Literature DB >> 114612

Responses of primate spinothalamic neurons to graded and to repeated noxious heat stimuli.

D R Kenshalo, R B Leonard, J M Chung, W D Willis.   

Abstract

1. The responses of primate spinothalamic tract cells innervating the glabrous skin of the foot to noxious thermal stimuli have been examined. 2. Of the 41 cells studied, 98% responded to noxious thermal stimuli. Heating the cutaneous receptive field with a series of stimuli from 35 to 43, 47, and 50 degrees C produced a graded increase in discharge rate. The responses were characterized by an onset, which occurred after the temperature change had either slowed or stopped, an acceleration in the discharge up to a peak, and then an adaptation to a new base-line level. The time constants of adaptation were faster than those reported for C polymodal nociceptors. 3. No systematic differences were found in the responses to noxious thermal stimuli of cells with wide dynamic range receptive fields and of cells with narrow dynamic range, high-threshold receptive fields. There were also no differences in the responses of cells located in the marginal zone and of cells located in the neck of the dorsal horn. 4. The relationship between peak frequency and final skin temperature with a 30 s stimulus duration can best be described by a power function with an exponent of 2.1. An increase in the stimulus duration to 120 s resulted in an increase in the exponent of the power function to 3.2. 5. Repetition of the series of 30-s heat stimuli resulted in an increase in peak frequency, total impulse count, and background activity. Repetition of stimuli having a duration of 120 s produced an increase in the peak frequency at 43 and 45 degrees C, a smaller increase at 47 degrees C, and a decrease at 50 degrees C. Background activity was increased by the lower temperature stimuli, but was decreased following higher temperature stimuli. 6. In six additional cells, the skin was heated with three consecutive presentations at each temperature level (43, 45, 47, and 50 degrees C) for 30 s. No change was observed in the peak frequencies of the responses to successive stimuli of the same intensity. However, the exponent of the power function relating the average peak frequency for the six cells to changes in skin temperature was 3.9. This exponent was larger than that seen when two series of graded heat stimuli of 120 s duration were used, indicating more sensitization despite the fact the total time of exposure to noxious heat was less. 7. A role for both high-threshold and wide dynamic range spinothalamic cells in transmitting nociceptive information to the diencephalon is postulated.

Mesh:

Year:  1979        PMID: 114612     DOI: 10.1152/jn.1979.42.5.1370

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


  12 in total

1.  Termination zones of functionally characterized spinothalamic tract neurons within the primate posterior thalamus.

Authors:  Steve Davidson; Xijing Zhang; Sergey G Khasabov; Donald A Simone; Glenn J Giesler
Journal:  J Neurophysiol       Date:  2008-08-13       Impact factor: 2.714

2.  Determinants of laser-evoked EEG responses: pain perception or stimulus saliency?

Authors:  G D Iannetti; N P Hughes; M C Lee; A Mouraux
Journal:  J Neurophysiol       Date:  2008-06-04       Impact factor: 2.714

3.  Analgesic effectiveness of ketorolac compared to meperidine in the rat formalin test.

Authors:  B C Randolph; M A Peters
Journal:  Anesth Prog       Date:  1997

Review 4.  Neuroanatomy of the pain system and of the pathways that modulate pain.

Authors:  W D Willis; K N Westlund
Journal:  J Clin Neurophysiol       Date:  1997-01       Impact factor: 2.177

5.  Responses of spinothalamic tract cells in the superficial dorsal horn of the primate lumbar spinal cord.

Authors:  D G Ferrington; L S Sorkin; W D Willis
Journal:  J Physiol       Date:  1987-07       Impact factor: 5.182

Review 6.  Combination therapy for neuropathic pain: a review of current evidence.

Authors:  Yakov Vorobeychik; Vitaly Gordin; Jianren Mao; Lucy Chen
Journal:  CNS Drugs       Date:  2011-12-01       Impact factor: 5.749

7.  Temporal summation of heat pain in humans: Evidence supporting thalamocortical modulation.

Authors:  Tuan D Tran; Heng Wang; Animesh Tandon; Luis Hernandez-Garcia; Kenneth L Casey
Journal:  Pain       Date:  2010-05-21       Impact factor: 6.961

8.  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

Review 9.  Pain management: physiopathology, future research and endpoints.

Authors:  M Sosnowski
Journal:  Support Care Cancer       Date:  1993-03       Impact factor: 3.603

10.  Prolonged noxious mechanical stimulation of the rat's tail: responses and encoding properties of dorsal horn neurones.

Authors:  F Cervero; H O Handwerker; J M Laird
Journal:  J Physiol       Date:  1988-10       Impact factor: 5.182

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