Evidence map›Paper›PMID 30217504›Full record

ArticleAlcohol (Fayetteville, N.Y.)2019

Mesenchymal stem cell treatment attenuates liver and lung inflammation after ethanol intoxication and burn injury.

Brenda J Curtis, Jill A Shults, Devin M Boe, Luis Ramirez, Elizabeth J Kovacs

Open access · greenAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 17 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

5 authors at 3 institutions in 1 country.

Brenda J CurtisBurn Research and Alcohol Research Programs, Department of Surgery, Division of GI, Trauma and Endocrine Surgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO, United States.
Jill A ShultsAlcohol Research Program, Burn and Shock Trauma Research Institute, Department of Surgery, Loyola University Chicago, Health Sciences Campus, Stritch School of Medicine, Maywood, IL, United States.
Devin M BoeBurn Research and Alcohol Research Programs, Department of Surgery, Division of GI, Trauma and Endocrine Surgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO, United States.
Luis RamirezAlcohol Research Program, Burn and Shock Trauma Research Institute, Department of Surgery, Loyola University Chicago, Health Sciences Campus, Stritch School of Medicine, Maywood, IL, United States.
Elizabeth J KovacsBurn Research and Alcohol Research Programs, Department of Surgery, Division of GI, Trauma and Endocrine Surgery, University of Colorado Denver, Anschutz Medical Campus, Aurora, CO, United States. Electronic address: Elizabeth.Kovacs@UCDenver.edu.
Loyola University Chicago · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Colorado Denver · US

Funding

Ethanol Effects on Recovery after InjuryR01GM115257 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI KOVACS, ELIZABETH J. · 2015 to 2018
$1.7M
Binge alcohol intoxication, mesenchymal stem cells and lung inflammationR21AA023193 · NIAAA · UNIVERSITY OF COLORADO DENVER · PI KOVACS, ELIZABETH J. · 2015 to 2016
$402k
Ethanol, Lung Mesenchymal Stem Cells and Pulmonary Inflammation After Burn InjuryF31AA022566 · NIAAA · LOYOLA UNIVERSITY CHICAGO · PI SHULTS, JILL ANN · 2013 to 2015
$77k
NIAAA NIH HHS F31 AA022566NIAAA NIH HHS R21 AA023193NIGMS NIH HHS R01 GM115257
6 · The paper itself

Abstract

Cutaneous burn injury is one of the most devastating injuries one can obtain, with tissue damage extending beyond the skin wound to distal organs, including the gastrointestinal tract, liver, and lungs. Multiple organ failure is a leading cause of death after burn injury, resulting in excessive systemic and localized inflammation directly contributing to end organ damage. We postulated that the gut-liver-lung inflammatory axis underscores multiple organ failure in the context of burn injury and is hyper-activated when ethanol intoxication precedes burn. Mesenchymal stem cells (MSCs) are regenerative and anti-inflammatory, and MSC treatment has been shown to be beneficial in several immune disorders and injury models. Our objective was to determine whether intravenous infusion of exogenous bone marrow-derived MSCs could reduce post-burn and intoxication pulmonary, hepatic, and systemic inflammation. Vehicle- or ethanol- (1.6 g/kg) treated mice were subjected to sham or 15% total body surface area scald burn. One hour post-injury, mice were given 5 × 10

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsBinge DrinkingBurnsChemokinesCytokinesDisease Models, AnimalEthanolFlow CytometryHepatitis, AlcoholicIn Situ Nick-End LabelingMaleMiceMice, Inbred C57BLPneumoniaPolymerase Chain ReactionChemokinesCytokinesEthanolAlcoholApoptosisBurn injuryLiverLungMesenchymal stem cells

Identifiers

PMID30217504
PMCPMC6411458
OpenAlexW2890389264

What OpenQuestion holds

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LicenceTDM
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.