JN Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 63: 473-490, 1990;
0022-3077/90 $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 Bernard, J. F.
Right arrow Articles by Besson, J. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bernard, J. F.
Right arrow Articles by Besson, J. M.

Journal of Neurophysiology, Vol 63, Issue 3 473-490, Copyright © 1990 by APS


ARTICLES

The spino(trigemino)pontoamygdaloid pathway: electrophysiological evidence for an involvement in pain processes

J. F. Bernard and J. M. Besson
Unite de Recherches de Physiopharmacologie du Systeme Nerveux, Institut National de la Sante et de la Recherche Medicale, U161, Paris, France.

1. Neurons were recorded in the parabrachial (PB) area, located in the dorsolateral region of the pons (with the use of extracellular micropipette), in the anesthetized rat. Parabrachioamygdaloid (PA) neurons (n = 67) were antidromically identified after stimulation in the centralis nucleus of the amygdala (Ce). The axons of these neurons exhibit a very slow conduction velocity, between 0.26 and 1.1 m/s, i.e., in the unmyelinated range. 2. These PA neurons were located in a restricted region of the PB area: the subnuclei external lateral (PBel) and external medial (PBem). A relative somatotopic organization was found in this region. 3. These units were separated into two groups: 1) a group of nociceptive-specific (NS) neurons (69%), which responded exclusively to noxious stimuli, and 2) a group of nonresponsive (NR) neurons (31%). 4. The NS neurons exhibited low or lacked spontaneous activity. They responded exclusively to mechanical (pinch or squeeze) and/or thermal (waterbath or waterjet greater than 44 degrees C) noxious stimuli with a marked and sustained activation with a rapid onset and generally without afterdischarge. Noxious thermal stimuli generally induced a stronger response than the noxious mechanical stimuli. These neurons exhibited a clear capacity to encode thermal stimuli in the noxious range: 1) the stimulus-response function was always positive and monotonic; 2) the slope of the curve progressively increased up to a maximum where it was very steep, then the steepness of the slope decreased close to the maximum response; and 3) the mean threshold was 44.1 +/- 2 degrees C, and the point of steepest slope of the mean curve was around 47 degrees C. 5. The excitatory receptive fields of the NS neurons were large in the majority (70%) of the cases and included several areas of the body. A more marked activation was often obtained from stimuli applied to one part of the body, denoted as the preferential receptive field (PRF). In the other cases (30%), the excitatory receptive field was relatively small (SRF) and restricted to one part of the body (the tail, a paw, a hemiface, or the tongue). Both the PRF and SRF were more often located on the contralateral side. In addition, noxious stimuli applied outside the excitatory receptive field were found to strongly inhibit the responses of NS neurons. 6. All the NS neurons responded to intense transcutaneous electrical stimulation applied to the PRF or SRF with two peaks of activation.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
Cereb CortexHome page
A. Hennenlotter, C. Dresel, F. Castrop, A. O. Ceballos Baumann, A. M. Wohlschlager, and B. Haslinger
The Link between Facial Feedback and Neural Activity within Central Circuitries of Emotion--New Insights from Botulinum Toxin-Induced Denervation of Frown Muscles
Cereb Cortex, June 17, 2008; (2008) bhn104v1.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
Y. Carrasquillo and R. W. Gereau IV
Activation of the Extracellular Signal-Regulated Kinase in the Amygdala Modulates Pain Perception
J. Neurosci., February 14, 2007; 27(7): 1543 - 1551.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. E. Wilensky, G. E. Schafe, M. P. Kristensen, and J. E. LeDoux
Rethinking the Fear Circuit: The Central Nucleus of the Amygdala Is Required for the Acquisition, Consolidation, and Expression of Pavlovian Fear Conditioning
J. Neurosci., November 29, 2006; 26(48): 12387 - 12396.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
T. F. Finnegan, S.-R. Chen, and H.-L. Pan
{micro} Opioid Receptor Activation Inhibits GABAergic Inputs to Basolateral Amygdala Neurons Through Kv1.1/1.2 Channels
J Neurophysiol, April 1, 2006; 95(4): 2032 - 2041.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
P. Boscan, M. Dutschmann, H. Herbert, and J. F. R. Paton
Neurokininergic Mechanism within the Lateral Crescent Nucleus of the Parabrachial Complex Participates in the Heart-Rate Response to Nociception
J. Neurosci., February 9, 2005; 25(6): 1412 - 1420.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
T. F. Finnegan, S.-R. Chen, and H.-L. Pan
Effect of the {micro} Opioid on Excitatory and Inhibitory Synaptic Inputs to Periaqueductal Gray-Projecting Neurons in the Amygdala
J. Pharmacol. Exp. Ther., February 1, 2005; 312(2): 441 - 448.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
D. Pare, G. J. Quirk, and J. E. Ledoux
New Vistas on Amygdala Networks in Conditioned Fear
J Neurophysiol, July 1, 2004; 92(1): 1 - 9.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. Gauriau and J.-F. Bernard
Posterior Triangular Thalamic Neurons Convey Nociceptive Messages to the Secondary Somatosensory and Insular Cortices in the Rat
J. Neurosci., January 21, 2004; 24(3): 752 - 761.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
L. Becerra, M. Iadarola, and D. Borsook
CNS Activation by Noxious Heat to the Hand or Foot: Site-Dependent Delay in Sensory But Not Emotion Circuitry
J Neurophysiol, January 1, 2004; 91(1): 533 - 541.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
V. Neugebauer and W. Li
Differential Sensitization of Amygdala Neurons to Afferent Inputs in a Model of Arthritic Pain
J Neurophysiol, February 1, 2003; 89(2): 716 - 727.
[Abstract] [Full Text] [PDF]


Home page
Mol. Interv.Home page
D. D. Price
Central Neural Mechanisms that Interrelate Sensory and Affective Dimensions of Pain
Mol. Interv., October 1, 2002; 2(6): 392 - 403.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
V. Neugebauer and W. Li
Processing of Nociceptive Mechanical and Thermal Information in Central Amygdala Neurons With Knee-Joint Input
J Neurophysiol, January 1, 2002; 87(1): 103 - 112.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Roentgenol.Home page
R. K. Fulbright, C. J. Troche, P. Skudlarski, J. C. Gore, and B. E. Wexler
Functional MR Imaging of Regional Brain Activation Associated with the Affective Experience of Pain
Am. J. Roentgenol., November 1, 2001; 177(5): 1205 - 1210.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. Bourgeais, L. Monconduit, L. Villanueva, and J.-F. Bernard
Parabrachial Internal Lateral Neurons Convey Nociceptive Messages from the Deep Laminas of the Dorsal Horn to the Intralaminar Thalamus
J. Neurosci., March 15, 2001; 21(6): 2159 - 2165.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
H. Bester, C. De Felipe, and S. P. Hunt
The NK1 Receptor Is Essential for the Full Expression of Noxious Inhibitory Controls in the Mouse
J. Neurosci., February 1, 2001; 21(3): 1039 - 1046.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
A. Malick, R. M. Strassman, and R. Burstein
Trigeminohypothalamic and Reticulohypothalamic Tract Neurons in the Upper Cervical Spinal Cord and Caudal Medulla of the Rat
J Neurophysiol, October 1, 2000; 84(4): 2078 - 2112.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
D. D. Price
Psychological and Neural Mechanisms of the Affective Dimension of Pain
Science, June 9, 2000; 288(5472): 1769 - 1772.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H. Bester, V. Chapman, J.-M. Besson, and J.-F. Bernard
Physiological Properties of the Lamina I Spinoparabrachial Neurons in the Rat
J Neurophysiol, April 1, 2000; 83(4): 2239 - 2259.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
M. Rousseaux, F. Cassim, B. Bayle, and E. Laureau
Analysis of the Perception of and Reactivity to Pain and Heat in Patients With Wallenberg Syndrome and Severe Spinothalamic Tract Dysfunction
Stroke, October 1, 1999; 30(10): 2223 - 2229.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
C. Shi and M. Davis
Pain Pathways Involved in Fear Conditioning Measured with Fear-Potentiated Startle: Lesion Studies
J. Neurosci., January 1, 1999; 19(1): 420 - 430.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
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]


Home page
J. Neurophysiol.Home page
C. B. Halsell and S. P. Travers
Anterior and Posterior Oral Cavity Responsive Neurons Are Differentially Distributed Among Parabrachial Subnuclei in Rat
J Neurophysiol, August 1, 1997; 78(2): 920 - 938.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. Jasmin, A. R. Burkey, J. P. Card, and A. I. Basbaum
Transneuronal Labeling of a Nociceptive Pathway, the Spino-(Trigemino-)Parabrachio-Amygdaloid, in the Rat
J. Neurosci., May 15, 1997; 17(10): 3751 - 3765.
[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