HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Dynorphin-independent spinal cannabinoid antinociception.

Abstract
Spinal antinociception produced by delta 9-tetrahydro-cannabinol (Delta(9)-THC) and other cannabinoid agonists has been suggested to be mediated by the release of dynorphin acting at the kappa opioid receptor. Alternatively, as cannabinoid receptors are distributed appropriately in the pain transmission pathway, cannabinoid agonists might act directly at the spinal level to inhibit nociception, without requiring dynorphin release. Here, these possibilities were explored using mice with a deletion of the gene encoding prodynorphin. Antinociceptive dose-response curves were constructed for spinal Delta(9)-THC and WIN 55,212-2 in prodynorphin knock-out mice and in wild-type littermates. WIN 55,212-2 and Delta(9)-THC were equipotent in the wild-type and prodynorphin knock-out mice. Spinal pretreatment with a kappa opioid receptor antagonist, nor-binaltorphimine (nor-BNI), did not alter the dose-response curves for either WIN 55,212-2 or Delta(9)-THC in prodynorphin knock-out and wild-type mice. However, the same dose of nor-BNI used blocked U50,488H-induced antinociception in both wild-type and prodynorphin knock-out mice, confirming kappa opioid receptor activity. Pretreatment with SR141716A, a cannabinoid receptor antagonist blocked the antinociceptive actions of both WIN 55,212-2 and Delta(9)-THC. These data support the conclusion that antinociception produced by spinal cannabinoids are likely to be mediated directly through activation of cannabinoid receptors without the requirement for dynorphin release or activation of kappa opioid receptors.
AuthorsL R Gardell, M H Ossipov, T W Vanderah, J Lai, F Porreca
JournalPain (Pain) Vol. 100 Issue 3 Pg. 243-248 (Dec 2002) ISSN: 0304-3959 [Print] United States
PMID12467995 (Publication Type: Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Analgesics
  • Analgesics, Non-Narcotic
  • Benzoxazines
  • Morpholines
  • Naphthalenes
  • norbinaltorphimine
  • (3R)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone
  • Naltrexone
  • Dynorphins
  • Dronabinol
Topics
  • Analgesics (administration & dosage)
  • Analgesics, Non-Narcotic (administration & dosage)
  • Animals
  • Benzoxazines
  • Dose-Response Relationship, Drug
  • Dronabinol (administration & dosage)
  • Dynorphins (deficiency)
  • Injections, Spinal
  • Male
  • Mice
  • Mice, Knockout
  • Morpholines (administration & dosage)
  • Naltrexone (analogs & derivatives)
  • Naphthalenes (administration & dosage)
  • Pain (drug therapy)
  • Pain Measurement (drug effects)
  • Reference Values
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Single-Blind Method
  • Species Specificity
  • Spinal Cord (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: