Evidence map›Paper›PMID 29117570›Full record

ArticleCell reports2017

Oxytocin Modulates Nociception as an Agonist of Pain-Sensing TRPV1.

Yelena Nersesyan, Lusine Demirkhanyan, Deny Cabezas-Bratesco, Victoria Oakes, Ricardo Kusuda, Tyler Dawson, Xiaohui Sun, Chike Cao, Alejandro Martin Cohen, Bharath Chelluboina and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 2 pooled it
13.9field-weighted citation impact, top 1% 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

69 citing papers in PubMed, 2 syntheses or guidelines pooled it, 120 citations in OpenAlex.

  1. Pooled it
  2. The Impact of TRPV1 on Cancer Pathogenesis and Therapy: A Systematic Review.International journal of biological sciences · 2021
    Pooled it
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  10. Acute, chronic and conditioned effects of intranasal oxytocin in the mu-opioid receptor knockout mouse model of autism: Social context matters.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
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9 more citing papers are in PubMed but not listed here.

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

15 authors at 9 institutions in 7 countries.

Yelena NersesyanDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, 1 Illini Drive, Peoria, IL 61605, USA.
Lusine DemirkhanyanDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, 1 Illini Drive, Peoria, IL 61605, USA.
Deny Cabezas-BratescoInstituto de Fisiologia, Facultad de Medicina, Universidad Austral de Chile, and Millennium Nucleus of Ion Channels-Associated Diseases (MiNICAD), Valdivia 5110566, Chile.
Victoria OakesDepartment of Chemistry, King's College London, Britannia House, 7 Trinity Street, London, SE1 1DB, UK.
Ricardo KusudaDepartment of Anesthesia, Friedrich-Alexander University Erlangen-Nürnberg, Krankenhausstrasse 12, 91054 Erlangen, Germany; Department of Pharmacology, Ribeirão Preto Medical School, University of São Paulo, Av. Bandeirantes 3900, 14049-900 Ribeirão Preto, Brazil.
Tyler DawsonDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, 1 Illini Drive, Peoria, IL 61605, USA.
Xiaohui SunDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, 1 Illini Drive, Peoria, IL 61605, USA; College of Pharmaceutical Sciences, Soochow University, Suzhou, Jiangsu 215123, China.
Chike CaoIon Channel Research Unit, Duke University Medical Center, Durham, NC 27710, USA.
Alejandro Martin CohenDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, Dalhousie University, 5850 College Street, P.O. Box 15000, Halifax, NS B3H 4R2, Canada.
Bharath ChelluboinaDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, 1 Illini Drive, Peoria, IL 61605, USA.
Krishna Kumar VeeravalliDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, 1 Illini Drive, Peoria, IL 61605, USA.
Katharina ZimmermannDepartment of Anesthesia, Friedrich-Alexander University Erlangen-Nürnberg, Krankenhausstrasse 12, 91054 Erlangen, Germany.
Carmen DomeneDepartment of Chemistry, King's College London, Britannia House, 7 Trinity Street, London, SE1 1DB, UK; Chemistry Research Laboratory, Mansfield Road, University of Oxford, Oxford, OX1 3TA, UK.
Sebastian BrauchiInstituto de Fisiologia, Facultad de Medicina, Universidad Austral de Chile, and Millennium Nucleus of Ion Channels-Associated Diseases (MiNICAD), Valdivia 5110566, Chile.
Eleonora ZakharianDepartment of Cancer Biology and Pharmacology, University of Illinois College of Medicine, 1 Illini Drive, Peoria, IL 61605, USA. Electronic address: zakharel@uic.edu.
Illinois College · USAustral University of Chile · CLDalhousie University · CADuke University Hospital · USFriedrich-Alexander-Universität Erlangen-Nürnberg · DEKing's College London · GBUniversidade de São Paulo · BRUniversity of Illinois Urbana-Champaign · USUniversity of Oxford · GB

Funding

TRP channels in supramolecular complexes with Inorganic Polyphosphate and PolyhydR01GM098052 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ZAKHARIAN, ELEONORA · 2011 to 2015
$1.5M
NIGMS NIH HHS R01 GM098052
6 · The paper itself

Abstract

Oxytocin is a hormone with various actions. Oxytocin-containing parvocellular neurons project to the brainstem and spinal cord. Oxytocin release from these neurons suppresses nociception of inflammatory pain, the molecular mechanism of which remains unclear. Here, we report that the noxious stimulus receptor TRPV1 is an ionotropic oxytocin receptor. Oxytocin elicits TRPV1 activity in native and heterologous expression systems, regardless of the presence of the classical oxytocin receptor. In TRPV1 knockout mice, DRG neurons exhibit reduced oxytocin sensitivity relative to controls, and oxytocin injections significantly attenuate capsaicin-induced nociception in in vivo experiments. Furthermore, oxytocin potentiates TRPV1 in planar lipid bilayers, supporting a direct agonistic action. Molecular modeling and simulation experiments provide insight into oxytocin-TRPV1 interactions, which resemble DkTx. Together, our findings suggest the existence of endogenous regulatory pathways that modulate nociception via direct action of oxytocin on TRPV1, implying its analgesic effect via channel desensitization.

Indexed as

AnimalsCalciumCapsaicinCells, CulturedEvoked PotentialsFemaleGanglia, SpinalHEK293 CellsHumansMaleMiceMice, Inbred C57BLMice, KnockoutNeuronsNociceptionOxytocinCalciumCapsaicincapsazepineOxytocinReceptors, OxytocinTRPV1 receptorTRPV Cation ChannelsMD simulationsmolecular dynamics simulationsnociceptionoxytocinoxytocin receptorplanar lipid bilayerstransient receptor potential vanilloid 1TRPV1 ion channel

Identifiers

PMID29117570
PMCPMC5701661
OpenAlexW2767886902

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.