Evidence map›Paper›PMID 32306507›Full record

ArticleMolecular nutrition & food research2020

Inhibition of 5-Lipoxygenase-Derived Leukotrienes and Hemiketals as a Novel Anti-Inflammatory Mechanism of Urolithins.

Juan Antonio Giménez-Bastida, Antonio González-Sarrías, Juan Carlos Espín, Claus Schneider

Open access · greenAbstract read
In one paragraph

Article in Molecular nutrition & food research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Saudi journal of biological sciences · 2023
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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

4 authors at 2 institutions in 2 countries.

Juan Antonio Giménez-BastidaDepartment of Pharmacology and Vanderbilt Institute of Chemical Biology, Vanderbilt University Medical School, Nashville, TN, 37232, USA.ORCID 0000-0002-1244-8764
Antonio González-SarríasLaboratory of Food and Health, Research Group on Quality, Safety and Bioactivity of Plant Foods, Dept. Food Science and Technology, CEBAS-CSIC, P.O. Box 164, Murcia, Campus de Espinardo, 30100, Spain.ORCID 0000-0002-3407-0678
Juan Carlos EspínLaboratory of Food and Health, Research Group on Quality, Safety and Bioactivity of Plant Foods, Dept. Food Science and Technology, CEBAS-CSIC, P.O. Box 164, Murcia, Campus de Espinardo, 30100, Spain.ORCID 0000-0002-1068-8692
Claus SchneiderDepartment of Pharmacology and Vanderbilt Institute of Chemical Biology, Vanderbilt University Medical School, Nashville, TN, 37232, USA.ORCID 0000-0003-4215-967X
Centro de Edafología y Biología Aplicada del Segura · ESVanderbilt University · US

Funding

Convergence of the COX-2 and 5-lipoxygenase pathwaysR01GM076592 · NIGMS · VANDERBILT UNIVERSITY · PI SCHNEIDER, CLAUS · 2007 to 2021
$4.0M
American Heart Association-American Stroke Association 16POST30690001NIGMS NIH HHS R01 GM076592
6 · The paper itself

Abstract

scopeUrolithins (Uro), gut microbial metabolites derived from ellagic acid (EA), reach significant concentrations in the human colon. Uro-A exerts anti-inflammatory activity in animal models of inflammatory bowel diseases (IBDs). It is hypothesized that Uro can modulate the biosynthesis of leukocyte-derived inflammatory eicosanoids from the 5-lipoxygenase (5-LOX), cyclooxygenase-2 (COX-2), and 5-LOX/COX-2 pathways, relevant in the onset and progression of IBDs, including 5-hydroxyeicosatetraenoic acids (5-HETEs), leukotriene-B METHODS AND

resultsLeukocytes, obtained from six healthy donors, are stimulated with lipopolysaccharide and calcium ionophore A23187. Uro, at concentrations found in the human colon (1-15 µm), decrease eicosanoid biosynthesis and COX-2 levels in the activated leukocytes. In contrast, EA and conjugated Uro (glucuronides and sulfates) are inactive. Uro-A and isourolithin-A reduce the formation of the 5-LOX/COX-2 products HKE

conclusionsThe results show that physiologically relevant colonic Uro target eicosanoid biosynthetic pathways. The effect on HKs and LTB

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalArachidonate 5-LipoxygenaseCoumarinsCyclooxygenase 2DinoprostoneEicosanoidsHumansHydrolyzable TanninsHydroxyeicosatetraenoic AcidsLeukocytesLeukotriene B4MiceRAW 264.7 Cells3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one5-hydroxy-6,8,11,14-eicosatetraenoic acidAnti-Inflammatory Agents, Non-SteroidalArachidonate 5-LipoxygenaseCoumarinsCyclooxygenase 2DinoprostoneEicosanoidsHydrolyzable TanninsHydroxyeicosatetraenoic AcidsLeukotriene B4PTGS2 protein, humanurolithin Burolithin C5-lipoxygenasecyclooxygenase-2eicosanoidinflammatory bowel diseaseurolithins

Identifiers

PMID32306507
PMCPMC7297467
OpenAlexW3017034669

What OpenQuestion holds

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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.