Evidence map›Paper›PMID 26121396›Full record

ArticleMolecules (Basel, Switzerland)2015

Redox-Active Profile Characterization of Remirea maritima Extracts and Its Cytotoxic Effect in Mouse Fibroblasts (L929) and Melanoma (B16F10) Cells.

Grace Anne A Dória, Anderson R Santos, Leonardo S Bittencourt, Rafael C Bortolin, Paula P Menezes, Bruno S Vasconcelos, Rebeca O Souza, Maria José V Fonseca, Alan Diego C Santos, Shanmugam Saravanan and 6 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2015. 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
0.8field-weighted citation impact, top 33% 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. Review
  2. Article
  3. 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

16 authors at 3 institutions in 1 country.

Grace Anne A DóriaDepartament of Pharmacy, Federal University of Sergipe, Av. Marechal Rondon, Jardim Rosa Elze, 49100-000 São Cristóvão, Sergipe, Brazil. gracedoria@hotmail.com.
Anderson R SantosDepartament of Pharmacy, Federal University of Sergipe, Av. Marechal Rondon, Jardim Rosa Elze, 49100-000 São Cristóvão, Sergipe, Brazil. andersonfarmacia@yahoo.com.br.
Leonardo S BittencourtDepartament of Biochemistry, Federal University of Rio Grande do Sul, 90040-060 Porto Alegre, Rio Grande do Sul, Brazil. lsbittencourt@hotmail.com.
Rafael C BortolinDepartament of Biochemistry, Federal University of Rio Grande do Sul, 90040-060 Porto Alegre, Rio Grande do Sul, Brazil. rafaelbortolin@hotmail.com.
Paula P MenezesDepartament of Pharmacy, Federal University of Sergipe, Av. Marechal Rondon, Jardim Rosa Elze, 49100-000 São Cristóvão, Sergipe, Brazil. paulamenezes_16@yahoo.com.br.
Bruno S VasconcelosDepartament of Pharmacy, Federal University of Sergipe, Av. Marechal Rondon, Jardim Rosa Elze, 49100-000 São Cristóvão, Sergipe, Brazil. bruninho_farma@hotmail.com.
Rebeca O SouzaDepartament of Pharmacy, University of São Paulo, 14040-900 Ribeirão Preto, São Paulo, Brazil. rebecapharma@yahoo.com.br.
Maria José V FonsecaDepartament of Pharmacy, University of São Paulo, 14040-900 Ribeirão Preto, São Paulo, Brazil. magika@fcfrp.usp.br.
Alan Diego C SantosDepartament of Physiology and Chemistry, Federal University of Sergipe, 49100-000 São Cristóvão, Sergipe, Brazil. alandiego0@yahoo.com.br.
Shanmugam SaravananDepartament of Pharmacy, Federal University of Sergipe, Av. Marechal Rondon, Jardim Rosa Elze, 49100-000 São Cristóvão, Sergipe, Brazil. saranflora04@gmail.com.
Francilene A SilvaDepartament of Pharmacy, Federal University of Sergipe, Av. Marechal Rondon, Jardim Rosa Elze, 49100-000 São Cristóvão, Sergipe, Brazil. farmsilva@hotmail.com.
Daniel P GelainDepartament of Biochemistry, Federal University of Rio Grande do Sul, 90040-060 Porto Alegre, Rio Grande do Sul, Brazil. dgelain@yahoo.com.br.
José Cláudio F MoreiraDepartament of Biochemistry, Federal University of Rio Grande do Sul, 90040-060 Porto Alegre, Rio Grande do Sul, Brazil. 00006866@ufrgs.br.
Ana Paula N PrataDepartament of Biology, Federal University of Sergipe, 49100-000 São Cristóvão, Sergipe, Brazil. apprata@yahoo.com.br.
Lucindo J Quintans-JúniorDepartament of Physiology and Chemistry, Federal University of Sergipe, 49100-000 São Cristóvão, Sergipe, Brazil.
Adriano A S AraújoDepartament of Pharmacy, Federal University of Sergipe, Av. Marechal Rondon, Jardim Rosa Elze, 49100-000 São Cristóvão, Sergipe, Brazil. left.ufs@hotmail.com.
Universidade Federal de Sergipe · BRUniversidade Federal do Rio Grande do Sul · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Remirea maritima is a tropical plant with a reticulated root system belonging to the family Cyperaceae, also known to have biologically active secondary metabolites. However, very few data on R. maritima's biological actions are available and there are no reports regarding the redox-active profile of this plant. In this study, we examined the total phenolic content of Remirea maritima hydroalcoholic (RMHA) extracts, redox properties against different reactive species generated in vitro and their cytotoxic effect against fibroblasts (L929) and melanoma (B16F10) cells. Total reactive antioxidant potential index (TRAP) and total antioxidant reactivity (TAR) results revealed that RMHA at all concentrations tested showed significant antioxidant capacity. RMHA was also effective against hydroxyl radical formation, reduction of Fe3+ to Fe2+ and in scavenging nitric oxide (NO) radicals. In vitro, the level of lipid peroxidation was reduced by RMHA extract and the data showed significant oxidative damage protection. The RMHA cytotoxicity was evaluated by a neutral red assay in fibroblast (L929) and melanome (B16F10) cells. The obtained results showed that the RMHA (40 and 80 µg/mL, respectively) reduced 70% of the viable cells. In conclusion, this study represents the first report regarding the antioxidant and anti-proliferative potential of R. maritima against B16F10 melanoma cells.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicCell LineCell Line, TumorCyperaceaeFibroblastsMelanoma, ExperimentalMiceOxidation-ReductionPlant ExtractsAntineoplastic Agents, PhytogenicPlant Extractscellular viabilitycytotoxicityfree radicalsoxidative stressRemirea maritimatotal phenol

Identifiers

PMID26121396
PMCPMC6331889
OpenAlexW1660374452

What OpenQuestion holds

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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.