Evidence map›Paper›PMID 28572613›Full record

ArticleScientific reports2017

Mesenchymal stem cells correct haemodynamic dysfunction associated with liver injury after extended resection in a pig model.

Hans-Michael Tautenhahn, Sandra Brückner, Christiane Uder, Silvio Erler, Madlen Hempel, Martin von Bergen, Janine Brach, Sandra Winkler, Franziska Pankow, Claudia Gittel and 8 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
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

18 authors at 8 institutions in 1 country.

Hans-Michael TautenhahnClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Sandra BrücknerClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Christiane UderClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Silvio ErlerInstitute of Biology, Molecular Ecology, Martin-Luther-University Halle-Wittenberg, Hoher Weg 4, 06099, Halle, Germany.ORCID 0000-0002-9425-8103
Madlen HempelClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Martin von BergenDepartment of Molecular Systems Biology, Helmholtz Centre for Environmental Research, Permoser Strasse 15, 04318, Leipzig, Germany.
Janine BrachClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Sandra WinklerClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Franziska PankowClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Claudia GittelLarge Animal Clinic for Surgery, University of Leipzig, An den Tierkliniken 21, 04103, Leipzig, Germany.
Manja BaunackLarge Animal Clinic for Surgery, University of Leipzig, An den Tierkliniken 21, 04103, Leipzig, Germany.
Undine LangeClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Johannes BroschewitzClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Matthias DollingerDepartment of Medicine I, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.
Michael BartelsClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany.
Uta PietschDepartment of Anaesthesiology and Intensive Care, University Hospital Leipzig, Liebigstraße 20, 04103, Leipzig, Germany.
Kerstin AmannDepartment of Nephropathology, University Hospital Erlangen, Krankenhausstr. 8-10, 91054, Erlangen, Germany.
Bruno ChristClinics of Visceral, Transplantation, Thoracic and Vascular Surgery, University of Leipzig, Liebigstraße 21, 04103, Leipzig, Germany. bruno.christ@medizin.uni-leipzig.de.ORCID 0000-0001-8213-9548
Leipzig University · DEUniversity Hospital Leipzig · DEHelios Park-Klinikum Leipzig · DEHelmholtz Centre for Environmental Research · DEJena University Hospital · DEMartin Luther University Halle-Wittenberg · DEUniversitätsklinikum Erlangen · DEUniversity Hospital Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In patients, acute kidney injury (AKI) is often due to haemodynamic impairment associated with hepatic decompensation following extended liver surgery. Mesenchymal stem cells (MSCs) supported tissue protection in a variety of acute and chronic diseases, and might hence ameliorate AKI induced by extended liver resection. Here, 70% liver resection was performed in male pigs. MSCs were infused through a central venous catheter and haemodynamic parameters as well as markers of acute kidney damage were monitored under intensive care conditions for 24 h post-surgery. Cytokine profiles were established to anticipate the MSCs' potential mode of action. After extended liver resection, hyperdynamic circulation, associated with hyponatraemia, hyperkalaemia, an increase in serum aldosterone and low urine production developed. These signs of hepatorenal dysfunction and haemodynamic impairment were corrected by MSC treatment. MSCs elevated PDGF levels in the serum, possibly contributing to circulatory homeostasis. Another 14 cytokines were increased in the kidney, most of which are known to support tissue regeneration. In conclusion, MSCs supported kidney and liver function after extended liver resection. They probably acted through paracrine mechanisms improving haemodynamics and tissue homeostasis. They might thus provide a promising strategy to prevent acute kidney injury in the context of post-surgery acute liver failure.

Indexed as

HemodynamicsMesenchymal Stem Cell TransplantationAcute Kidney InjuryAnimalsBlood PressureDisease Models, AnimalLiverMaleParacrine CommunicationSus scrofa

Identifiers

PMID28572613
PMCPMC5454025
OpenAlexW2619274596

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.