Evidence map›Paper›PMID 39970160›Full record

ArticlePloS one2025

Sodium propionate decreases implant-induced foreign body response in mice.

Deivenita Juliana Alves Carvalho do Carmo, Marcela Guimarães Takahashi Lazari, Letícia Cristine Cardoso Dos Santos, Pedro Augusto Carvalho Costa, Itamar Couto Guedes Jesus, Silvia Guatimosim, Pedro Pires Goulart Guimaraes, Silvia Passos Andrade, Paula Peixoto Campos

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Dual Beneficial Effects of Topical l-Glutamine on Oral Mucositis in 5-Fluorouracil-Treated Mice.Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology · 2026
    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

9 authors.

Deivenita Juliana Alves Carvalho do CarmoDepartment of General Pathology, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.
Marcela Guimarães Takahashi LazariDepartment of General Pathology, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.
Letícia Cristine Cardoso Dos SantosDepartment of General Pathology, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.
Pedro Augusto Carvalho CostaDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.ORCID 0000-0002-3240-7513
Itamar Couto Guedes JesusDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.
Silvia GuatimosimDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.
Pedro Pires Goulart GuimaraesDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.ORCID 0000-0003-4534-2779
Silvia Passos AndradeDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.
Paula Peixoto CamposDepartment of General Pathology, Institute of Biological Sciences, Federal University of Minas Gerais, Campus UFMG, Belo Horizonte, Minas Gerais, Brazil.ORCID 0000-0003-2016-2210

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The short-chain fatty acid (SCFA) propionate, beyond its actions on the intestine, has been able to lower inflammation and modulate angiogenesis and fibrogenesis in pathological conditions in experimental animal models. Its effects on foreign body reaction (FBR), an abnormal healing process induced by implantation of medical devices, have not been investigated. We have evaluated the effects of sodium propionate (SP) on inflammation, neovascularization and remodeling on a murine model of implant-induced FBR. Polyether-polyurethane sponge discs implanted subcutaneously in C57BL/6 mice provided the scaffold for the formation of the fibrovascular tissue. Fifteen-day old implants of the treated group (SP, 100 mg/kg for 14 days) presented a decrease in the inflammatory response as evaluated by cellular influx (flow cytometry; Neutrophils 54%; Lymphocytes 25%, Macrophages 40%). Myeloperoxidase activity, TNF-α levels and mast cell number were also lower in the treated group relative to the control group. Angiogenesis was evaluated by blood vessel number and VEGF levels, which were downregulated by the treatment. Moreover, the number of foreign body giant cells HE (FBGC) and the thickness of the collagenous capsule were reduced by 58% and 34%, respectively. Collagen deposition inside the implant, TGF-β1 levels, α-SMA and TGF-β1 expression were also reduced. These effects may indicate that SP holds potential as a therapeutic agent for attenuating adverse remodeling processes associated with implantable devices, expanding its applications in biomedical contexts.

Indexed as

Foreign-Body ReactionPropionatesProstheses and ImplantsAnimalsCollagenMaleMiceMice, Inbred C57BLTransforming Growth Factor beta1Tumor Necrosis Factor-alphaVascular Endothelial Growth Factor ACollagenPropionatesTransforming Growth Factor beta1Tumor Necrosis Factor-alphaVascular Endothelial Growth Factor A

Identifiers

PMID39970160
PMCPMC11838875

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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.