Evidence map›Paper›PMID 27764229›Full record

ArticlePloS one2016

Oral Administration of Linoleic Acid Induces New Vessel Formation and Improves Skin Wound Healing in Diabetic Rats.

Hosana G Rodrigues, Marco A R Vinolo, Fabio T Sato, Juliana Magdalon, Carolina M C Kuhl, Ana S Yamagata, Ana Flávia M Pessoa, Gabriella Malheiros, Marinilce F Dos Santos, Camila Lima and 6 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 65 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 3 countries.

Hosana G RodriguesSchool of Applied Sciences, University of Campinas, Limeira, Brazil.
Marco A R VinoloDepartment of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas, Campinas, Brazil.
Fabio T SatoDepartment of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas, Campinas, Brazil.
Juliana MagdalonDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Carolina M C KuhlSchool of Applied Sciences, University of Campinas, Limeira, Brazil.
Ana S YamagataDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Ana Flávia M PessoaCell and Developmental Biology Department, Institute of Biomedical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Gabriella MalheirosCell and Developmental Biology Department, Institute of Biomedical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Marinilce F Dos SantosCell and Developmental Biology Department, Institute of Biomedical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Camila LimaDepartment of Clinical and Toxicology Analyses, School of Pharmaceutical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Sandra H FarskyDepartment of Clinical and Toxicology Analyses, School of Pharmaceutical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Niels O S CamaraDepartment of Immunology, Institute of Biomedical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Maria R WillinerFood Sciences and Nutrition, School of Biochemistry and Biological Sciences, National University of Litoral, Santa Fé, Argentina.
Claudio A BernalFood Sciences and Nutrition, School of Biochemistry and Biological Sciences, National University of Litoral, Santa Fé, Argentina.
Philip C CalderHuman Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
Rui CuriDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, Sao Paulo University, Sao Paulo, Brazil.
Universidade de São Paulo · BRUniversidade Estadual de Campinas (UNICAMP) · BRNational University of the Littoral · ARUniversity Hospital Southampton NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImpaired wound healing has been widely reported in diabetes. Linoleic acid (LA) accelerates the skin wound healing process in non-diabetic rats. However, LA has not been tested in diabetic animals.

objectivesWe investigated whether oral administration of pure LA improves wound healing in streptozotocin-induced diabetic rats.

methodsDorsal wounds were induced in streptozotocin-induced type-1 diabetic rats treated or not with LA (0.22 g/kg b.w.) for 10 days. Wound closure was daily assessed for two weeks. Wound tissues were collected at specific time-points and used to measure fatty acid composition, and contents of cytokines, growth factors and eicosanoids. Histological and qPCR analyses were employed to examine the dynamics of cell migration during the healing process.

resultsLA reduced the wound area 14 days after wound induction. LA also increased the concentrations of cytokine-induced neutrophil chemotaxis (CINC-2αβ), tumor necrosis factor-α (TNF-α) and leukotriene B4 (LTB4), and reduced the expression of macrophage chemoattractant protein-1 (MCP-1) and macrophage inflammatory protein-1 (MIP-1). These results together with the histological analysis, which showed accumulation of leukocytes in the wound early in the healing process, indicate that LA brought forward the inflammatory phase and improved wound healing in diabetic rats. Angiogenesis was induced by LA through elevation in tissue content of key mediators of this process: vascular-endothelial growth factor (VEGF) and angiopoietin-2 (ANGPT-2).

conclusionsOral administration of LA hastened wound closure in diabetic rats by improving the inflammatory phase and angiogenesis.

Indexed as

Administration, OralAngiopoietin-2AnimalsCell MovementCytokinesDiabetes Mellitus, ExperimentalGene Expression RegulationLinoleic AcidNeovascularization, PhysiologicRatsStreptozocinVascular Endothelial Growth Factor AWound HealingAngiopoietin-2CytokinesLinoleic AcidStreptozocinVascular Endothelial Growth Factor Avascular endothelial growth factor A, rat

Identifiers

PMID27764229
PMCPMC5072690
OpenAlexW2536983686

What OpenQuestion holds

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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.