Evidence map›Paper›PMID 28800748›Full record

ArticleBMC pharmacology & toxicology2017

Short-term treatment with taurolidine is associated with liver injury.

René Fahrner, Anika Möller, Adrian T Press, Andreas Kortgen, Michael Kiehntopf, Falk Rauchfuss, Utz Settmacher, Alexander S Mosig

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 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
0.6field-weighted citation impact, top 32% 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, 16 citations in OpenAlex.

  1. Review
  2. In vitro liver models for toxicological research.Drug metabolism and pharmacokinetics · 2025
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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

8 authors at 1 institution in 1 country.

René FahrnerDepartment of General, Visceral and Vascular Surgery, University Hospital Jena, 07747, Jena, Germany. rene.fahrner@med.uni-jena.de.
Anika MöllerDepartment of General, Visceral and Vascular Surgery, University Hospital Jena, 07747, Jena, Germany.
Adrian T PressCenter for Sepsis Control and Care (CSCC), University Hospital Jena, 07747, Jena, Germany.
Andreas KortgenCenter for Sepsis Control and Care (CSCC), University Hospital Jena, 07747, Jena, Germany.
Michael KiehntopfCenter for Sepsis Control and Care (CSCC), University Hospital Jena, 07747, Jena, Germany.
Falk RauchfussDepartment of General, Visceral and Vascular Surgery, University Hospital Jena, 07747, Jena, Germany.
Utz SettmacherDepartment of General, Visceral and Vascular Surgery, University Hospital Jena, 07747, Jena, Germany.
Alexander S MosigCenter for Sepsis Control and Care (CSCC), University Hospital Jena, 07747, Jena, Germany.
Jena University Hospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTaurolidine has been used for peritonitis, oncological and catheter-lock treatment because of its anti-inflammatory properties. It has been suggested that taurolidine has no severe side-effects, but after long-term use morphological and functional changes of the liver were reported. The aim of this study was to investigate the effect of short-term use of taurolidine on the liver.

methodsIn HepaRG cell cultures and on a novel liver biochip dose-dependent effects of taurolidine treatment on hepatocyte adherence and cell viability was investigated. Furthermore, liver enzymes and interleukin- (IL-) 6 were measured in supernatants. Male rats were treated with low- or high-dose taurolidine, respectively, and compared to controls with physiological saline solution administration regarding blood serum parameters and histology.

resultsIn HepaRG cell cultures, hepatocyte adherence was significantly decreased, cell death and cleaved caspase-3 were significantly increased after administration of taurolidine in a dose-dependent manner. High-dose application of taurolidine led to elevated liver enzymes and IL-6 secretion in hepatic organoid. After 24 h a significant increase of serum GLDH and ASAT was observed in rats treated with high-dose taurolidine treatment.

conclusionsOur results suggest that taurolidine caused liver injury after short-term use in in vitro and in vivo models probably due to direct toxic effects on hepatocytes. Therefore, the taurolidine dose should be titrated in further investigations regarding liver injury and inflammation.

Indexed as

AnimalsAspartate AminotransferasesCaspase 3Cell AdhesionCell LineCell SurvivalChemical and Drug Induced Liver Injury, ChronicCytokinesGlutamate DehydrogenaseHumansLiverMaleRats, Inbred LewTaurineThiadiazinesAspartate AminotransferasesCASP3 protein, humanCaspase 3CytokinesGlutamate DehydrogenaseTaurinetaurolidineThiadiazinesCytokinesLiver biochipLiver enzymesLiver injuryTaurolidine

Identifiers

PMID28800748
PMCPMC5553585
OpenAlexW2743562019

What OpenQuestion holds

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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.