Cocaine continues to be one of the most commonly abused illicit drugs in the US. Pre-clinical literature suggests that targeting glucagon-like peptide-1 receptors (GLP-1Rs) in the brain may represent a novel approach to treating cocaine use disorder. Specifically, GLP-1R agonists, which are FDA-approved for treating diabetes and obesity, have been shown to reduce voluntary drug taking and seeking in preclinical models of cocaine use disorder. However, the exact neural circuits and cell types that mediate the suppressive effects of GLP-1R agonists on cocaine-seeking behaviour are mostly unknown.
New research from the University of Pennsylvania School of Nursing (Penn Nursing) has discovered that GLP-1Rs are expressed on specific cell types and neural circuits in the brain that reduce cocaine-seeking behaviour. Investigators have also discovered that GLP-1Rs are expressed primarily on GABAergic neurons in the hindbrain and that the efficacy of the GLP-1R agonist exendin-4 to reduce cocaine-seeking depends, in part, on activation of these GABA circuits.
Moreover, activating these endogenous anti-craving circuits in the brain using viral-mediated gene delivery methods was sufficient to reduce cocaine-seeking behaviour. These findings highlight GLP-1R-expressing anti-craving circuits in the brain that could serve as potential targets to reduce cocaine craving-induced relapse. The findings are published in the journal Molecular Psychiatry.
‘Overall, the translational implications of these findings are profound in that they support GLP-1R-focused therapeutic approaches for the treatment of cocaine craving and relapse,’ says lead investigator Heath Schmidt, PhD, associate professor of Nursing at Penn Nursing.
Disclaimer: Psychreg is mainly for information purposes only. Materials on this website are not intended to be a substitute for professional advice, diagnosis, medical treatment, or therapy. Never disregard professional psychological or medical advice nor delay in seeking professional advice or treatment because of something you have read on this website. Read our full disclaimer here.