Evidence map›Paper›PMID 25635877›Full record

ArticlePloS one2015

Eugenol inhibits the GABAA current in trigeminal ganglion neurons.

Sang Hoon Lee, Jee Youn Moon, Sung Jun Jung, Jin Gu Kang, Seung Pyo Choi, Jun Ho Jang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Eugenol and lidocaine inhibit voltage-gated NaFrontiers in pharmacology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Synergistic Herb-Herb Interaction of the Antinociceptive and Anti-Inflammatory Effects ofEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
  8. Article
  9. Article
  10. Review
  11. Review
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 4 institutions in 1 country.

Sang Hoon LeeDepartment of Biomedical Science, Graduate School of Biomedical Science; Engineering, Hanyang University, Seoul, Republic of Korea.
Jee Youn MoonDepartment of Anesthesiology and Pain Medicine, Seoul National University Hospital College of Medicine, Seoul, Republic of Korea.
Sung Jun JungDepartment of Physiology, Medical School, Hanyang University, Seoul, Republic of Korea.
Jin Gu KangDepartment of Anaesthesiology and Pain Medicine, Hallim University, Dongtan Sacred Heart Hospital, Kyunggi-do, Republic of Korea.
Seung Pyo ChoiDepartment of Anesthesiology and Pain Medicine, Seoul National University Hospital College of Medicine, Seoul, Republic of Korea.
Jun Ho JangDepartment of Biomedical Science, Graduate School of Biomedical Science; Engineering, Hanyang University, Seoul, Republic of Korea.
Hanyang University · KRSeoul National University Hospital · KRHallym University Dongtan Sacred Heart Hospital · KRHanyang University Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eugenol has sedative, antioxidant, anti-inflammatory, and analgesic effects, but also serves as an irritant through the regulation of a different set of ion channels. Activation of gamma aminobutyric acid (GABA) receptors on sensory neurons leads to the stabilization of neuronal excitability but contributes to formalin-induced inflammatory pain. In this study, we examined the effect of eugenol on the GABA-induced current in rat trigeminal ganglia (TG) neurons and in human embryonic kidney (HEK) 293 cells expressing the GABAA receptor α1β2γ2 subtype using the whole-cell patch clamp technique. RT-PCR and Western blot analysis were used to confirm the expression of GABAA receptor γ2 subunit mRNA and protein in the TG and hippocampus. Eugenol decreased the amplitude ratio of the GABA-induced current to 27.5 ± 3.2% (p < 0.05) in TG neurons, which recovered after a 3-min washout. In HEK 293 cells expressing the α1β2γ2 subtype, eugenol inhibited GABA-induced currents in a dose-dependent manner. Application of eugenol also decreased the GABA response in the presence of a G-protein blocker. Eugenol pretreatment with different concentrations of GABA resulted in similar inhibition of the GABA-induced current in a non-competitive manner. In conclusion, eugenol inhibits the GABA-induced current in TG neurons and HEK 293 cells expressing the GABAA receptor in a reversible, dose-dependent, and non-competitive manner, but not via the G-protein pathway. We suggest that the GABAA receptor could be a molecular target for eugenol in the modulation of nociceptive information.

Indexed as

AnimalsEugenolHEK293 CellsHumansIon Channel GatingMaleNeuronsRats, Sprague-DawleyReceptors, GABA-ATrigeminal GanglionEugenolReceptors, GABA-A

Identifiers

PMID25635877
PMCPMC4311912
OpenAlexW2083061108

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.