JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 54: 491-501, 1985;
0022-3077/85 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shea, V. K.
Right arrow Articles by Perl, E. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shea, V. K.
Right arrow Articles by Perl, E. R.

Journal of Neurophysiology, Vol 54, Issue 3 491-501, Copyright © 1985 by APS


ARTICLES

Sensory receptors with unmyelinated (C) fibers innervating the skin of the rabbit's ear

V. K. Shea and E. R. Perl

The cutaneous receptive properties of unmyelinated (C) fibers of the rabbit's great auricular nerve were determined by single-unit recordings. The majority of C-fiber units could be excited by cutaneous stimulation, and such sensory units fell into three major categories on the basis of responses to mechanical and thermal stimulation of their cutaneous receptive fields: low-threshold mechanoreceptors, nociceptors, or specific thermoreceptors. The majority of afferent elements were nociceptive, and all nociceptors responded to strong mechanical stimulation. Three types of nociceptors could be distinguished by their responses to thermal stimuli. Polymodal nociceptors responded to heat with thresholds of 40-55 degrees C and typically displayed enhanced responses or sensitization after noxious heating of their receptive fields. High-threshold mechanoreceptors failed to respond promptly to heat before noxious cutaneous stimulation which, however, elicited subsequent back-ground activity or sensitivity to heat. A third type of nociceptor responded to cold but not to heat. Low-threshold mechanoreceptors were identified by their brisk responses to very gentle, slowly moving mechanical stimulation of their receptive fields, and were readily distinguished from any element classified as nociceptive by their lower mechanical thresholds. Rapid innocuous warming or cooling excited some of the low-threshold mechanoreceptors. Specific thermoreceptors, both warming and cooling types, were rare, insensitive to mechanical stimulation, and responded to very slight changes in temperature. In contrast to the sensitization to heat, which was characteristic of most nociceptors, specific warming receptors displayed depressed thermal responses after noxious heating of their receptive fields. These results provide further evidence of the similarity of C-fiber receptors innervating hairy skin of different species. Some differences from past reports and additional features are described.


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
M. D. Boada and C. J. Woodbury
Physiological Properties of Mouse Skin Sensory Neurons Recorded Intracellularly In Vivo: Temperature Effects on Somal Membrane Properties
J Neurophysiol, August 1, 2007; 98(2): 668 - 680.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
K. M. Albers, C. J. Woodbury, A. M. Ritter, B. M. Davis, and H. R. Koerber
Glial cell line-derived neurotrophic factor expression in skin alters the mechanical sensitivity of cutaneous nociceptors.
J. Neurosci., March 15, 2006; 26(11): 2981 - 2990.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H. Xing, J. Ling, M. Chen, and J. G. Gu
Chemical and Cold Sensitivity of Two Distinct Populations of TRPM8-Expressing Somatosensory Neurons
J Neurophysiol, February 1, 2006; 95(2): 1221 - 1230.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. Wessberg, H. Olausson, K. W. Fernstrom, and A. B. Vallbo
Receptive Field Properties of Unmyelinated Tactile Afferents in the Human Skin
J Neurophysiol, March 1, 2003; 89(3): 1567 - 1575.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
E. R. Perl
Causalgia, pathological pain, and adrenergic receptors
PNAS, July 6, 1999; 96(14): 7664 - 7667.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. B. Vallbo, H. Olausson, and J. Wessberg
Unmyelinated Afferents Constitute a Second System Coding Tactile Stimuli of the Human Hairy Skin
J Neurophysiol, June 1, 1999; 81(6): 2753 - 2763.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
Z. D. Prete and P. Grigg
Responses of Rapidly Adapting Afferent Neurons to Dynamic Stretch of Rat Hairy Skin
J Neurophysiol, August 1, 1998; 80(2): 745 - 754.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
J Sato and E. Perl
Adrenergic excitation of cutaneous pain receptors induced by peripheral nerve injury
Science, March 29, 1991; 251(5001): 1608 - 1610.
[Abstract] [PDF]


Home page
ScienceHome page
Y Sugiura, C. Lee, and E. Perl
Central projections of identified, unmyelinated (C) afferent fibers innervating mammalian skin
Science, October 17, 1986; 234(4774): 358 - 361.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online