Evidence map›Paper›PMID 25337194›Full record

ArticleInternational journal of clinical and experimental pathology2014

Remodeling of the thoracic aorta after bone marrow cell transplantation.

Alyne Felix, Nemesis Monteiro, Vinícius Novaes Rocha, Genilza Oliveira, Alan Cesar Moraes, Cherley Andrade, Ana Lucia Nascimento, Laís de Carvalho, Alessandra Thole, Jorge Carvalho

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Alyne FelixLaboratory of Ultrastructure and Tissue Biology, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Nemesis MonteiroLaboratory of Ultrastructure and Tissue Biology, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Vinícius Novaes RochaLaboratory of Ultrastructure and Tissue Biology, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Genilza OliveiraLaboratory of Cell Culture, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Alan Cesar MoraesLaboratory of Ultrastructure and Tissue Biology, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Cherley AndradeLaboratory of Ultrastructure and Tissue Biology, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Ana Lucia NascimentoLaboratory of Ultrastructure and Tissue Biology, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Laís de CarvalhoLaboratory of Cell Culture, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Alessandra TholeLaboratory of Cell Culture, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.
Jorge CarvalhoLaboratory of Ultrastructure and Tissue Biology, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro Rio de Janeiro, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells are characterized by their ability to differentiate into multiple cell lineages and display the paracrine effect. The aim of this work was to evaluate the effect of therapy with bone marrow cells (BMCs) on blood glucose, lipid metabolism and aortic wall remodeling in mice through the administration of a high fat diet and subsequent BMCs transplantation. C57BL/6 mice were fed a control diet (CO group) or an atherogenic diet (AT group). After 16 weeks, the AT group was divided into four groups: an AT 14 days group and AT 21 days group, that were given an injection of vehicle and sacrificed at 14 and 21 days after, respectively; AT-BMC 14 days group and AT-BMC 21 days group that was given an injection of BMCs and sacrificed at 14 and 21 days after. The CO group was sacrificed along with other groups. The BMCs transplant had reduced blood glucose, triglycerides and total cholesterol. The Qa (1/mm(2)) was quantitatively reduced in AT 14 days group, AT 21 days group and was high in AT-BMC 21 days group. The AT 21 days group exhibited increased tunica media and elastic system fibers. The immunolabeling for α-SMA and VEGF showed less immunolabeling in transplanted groups with BMCs. The immunostaining for PCNA seems to be more expressive in the group AT-BMC 21 days group. To conclude, our results support the concept that in mice, the injection of BMCs improve glucose levels, lipid metabolism and remodeling of the aortic wall in animals using atherogenic diet.

Indexed as

Bone Marrow TransplantationVascular RemodelingActinsAnimalsAorta, ThoracicAortic DiseasesAtherosclerosisBiomarkersBlood GlucoseDiet, High-FatDisease Models, AnimalLipidsMaleMice, Inbred C57BLProliferating Cell Nuclear AntigenTime FactorsActa2 protein, mouseActinsBiomarkersBlood GlucoseLipidsProliferating Cell Nuclear AntigenVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseaorta remodelingatherogenic dietBone marrow cells

Identifiers

PMID25337194
PMCPMC4203165

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.