Evidence map›Paper›PMID 25445722›Full record

ArticleToxicology letters2015

Dissolution of lipids from mucus: a possible mechanism for prompt disruption of gut barrier function by alcohol.

Xiaofa Qin, Edwin A Deitch

Open access · greenAbstract read
In one paragraph

Article in Toxicology letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Engineering the Mucus Barrier.Annual review of biomedical engineering · 2018
    Review
  13. Article
  14. Article
  15. 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

2 authors at 1 institution in 1 country.

Xiaofa QinDepartment of Surgery, Rutgers-New Jersey Medical School, Newark, NJ 07103, USA. Electronic address: xiaofa_qin@yahoo.com.
Edwin A DeitchDepartment of Surgery, Rutgers-New Jersey Medical School, Newark, NJ 07103, USA.
Rutgers, The State University of New Jersey · US

Funding

Shock, Trauma and Gut Origin SepsisR01GM059841 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI DEITCH, EDWIN A · 1999 to 2012
$5.6M
NIGMS NIH HHS GM 59841NIGMS NIH HHS R01 GM059841
6 · The paper itself

Abstract

Acute and/or chronic alcohol ingestion has been shown to exacerbate the morbidity and mortality rate associated with acute mechanical and/or thermal trauma. While alcohol ingestion can affect many organs and systems, clinical and preclinical studies indicate that alcohol ingestion can cause a 'leaky gut' syndrome which in turn contributes to infection and systemic organ dysfunction. This study investigated the acute effect of alcohol on gut barrier function. Using an in vivo isolated gut sac model of naïve male rats, each individual gut sac was injected with different concentrations (0, 5, 10, 20, and 40%, v/v) of alcohol. After different times of alcohol exposure, each isolated gut segment was harvested and intestinal permeability and mucosal surface hydrophobicity (a physiologic marker of mucus barrier function) were measured as well as luminal DNA, mucus, protein and free fatty acids. The results showed that alcohol caused dose-dependent and time-dependent increases in gut permeability and decreases in mucosal surface hydrophobicity, with significant changes to be observed 5 min after treatment with 10% alcohol. In addition, it is further found that these changes in permeability and hydrophobicity are more closely associated with increased intestinal luminal free fatty acids levels but not protein or DNA levels. These results suggest that alcohol may cause loss of gut barrier function by extracting and dissolving lipids from the mucus with a resultant decrease in mucosal surface hydrophobicity, which is a critical component of gut barrier function.

Indexed as

AnimalsCentral Nervous System DepressantsDNADose-Response Relationship, DrugEthanolFatty Acids, NonesterifiedGastric MucosaGastrointestinal TractIn Vitro TechniquesLipidsMaleMucusPermeabilityRatsRats, Sprague-DawleyStomachCentral Nervous System DepressantsDNAEthanolFatty Acids, NonesterifiedLipidsAlcoholFree fatty acidsGut permeabilityMucosal hydrophobicityMucus

Identifiers

PMID25445722
PMCPMC4291284
OpenAlexW1993023619

What OpenQuestion holds

Textmetadata
LicenceTDM
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.