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The delta opioid receptor is a Gi-protein-coupled receptor (GPCR) with a broad expression pattern both in the central nervous system and the body. The receptor has been investigated as a potential target for a multitude of significant diseases including migraine, alcohol use disorder, ischemia, and neurodegenerative diseases. Despite multiple attempts, delta opioid receptor-selective molecules have not been translated into the clinic. Yet, the therapeutic promise of the delta opioid receptor remains and thus there is a need to identify novel delta opioid receptor ligands to be optimized and selected for clinical trials. Here, we highlight recent developments involving the delta opioid receptor, the closely related mu and kappa opioid receptors, and in the broader area of the GPCR drug discovery research. We focus on the validity and utility of the available delta opioid receptor structures. We also discuss the increased ability to perform ultra-large-scale docking studies on GPCRs, the rise in high-resolution cryo-EM structures, and the increased prevalence of machine learning and artificial intelligence in drug discovery. Overall, we pose that there are multiple opportunities to enable in silico drug discovery at the delta opioid receptor to identify novel delta opioid modulators potentially with unique pharmacological properties, such as biased signaling.
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http://dx.doi.org/10.3390/ph15070873 | DOI Listing |
Open Life Sci
September 2025
Physiology and Physiopathology Team, Faculty of Sciences, Genomic of Human Pathologies Research Centre, Mohammed V University in Rabat, Rabat, Morocco.
The legalization of cannabis for industrial and medicinal purposes has significantly expanded worldwide. This study delves into the analgesic potential toxicity study of chloroformic extract from the Moroccan L. () cultivar, Khardala (KH extract).
View Article and Find Full Text PDFBioorg Med Chem
August 2025
Department of Medicinal Chemistry, School of Pharmacy, Fudan University, No. 826 Zhangheng Road, Shanghai 201203, China. Electronic address:
The delta opioid receptor (DOR) is a promising target for developing analgesics with fewer side effects compared to mu opioid receptor (MOR) agonists. However, non-peptidyl DOR-selective agonists remain limited. Using the "message-address" concept in opioid ligand design, we designed and synthesized a series of para-substituted N-cyclopropylmethyl-7α-phenyl-6,14-endoetheno-tetrahydronorthebaines to explore their binding affinity and selectivity for DOR over MOR and kappa opioid receptor (KOR).
View Article and Find Full Text PDFCurr Res Pharmacol Drug Discov
August 2025
Department of Drug and Health Sciences, University of Catania, Catania, Italy.
In neuropathic pain (NP), a dysregulation of glial functions in the central and peripheral nervous systems has been described, and the balance between pro-inflammatory and anti-inflammatory mediators is lost in the transition from acute to chronic pain. This raises the possibility to resolve pain via the induction of anti-inflammatory cytokines that have a protective role against neuroinflammatory events. Transforming growth factor-β1 (TGF-β1), an anti-inflammatory cytokine is able to counteract the development of chronic NP.
View Article and Find Full Text PDFIr J Med Sci
August 2025
Department of Anesthesiology and Reanimation, Istanbul Haseki Training and Research Hospital, Ugur Mumcu, Sultangazi, Istanbul, Turkey.
Background: Pain management in intensive care is challenging due to multiple potential causes. The physiological consequences of uncontrolled pain can adversely affect treatment. Reliable, objective pain monitoring may therefore improve care.
View Article and Find Full Text PDFJ Pharmacol Exp Ther
July 2025
Department of Pharmacology, University of Texas HealthScience Center at San Antonio, San Antonio, Texas; Addiction Research, Treatment & Training Center of Excellence, University of Texas HealthScience Center at San Antonio, San Antonio, Texas; Department of Psychiatry, University of Texas Health
The mu-opioid receptor agonists methadone and buprenorphine are effective for treating opioid use disorder (OUD); however, both drugs are diverted and misused and withdrawal signs can emerge when treatment is tapered or discontinued. Mu-opioid and cannabinoid type 1 receptors are colocalized in several brain regions, and cannabinoids have been proposed as potential treatments for opioid withdrawal. This study tested Δ-tetrahydrocannabinol (THC) and cannabidiol (CBD), alone and in mixtures, for treating the behavioral and physiological signs of morphine withdrawal in 3 male rhesus monkeys.
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