WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
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 Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (68)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Manning, B. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Manning, B. H.

 Previous Article  |  Next Article 

The Journal of Neuroscience, November 15, 1998, 18(22):9453-9470

A Lateralized Deficit in Morphine Antinociception after Unilateral Inactivation of the Central Amygdala

Barton H. Manning

Department of Neurology, University of California, San Francisco, San Francisco, California 94143-0114

The amygdala is a forebrain region that is receiving increasing attention as a modulator of pain sensation. The amygdala contributes to antinociception elicited by both psychological factors (e.g., fear) and exogenous opioid agonists. Unlike the midbrain periaqueductal gray matter (PAG) or rostral ventromedial medulla, the amygdala is a pain-modulating region that has clear bilateral representation in the brain, making it possible to determine whether pain-modulating effects of this region are lateralized with respect to the peripheral origin of noxious stimulation. Unilateral inactivation of the central nucleus of the amygdala (Ce) plus adjacent portions of the basolateral amygdaloid complex (with either the excitotoxin NMDA or the GABAA agonist muscimol) reduced the ability of morphine to suppress prolonged, formalin-induced pain derived from the hindpaw ipsilateral, but not contralateral, to the inactivated region. This effect was evident regardless of the nociceptive scoring method used (weighted scores or flinch-frequency method) and was not accompanied by a concurrent reduction in morphine-induced hyperlocomotion. Unilateral lesions restricted to the basolateral amygdaloid complex (i.e., not including the Ce) did not reduce the ability of morphine to suppress formalin-induced pain derived from either hindpaw. The results constitute the first report of a lateralized deficit in opioid antinociception after unilateral inactivation of a specific brain area and show the first clear neuroanatomical dissociation between antinociceptive and motor effects of systemically administered morphine in the rat. The amygdala appears to modulate nociceptive signals entering the ipsilateral spinal dorsal horn, probably through monosynaptic connections with ipsilateral portions of the PAG.

Key words: pain; antinociception; analgesia; morphine; opioid; formalin test; amygdala; central nucleus; lesion; NMDA; muscimol; inactivation; fear; defense reaction


Copyright © 1998 Society for Neuroscience  0270-6474/98/18229453-18$05.00/0


This article has been cited by other articles:


Home page
Arch Gen PsychiatryHome page
D. J. Scott, C. S. Stohler, C. M. Egnatuk, H. Wang, R. A. Koeppe, and J.-K. Zubieta
Placebo and Nocebo Effects Are Defined by Opposite Opioid and Dopaminergic Responses
Arch Gen Psychiatry, February 1, 2008; 65(2): 220 - 231.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. E. Harris, D. J. Clauw, D. J. Scott, S. A. McLean, R. H. Gracely, and J.-K. Zubieta
Decreased Central {micro}-Opioid Receptor Availability in Fibromyalgia
J. Neurosci., September 12, 2007; 27(37): 10000 - 10006.
[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
Arch Gen PsychiatryHome page
E. Geuze, H. G. M. Westenberg, A. Jochims, C. S. de Kloet, M. Bohus, E. Vermetten, and C. Schmahl
Altered Pain Processing in Veterans With Posttraumatic Stress Disorder
Arch Gen Psychiatry, January 1, 2007; 64(1): 76 - 85.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
L. Becerra, K. Harter, R. G. Gonzalez, and D. Borsook
Functional magnetic resonance imaging measures of the effects of morphine on central nervous system circuitry in opioid-naive healthy volunteers.
Anesth. Analg., July 1, 2006; 103(1): 208 - 216.
[Abstract] [Full Text] [PDF]


Home page
Arch Gen PsychiatryHome page
C. Schmahl, M. Bohus, F. Esposito, R.-D. Treede, F. Di Salle, W. Greffrath, P. Ludaescher, A. Jochims, K. Lieb, K. Scheffler, et al.
Neural correlates of antinociception in borderline personality disorder.
Arch Gen Psychiatry, June 1, 2006; 63(6): 659 - 666.
[Abstract] [Full Text] [PDF]


Home page
ptjournalHome page
S. Jorge, C. A Parada, S. H Ferreira, and C. H Tambeli
Interferential Therapy Produces Antinociception During Application in Various Models of Inflammatory Pain
Physical Therapy, June 1, 2006; 86(6): 800 - 808.
[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. 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
NeuroscientistHome page
V. Neugebauer, W. Li, G. C. Bird, and J. S. Han
The Amygdala and Persistent Pain
Neuroscientist, June 1, 2004; 10(3): 221 - 234.
[Abstract] [PDF]


Home page
J. Neurophysiol.Home page
W. Li and V. Neugebauer
Differential Roles of mGluR1 and mGluR5 in Brief and Prolonged Nociceptive Processing in Central Amygdala Neurons
J Neurophysiol, January 1, 2004; 91(1): 13 - 24.
[Abstract] [Full Text]


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
J. Neurosci.Home page
V. Neugebauer, W. Li, G. C. Bird, G. Bhave, and R. W. Gereau IV
Synaptic Plasticity in the Amygdala in a Model of Arthritic Pain: Differential Roles of Metabotropic Glutamate Receptors 1 and 5
J. Neurosci., January 1, 2003; 23(1): 52 - 63.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. E. Cain, B. S. Kapp, and C. B. Puryear
The Contribution of the Amygdala to Conditioned Thalamic Arousal
J. Neurosci., December 15, 2002; 22(24): 11026 - 11034.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J.-K. Zubieta, Y. R. Smith, J. A. Bueller, Y. Xu, M. R. Kilbourn, D. M. Jewett, C. R. Meyer, R. A. Koeppe, and C. S. Stohler
{micro}-Opioid Receptor-Mediated Antinociceptive Responses Differ in Men and Women
J. Neurosci., June 15, 2002; 22(12): 5100 - 5107.
[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
J. Neurosci.Home page
B. H. Manning, N. M. Merin, I. D. Meng, and D. G. Amaral
Reduction in Opioid- and Cannabinoid-Induced Antinociception in Rhesus Monkeys after Bilateral Lesions of the Amygdaloid Complex
J. Neurosci., October 15, 2001; 21(20): 8238 - 8246.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
J.-K. Zubieta, Y. R. Smith, J. A. Bueller, Y. Xu, M. R. Kilbourn, D. M. Jewett, C. R. Meyer, R. A. Koeppe, and C. S. Stohler
Regional Mu Opioid Receptor Regulation of Sensory and Affective Dimensions of Pain
Science, July 13, 2001; 293(5528): 311 - 315.
[Abstract] [Full Text]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. P. Johansen, H. L. Fields, and B. H. Manning
The affective component of pain in rodents: Direct evidence for a contribution of the anterior cingulate cortex
PNAS, June 12, 2001; (2001) 141218998.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. P. Johansen, H. L. Fields, and B. H. Manning
The affective component of pain in rodents: Direct evidence for a contribution of the anterior cingulate cortex
PNAS, July 3, 2001; 98(14): 8077 - 8082.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-