Literature DB >> 825619

Response of unmyelinated (C) polymodal nociceptors to thermal stimuli applied to monkey's face.

R E Beitel, R Dubner.   

Abstract

1. The response of C polymodal nociceptors to thermal and mechanical stimuli applied to the monkey's face was recorded extracellulary in the trigeminal ganglion in rhesus monkeys anesthetized with sodium pentobarbital. Conduction velocities, determined from electrical stimulation of receptive fields (RFs), were in the range for unmyelinated C fibers (mean=0.82 m/s, n=20; SD=+/-0.17). With two exceptions cutaneous RFs were single spots (median=2 mm2; n=37) and usually were identical for thermal and mechanical stimuli. The median force threshold for the sample of units was 1.2 g (von Frey technique; n = 39; range = 0.07-8.5 g). 2. Discharges to thermal stimuli were investigated with a feedback-controlled contact thermode which permitted temperature changes less than or equal 12.0 degrees C/s. Thermal thresholds ranged from 38 degree to 49 degree C (median=46 degrees C; n=37), and maximum discharge frequencies were obtained in the noxious heat range (45-55 degrees C). For a graded series of 5 s duration stimuli from an adapting temperature of 35 degrees C, the number of impulses increased as a monotonic function of stimulus intensity over the range from threshold temperature to 50-53 degrees C. Many stimulus-response functions were positively accelerated, and linear regression analyses showed that most units examined were best fit by nonlinear functions. 3. The typical pattern of activity to 5 s duration temperature shifts into the noxious heat range was a short accelerating burst of impulses followed by deceleration to a lower rate of discharge prior to termination of the stimulus. The temporal profile of the discharge of impulses was virtually identical at different adapting temperatures. In units tested with 30 s duration stimuli at 2-6 degrees C above threshold, the mean frequency of discharge during the final 25 s was 1.46 impulses/s (n=6; SD=+/-0.89). 4. Application of noxious heat stimuli a few degrees above threshold temperature typically sensitized or enhanced the response of the unit to subsequent application of heat stimuli. The signs of sensitization consisted of a decrease in threshold temperature, increased frequency of discharge, decreased latency to the first impulse, and afterdischarges. Units failed to respond throughout the duration of 30 s stimuli if the final temperature exceeded 50 degrees C. Depressed responses were sometimes produced by application of intense (greater than or equal 55 degrees C) stimuli, presumably as a result of partial inactivation of the receptor. 5. In a correlative analysis, the latency and pattern of discharge in a sample of units were compared with escape responses in two monkeys to temperature shifts into the noxious heat range (49 and 51 degrees C). The analysis revealed that the discharge of C polymodal nociceptors alone cannot account for fast escape responses, but the discharge may contribute to escape responses which occur more than 3.5 s after the onset of stimulation.

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Year:  1976        PMID: 825619     DOI: 10.1152/jn.1976.39.6.1160

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  31 in total

1.  Functional properties of tooth pulp neurons responding to thermal stimulation.

Authors:  D K Ahn; E A Doutova; K McNaughton; A R Light; M Närhi; W Maixner
Journal:  J Dent Res       Date:  2012-01-17       Impact factor: 6.116

2.  An investigation of the gate control theory of pain using the experimental pain stimulus of potassium iontophoresis.

Authors:  S A Humphries; M H Johnson; N R Long
Journal:  Percept Psychophys       Date:  1996-07

3.  C-polymodal nociceptors activated by noxious low temperature in human skin.

Authors:  M Campero; J Serra; J L Ochoa
Journal:  J Physiol       Date:  1996-12-01       Impact factor: 5.182

4.  Biophysical and functional consequences of receptor-mediated nerve fiber transformation.

Authors:  D L Tanelian; V S Markin
Journal:  Biophys J       Date:  1997-03       Impact factor: 4.033

5.  Testing Assumptions in Human Pain Models: Psychophysical Differences Between First and Second Pain.

Authors:  Nathanial R Eckert; Charles J Vierck; Corey B Simon; Yenisel Cruz-Almeida; Roger B Fillingim; Joseph L Riley
Journal:  J Pain       Date:  2016-11-22       Impact factor: 5.820

6.  Thermal perception on lingual and labial skin.

Authors:  B G Green
Journal:  Percept Psychophys       Date:  1984-09

7.  Thermal nociceptive properties of trigeminal afferent neurons in rats.

Authors:  Jason M Cuellar; Neil A Manering; Mikhail Klukinov; Michael I Nemenov; David C Yeomans
Journal:  Mol Pain       Date:  2010-07-07       Impact factor: 3.395

8.  Cutaneous sensory afferents recorded from the nervus intramandibularis of Gallus gallus var domesticus.

Authors:  M J Gentle
Journal:  J Comp Physiol A       Date:  1989-02       Impact factor: 1.836

9.  Discharge patterns of afferent cutaneous nerve fibers from the rat's tail during prolonged noxious mechanical stimulation.

Authors:  H O Handwerker; F Anton; P W Reeh
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

10.  Parallels between properties of high-threshold mechanoreceptors of the goat oral mucosa and human pain report.

Authors:  B Cooper; B Loughner; R M Friedman; M W Heft; J LaBanc; A Fonte
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

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