Evidence map›Paper›PMID 27999878›Full record

ArticleArchives of toxicology2017

In vivo imaging of systemic transport and elimination of xenobiotics and endogenous molecules in mice.

Raymond Reif, Ahmed Ghallab, Lynette Beattie, Georgia Günther, Lars Kuepfer, Paul M Kaye, Jan G Hengstler

Open access · hybridAbstract read
In one paragraph

Article in Archives of toxicology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 58 citations in OpenAlex.

  1. A 3D In Vitro Model of the Human Hepatobiliary Junction.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  11. Intravital Imaging of Inflammatory Response in Liver Disease.Frontiers in cell and developmental biology · 2022
    Review
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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

7 authors at 5 institutions in 4 countries.

Raymond ReifLeibniz Research Centre for Working Environment and Human Factors, Technical University Dortmund, Dortmund, Germany. reif@ifado.de.
Ahmed GhallabLeibniz Research Centre for Working Environment and Human Factors, Technical University Dortmund, Dortmund, Germany. ghallab@ifado.de.ORCID http://orcid.org/0000-0003-0695-3403
Lynette BeattieCentre for Immunology and Infection, University of York, York, UK.
Georgia GüntherLeibniz Research Centre for Working Environment and Human Factors, Technical University Dortmund, Dortmund, Germany.
Lars KuepferComputational Systems Biology, Bayer Technology Services GmbH, Leverkusen, Germany.
Paul M KayeCentre for Immunology and Infection, University of York, York, UK.
Jan G HengstlerLeibniz Research Centre for Working Environment and Human Factors, Technical University Dortmund, Dortmund, Germany. hengstler@ifado.de.
TU Dortmund University · DEBayer (Germany) · DEQIMR Berghofer Medical Research Institute · AUSouth Valley University · EGUniversity of York · GB

Funding

Medical Research Council G1000230
6 · The paper itself

Abstract

We describe a two-photon microscopy-based method to evaluate the in vivo systemic transport of compounds. This method comprises imaging of the intact liver, kidney and intestine, the main organs responsible for uptake and elimination of xenobiotics and endogenous molecules. The image quality of the acquired movies was sufficient to distinguish subcellular structures like organelles and vesicles. Quantification of the movement of fluorescent dextran and fluorescent cholic acid derivatives in different organs and their sub-compartments over time revealed significant dynamic differences. Calculated half-lives were similar in the capillaries of all investigated organs but differed in the specific sub-compartments, such as parenchymal cells and bile canaliculi of the liver, glomeruli, proximal and distal tubules of the kidney and lymph vessels (lacteals) of the small intestine. Moreover, tools to image immune cells, which can influence transport processes in inflamed tissues, are described. This powerful approach provides new possibilities for the analysis of compound transport in multiple organs and can support physiologically based pharmacokinetic modeling, in order to obtain more precise predictions at the whole body scale.

Indexed as

AcetaminophenAnimalsChemical and Drug Induced Liver InjuryHepatocytesIntestinesKidneyKupffer CellsLiverMaleMice, TransgenicMicroscopyVideo RecordingXenobioticsAcetaminophenXenobioticsBile canaliculiDrug transportGlomerulusHepatocyteIntravital imagingLactealRenal tubules

Identifiers

PMID27999878
PMCPMC5316407
OpenAlexW2566048187

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.