental Biology and Medicine Aims and scope

Abstract

We studied the effect of ultralow doses of theophylline and morphine, modulators of receptors and intracellular signal systems, on ion permeability of membranes. Theophylline and morphine in ultralow doses blocked the neuronal responses to these agents applied in physiological concentrations. Theophylline in ultralow doses attenuated, but did not completely block neuronal reaction to morphine. These findings suggest that ultralow doses of various substances producing no appreciable physiological changes can activate mechanisms providing optimum response to strong factors.

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

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  1. T. A. Zapara, I. F. Pavlov, and O. I. Epshtein, Byull. Eksp. Biol. Med., 10,No. 128, 392-398 (1999).

    Google Scholar 

  2. M. O. Samoilov, Brain and Adaptation: Molecular and Cellular Mechanisms [in Russian], St. Petersburg (1999).

  3. A. D. Shcherbatko, Intracellular Signaling [in Russian], Ed. P. G. Kostyuk, Moscow (1988).

  4. W. A. Catterall, Science, 242, 50-61 (1988).

    Google Scholar 

  5. M. K. Leung and G. B. Stefano, Progr. Neurobiol., 28, 131-159 (1987).

    Google Scholar 

  6. E. Neher, Neuroscience, 26,No. 3, 727-734 (1988).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Epstein, O.I., Shtark, M.B., Zapara, T.A. et al. Reaction of Neurons to Alkaloid Agonists of Opioid Receptors during Modulation of Phosphodiesterases. Bulletin of Experimental Biology and Medicine 135 (Suppl 7), 17–19 (2003). https://doi.org/10.1023/A:1024745705881

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1024745705881

Navigation