Evidence map›Paper›PMID 30683148›Full record

ArticleBMC research notes2019

High dose gabapentin does not alter tumor growth in mice but reduces arginase activity and increases superoxide dismutase, IL-6 and MCP-1 levels in Ehrlich ascites.

Plinio da Cunha Leal, Ed Carlos Rey Moura, Rachel Jorge Dino Cossetti, Johnny Ramos do Nascimento, Izabel Cristina Portela Bogéa Serra, Bruno de Paulo Ribeiro, Andre Álvares Marques Vale, Ana Paula Silva de Azevedo Dos Santos, Flavia Raquel Fernandes do Nascimento, Rioko Kimiko Sakata

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Pharmaceuticals (Basel, Switzerland) · 2024
    Article
  2. Article
  3. Second Generation of Antiepileptic Drugs and Oxidative Stress.International journal of molecular sciences · 2023
    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

10 authors at 3 institutions in 1 country.

Plinio da Cunha LealFederal University of Maranhão, São Luís, MA, Brazil. pliniocunhaleal@hotmail.com.
Ed Carlos Rey MouraFederal University of Maranhão, São Luís, MA, Brazil.
Rachel Jorge Dino CossettiFederal University of Maranhão, São Luís, MA, Brazil.
Johnny Ramos do NascimentoFederal University of Maranhão, São Luís, MA, Brazil.
Izabel Cristina Portela Bogéa SerraFederal University of Maranhão, São Luís, MA, Brazil.
Bruno de Paulo RibeiroFederal University of Maranhão, São Luís, MA, Brazil.
Andre Álvares Marques ValeFederal University of Maranhão, São Luís, MA, Brazil.
Ana Paula Silva de Azevedo Dos SantosFederal University of Maranhão, São Luís, MA, Brazil.
Flavia Raquel Fernandes do NascimentoFederal University of Maranhão, São Luís, MA, Brazil.
Rioko Kimiko SakataFederal University of São Paulo, São Paulo, SP, Brazil.
Universidade Federal do Maranhão · BRCentro Infantil Boldrini · BRUniversidade Federal de São Paulo · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico grant no 305608/2015-0Fundação de Amparo à Pesquisa do Estado do Maranhão grant no 00572/14Fundação de Amparo à Pesquisa do Estado do Maranhão grant no 01354/16Fundação de Amparo à Pesquisa do Estado do Maranhão grant no BD-01310/15
6 · The paper itself

Abstract

objectivesThe purpose of this study was to evaluate the effect of gabapentin on Ehrlich tumor growth in Swiss mice, a highly aggressive and inflammatory tumor model. Mice were grouped into sets of 5 animals and treated from days 2 to 8 with gabapentin 30 mg/kg body weight (G30) or 100 mg/kg body weight (G100), or normal sterile saline (control).

resultsThe mice were euthanized on day 10. Tumor growth, tumoricidal agents and inflammatory cytokines levels were assessed. At day 10, G30 and G100 mice gained weight, but there were no differences in tumor cell count or in ascites volume. In G100, there was a reduction in arginase and an increase in SOD activities. There was an increase in IL-6 and MCP-1 levels, especially in G100, but no alterations in TNF-α. There was no direct evidence of tumor induction by gabapentin. However, the findings suggest that its use modulates immune response to a more effector and less deleterious profile, with increase in activity of anti-oxidant enzymes and in cytokines that favor activation of macrophages, which could improve the general status of the tumor host.

Indexed as

Breast NeoplasmsCarcinoma, Ehrlich TumorInterleukin-6AnalgesicsAnimalsArginaseChemokine CCL2Disease Models, AnimalFemaleGabapentinMiceSuperoxide DismutaseWeight GainAnalgesicsArginaseCcl2 protein, mouseChemokine CCL2GabapentinInterleukin-6interleukin-6, mouseSuperoxide DismutaseArginineCytokineEhrlich tumorGabapentinSODTumor growth

Identifiers

PMID30683148
PMCPMC6347815
OpenAlexW2913854503

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.