Evidence map›Paper›PMID 26490459›Full record

ArticlePflugers Archiv : European journal of physiology2016

Acute and chronic nociceptive phases observed in a rat hind paw ischemia/reperfusion model depend on different mechanisms.

J Z Klafke, M A da Silva, M F Rossato, S Dal Toé de Prá, F K Rigo, C I B Walker, G V Bochi, R N Moresco, J Ferreira, G Trevisan

Abstract read
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In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Pain in Hemophilia: Unexplored Role of Oxidative Stress.Antioxidants (Basel, Switzerland) · 2022
    Review
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  11. Article
  12. Review
  13. Analgesic effects of Phα1β toxin: a review of mechanisms of action involving pain pathways.The journal of venomous animals and toxins including tropical diseases · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
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  19. Article
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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

10 authors at 7 institutions in 2 countries.

J Z KlafkeGrupo Multidisciplinar de Saúde, Programa de Pós-Graduação em Atenção Integral à Saúde, Universidade de Cruz Alta (UNICRUZ), 98020-290, Cruz Alta, RS, Brazil.
M A da SilvaDepartamento de Saúde, Curso de Biomedicina, Faculdade de Educação e Cultura de Vilhena, 76980-000, Vilhena, RO, Brazil.
M F RossatoPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica, Departamento de Química, Universidade Federal de Santa Maria (UFSM), 97105-900, Santa Maria, RS, Brazil.
S Dal Toé de PráPrograma de Pós-Graduação em Ciências da Saúde, Universidade do Extremo Sul Catarinense (UNESC), Avenida Universitária, 1105, room 21, building S, 88806-000, Criciúma, SC, Brazil.
F K RigoPrograma de Pós-Graduação em Biomedicina do Instituto de Ensino e Pesquisa da Santa Casa de Belo Horizonte, Departamento de Biomedicina e Medicina (IEPBH), Belo Horizonte, MG, Brazil.
C I B WalkerDepartamento de Saúde (Farmácia), Universidade Federal do Sergipe (UFS), 49400-000, Lagarto, SE, Brazil.
G V BochiPrograma de Pós-Graduação em Farmacologia, Departamento de Fisiologia e Farmacologia, Universidade Federal de Santa Maria (UFSM), 97105-900, Santa Maria, RS, Brazil.
R N MorescoPrograma de Pós-Graduação em Farmacologia, Departamento de Fisiologia e Farmacologia, Universidade Federal de Santa Maria (UFSM), 97105-900, Santa Maria, RS, Brazil.
J FerreiraLaboratório de Bioquímica Clínica, Departamento de Análises Clínicas e Toxicológicas, Universidade Federal de Santa Maria (UFSM), 97105-900, Santa Maria, RS, Brazil. ferreiraj99@gmail.com.
G TrevisanPrograma de Pós-Graduação em Ciências da Saúde, Universidade do Extremo Sul Catarinense (UNESC), Avenida Universitária, 1105, room 21, building S, 88806-000, Criciúma, SC, Brazil. gabitrev@hotmail.com.
Universidade Federal de Santa Maria · BRUniversidade do Extremo Sul Catarinense · BRCultura · MXInstituto de Ensino e Pesquisa Santa Casa · BRUniversidade Federal de Santa Catarina · BRUniversidade Federal de Sergipe · BRUniversity of Cruz Alta · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex regional pain syndrome type 1 (CRPS1) may be evoked by ischemia/reperfusion, eliciting acute and chronic pain that is difficult to treat. Despite this, the underlying mechanism of CRPS1 has not been fully elucidated. Therefore, the goal of this study is to evaluate the involvement of inflammation, oxidative stress, and the transient receptor potential ankyrin 1 (TRPA1) channel, a chemosensor of inflammation and oxidative substances, in an animal model of chronic post-ischemia pain (CPIP). Male Wistar rats were subjected to 3 h hind paw ischemia/reperfusion (CPIP model). Different parameters of nociception, inflammation, ischemia, and oxidative stress were evaluated at 1 (acute) and 14 (chronic) days after CPIP. The effect of a TRPA1 antagonist and the TRPA1 immunoreactivity were also observed after CPIP. In the CPIP acute phase, we observed mechanical and cold allodynia; increased levels of tumor necrosis factor-α (hind paw), ischemia-modified albumin (IMA) (serum), protein carbonyl (hind paw and spinal cord), lactate (serum), and 4-hydroxy-2-nonenal (4-HNE, hind paw and spinal cord); and higher myeloperoxidase (MPO) and N-acetyl-β-D-glucosaminidase (NAGase) activities (hind paw). In the CPIP chronic phase, we detected mechanical and cold allodynia and increased levels of IMA (serum), protein carbonyl (hind paw and spinal cord), and 4-HNE (hind paw and spinal cord). TRPA1 antagonism reduced mechanical and cold allodynia 1 and 14 days after CPIP, but no change in TRPA1 immunoreactivity was observed. Different mechanisms underlie acute (inflammation and oxidative stress) and chronic (oxidative stress) phases of CPIP. TRPA1 activation may be relevant for CRPS1/CPIP-induced acute and chronic pain.

Indexed as

NociceptionAcetylglucosaminidaseAcute PainAldehydesAnimalsChronic PainCold TemperatureHindlimbHyperalgesiaLactic AcidMaleOxidative StressPeroxidaseProtein CarbonylationRatsRats, Wistar4-hydroxy-2-nonenalAcetylglucosaminidaseAldehydesLactic AcidPeroxidaseSerum AlbuminTRPA1 Cation ChannelTrpa1 protein, ratTRPC Cation ChannelsTumor Necrosis Factor-alpha4-HNEAllodyniaCRPS 1HC-030031NeuropathyPain

Identifiers

PMID26490459
OpenAlexW1883850239

What OpenQuestion holds

Textmetadata
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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.