Evidence map›Paper›PMID 28740200›Full record

ArticleScientific reports2017

Physiologically-based modelling in mice suggests an aggravated loss of clearance capacity after toxic liver damage.

Arne Schenk, Ahmed Ghallab, Ute Hofmann, Reham Hassan, Michael Schwarz, Andreas Schuppert, Lars Ole Schwen, Albert Braeuning, Donato Teutonico, Jan G Hengstler and 1 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 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

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  8. Frontiers in bioengineering and biotechnology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 8 institutions in 3 countries.

Arne SchenkJoint Research Center for Computational Biomedicine, RWTH Aachen University, Aachen, Germany.
Ahmed GhallabLeibniz Research Centre for Working Environment and Human Factors at the Technical University Dortmund, Dortmund, Germany.
Ute HofmannDr. Margarete Fischer-Bosch Institute of Clinical Pharmacology and University of Tuebingen, Stuttgart, Germany.
Reham HassanLeibniz Research Centre for Working Environment and Human Factors at the Technical University Dortmund, Dortmund, Germany.
Michael SchwarzGerman Federal Institute for Risk Assessment, Dept. Food Safety, Berlin, Germany.
Andreas SchuppertJoint Research Center for Computational Biomedicine, RWTH Aachen University, Aachen, Germany.
Lars Ole SchwenFraunhofer MEVIS, Bremen, Germany.ORCID 0000-0003-0195-9603
Albert BraeuningGerman Federal Institute for Risk Assessment, Dept. Food Safety, Berlin, Germany.
Donato TeutonicoSystems Pharmacology, Bayer AG, Leverkusen, Germany.
Jan G HengstlerLeibniz Research Centre for Working Environment and Human Factors at the Technical University Dortmund, Dortmund, Germany.
Lars KuepferSystems Pharmacology, Bayer AG, Leverkusen, Germany. lars.kuepfer@bayer.com.
Bayer (Germany) · DEFederal Institute for Risk Assessment · DESouth Valley University · EGDr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology · DEFraunhofer Institute for Digital Medicine · DEInstitut de Relations Internationales et Stratégiques · FRRWTH Aachen University · DETU Dortmund University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diseases and toxins may lead to death of active liver tissue, resulting in a loss of total clearance capacity at the whole-body level. However, it remains difficult to study, whether the loss of metabolizing tissue is sufficient to explain loss of metabolic capacity of the liver or whether the surviving tissue undergoes an adaptive response to compensate the loss. To understand the cellular impact of toxic liver damage in an in vivo situation, we here used physiologically-based pharmacokinetic modelling to investigate pharmacokinetics of a specifically designed drug cocktail at three different sampling sites of the body in healthy mice and mice treated with carbon tetrachloride (CCl

Indexed as

AnimalsCarbon TetrachlorideChemical and Drug Induced Liver InjuryDrug DesignLiverMaleMiceMice, Inbred C57BLPharmaceutical PreparationsTissue DistributionCarbon TetrachloridePharmaceutical Preparations

Identifiers

PMID28740200
PMCPMC5524914
OpenAlexW2737338770

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.