Evidence map›Paper›PMID 28706420›Full record

ArticleWorld journal of gastroenterology2017

Rodrigo de Oliveira Formiga, Zelma Glebya Maciel Quirino, Margareth de Fátima Formiga Melo Diniz, Alexsandro Fernandes Marinho, Josean Fechine Tavares, Leônia Maria Batista

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.1field-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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Antifungal activity and antidiarrheal activityWorld journal of gastroenterology · 2020
    Article
  4. 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 2 institutions in 2 countries.

Rodrigo de Oliveira FormigaRodrigo de Oliveira Formiga, Margareth de Fátima Formiga Melo Diniz, Alexsandro Fernandes Marinho, Josean Fechine Tavares, Leônia Maria Batista, Postgraduate Program in Natural Products and Bioactive Synthetics, Health Sciences Center, Federal University of Paraiba, João Pessoa 58051, PB, Brazil.
Zelma Glebya Maciel QuirinoRodrigo de Oliveira Formiga, Margareth de Fátima Formiga Melo Diniz, Alexsandro Fernandes Marinho, Josean Fechine Tavares, Leônia Maria Batista, Postgraduate Program in Natural Products and Bioactive Synthetics, Health Sciences Center, Federal University of Paraiba, João Pessoa 58051, PB, Brazil.
Margareth de Fátima Formiga Melo DinizRodrigo de Oliveira Formiga, Margareth de Fátima Formiga Melo Diniz, Alexsandro Fernandes Marinho, Josean Fechine Tavares, Leônia Maria Batista, Postgraduate Program in Natural Products and Bioactive Synthetics, Health Sciences Center, Federal University of Paraiba, João Pessoa 58051, PB, Brazil.
Alexsandro Fernandes MarinhoRodrigo de Oliveira Formiga, Margareth de Fátima Formiga Melo Diniz, Alexsandro Fernandes Marinho, Josean Fechine Tavares, Leônia Maria Batista, Postgraduate Program in Natural Products and Bioactive Synthetics, Health Sciences Center, Federal University of Paraiba, João Pessoa 58051, PB, Brazil.
Josean Fechine TavaresRodrigo de Oliveira Formiga, Margareth de Fátima Formiga Melo Diniz, Alexsandro Fernandes Marinho, Josean Fechine Tavares, Leônia Maria Batista, Postgraduate Program in Natural Products and Bioactive Synthetics, Health Sciences Center, Federal University of Paraiba, João Pessoa 58051, PB, Brazil.
Leônia Maria BatistaRodrigo de Oliveira Formiga, Margareth de Fátima Formiga Melo Diniz, Alexsandro Fernandes Marinho, Josean Fechine Tavares, Leônia Maria Batista, Postgraduate Program in Natural Products and Bioactive Synthetics, Health Sciences Center, Federal University of Paraiba, João Pessoa 58051, PB, Brazil.
Creative Research Enterprises (United States) · USUniversidade Federal da Paraíba · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the acute toxicity, phytochemical profile, antidiarrheal activity and mechanisms of action of

methodsA castor oil-induced diarrhea model was used to evaluate antidiarrheal activity. Intestinal transit and gastric emptying protocols were used to evaluate a possible antimotility effect. K

resultsAll tested doses of the extract (62.5, 125, 250 and 500 mg/kg) possessed antidiarrheal activity, with a significant decrease of the evacuation index. This activity is possibly related to a reduced gastric emptying (125, 250 and 500 mg/kg) and to a decreased percentage of intestinal transit for all tested doses. That last effect seems to be modulated by nitric oxide, K

conclusionThe antidiarrheal effect of

Indexed as

AnimalsAntidiarrhealsCastor OilDiarrheaDisease Models, AnimalEthanolFemaleGastric EmptyingGastrointestinal TransitIntestinal MucosaIntestinal SecretionsKATP ChannelsMaleMaytenusMiceNitric OxideAntidiarrhealsCastor OilEthanolKATP ChannelsNitric OxidePlant ExtractsReceptors, AdrenergicAntidiarrheal activityCelastraceaeDiarrheaMaytenus erythroxylonMedicinal plants

Identifiers

PMID28706420
PMCPMC5487501
OpenAlexW2684823302

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.