Evidence map›Paper›PMID 35806458›Full record

ArticleInternational journal of molecular sciences2022

Improvement of Left Ventricular Graft Function Using an Iron-Chelator-Supplemented Bretschneider Solution in a Canine Model of Orthotopic Heart Transplantation.

Gábor Szabó, Sivakkanan Loganathan, Sevil Korkmaz-Icöz, Ágnes Balogh, Zoltan Papp, Paige Brlecic, Péter Hegedüs, Tamás Radovits, Matthias Karck, Béla Merkely and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
0.4field-weighted citation impact, top 38% 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, 2 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

11 authors at 3 institutions in 2 countries.

Gábor SzabóDepartment of Cardiac Surgery, University of Heidelberg, 69120 Heidelberg, Germany.
Sivakkanan LoganathanDepartment of Cardiac Surgery, University of Heidelberg, 69120 Heidelberg, Germany.
Sevil Korkmaz-IcözDepartment of Cardiac Surgery, University of Heidelberg, 69120 Heidelberg, Germany.
Ágnes BaloghDivision of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Zoltan PappDivision of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0002-4675-1542
Paige BrlecicDepartment of Cardiac Surgery, University of Heidelberg, 69120 Heidelberg, Germany.
Péter HegedüsDepartment of Cardiac Surgery, University of Halle (Saale), 06120 Halle, Germany.
Tamás RadovitsDepartment of Cardiac Surgery, University of Heidelberg, 69120 Heidelberg, Germany.
Matthias KarckDepartment of Cardiac Surgery, University of Heidelberg, 69120 Heidelberg, Germany.
Béla MerkelyDepartment of Cardiac Surgery, University of Halle (Saale), 06120 Halle, Germany.
Gábor VeresDepartment of Cardiac Surgery, University of Heidelberg, 69120 Heidelberg, Germany.
Heidelberg University · DEUniversity of Debrecen · HUSemmelweis University · HU

Funding

Köhler Research Grant, Dr. Franz Köhler Chemie GmBH, Alsbach-Hähnlein, Germany. Köhler Research GrantNational Development Agency National Development Agency of Hungary (TÁMOP)
6 · The paper itself

Abstract

Demand for organs is increasing while the number of donors remains constant. Nevertheless, not all organs are utilized due to the limited time window for heart transplantation (HTX). Therefore, we aimed to evaluate whether an iron-chelator-supplemented Bretschneider solution could protect the graft in a clinically relevant canine model of HTX with prolonged ischemic storage. HTX was performed in foxhounds. The ischemic time was standardized to 4 h, 8 h, 12 h or 16 h, depending on the experimental group. Left ventricular (LV) and vascular function were measured. Additionally, the myocardial high energy phosphate and iron content and the in-vitro myocyte force were evaluated. Iron chelator supplementation proved superior at a routine preservation time of 4 h, as well as for prolonged times of 8 h and longer. The supplementation groups recovered quickly compared to their controls. The LV function was preserved and coronary blood flow increased. This was also confirmed by in vitro myocyte force and vasorelaxation experiments. Additionally, the biochemical results showed significantly higher adenosine triphosphate content in the supplementation groups. The iron chelator LK614 played an important role in this mechanism by reducing the chelatable iron content. This study shows that an iron-chelator-supplemented Bretschneider solution effectively prevents myocardial/endothelial damage during short- as well as long-term conservation.

Indexed as

Heart TransplantationOrgan PreservationAnimalsDietary SupplementsDogsGlucoseHeartIronIron Chelating AgentsMannitolMyocardiumPotassium ChlorideProcaineVentricular Function, LeftBretschneider cardioplegic solutionGlucoseIronIron Chelating AgentsMannitolPotassium ChlorideProcainecustodioliron chelatororthotopic heart transplantation

Identifiers

PMID35806458
PMCPMC9267501
OpenAlexW4284676920

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.