|
|
||||||||
Journal of Neurophysiology, Vol 71, Issue 6 2430-2445, Copyright © 1994 by APS
ARTICLES |
C. Y. Chiang, J. W. Hu and B. J. Sessle
Department of Oral Physiology, Faculty of Dentistry, University of Toronto, Ontario, Canada.
1. The aim of this study was to test whether parabrachial area (PBA) stimulation exerts inhibitory influences on the spontaneous activity and responses evoked by skin and deep afferent inputs in trigeminal subnucleus caudalis (Vc) neurons, and to compare these effects with those of nucleus raphe magnus (NRM) stimulation. A total of 92 nonnociceptive and nociceptive Vc neurons was recorded in urethan/alpha-chloralose-anesthetized rats. Each neuron was functionally classified as low-threshold mechanoceptive (LTM), wide dynamic range (WDR), nociceptive-specific (NS), nociceptive convergent with both skin and deep inputs (S+D), or deep nociceptive (D); the LTM neurons could be subdivided as rapidly adapting (RA) or slowly adapting (SA). Conditioning stimulation was applied to histologically verified sites in PBA and NRM. 2. The spontaneous or evoked activity of all classes of neurons could be inhibited by PBA as well as by NRM stimulation, but generally the incidence and magnitude of inhibition were lower for the LTM neurons. Occasionally, facilitation of neuronal activity was also produced by PBA and NRM stimulation. 3. The spontaneous activity of 11 LTM neurons (6 RA, 5 SA), 13 nociceptive neurons (6 WDR, 7 NS), and 5 D neurons was tested with stimulation of PBA or NRM or both. LTM spontaneous activity was more significantly inhibited by NRM stimulation than by PBA stimulation, whereas both NRM and PBA stimulation had similar and significant inhibitory effects on NS, WDR, and D neurons. 4. The evoked nonnociceptive responses of 28 LTM neurons (16 RA, 12 SA) and of 6 WDR neurons were also tested with stimulation of PBA or NRM or both. The magnitudes of inhibition of the responses produced by PBA conditioning stimulation were statistically significantly less than those induced by NRM conditioning stimulation. 5. The cutaneous and deep nociceptive responses of cutaneous nociceptive neurons (9 NS, 19 WDR) and seven D neurons, respectively, were also tested with PBA and NRM stimulation. There was a significant difference in potency between PBA- and NRM-induced inhibition, but no difference in the magnitude of inhibitory effects among NS, WDR, and D neurons. For both PBA and NRM conditioning stimulation, graded increases in intensities of stimulation produced linear increases in inhibitory effects on nociceptive responses; an increase in stimulation frequency from 5 to 400 Hz also produced increases in inhibition of the nociceptive responses. 6. In five S+D nociceptive convergent neurons, the responses elicited by deep inputs were more powerfully inhibited by PBA stimulation than those elicited by cutaneous inputs.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
R. Benoliel, J. Epstein, E. Eliav, R. Jurevic, and S. Elad Orofacial Pain in Cancer: Part I--Mechanisms J. Dent. Res., June 1, 2007; 86(6): 491 - 505. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Foo and P. Mason Sensory suppression during feeding PNAS, November 15, 2005; 102(46): 16865 - 16869. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Mason DECONSTRUCTING ENDOGENOUS PAIN MODULATIONS J Neurophysiol, September 1, 2005; 94(3): 1659 - 1663. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Y. Chiang, S. Zhang, Y. F. Xie, J. W. Hu, J. O. Dostrovsky, M. W. Salter, and B. J. Sessle Endogenous ATP Involvement in Mustard-Oil-Induced Central Sensitization in Trigeminal Subnucleus Caudalis (Medullary Dorsal Horn) J Neurophysiol, September 1, 2005; 94(3): 1751 - 1760. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Belforte and J. H. Pazo Striatal Inhibition of Nociceptive Responses Evoked in Trigeminal Sensory Neurons by Tooth Pulp Stimulation J Neurophysiol, March 1, 2005; 93(3): 1730 - 1741. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Hu, C. Y. Chiang, J. W. Hu, J. O. Dostrovsky, and B. J. Sessle P2X Receptors in Trigeminal Subnucleus Caudalis Modulate Central Sensitization in Trigeminal Subnucleus Oralis J Neurophysiol, October 1, 2002; 88(4): 1614 - 1624. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Y. Chiang, B. Hu, J. W. Hu, J. O. Dostrovsky, and B. J. Sessle Central Sensitization of Nociceptive Neurons in Trigeminal Subnucleus Oralis Depends on Integrity of Subnucleus Caudalis J Neurophysiol, July 1, 2002; 88(1): 256 - 264. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. Park, C. Y. Chiang, J. W. Hu, and B. J. Sessle Neuroplasticity Induced by Tooth Pulp Stimulation in Trigeminal Subnucleus Oralis Involves NMDA Receptor Mechanisms J Neurophysiol, May 1, 2001; 85(5): 1836 - 1846. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
K. Iwata, A. Tashiro, Y. Tsuboi, T. Imai, R. Sumino, T. Morimoto, R. Dubner, and K. Ren Medullary Dorsal Horn Neuronal Activity in Rats with Persistent Temporomandibular Joint and Perioral Inflammation J Neurophysiol, September 1, 1999; 82(3): 1244 - 1253. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Y. Chiang, S. J. Park, C. L. Kwan, J. W. Hu, and B. J. Sessle NMDA Receptor Mechanisms Contribute to Neuroplasticity Induced in Caudalis Nociceptive Neurons by Tooth Pulp Stimulation J Neurophysiol, November 1, 1998; 80(5): 2621 - 2631. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
I. D. Meng, J. W. Hu, and D. A. Bereiter Differential Effects of Morphine on Corneal-Responsive Neurons in Rostral Versus Caudal Regions of Spinal Trigeminal Nucleus in the Rat J Neurophysiol, May 1, 1998; 79(5): 2593 - 2602. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Y. Chiang, J. W. Hu, and B. J. Sessle NMDA Receptor Involvement in Neuroplastic Changes Induced By Neonatal Capsaicin Treatment in Trigeminal Nociceptive Neurons J Neurophysiol, November 1, 1997; 78(5): 2799 - 2803. [Abstract] [Full Text] [PDF] |
||||
![]() |
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 |