Opioid-galanin receptor heteromers differentiate the dopaminergic effects of morphine and methadone

Randal A. Serafini, Venetia Zachariou

Research output: Contribution to journalReview articlepeer-review

7 Scopus citations

Abstract

As the opioid addiction crisis reaches epidemic levels, the identification of opioid analgesics that lack abuse potential may provide a path to safer treatment of chronic pain. Preclinical studies have demonstrated that galanin affects physical dependence and rewarding actions associated with morphine. In the brain and periphery, galanin and opioids signal through their respective GPCRs, GalR1-3 and the μ-opioid receptor (MOR). In this issue of the JCI, Cai and collaborators reveal that heteromers between GalR1 and MOR in the rat ventral tegmental area attenuate the potency of methadone, but not other opioids, in stimulating the dopamine release that produces euphoria. These studies help us understand why some synthetic opioids, such as methadone, do not trigger the release of dopamine in the mesolimbic system but still possess strong analgesic properties.

Original languageEnglish
Pages (from-to)2653-2654
Number of pages2
JournalJournal of Clinical Investigation
Volume129
Issue number7
DOIs
StatePublished - 2019

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