Evidence map›Paper›PMID 42247579›Full record

ArticleJournal of medicinal chemistry2026

Development and Biological Characterization of Fluorescent Dynorphins for the Visualization of Kappa Opioid Receptors.

Predrag Kalaba, Monika Perisic Böhm, Filip D̵ikić, Nataša Tomašević, Ruth Drdla-Schutting, Simon Hasinger, Dylan M Ines, Alexandra Wolf, Mireia Belil-Catalina, Sharon D Bryant and 4 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Predrag KalabaInstitute of Biological Chemistry, Faculty of Chemistry, University of Vienna, Vienna 1090, Austria.ORCID 0000-0003-0480-2337
Monika Perisic BöhmInstitute of Biological Chemistry, Faculty of Chemistry, University of Vienna, Vienna 1090, Austria.ORCID 0009-0005-3413-1310
Filip D̵ikićDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna 1090, Austria.
Nataša TomaševićInstitute of Pharmacology, Center for Pharmacology and Physiology, Medical University of Vienna, Vienna 1090, Austria.
Ruth Drdla-SchuttingDepartment of Neurophysiology, Center for Brain Research, Medical University of Vienna, Vienna 1090, Austria.
Simon HasingerInstitute of Pharmacology, Center for Pharmacology and Physiology, Medical University of Vienna, Vienna 1090, Austria.ORCID 0000-0002-6356-5442
Dylan M InesInstitute of Biological Chemistry, Faculty of Chemistry, University of Vienna, Vienna 1090, Austria.
Alexandra WolfDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna 1090, Austria.
Mireia Belil-CatalinaInstitute of Biological Chemistry, Faculty of Chemistry, University of Vienna, Vienna 1090, Austria.
Sharon D BryantInte:Ligand GmbH, Vienna 1070, Austria.
Mariana SpeteaDepartment of Pharmaceutical Chemistry, Institute of Pharmacy and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innsbruck 6020, Austria.ORCID 0000-0002-2379-5358
Christian W GruberInstitute of Pharmacology, Center for Pharmacology and Physiology, Medical University of Vienna, Vienna 1090, Austria.ORCID 0000-0001-6060-7048
Markus MuttenthalerInstitute of Biological Chemistry, Faculty of Chemistry, University of Vienna, Vienna 1090, Austria.ORCID 0000-0003-1996-4646
Erik KeimpemaDepartment of Molecular Neurosciences, Center for Brain Research, Medical University of Vienna, Vienna 1090, Austria.ORCID 0000-0002-7555-6762

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The kappa opioid receptor (KOR) controls a wide variety of biological processes, including pain and reward responses. However, its precise spatiotemporal location remains poorly understood due to limited selective molecular tools. We addressed this problem by developing dynorphin-based fluorescent KOR tracers that are selective for KOR over its closely related mu- and delta-family members (MOR, DOR). Our lead tracer is highly selective for KOR (>360-fold over MOR and DOR) and can effectively visualize KORs in the somatodendritic compartment of cultured primary cortical neurons, as well as in superficial layer neurons of the spinal cord dorsal horn. Furthermore, it blocked the KOR agonist U50,488-induced reduction in the excitatory drive of spinal cord neurons. The developed tracer can also be immobilized with paraformaldehyde and used for

Indexed as

DynorphinsFluorescent DyesReceptors, Opioid, kappaAnimalsCells, CulturedHumansNeuronsRatsSpinal CordDynorphinsFluorescent DyesReceptors, Opioid, kappa

Identifiers

PMID42247579
PMCPMC13312453

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Registered trials

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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 OpenQuestion graph.