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. 1980 Feb;299:233–245. doi: 10.1113/jphysiol.1980.sp013122

Mechanical and thermal responses of polymodal receptors recorded from the superior spermatic nerve of dogs.

T Kumazawa, K Mizumura
PMCID: PMC1279222  PMID: 7381767

Abstract

1. One hundred and fifty-three units were recorded from the superior spermatic nerve of dogs and were tested with mechanical, chemical or heat stimulation. Among 104 units tested with all three methods of stimulation ninety-three units responded to all of them; thus 90% of the superior spermatic nerve units are considered to be polymodal receptors. Only mechanical and thermal responses are reported in this paper. 2. Conduction velocities measured at the nerve trunk in the abdominal cavity were mostly within the A-delta fibre range (average conduction velocity: 11.1 m.s-1, n = 63), but in the receptive region much delay was observed. In contrast to the cutaneous polymodal receptors, polymodal receptors in the superior spermatic nerve usually had multiple receptive sites, up to nine in number. 3. Mechanical responses of these polymodal receptors consisted of dynamic and steady-state responses and sometimes were followed by after-discharges. Maximum responses were obtained with a noxious intensity of stimulation, but thresholds scattered over a wide range including non-noxious intensities. 4. In response to heating, these polymodal units gave an irregular discharge that increased roughly in parallel to temperature rise with an average threshold and S.E. of mean, 42.6+/-0.4 degrees C (n = 73). They showed sensitization or deactivation or both on repetition of heating. Cooling the receptive site caused only transient and weak responses, if any.

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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. Bradykinin and serotonin effects on various types of cutaneous nerve fibers. Pflugers Arch. 1974 Mar 11;347(3):209–222. doi: 10.1007/BF00592598. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. Beitel R. E., Dubner R. Response of unmyelinated (C) polymodal nociceptors to thermal stimuli applied to monkey's face. J Neurophysiol. 1976 Nov;39(6):1160–1175. doi: 10.1152/jn.1976.39.6.1160. [DOI] [PubMed] [Google Scholar]
  4. Bessou P., Perl E. R. Amovement receptor of the small intestine. J Physiol. 1966 Jan;182(2):404–426. doi: 10.1113/jphysiol.1966.sp007829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. Croze S., Duclaux R., Kenshalo D. R. The thermal sensitivity of the polymodal nociceptors in the monkey. J Physiol. 1976 Dec;263(3):539–562. doi: 10.1113/jphysiol.1976.sp011644. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Duclaux R., Mei N., Ranieri F. Conduction velocity along the afferent vagal dendrites: a new type of fibre. J Physiol. 1976 Sep;260(2):487–495. doi: 10.1113/jphysiol.1976.sp011527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. FJALLBRANT N., IGGO A. The effect of histamine, 5-hydroxytryptamine and acetylcholine on cutaneous afferent fibres. J Physiol. 1961 May;156:578–590. doi: 10.1113/jphysiol.1961.sp006694. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fitzgerald M., Lynn B. The sensitization of high threshold mechanoreceptors with myelinated axons by repeated heating. J Physiol. 1977 Feb;265(2):549–563. doi: 10.1113/jphysiol.1977.sp011730. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Floyd K., Hick V. E., Morrison J. F. Mechanosensitive afferent units in the hypogastric nerve of the cat. J Physiol. 1976 Jul;259(2):457–471. doi: 10.1113/jphysiol.1976.sp011476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Floyd K., Morrison J. F. Splanchnic mechanoreceptors in the dog. Q J Exp Physiol Cogn Med Sci. 1974 Oct;59(4):361–366. doi: 10.1113/expphysiol.1974.sp002279. [DOI] [PubMed] [Google Scholar]
  12. HENSEL H., IGGO A., WITT I. A quantitative study of sensitive cutaneous thermoreceptors with C afferent fibres. J Physiol. 1960 Aug;153:113–126. doi: 10.1113/jphysiol.1960.sp006522. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. IGGO A. Cutaneous heat and cold receptors with slowly conducting (C) afferent fibres. Q J Exp Physiol Cogn Med Sci. 1959 Oct;44:362–370. doi: 10.1113/expphysiol.1959.sp001417. [DOI] [PubMed] [Google Scholar]
  14. IGGO A. The electrophysiological identification of single nerve fibres, with particular reference to the slowest-conducting vagal afferent fibres in the cat. J Physiol. 1958 Jun 18;142(1):110–126. doi: 10.1113/jphysiol.1958.sp006002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kumazawa T., Mizumura K. Chemical responses of polymodal receptors of the scrotal contents in dogs. J Physiol. 1980 Feb;299:219–231. doi: 10.1113/jphysiol.1980.sp013121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kumazawa T., Mizumura K. The polymodal C-fiber receptor in the muscle of the dog. Brain Res. 1976 Jan 23;101(3):589–593. doi: 10.1016/0006-8993(76)90483-2. [DOI] [PubMed] [Google Scholar]
  17. Kumazawa T., Mizumura K. The polymodal receptors in the testis of dog. Brain Res. 1977 Nov 18;136(3):553–558. doi: 10.1016/0006-8993(77)90080-4. [DOI] [PubMed] [Google Scholar]
  18. Kumazawa T., Mizumura K. Thin-fibre receptors responding to mechanical, chemical, and thermal stimulation in the skeletal muscle of the dog. J Physiol. 1977 Dec;273(1):179–194. doi: 10.1113/jphysiol.1977.sp012088. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. 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]
  20. Morrison J. F. Splanchnic slowly adapting mechanoreceptors with punctate receptive fields in the mesentery and gastrointestinal tract of the cat. J Physiol. 1973 Sep;233(2):349–361. doi: 10.1113/jphysiol.1973.sp010311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. NIIJIMA A. Multi-visceral supply of a single myelinated splanchnic nerve fiber in the toad. Jpn J Physiol. 1961 Aug 15;11:427–442. doi: 10.2170/jjphysiol.11.427. [DOI] [PubMed] [Google Scholar]
  22. Perl E. R., Kumazawa T., Lynn B., Kenins P. Sensitization of high threshold receptors with unmyelinated (C) afferent fibers. Prog Brain Res. 1976;43:263–277. doi: 10.1016/S0079-6123(08)64359-9. [DOI] [PubMed] [Google Scholar]
  23. Peterson D. F., Brown A. M. Functional afferent innervation of testis. J Neurophysiol. 1973 May;36(3):425–433. doi: 10.1152/jn.1973.36.3.425. [DOI] [PubMed] [Google Scholar]
  24. WITT I., GRIFFIN J. P. Afferent cutaneous C-fibre reactivity to repeated thermal stimuli. Nature. 1962 May 26;194:776–777. doi: 10.1038/194776a0. [DOI] [PubMed] [Google Scholar]

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