ArticleExperimental brain research2025
Supraspinal kappa-opioid receptors: new therapeutic strategies for pain, pruritus, and negative emotions.
Article in Experimental brain research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- κ-Opioid Receptor Agonists as Robust Pain-Modulating Agents: Mechanisms and Therapeutic Potential in Pain Modulation.Journal of clinical medicine · 2025Review
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Authors and funding
9 authors.
Funding
Abstract
Research on kappa-opioid receptor (KOR) regulation of pain and itching has focused primarily on spinal and peripheral levels. However, the role of central KOR in this process, as well as the mechanisms exacerbating negative emotional responses to pain and itching, remains unknown. Therefore, this study aimed to utilize the advantages of intracerebroventricular (i.c.v.) administration of U50488H to explore supraspinal KOR activation on pain, itching, and negative emotions. U50488H, a prototypical KOR agonist, was administered i.c.v., with physiological saline as the control. The Hargreaves test and intradermal injection of histamine and chloroquine were conducted to assess thermal pain and itch behavior, respectively. The elevated plus maze (EPM), open field test (OFT), and tail suspension test (TST) were performed to evaluate negative emotions. i.c.v. administration of U50488H increased thermal pain latencies, reduced scratching behavior, and decreased locomotor activity in the central zone of the OFT and in the open arms of the EPM, while increasing immobility in the TST. i.c.v. pretreatment with the KOR antagonist nor-Binaltorphimine dihydrochloride reversed all of the above behaviors. In conclusion, central administration of U50488H can exhibit analgesic and antipruritic effects while also inducing negative emotional responses. Our results highlight the potential of supraspinal KOR as a promising therapeutic target in the combined treatment of pain, pruritus, and negative emotions.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.