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The Journal of Neuroscience, January 1, 1998, 18(1):451-457
Hypoactivity of the Spinal Cannabinoid System Results in
NMDA-Dependent Hyperalgesia
Jennelle Durnett
Richardson1,
Lin
Aanonsen3, and
Kenneth M.
Hargreaves1, 2
Departments of 1 Pharmacology and
2 Restorative Sciences, University of Minnesota,
Minneapolis, Minnesota 55455, and 3 Department of Biology,
Macalester College, St. Paul, Minnesota 55105
Cannabinoids, such as 9-THC, are capable of
inhibiting nociception, i.e., pain transmission, at least in part, by
interacting with spinal Gi/Go-coupled
cannabinoid receptors. What is not known, however, is the
antinociceptive role of endogenous spinal cannabinoids. If endogenous cannabinoids modulate basal nociceptive thresholds, then
alterations in this system could be involved in the etiology of certain
pain states. In this report we provide evidence for tonic modulation of
basal thermal nociceptive thresholds by the spinal cannabinoid system.
Administration of oligonucleotides directed against CB1
cannabinoid receptor mRNA significantly reduced spinal cannabinoid
binding sites and produced significant hyperalgesia when compared with
a randomer oligonucleotide control. A second method used to reduce
activity of the spinal cannabinoid receptor was intrathecal
administration of the cannabinoid receptor antagonist SR 141716A. SR
141716A evoked thermal hyperalgesia with an ED50 of 0.0012 fmol. The SR 141716A-induced hyperalgesia was dose-dependently blocked
by the administration of D-AP-5 or MK-801, two antagonists to the NMDA receptor. These results indicate that there is tonic activation of the spinal cannabinoid system under normal conditions. Furthermore, hypoactivity of the spinal cannabinoid system results in
an NMDA-dependent hyperalgesia and thus may participate in the etiology
of certain chronic pain states.
Key words:
endogenous cannabinoid; SR 141716A; glutamate; NMDA; hyperalgesia; nociceptive threshold; tonic; spinal cord
Copyright © 1998 Society for Neuroscience 0270-6474/98/181451-07$05.00/0
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