Evidence map›Paper›PMID 28826482›Full record

ArticleeLife2017

Anti-nociceptive action of peripheral mu-opioid receptors by G-beta-gamma protein-mediated inhibition of TRPM3 channels.

Sandeep Dembla, Marc Behrendt, Florian Mohr, Christian Goecke, Julia Sondermann, Franziska M Schneider, Marlene Schmidt, Julia Stab, Raissa Enzeroth, Michael G Leitner and 11 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
8.1field-weighted citation impact, top 2% of its field
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

65 citing papers in PubMed, 116 citations in OpenAlex.

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  14. Navigating the Controversies: Role of TRPM Channels in Pain States.International journal of molecular sciences · 2024
    Review
  15. TRPM3, TRPM4, and TRPM5 as thermo-sensitive channels.The journal of physiological sciences : JPS · 2024
    Review
  16. Pathology of pain and its implications for therapeutic interventions.Signal transduction and targeted therapy · 2024
    Review
  17. Article
  18. TRPM channels in health and disease.Nature reviews. Nephrology · 2024
    Review
  19. Role of TRP Channels in Metabolism-Related Diseases.International journal of molecular sciences · 2024
    Review
  20. Article

5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 8 institutions in 3 countries.

Sandeep Dembla *Institut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Marc Behrendt *Institut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Florian MohrInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Christian GoeckeInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Julia SondermannMax-Planck-Institut für Experimentelle Medizin, Göttingen, Germany.
Franziska M SchneiderInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Marlene SchmidtInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Julia StabExperimentelle und Klinische Pharmakologie und Toxikologie, Universität des Saarlandes, Homburg, Germany.
Raissa EnzerothInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Michael G LeitnerInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Paulina Nuñez-BadinezDepartment of Neurophysiology, Center of Biomedicine and Medical Technology Mannheim, Medical Faculty Mannheim Heidelberg University, Mannheim, Germany.
Jochen SchwenkInstitute of Physiology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Bernd NürnbergAbteilung für Pharmakologie und Experimentelle Therapie, Institut für Experimentelle und Klinische Pharmakologie und Toxikologie, Universität Tübingen, Tübingen, Germany.
Alejandro CohenProteomics and Mass Spectrometry Core Facility, Life Sciences Research Institute, Dalhousie University, Halifax, Nova Scotia, Canada.
Stephan E PhilippExperimentelle und Klinische Pharmakologie und Toxikologie, Universität des Saarlandes, Homburg, Germany.
Wolfgang GreffrathDepartment of Neurophysiology, Center of Biomedicine and Medical Technology Mannheim, Medical Faculty Mannheim Heidelberg University, Mannheim, Germany.
Moritz BünemannInstitut für Pharmakologie und Klinische Pharmazie, Philipps-Universität Marburg, Marburg, Germany.
Dominik OliverInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.
Eleonora ZakharianDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, Peoria, United States.
Manuela SchmidtMax-Planck-Institut für Experimentelle Medizin, Göttingen, Germany.ORCID http://orcid.org/0000-0003-1972-3519
Johannes OberwinklerInstitut für Physiologie und Pathophysiologie, Philipps-Universität Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-8541-3626
Philipps University of Marburg · DEHeidelberg University · DESaarland University · DEDalhousie University · CAMax Planck Institute of Experimental Medicine · DEUniversity of Freiburg · DEUniversity of Illinois Urbana-Champaign · USUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Opioids, agonists of µ-opioid receptors (µORs), are the strongest pain killers clinically available. Their action includes a strong central component, which also causes important adverse effects. However, µORs are also found on the peripheral endings of nociceptors and their activation there produces meaningful analgesia. The cellular mechanisms downstream of peripheral µORs are not well understood. Here, we show in neurons of murine dorsal root ganglia that pro-nociceptive TRPM3 channels, present in the peripheral parts of nociceptors, are strongly inhibited by µOR activation, much more than other TRP channels in the same compartment, like TRPV1 and TRPA1. Inhibition of TRPM3 channels occurs via a short signaling cascade involving Gβγ proteins, which form a complex with TRPM3. Accordingly, activation of peripheral µORs in vivo strongly attenuates TRPM3-dependent pain. Our data establish TRPM3 inhibition as important consequence of peripheral µOR activation indicating that pharmacologically antagonizing TRPM3 may be a useful analgesic strategy.

Indexed as

Analgesics, OpioidAnimalsBehavior Rating ScaleCalciumCalcium SignalingGanglia, SpinalGTP-Binding Protein beta SubunitsGTP-Binding Protein gamma SubunitsHEK293 CellsHumansMaleMiceMice, Inbred C57BLNeuronsNociceptorsPainAnalgesics, OpioidCalciumG-protein Beta gammaGTP-Binding Protein beta SubunitsGTP-Binding Protein gamma SubunitsReceptors, OpioidReceptors, Opioid, muTRPA1 Cation ChannelTrpa1 protein, mouseTRPM3 protein, mouseTRPM Cation ChannelsTRPV1 protein, mouseTRPV Cation ChannelsanalgesiaG-proteinMOPmouseneurosciencepainperipheral opioid receptorsTRPM3

Identifiers

PMID28826482
PMCPMC5593507
OpenAlexW2746622153

What OpenQuestion holds

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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.