Evidence map›Paper›PMID 26439723›Full record

ArticleEuropean journal of nutrition2017

Gastrointestinal stability of urolithins: an in vitro approach.

Pedro Mena, Margherita Dall'Asta, Luca Calani, Furio Brighenti, Daniele Del Rio

Abstract read
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In one paragraph

Article in European journal of nutrition, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Transformation of Oligomeric Ellagitannins, Typical forJournal of agricultural and food chemistry · 2020
    Article
  9. Review
  10. Ellagic Acid-Derived Urolithins as Modulators of Oxidative Stress.Oxidative medicine and cellular longevity · 2020
    Review
  11. Stability of Principal Hydrolysable Tannins fromMolecules (Basel, Switzerland) · 2019
    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

5 authors at 2 institutions in 2 countries.

Pedro MenaThe Laboratory of Phytochemicals in Physiology, LS9 InterLab Group, Department of Food Science, University of Parma, Parma, Italy. pedromiguel.menaparreno@unipr.it.
Margherita Dall'AstaThe Laboratory of Phytochemicals in Physiology, LS9 InterLab Group, Department of Food Science, University of Parma, Parma, Italy.
Luca CalaniThe Laboratory of Phytochemicals in Physiology, LS9 InterLab Group, Department of Food Science, University of Parma, Parma, Italy.
Furio BrighentiHuman Nutrition Unit, Department of Food Science, University of Parma, Via Volturno 39, 43125, Parma, Italy.
Daniele Del RioThe Laboratory of Phytochemicals in Physiology, LS9 InterLab Group, Department of Food Science, University of Parma, Parma, Italy.
University of Parma · ITUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeUrolithins are bioactive ellagitannin-derived metabolites showing a wide phenotypic variation in their production by the gut microbiota. This work represents a first in vitro step toward the development of new strategies focused on the oral supplementation of urolithins with the aim of overcoming their selective production and making their putative health benefits available for the whole population.

methodsIn order to study their gastrointestinal stability, urolithin A, urolithin B, and urolithin B-glucuronide, as well as ellagic acid, were subjected to a simulated gastrointestinal digestion model consisting of oral, gastric, and pancreatic steps followed by a 24-h fecal fermentation. The effect of the entero-hepatic recirculation on urolithin B-glucuronide, a phase II metabolite, was also investigated.

resultsUrolithin B was the molecule able to resist to a greater extent the conditions of the gastrointestinal tract, while urolithin A and ellagic acid were drastically unstable during the colonic step. Conjugation with glucuronic acid, ideally occurring in the liver, conferred to urolithin B an increased stability, which may be interesting in the framework of entero-hepatic recirculation.

conclusionThis set of experiments lets hypothesize that orally supplemented urolithins may come into contact with the colonic epithelium and become accessible for uptake or exert local anti-inflammatory activity, overcoming the limitations of enterotypes unable to convert ellagitannins into these putatively beneficial metabolites.

Indexed as

Gastrointestinal MicrobiomeChemical PhenomenaColonCoumarinsDigestionEllagic AcidFecesFermentationGastrointestinal TractGlucuronidesHumansHydrolyzable TanninsModels, Biological3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-oneCoumarinsEllagic AcidGlucuronidesHydrolyzable Tanninsurolithin BBioaccessibilityColonic fermentationEllagic acidEllagitanninGastrointestinal tractMicrobial metabolite

Identifiers

PMID26439723
OpenAlexW1866078022

What OpenQuestion holds

Textmetadata
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.