Effects of inflammatory pain on CB1 receptor in the midbrain periaqueductal gray

Introduction:The periaqueductal gray (PAG) mediates the antinociceptive properties of analgesics, including opioids and cannabinoids. Administration of either opioids or cannabinoids into the PAG induces antinociception. However, most studies characterizing the antinociceptive properties of cannabinoids in the PAG have been conducted in naive animals. Few studies have reported on the role of CB1 receptors in the PAG during conditions which would prompt the administration of analgesics, namely, during pain states.Objectives:To examine inflammatory pain-induced changes in CB1 receptor expression and function in the midbrain periaqueductal gray.Methods:In this study, we used the Complete Freund Adjuvant model to characterize CB1 receptor expression and G-protein coupling during persistent inflammatory pain.Results:Inflammatory pain induced an upregulation in the expression of synaptic CB1 receptors in the PAG. Despite this pain-induced change in CB1 expression, there was no corresponding upregulation of CB1 mRNA after the induction of inflammatory pain, suggesting a pain-induced recruitment of CB1 receptors to the synaptic sites within PAG neurons or increased coupling efficiency between the receptor and effector systems. Inflammatory pain also enhanced ventrolateral PAG CB1 receptor activity, as there was an increase in CP55,940-stimulated G-protein activation compared with pain-naive control animals.Conclusion:These findings complement a growing body of evidence which demonstrate pain-induced changes in brain regions that are responsible for both the analgesic and rewarding properties of analgesic pharmacotherapies. Because much of our understanding of the pharmacology of cannabinoids is based on studies which use largely pain-naive male animals, this work fills in important gaps in the knowledge base by incorporating pain-induced adaptations and cannabinoid pharmacology in females.

Automated summary

This study investigated the changes in CB1 receptor expression and G-protein coupling in the periaqueductal gray during persistent inflammatory pain. The results showed an upregulation of synaptic CB1 receptors and enhanced CB1 receptor activity in the ventrolateral PAG during inflammatory pain. These findings contribute to a better understanding of pain-induced adaptations and cannabinoid pharmacology in both male and female animals.