Evidence map›Paper›PMID 32960290›Full record

Trial reportEuropean journal of nutrition2021

Comparative studies of urolithins and their phase II metabolites on macrophage and neutrophil functions.

Aneta Bobowska, Sebastian Granica, Agnieszka Filipek, Matthias F Melzig, Thomas Moeslinger, Jürgen Zentek, Aleksandra Kruk, Jakub P Piwowarski

Open access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in European journal of nutrition, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.0field-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

31 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  3. Metabolic fate of rambutan (Food chemistry: X · 2026
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  12. Saudi journal of biological sciences · 2023
    Article
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  17. Preventive and Therapeutic Effects ofInternational journal of molecular sciences · 2023
    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

8 authors at 3 institutions in 3 countries.

Aneta BobowskaDepartment of Pharmacognosy and Molecular Basis of Phytotherapy, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097, Warsaw, Poland.
Sebastian GranicaDepartment of Pharmacognosy and Molecular Basis of Phytotherapy, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097, Warsaw, Poland.
Agnieszka FilipekDepartment of Pharmacognosy and Molecular Basis of Phytotherapy, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097, Warsaw, Poland.
Matthias F MelzigDepartment of Pharmaceutical Biology, Institute of Pharmacy, Freie Universität Berlin, Berlin, Germany.
Thomas MoeslingerInstitute of Physiology, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Jürgen ZentekInstitute of Animal Nutrition, Freie Universität Berlin, Berlin, Germany.
Aleksandra KrukDepartment of Pharmacognosy and Molecular Basis of Phytotherapy, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097, Warsaw, Poland.
Jakub P PiwowarskiDepartment of Pharmacognosy and Molecular Basis of Phytotherapy, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097, Warsaw, Poland. jakub.piwowarski@wum.edu.pl.ORCID http://orcid.org/0000-0002-5011-0983
Medical University of Warsaw · PLFreie Universität Berlin · DEMedical University of Vienna · AT

Funding

Polish Ministry of Science and Higher Education Iuventus Plus [IP2015 062274]
6 · The paper itself

Abstract

purposeEllagitannins are high molecular weight polyphenols present in high quantities in various food products. They are metabolized by human and animal gut microbiota to postbiotic metabolites-urolithins, bioavailable molecules of a low molecular weight. Following absorption in the gut, urolithins rapidly undergo phase II metabolism. Thus, to fully evaluate the mechanisms of their biological activity, the in vitro studies should be conducted for their phase II conjugates, mainly glucuronides. The aim of the study was to comparatively determine the influence of urolithin A, iso-urolithin A, and urolithin B together with their respective glucuronides on processes associated with the inflammatory response.

methodsThe urolithins obtained by chemical synthesis or isolation from microbiota cultures were tested with their respective glucuronides isolated from human urine towards modulation of inflammatory response in THP-1-derived macrophages, RAW 264.7 macrophages, PBMCs-derived macrophages, and primary neutrophils.

resultsUrolithin A was confirmed to be the most active metabolite in terms of LPS-induced inflammatory response inhibition (TNF-α attenuation, IL-10 induction). The observed strong induction of ERK1/2 phosphorylation has been postulated as the mechanism of its action. None of the tested glucuronide conjugates was active in terms of pro-inflammatory TNF-α inhibition and anti-inflammatory IL-10 and TGF-β1 induction.

conclusionComparative studies of the most abundant urolithins and their phase II conjugates conducted on human and murine immune cells unambiguously confirmed urolithin A to be the most active metabolite in terms of inhibition of the inflammatory response. Phase II metabolism was shown to result in the loss of urolithins' pharmacological properties.

Indexed as

Gastrointestinal MicrobiomeNeutrophilsAnimalsAnti-Inflammatory AgentsCoumarinsHumansHydrolyzable TanninsMacrophagesMiceAnti-Inflammatory AgentsCoumarinsHydrolyzable TanninsEllagitanninsInflammationPhase II metabolismPostbioticsUrolithins

Identifiers

PMID32960290
PMCPMC8137622
OpenAlexW3087154711

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.