Evidence map›Paper›PMID 31835656›Full record

ArticleInternational journal of molecular sciences2019

Fingolimod Plays Role in Attenuation of Myocardial Injury Related to Experimental Model of Cardiac Arrest and Extracorporeal Life Support Resuscitation.

Naseer Ahmed, Abid H Laghari, Bashar AlBkhoor, Sobia Tabassum, Sultan Ayoub Meo, Nazeer Muhammad, Daniele Linardi, Abeer A Al-Masri, Guido Fumagalli, Giovanni Battista Luciani and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

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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

12 authors at 6 institutions in 4 countries.

Naseer AhmedDepartment of Biological and Biomedical Sciences, The Aga Khan University, Karachi 74800, Pakistan.
Abid H LaghariDepartment of Medicine, section of Cardiology, Aga Khan University, Karachi 74800, Pakistan.
Bashar AlBkhoorQueen Ali Heart Institute, Amman 111881, Jordan.ORCID 0000-0001-7129-098X
Sobia TabassumDepartment of Biological Sciences, International Islamic University, Islamabad 44000, Pakistan.
Sultan Ayoub MeoDepartment of Physiology, College of Medicine, King Saud University, Riyadh 11461, Saudi Arabia.
Nazeer MuhammadCOMSATS University Islamabad, Wah Campus, Rawalpindi 47040, Pakistan.ORCID 0000-0002-4056-9854
Daniele LinardiDepartment of Surgery, Cardiac Surgery Division, University of Verona Medical School, 37129 Verona, Italy.
Abeer A Al-MasriDepartment of Physiology, College of Medicine, King Saud University, Riyadh 11461, Saudi Arabia.
Guido FumagalliDepartment of Diagnostics and Public Health, Section of Pharmacology, University of Verona Medical School, 37134 Verona, Italy.
Giovanni Battista LucianiDepartment of Surgery, Cardiac Surgery Division, University of Verona Medical School, 37129 Verona, Italy.
Giuseppe FaggianDepartment of Surgery, Cardiac Surgery Division, University of Verona Medical School, 37129 Verona, Italy.
Alessio RungatscherDepartment of Surgery, Cardiac Surgery Division, University of Verona Medical School, 37129 Verona, Italy.
University of Verona · ITAga Khan University · PKKing Saud University · SACOMSATS University Islamabad · PKInternational Islamic University, Islamabad · PKJordan Hospital · JO

Funding

King Saud University RGP-VPP 181
6 · The paper itself

Abstract

backgroundSudden cardiac arrest is a major global health concern, and survival of patients with ischemia-reperfusion injury is a leading cause of myocardial dysfunction. The mechanism of this phenomenon is not well understood because of the complex pathophysiological nature of the disease. Aim of the study was to investigate the cardioprotective role of fingolimod in an in vivo model of cardiac arrest and resuscitation.

methodsIn this study, an in vivo rat model of cardiac arrest using extracorporeal membrane oxygenation resuscitation monitored by invasive hemodynamic measurement was developed. At the beginning of extracorporeal life support (ECLS), animals were randomly treated with fingolimod (Group A,

resultsTreatment with fingolimod resulted in activation of survival pathways resulting into reduced inflammation, myocardial oxidative stress and apoptosis of cardiomyocytes. This led to significant improvement in systolic and diastolic functions of the left ventricle and improved contractility index.

conclusionsSphingosine1phosphate receptor activation with fingolimod improved cardiac function after cardiac arrest supported with ECLS. Present study findings strongly support a cardioprotective role of fingolimod through sphingosine-1-phosphate receptor activation during reperfusion after circulatory arrest.

Indexed as

Cardiopulmonary ResuscitationAnimalsApoptosisbcl-2-Associated X ProteinBiomarkersCollagenDisease Models, AnimalFingolimod HydrochlorideHeart ArrestHemodynamicsInflammation MediatorsMyocardiumNeutrophil InfiltrationNitrosative StressNucleotidesOxidative Stressbcl-2-Associated X ProteinBiomarkersCollagenFingolimod HydrochlorideInflammation MediatorsNucleotidescardiac arrestcardioprotectionextracorporeal life supportfingolimodresuscitation

Identifiers

PMID31835656
PMCPMC6940876
OpenAlexW2994707330

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.