JN AJP: Cell Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 70: 2260-2275, 1993;
0022-3077/93 $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 Peppel, P.
Right arrow Articles by Anton, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Peppel, P.
Right arrow Articles by Anton, F.

Journal of Neurophysiology, Vol 70, Issue 6 2260-2275, Copyright © 1993 by APS


ARTICLES

Responses of rat medullary dorsal horn neurons following intranasal noxious chemical stimulation: effects of stimulus intensity, duration, and interstimulus interval

P. Peppel and F. Anton
Department of Physiology and Biocybernetics, University of Erlangen/Nurnberg, Germany.

1. Most quantitative examinations of nociception are performed with thermal or mechanical stimuli. Because nociceptive processing mechanisms may depend on the modality of the stimuli, comparable studies on chemonociception are necessary. 2. We examined the activity of chemonociceptive medullary dorsal horn neurons in halothane-anesthetized rats. For controlled noxious chemical stimulation, defined CO2 pulses were applied to the nasal mucosa. The effects of stimulus intensity, duration, and interstimulus interval (ISI) were tested by performing three different CO2 stimulation protocols (see below). 3. The recorded neurons were characterized by intranasal and facial stimuli of different modalities. The cells received input from intranasal A delta- and/or C-fibers. All tested neurons also responded to other intranasally applied irritants, e.g., mustard oil. Furthermore, the units were sensitive to intranasal high-threshold mechanical stimulation and to facial mechanical stimulation. According to the properties of their facial mechanoreceptive fields, the units were classified as wide dynamic range (WDR) or nociceptive specific (NS) neurons. The majority of the cells also responded to facially applied noxious heat stimuli, so that most of the recorded neurons were found to be multimodal. Some of the neurons, in addition, had convergent input from primary afferents innervating the maxillary tooth pulps or the cornea and periorbital structures. 4. In the first stimulation protocol we presented four different CO2 concentrations (25, 50, 75, and 100%; stimulus duration 2 s). In total, each concentration was applied 10 times (2 trains of 5 stimuli). Stimulus response functions (SRFs) were computed with average responses to identical stimuli. All but 2 of the 23 tested neurons displayed enhanced responses after stimulation with increasing intensities. In general, WDR cells (n = 15) discharged more vigorously to the same CO2 concentration than NS cells (n = 8). WDR neurons discriminated more reliably between stimulus intensities in the low to moderate range (25-50% CO2) than NS cells. Both categories of neurons, however, discriminated equally well in the moderate- to high-intensity range (50-75% CO2). The discriminatory capacity of WDR and NS neurons was reduced in the highest concentration range (75-100% CO2). The proportion of NS neurons significantly discriminating between these intensities tended to be higher compared with WDR neurons when stimuli were applied with long ISIs (120 s). 5. To examine the effects of the duration of the ISI, identical test sequences were performed with ISIs of 30 and 120 s. (ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
D. A. Bereiter, K. Okamoto, A. Tashiro, and H. Hirata
Endotoxin-Induced Uveitis Causes Long-Term Changes in Trigeminal Subnucleus Caudalis Neurons
J Neurophysiol, December 1, 2005; 94(6): 3815 - 3825.
[Abstract] [Full Text] [PDF]


Home page
Chem SensesHome page
P. M. Wise, C. J. Wysocki, and T. Radil
Time-Intensity Ratings of Nasal Irritation from Carbon Dioxide
Chem Senses, November 1, 2003; 28(9): 751 - 760.
[Abstract] [Full Text] [PDF]


Home page
Chem SensesHome page
J.-M. Dessirier, M. O'Mahony, M. Iodi-Carstens, and E. Carstens
Sensory Properties of Citric Acid: Psychophysical Evidence for Sensitization, Self-desensitization, Cross-desensitization and Cross-stimulus-induced Recovery Following Capsaicin
Chem Senses, December 1, 2000; 25(6): 769 - 780.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. T. Simons, J. -M. Dessirier, M. I. Carstens, M. O'Mahony, and E. Carstens
Neurobiological and Psychophysical Mechanisms Underlying the Oral Sensation Produced by Carbonated Water
J. Neurosci., September 15, 1999; 19(18): 8134 - 8144.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. Carstens, N. Kuenzler, and H. O. Handwerker
Activation of Neurons in Rat Trigeminal Subnucleus Caudalis by Different Irritant Chemicals Applied to Oral or Ocular Mucosa
J Neurophysiol, August 1, 1998; 80(2): 465 - 492.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
I. D. Meng, J. W. Hu, A. P. Benetti, and D. A. Bereiter
Encoding of Corneal Input in Two Distinct Regions of the Spinal Trigeminal Nucleus in the Rat: Cutaneous Receptive Field Properties, Responses to Thermal and Chemical Stimulation, Modulation by Diffuse Noxious Inhibitory Controls, and Projections to the Parabrachial Area
J Neurophysiol, January 1, 1997; 77(1): 43 - 56.
[Abstract] [Full Text] [PDF]




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