Evidence map›Paper›PMID 25849615›Full record

ArticleNeuroscience2015

The role of TRPM2 in hydrogen peroxide-induced expression of inflammatory cytokine and chemokine in rat trigeminal ganglia.

M-K Chung, J Asgar, J Lee, M S Shim, C Dumler, J Y Ro

Abstract read
In one paragraph

Article in Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. TLR4 induced TRPM2 mediated neuropathic pain.Frontiers in pharmacology · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Chemokines and Pain in the Trigeminal System.Frontiers in pain research (Lausanne, Switzerland) · 2021
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Oxidative medicine and cellular longevity · 2019
    Article
  18. Review
  19. Article
  20. Article
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

6 authors at 1 institution in 1 country.

M-K ChungUniversity of Maryland School of Dentistry, Department of Neural and Pain Sciences, Program in Neuroscience, United States.
J AsgarUniversity of Maryland School of Dentistry, Department of Neural and Pain Sciences, Program in Neuroscience, United States.
J LeeUniversity of Maryland School of Dentistry, Department of Neural and Pain Sciences, Program in Neuroscience, United States.
M S ShimUniversity of Maryland School of Dentistry, Department of Neural and Pain Sciences, Program in Neuroscience, United States.
C DumlerUniversity of Maryland School of Dentistry, Department of Neural and Pain Sciences, Program in Neuroscience, United States.
J Y RoUniversity of Maryland School of Dentistry, Department of Neural and Pain Sciences, Program in Neuroscience, United States. Electronic address: jro@umaryland.edu.
University of Maryland, Baltimore · US

Funding

Peripheral Receptor Mechanisms in Orofacial Muscle PainR01DE016062 · NIDCR · UNIVERSITY OF MARYLAND BALTIMORE · PI RO, JIN Y · 2005 to 2022
$5.6M
Genetic and post-translational modifications of TRPV1 in craniofacial painR01DE023846 · NIDCR · UNIVERSITY OF MARYLAND BALTIMORE · PI CHUNG, MAN-KYO · 2014 to 2018
$1.9M
NIDCR NIH HHS DE016062NIDCR NIH HHS DE023846NIDCR NIH HHS R01 DE016062NIDCR NIH HHS R01 DE023846
6 · The paper itself

Abstract

Trigeminal ganglia (TG) contain neuronal cell bodies surrounded by satellite glial cells. Although peripheral injury is well known to induce changes in gene expression within sensory ganglia, detailed mechanisms whereby peripheral injury leads to gene expression within sensory ganglia are not completely understood. Reactive oxygen species (ROS) are an important modulator of hyperalgesia, but the role of ROS generated within sensory ganglia is unclear. Since ROS are known to affect transcription processes, ROS generated within sensory ganglia could directly influence gene expression and induce cellular changes at the soma level. In this study, we hypothesized that peripheral inflammation leads to cytokine and chemokine production and ROS generation within TG and that transient receptor potential melastatin (TRPM2), a well known oxidative sensor, contributes to ROS-induced gene regulation within TG. The masseter injection of complete Freund's adjuvant (CFA) resulted in a significantly elevated level of ROS within TG of the inflamed side with a concurrent increase in cytokine expression in TG. Treatment of TG cultures with H2O2 significantly up-regulated mRNA and protein levels of cytokine/chemokine such as interleukin 6 (IL-6) and chemokine (C-X-C motif) ligand 2 (CXCL2). TRPM2 was expressed in both neurons and non-neuronal cells in TG, and pretreatment of TG cultures with 2-aminoethoxydiphenyl borate (2-APB), an inhibitor of TRPM2, or siRNA against TRPM2 attenuated H2O2-induced up-regulation of IL-6 and CXCL2. These results suggested that activation of TRPM2 could play an important role in the modulation of cytokine/chemokine expression within TG under oxidative stress and that such changes may contribute to amplification of nociceptive signals leading to pathological pain conditions.

Indexed as

AnimalsBoron CompoundsCells, CulturedCoculture TechniquesCytokinesFreund's AdjuvantFunctional LateralityHydrogen PeroxideInflammationMaleNeurogliaNeuronsOxidantsPhosphopyruvate HydrataseRatsRats, Sprague-Dawley2-aminoethoxydiphenyl borateBoron CompoundsCytokinesFreund's AdjuvantHydrogen PeroxideOxidantsPhosphopyruvate HydrataseReactive Oxygen SpeciesRNA, MessengerTrpm2 protein, ratTRPM Cation ChannelsCXCL2IL-6myositisoxidative stresssatellite glial cells

Identifiers

PMID25849615
PMCPMC4882920
OpenAlexW1973184324

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.