The effect of probiotic Escherichia coli strain Nissle 1917 lipopolysaccharide on the 5-aminosalicylic acid transepithelial transport across Caco-2 cell monolayers
Jazyk angličtina Země Slovensko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23846256
DOI
10.4149/gpb_2013035
Knihovny.cz E-zdroje
- MeSH
- antiflogistika nesteroidní metabolismus MeSH
- biologický transport účinky léků MeSH
- Caco-2 buňky MeSH
- epitelové buňky cytologie účinky léků metabolismus MeSH
- Escherichia coli chemie MeSH
- intracelulární prostor účinky léků metabolismus MeSH
- kultivační média speciální chemie MeSH
- lidé MeSH
- lipopolysacharidy farmakologie MeSH
- mesalamin metabolismus MeSH
- permeabilita účinky léků MeSH
- probiotika chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antiflogistika nesteroidní MeSH
- kultivační média speciální MeSH
- lipopolysacharidy MeSH
- mesalamin MeSH
The object of this study was to investigate the effect of probiotic Escherichia coli strain Nissle 1917 (EcN) (i) EcN lipopolysaccharide (EcN LPS) and (ii) bacteria-free supernatant of EcN suspension (EcN supernatant) on in vitro transepithelial transport of mesalazine (5-aminosalicylic acid, 5-ASA), the most commonly prescribed anti-inflammatory drug in inflammatory bowel disease (IBD). Effect of co-administered EcN LPS (100 µg/ml) or EcN supernatant (50 µg/ml) on the 5-ASA transport (300 µmol/l) was studied using the Caco-2 monolayer (a human colon carcinoma cell line) as a model of human intestinal absorption. Permeability characteristics for absorptive and secretory transport of parent drug and its intracellularly-formed metabolite were determined. The quantification of 5-ASA and its main metabolite N-acetyl-5-amino-salicylic acid (N-Ac-5-ASA) was performed by high performance liquid chromatography. Obtained results suggest that neither EcN LPS nor EcN supernatant had effect on the total 5-ASA transport (secretory flux greater than absorptive flux) and on the transport of intracellularly formed N-Ac-5-ASA (preferentially transported in the secretory direction). The percent cumulative transport of the total 5-ASA alone or in combination with EcN LPS or EcN supernatant did not exceed 1%.
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