Direkt zum Inhalt
Merck
  • Dissolution of lipids from mucus: a possible mechanism for prompt disruption of gut barrier function by alcohol.

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

Toxicology letters (2014-12-03)
Xiaofa Qin, Edwin A Deitch
ZUSAMMENFASSUNG

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.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Essigsäure, glacial, ACS reagent, ≥99.7%
Sigma-Aldrich
Essigsäure, glacial, ReagentPlus®, ≥99%
Sigma-Aldrich
Perchlorsäure, ACS reagent, 70%
Sigma-Aldrich
Essigsäure, glacial, ≥99.99% trace metals basis
Sigma-Aldrich
Essigsäure -Lösung, suitable for HPLC
Sigma-Aldrich
Acetaldehyd, ACS reagent, ≥99.5%
Sigma-Aldrich
Acetaldehyd, natural, FG
Sigma-Aldrich
Perchlorsäure, 70%, 99.999% trace metals basis
Sigma-Aldrich
Perchlorsäure, ACS reagent, 60%
Sigma-Aldrich
Acetaldehyd, puriss. p.a., anhydrous, ≥99.5% (GC)
Supelco
Acetaldehyd, PESTANAL®, analytical standard
Sigma-Aldrich
Acetaldehyd, ReagentPlus®, ≥99.0% (GC)
Sigma-Aldrich
Essigsäure, suitable for luminescence, BioUltra, ≥99.5% (GC)
USP
Eisessig, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
5α-Androstan-17β-ol-3-on, ≥97.5%
Supelco
Essigsäure, analytical standard
Sigma-Aldrich
Acetaldehyd -Lösung, 50 wt. % in ethanol
Sigma-Aldrich
Essigsäure, ≥99.5%, FCC, FG
Sigma-Aldrich
Acetaldehyd -Lösung, 40 wt. % in H2O
Sigma-Aldrich
Essigsäure, natural, ≥99.5%, FG
Sigma-Aldrich
Acetaldehyd -Lösung, 5 M in THF
Sigma-Aldrich
5α-Androstan-17β-ol-3-on, purum, ≥99.0% (TLC)
Supelco
Perchlorsäure-Konzentrat, 0.01 M HClO4 in water (0.01N), eluent for IC
Sigma-Aldrich
Acetaldehyd -Lösung, 40 wt. % in isopropanol
Sigma-Aldrich
β-D-Allose, rare aldohexose sugar
Supelco
5α-Androstan-17β-ol-3-on, VETRANAL®, analytical standard
Sigma-Aldrich
Essigsäure-12C2, 99.9 atom % 12C
Millipore
Bifido Selektives Supplement B, suitable for microbiology