Evidence map›Paper›PMID 30248186›Full record

ArticleBritish journal of pharmacology2018

Alcohol binge disrupts the rat intestinal barrier: the partial protective role of oleoylethanolamide.

M Antón, A Rodríguez-González, A Ballesta, N González, A Del Pozo, F R de Fonseca, M L Gómez-Lus, J C Leza, B García-Bueno, J R Caso and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

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  18. DietaryExperimental and therapeutic medicine · 2021
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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

11 authors at 2 institutions in 1 country.

M AntónDepartment of Psychobiology and Behavioral Science Methods, Faculty of Psychology, Complutense University, Madrid (UCM), and Red de Trastornos Adictivos (RTA) Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
A Rodríguez-GonzálezDepartment of Psychobiology and Behavioral Science Methods, Faculty of Psychology, Complutense University, Madrid (UCM), and Red de Trastornos Adictivos (RTA) Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
A BallestaDepartment of Psychobiology and Behavioral Science Methods, Faculty of Psychology, Complutense University, Madrid (UCM), and Red de Trastornos Adictivos (RTA) Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
N GonzálezDepartment of Medicine Microbiology, Faculty of Medicine, UCM, Madrid, Spain.
A Del PozoDepartment of Psychobiology and Behavioral Science Methods, Faculty of Psychology, Complutense University, Madrid (UCM), and Red de Trastornos Adictivos (RTA) Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
F R de FonsecaDepartment of Psychobiology and Behavioral Science Methods, Faculty of Psychology, Complutense University, Madrid (UCM), and Red de Trastornos Adictivos (RTA) Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
M L Gómez-LusDepartment of Medicine Microbiology, Faculty of Medicine, UCM, Madrid, Spain.
J C LezaDepartment of Pharmacology and Toxicology, Faculty of Medicine, UCM, Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Imas12 and IUINQ, Madrid, Spain.
B García-BuenoDepartment of Pharmacology and Toxicology, Faculty of Medicine, UCM, Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Imas12 and IUINQ, Madrid, Spain.
J R CasoDepartment of Pharmacology and Toxicology, Faculty of Medicine, UCM, Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Imas12 and IUINQ, Madrid, Spain.
L OrioDepartment of Psychobiology and Behavioral Science Methods, Faculty of Psychology, Complutense University, Madrid (UCM), and Red de Trastornos Adictivos (RTA) Instituto de Salud Carlos III (ISCIII), Madrid, Spain.ORCID 0000-0002-9614-4062
Instituto de Salud Carlos III · ESCentro de Investigación Biomédica en Red de Salud Mental · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeChronic alcohol consumption alters the gut-brain axis, but little is known about alcohol binge episodes on the functioning of the intestinal barrier. We investigated the influence of ethanol binges on bacterial translocation, gut inflammation and immunity, and tight junction (TJ) structure and the ability of the biolipid oleoylethanolamide (OEA) to prevent ethanol binge-induced intestinal barrier dysfunction. EXPERIMENTAL APPROACH: OEA was injected i.p. before repeated ethanol administration by oral gavage. Plasma, spleen, liver and mesenteric lymph nodes (MLN) were collected in sterile conditions for determination of bacterial load. Immune/inflammatory parameters, TJ proteins and apoptotic markers were determined in colonic tissue by RT-PCR and Western blotting. TJ ultrastructure was examined by transmission electron microscopy. KEY

resultsEthanol binges induced bacterial translocation to the MLN (mainly) and spleen. Colonic tissues showed signs of inflammation, and activation of innate (Toll-like receptor-4) and adaptive (IgA) immune systems and TJ proteins (occludin and claudin-3) were decreased after ethanol binges. Pretreatment with OEA reduced intestinal inflammation and immune activation and partially preserved the TJ structure affected by alcohol binges but had no effect on alcohol-induced apoptosis. Ultrastructural analyses of colonic TJs revealed dilated TJs in all ethanol groups, with less electron-dense material in non-pretreated rats. The protective effects of i.p. OEA did not reduce bacterial translocation to the MLN. However, intragastric OEA administration significantly reduced plasma LPS levels and bacterial translocation to the MLN. CONCLUSION AND IMPLICATIONS: OEA-based pharmacotherapies could potentially be useful to treat disorders characterized by intestinal barrier dysfunction, including alcohol abuse.

Indexed as

AlcoholismAnimalsAnti-Inflammatory Agents, Non-SteroidalEndocannabinoidsEthanolInflammationIntestinal MucosaMaleOleic AcidsRatsRats, WistarAnti-Inflammatory Agents, Non-SteroidalEndocannabinoidsEthanolOleic Acidsoleoylethanolamide

Identifiers

PMID30248186
PMCPMC6255955
OpenAlexW2894501910

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.