Skip to main content
Log in

Nociceptor stimulation and PGE release by capsaicin

  • Published:
Naunyn-Schmiedeberg's Archives of Pharmacology Aims and scope Submit manuscript

Summary

  1. 1.

    Intraarterial injection of capsaicin (threshold dose 0.3 μg) into the isolated perfused rabbit ear causes a dose-dependent reflex fall in blood pressure by stimulation of chemosensitive nociceptors.

  2. 2.

    Infusion of capsaicin (1 and 10 μg/ml) into the isolated rabbit ear dose-dependently stimulates prostaglandin biosynthesis, equally in innervated and chronically denervated preparations, therefore mainly in extraneuronal tissue. The capsaicin-induced prostaglandin E release is dependent on the presence of extracellular Ca2+.

  3. 3.

    The nociceptive reflex fall in blood pressure induced by i.a. injection of bradykinin is progressively enhanced under infusion of 1 μg/ml capsaicin whereas that induced by acetylcholine is not. Its enhancement is explained by the capsaicin-induced increased amount of prostaglandin E at the nociceptor sites.

  4. 4.

    Infusion of 10 μg/ml capsaicin renders the nociceptors insensitive to effects of bradykinin and acetylcholine.

  5. 5.

    Although the stimulation of nociceptors by capsaicin in a small dose includes the release of prostaglandin E from the surrounding tissue, it cannot be said whether a prostaglandin-mediated mechanism is also involved in the long lasting functional impairment of chemosensitive fibres induced by high doses of capsaicin.

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

  • Beck, P. W., Handwerker, H. O.: Bradykinin and serotonin effects on various types of cutaneous nerve fibres. Pflügers Arch. Ges. Physiol.347, 209–222 (1974)

    Google Scholar 

  • Coleridge, H. M., Coleridge, J. C. G., Kidd, C.: Role of the pulmonary arterial baroreceptors in the effects produced by capsaicin in the dog. J. Physiol. (Lond.)170, 272–285 (1964)

    Google Scholar 

  • Collier, H. O. J., McDonald-Gibson, W. J., Saeed, S. A.: Stimulation of prostaglandin biosynthesis by drugs: Effects in vitro of some drugs affecting gut function. Br. J. Pharmacol.58, 193–199 (1976)

    Google Scholar 

  • Damas, J., Deby, C.: Sur la liberation des prostaglandines et de leur précurseurs, par la bradykinine. Arch. Int. Physiol. Biochim.84, 293–304 (1976)

    Google Scholar 

  • Fjällebrant, N., Iggo, A.: The effect of histamine, 5-hydroxytryptamine and acetylcholine on cutaneous afferent fibres. J. Physiol. (Lond.)156, 578–590 (1961)

    Google Scholar 

  • Gamse, R., Molnar, A., Lembeck, F.: Substance P release from spinal cord slices by capsaicin. Life Sci.25, 629–636 (1979)

    Google Scholar 

  • Hökfelt, T., Kellerth, J. O., Nilsson, G., Pernow, B.: Experimental immunohistochemical studies on the localization and distribution of substance P in cat primary sensory neurones. Brain Res.100, 235–252 (1975)

    Google Scholar 

  • Jancsó, N., Jancsó-Gábor, A., Szolcsányi, J.: Direct evidence for neurogenic inflammation and its prevention by denervation and by pretreatment with capsaicin. Br. J. Pharmacol. Chemother.31, 138–151 (1967)

    Google Scholar 

  • Jancsó, N., Jancsó-Gábor, A., Szolcsányi, J.: The role of sensory nerve endings in neurogenic inflammation induced in human skin and the eye and paw of the rat. Br. J. Pharmacol. Chemother.32, 32–41 (1968)

    Google Scholar 

  • Jessell, T. M., Mudge, A. W., Leeman, S. E., Yaksh, T. L.: Release of substance P and somatostatin, in vivo, from primary afferent terminals in mammalian spinal cord. Proc. Soc. Neurosci.5, 611 (1979)

    Google Scholar 

  • Joó, F., Szolcsányi, J., Jancsó-Gábor, A.: Mitochondrial alterations in the spinal ganglion cells of the rat accompanying the longlasting sensory disturbance induced by capsaicin. Life Sci.8, 621–626 (1969)

    Google Scholar 

  • Juan, H.: Mechanism of action of bradykinin-induced release of prostaglandin E. Naunyn-Schmiedeberg's Arch. Pharmacol.300, 77–85 (1977)

    Google Scholar 

  • Juan, H.: Inhibition of the algesic effect of bradykinin and acetylcholine by mepacrine. Naunyn-Schmiedeberg's Arch. Pharmacol.301, 23–27 (1977a)

    Google Scholar 

  • Juan, H.: Prostaglandins as modulators of pain. Gen. Pharmacol.9, 403–409 (1978)

    Google Scholar 

  • Juan, H.: Role of calcium in prostaglandin E release induced by bradykinin and the ionophore A 23187. Naunyn-Schmiedeberg's Arch. Pharmacol.307, 177–183 (1979)

    Google Scholar 

  • Juan, H., Lembeck, F.: Action of peptides and other algesic agents on paravascular pain receptors of the isolated perfused rabbit ear. Naunyn-Schmiedeberg's Arch. Pharmacol.283, 151–164 (1974)

    Google Scholar 

  • Juan, H., Lembeck, F.: Release of prostaglandins from the isolated perfused rabbit ear by bradykinin and acetylcholine. Agents Actions6, 642–645 (1976)

    Google Scholar 

  • Juan, H., Lembeck, F.: Prostaglandin F reduces the algesic effect of bradykinin by antagonizing the pain enhancing action of endogenously released prostaglandin E. Br. J. Pharmacol.59, 385–391 (1977)

    Google Scholar 

  • Lembeck, F., Juan, H.: Interaction of prostaglandins and indomethacin with algesic substances. Naunyn-Schmiedeberg's Arch. Pharmacol.285, 301–313 (1974)

    Google Scholar 

  • Lembeck, F., Holzer, P.: Substance P as neurogenic mediator of antidromic vasodilation and neurogenic plasma extravasation. Naunyn-Schmiedeberg's Arch. Pharmacol.310, 175–183 (1979)

    Google Scholar 

  • Lembeck, F., Popper, H., Juan, H.: Release of prostaglandins by bradykinin as an intrinsic mechanism of its algesic effect. Naunyn-Schmiedeberg's Arch. Pharmacol.294, 69–73 (1976)

    Google Scholar 

  • Pórszász, J., György, J. L., Pórszász-Gibiszer, K.: Cardiovascular and respiratory effects of capsaicin. Acta Physiol. Hung.8, 61–76 (1955)

    Google Scholar 

  • Pórszász, J., Such, Gy., Pórszász-Gibiszer, K.: Circulatory and respiratory chemoreflexes. Analysis of the site of action and receptor types of capsaicin. Acta Physiol. Hung.12, 189–205 (1957)

    Google Scholar 

  • Szolcsányi, J.: A pharmacological approach to elucidation of the role of different nerve fibres and receptor endings in mediation of pain. J. Physiol. (Paris)73, 251–259 (1977)

    Google Scholar 

  • Szolcsányi, J.: Effect of pain producing chemical agents on the single fiber activity of slowly conducting afferent fibres. Acta Physiol. Acad. Sci. Hung. (in press, 1980)

  • Szolcsányi, J., Jancsó-Gábor, A., Joó, E.: Functional and fine structural characteristics of the sensory neuron blocking effect of capsaicin. Naunyn-Schmiedeberg's Arch. Pharmacol.287, 157–169 (1975)

    Google Scholar 

  • Toh, C. C., Lee, T. S., Kiang, A. K.: The pharmacological actions of capsaicin and analogues. Br. J. Pharmacol.10, 175–182 (1955)

    Google Scholar 

  • Vargaftig, B. B.: The pharmacology of slow reacting substance C and of arachidonic acid. Agents Actions3, 357–365 (1973)

    Google Scholar 

  • Virus, M., Gebhart, F.: Pharmacological actions of capsaicin: Apparent involvement of substance P and serotonin. Life Sci.25, 1273–1284 (1979)

    Google Scholar 

  • Youlten, L. J. F., McCall, E.: Prostaglandins, completment and cellular migration in carageenin inflammation. In: The role of prostaglandins in inflammation, G. P. Lewis, ed.), pp. 26–33. Bern-Stuttgart-Wien: Huber 1976

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Juan, H., Lembeck, F., Seewann, S. et al. Nociceptor stimulation and PGE release by capsaicin. Naunyn-Schmiedeberg's Arch. Pharmacol. 312, 139–143 (1980). https://doi.org/10.1007/BF00569722

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00569722

Key words

Navigation