Evidence map›Paper›PMID 37667267›Full record

ArticleBMC pulmonary medicine2023

Changes in the levels of free sialic acid during ex vivo lung perfusion do not correlate with pulmonary function. Experimental model.

Claudia Hernández-Jiménez, Javier Martínez-Cortés, J Raúl Olmos-Zuñiga, Rogelio Jasso-Victoria, María Teresa López-Pérez, Néstor Emmanuel Díaz-Martínez, Marcelino Alonso-Gómez, Axel Edmundo Guzmán-Cedillo, Matilde Baltazares-Lipp, Miguel Gaxiola-Gaxiola and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2023. 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
0.1field-weighted citation impact, top 60% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

15 authors at 3 institutions in 1 country.

Claudia Hernández-JiménezDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico. claudia_herjim@yahoo.com.
Javier Martínez-CortésDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
J Raúl Olmos-ZuñigaExperimental Lung Transplant Unit of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Rogelio Jasso-VictoriaDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
María Teresa López-PérezNursing Research Coordination of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Néstor Emmanuel Díaz-MartínezDepartment of Medical and Pharmaceutical Biotechnology, Center for Research and Assistance in Technology and Design of the State of Jalisco, Jalisco, Mexico.
Marcelino Alonso-GómezDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Axel Edmundo Guzmán-CedilloDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Matilde Baltazares-LippDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Miguel Gaxiola-GaxiolaLaboratory of Morphology of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Adriana Méndez-BernalElectron Microscopy Unit, Faculty of Veterinary Medicine and Zootechnics, National Autonomous University of Mexico, Mexico City, Mexico.
Adrián Polo-JerézDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Juan Carlos Vázquez-MineroCardiothoracic Surgery Service of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Oscar Hernández-PérezDepartment of Physiology, School of Medicine, National Autonomous University of Mexico, Mexico City, Mexico.
Christopher O Fernández-SolísDepartment of Surgery Research of National Institute of Respiratory Diseases Ismael Cosío Villegas, Mexico City, Mexico.
Instituto Nacional de Enfermedades Respiratorias · MXUniversidad Nacional Autónoma de México · MXSecretaría de Salud de Jalisco · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEx vivo lung perfusion (EVLP) constitutes a tool with great research potential due to its advantages over in vivo and in vitro models. Despite its important contribution to lung reconditioning, this technique has the disadvantage of incurring high costs and can induce pulmonary endothelial injury through perfusion and ventilation. The pulmonary endothelium is made up of endothelial glycocalyx (EG), a coating of proteoglycans (PG) on the luminal surface. PGs are glycoproteins linked to terminal sialic acids (Sia) that can affect homeostasis with responses leading to edema formation. This study evaluated the effect of two ex vivo perfusion solutions on lung function and endothelial injury.

methodsWe divided ten landrace swine into two groups and subjected them to EVLP for 120 min: Group I (n = 5) was perfused with Steen® solution, and Group II (n = 5) was perfused with low-potassium dextran-albumin solution. Ventilatory mechanics, histology, gravimetry, and sialic acid concentrations were evaluated.

resultsBoth groups showed changes in pulmonary vascular resistance and ventilatory mechanics (p < 0.05, Student's t-test). In addition, the lung injury severity score was better in Group I than in Group II (p < 0.05, Mann-Whitney U); and both groups exhibited a significant increase in Sia concentrations in the perfusate (p < 0.05 t-Student) and Sia immunohistochemical expression.

conclusionsSia, as a product of EG disruption during EVLP, was found in all samples obtained in the system; however, the changes in its concentration showed no apparent correlation with lung function.

Indexed as

Lung InjuryN-Acetylneuraminic AcidAnimalsLungModels, TheoreticalPerfusionRespirationSwineN-Acetylneuraminic AcidExperimental modelEx vivo lung perfusionN-Acetylneuraminic acidOrgan preservation solution

Identifiers

PMID37667267
PMCPMC10478437
OpenAlexW4386422160

What OpenQuestion holds

Textmetadata
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.