Evidence map›Paper›PMID 24722818›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2014

Gallic acid functions as a TRPA1 antagonist with relevant antinociceptive and antiedematogenic effects in mice.

Gabriela Trevisan, Mateus F Rossato, Raquel Tonello, Carin Hoffmeister, Jonatas Z Klafke, Fernanda Rosa, Kelly V Pinheiro, Francielle V Pinheiro, Aline A Boligon, Margareth L Athayde and 1 more

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Article in Naunyn-Schmiedeberg's archives of pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 48 citations in OpenAlex.

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  19. Antinociceptive Activity of Methanolic Extract ofPain research & management · 2018
    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

11 authors at 4 institutions in 1 country.

Gabriela TrevisanGraduate Program in Biological Sciences: Toxicological Biochemistry, Department of Chemistry, Center of Natural and Exact Sciences, Federal University of Santa Maria (UFSM), Avenida Roraima, 1000, Camobi, Santa Maria-RS, 97105-900, Brazil, gabitrev@hotmail.com.
Mateus F Rossato
Raquel Tonello
Carin Hoffmeister
Jonatas Z Klafke
Fernanda Rosa
Kelly V Pinheiro
Francielle V Pinheiro
Aline A Boligon
Margareth L Athayde
Juliano Ferreira
Universidade Federal de Santa Maria · BRCentro de Estudos e Pesquisas em Educação, Cultura e Ação Comunitária · BRUniversidade Federal de Santa Catarina · BRUniversity of Cruz Alta · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transient receptor potential ankyrin 1 (TRPA1) has been identified as a relevant target for the development of novel analgesics. Gallic acid (GA) is a polyphenolic compound commonly found in green tea and various berries and possesses a wide range of biological activities. The goal of this study was to identify GA as a TRPA1 antagonist and observe its antinociceptive effects in different pain models. First, we evaluated the ability of GA to affect cinnamaldehyde-induced calcium influx. Then, we observed the antinociceptive and antiedematogenic effects of GA (3-100 mg/kg) oral administration after the intraplantar (i.pl.) injection of TRPA1 agonists (allyl isothiocyanate, cinnamaldehyde, or hydrogen peroxide-H2O2) in either an inflammatory pain model (carrageenan i.pl. injection) or a neuropathic pain model (chronic constriction injury) in male Swiss mice (25-35 g). GA reduced the calcium influx mediated by TRPA1 activation. Moreover, the oral administration of GA decreased the spontaneous nociception triggered by allyl isothiocyanate, cinnamaldehyde, and H2O2. Carrageenan-induced allodynia and edema were largely reduced by the pretreatment with GA. Moreover, the administration of GA was also capable of decreasing cold and mechanical allodynia in a neuropathic pain model. Finally, GA was absorbed after oral administration and did not produce any detectable side effects. In conclusion, we found that GA is a TRPA1 antagonist with antinociceptive properties in relevant models of clinical pain without detectable side effects, which makes it a good candidate for the treatment of painful conditions.

Indexed as

AcroleinAnalgesicsAnimalsAnti-Inflammatory AgentsAntioxidantsEdemaGallic AcidHydrogen PeroxideHyperalgesiaMaleMicePainPsychomotor PerformanceSciatic NerveSpinal CordTransient Receptor Potential ChannelsAcroleinAnalgesicsAnti-Inflammatory AgentsAntioxidantscinnamaldehydeGallic AcidHydrogen PeroxideTransient Receptor Potential ChannelsTRPA1 Cation ChannelTrpa1 protein, mouse

Identifiers

PMID24722818
OpenAlexW2054657321

What OpenQuestion holds

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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.