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Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1981 Jul;44(7):600–607. doi: 10.1136/jnnp.44.7.600

C nociceptor activity in human nerve during painful and non painful skin stimulation.

J Van Hees, J Gybels
PMCID: PMC491064  PMID: 7288447

Abstract

Percutaneous recordings from more than one hundred single C fibres have been performed in the radial nerve of conscious human subjects. All these fibres belong to the poly-modal C nociceptor group, being excited by mechanical and thermal and also by chemical stimulation. Conduction velocities showed a monophasic distribution with a mean value of 0.86 m/s (SD: 0.17). The mechanical threshold, measured with von Frey hairs, varied between 2.3 and 13.1 g. The receptive field was circular or elliptical; for 33 units the mean axes were 6 mm and 7 mm. Mechanically evoked C fibre discharge even up to more than 10 spikes/s was not necessarily accompanied by pain sensation. Nettle sting evoked an irregular C fibre discharge (maximum 10 spikes/s) accompanied by a pricking and burning sensation; the sensation of itch which was sometimes reported, was not correlated with the discharge frequency. C fibre activation by a chemical irritant (paint remover) also evoked an irregular discharge (maximum 3 to 6 spikes/s), accompanied by pricking and burning pain sensation. The C threshold for radiant heat usually lay below the subject's pain threshold. Increasing skin temperature produced increasing neural firing rate. The mean spike frequency rarely exceeded two spikes/s even with stimuli evoking strong heat pain. The occurrence of subjective heat pain response could be as well predicted from th C fibre spike frequency as from the skin temperature. It is concluded that nociceptive C input provoked by thermal or chemical stimuli correlates well with pain sensation. However, similar C input provided by mechanical stimulation which activates also A beta mechanoreceptors, did not necessarily produce pain sensation.

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Selected References

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

  1. Beck P. W., Handwerker H. O., Zimmermann M. Nervous outflow from the cat's foot during noxious radiant heat stimulation. Brain Res. 1974 Mar 8;67(3):373–386. doi: 10.1016/0006-8993(74)90488-0. [DOI] [PubMed] [Google Scholar]
  2. Bessou P., Perl E. R. Response of cutaneous sensory units with unmyelinated fibers to noxious stimuli. J Neurophysiol. 1969 Nov;32(6):1025–1043. doi: 10.1152/jn.1969.32.6.1025. [DOI] [PubMed] [Google Scholar]
  3. COLLIER H. O., CHESHER G. B. Identification of 5-hydroxytryptamine in the sting of the nettle (urtica dioica). Br J Pharmacol Chemother. 1956 Jun;11(2):186–189. doi: 10.1111/j.1476-5381.1956.tb01051.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Emmelin N., Feldberg W. The mechanism of the sting of the common nettle (urtica urens). J Physiol. 1947 Oct 15;106(4):440–455. doi: 10.1113/jphysiol.1947.sp004225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gybels J., Handwerker H. O., Van Hees J. A comparison between the discharges of human nociceptive nerve fibres and the subject's ratings of his sensations. J Physiol. 1979 Jul;292:193–206. doi: 10.1113/jphysiol.1979.sp012846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hagbarth K. E., Vallbo A. B. Mechanoreceptor activity recorded percutaneously with semi-microelectrodes in human peripheral nerves. Acta Physiol Scand. 1967 Jan-Feb;69(1):121–122. doi: 10.1111/j.1748-1716.1967.tb03498.x. [DOI] [PubMed] [Google Scholar]
  7. Handwerker H. O., Neher K. D. Characteristics of C-fibre receptors in the cat's foot responding to stepwise increase of skin temperature ot noxious levels. Pflugers Arch. 1976 Sep 30;365(2-3):221–229. doi: 10.1007/BF01067022. [DOI] [PubMed] [Google Scholar]
  8. Iggo A. Cutaneous and subcutaneous sense organs. Br Med Bull. 1977 May;33(2):97–102. doi: 10.1093/oxfordjournals.bmb.a071432. [DOI] [PubMed] [Google Scholar]
  9. KEELE C. A. Chemical causes of pain & itch. Proc R Soc Med. 1957 Jul;50(7):477–484. [PMC free article] [PubMed] [Google Scholar]
  10. Konietzny F., Hensel H. Letters and notes: Warm fiber activity in human skin nerves. Pflugers Arch. 1975 Sep 9;359(3):265–267. doi: 10.1007/BF00587384. [DOI] [PubMed] [Google Scholar]
  11. Kumazawa T., Perl E. R. Primate cutaneous sensory units with unmyelinated (C) afferent fibers. J Neurophysiol. 1977 Nov;40(6):1325–1338. doi: 10.1152/jn.1977.40.6.1325. [DOI] [PubMed] [Google Scholar]
  12. LaMotte R. H., Campbell J. N. Comparison of responses of warm and nociceptive C-fiber afferents in monkey with human judgments of thermal pain. J Neurophysiol. 1978 Mar;41(2):509–528. doi: 10.1152/jn.1978.41.2.509. [DOI] [PubMed] [Google Scholar]
  13. Melzack R., Wall P. D. Pain mechanisms: a new theory. Science. 1965 Nov 19;150(3699):971–979. doi: 10.1126/science.150.3699.971. [DOI] [PubMed] [Google Scholar]
  14. Torebjörk H. E. Afferent C units responding to mechanical, thermal and chemical stimuli in human non-glabrous skin. Acta Physiol Scand. 1974 Nov;92(3):374–390. doi: 10.1111/j.1748-1716.1974.tb05755.x. [DOI] [PubMed] [Google Scholar]
  15. Torebjörk H. E., Hallin R. G. Identification of afferent C units in intact human skin nerves. Brain Res. 1974 Mar 8;67(3):387–403. doi: 10.1016/0006-8993(74)90489-2. [DOI] [PubMed] [Google Scholar]
  16. Van Hees J., Gybels J. M. Pain related to single afferent C fibers from human skin. Brain Res. 1972 Dec 24;48:397–400. doi: 10.1016/0006-8993(72)90198-9. [DOI] [PubMed] [Google Scholar]

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