Sustained cannabinoid agonist treatment augments CGRP release in a PKA-dependent manner.

Abstract

Studies have shown that sustained cannabinoid treatment increases the sensitivity to painful heat stimuli (thermal hyperalgesia) and innocuous mechanical stimuli (tactile allodynia). It has been suggested that augmented release of pain neurotransmitters (such as calcitonin gene-related peptide, CGRP) might be responsible for this abnormal pain sensitization. We hypothesize that intracellular adaptations upon sustained cannabinoid treatment causes augmented release of CGRP from primary nociceptors leading to increased pain sensitivity. We show that sustained (24 h) cannabinoid agonist [(+)WIN 55,212-2] treatment of 7-day-old neonatal rat dorsal root ganglion neurons significantly augments basal CGRP release from these cells in a protein kinase A-dependent manner. Our results indicate that these intracellular compensatory adaptations may play a crucial trigger role in further neuronal system adaptations for modulation of pain.

• Authors: Suneeta Tumati, Henry I Yamamura, Paul A St John, Todd W Vanderah, William R Roeske, Eva V Varga
• Journal: Neuroreport (Neuroreport) Vol. 20 Issue 8 Pg. 815-9 (May 27 2009) ISSN: 1473-558X [Electronic] England
• PMID: 19387418 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Benzoxazines
• Cannabinoids
• Morpholines
• Naphthalenes
• (3R)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanone
• Cyclic AMP-Dependent Protein Kinases
• Calcitonin Gene-Related Peptide

Topics

• Animals
• Animals, Newborn
• Benzoxazines (pharmacology)
• Calcitonin Gene-Related Peptide (metabolism)
• Cannabinoids (pharmacology)
• Cells, Cultured
• Cyclic AMP-Dependent Protein Kinases (physiology)
• Drug Administration Schedule
• Ganglia, Spinal (drug effects, metabolism)
• Hyperalgesia (metabolism, physiopathology)
• Morpholines (pharmacology)
• Naphthalenes (pharmacology)
• Nociceptors (drug effects, metabolism)
• Pain (metabolism, physiopathology)
• Pain Threshold (drug effects, physiology)
• Rats
• Rats, Sprague-Dawley
• Sensory Receptor Cells (drug effects, metabolism)
• Time Factors
• Up-Regulation (physiology)