Source:http://linkedlifedata.com/resource/pubmed/id/16047471
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2005-7-28
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pubmed:abstractText |
The aim of this study was to investigate the effect of Clostridium difficile toxin A (TxA) on intestinal epithelial cell migration, apoptosis, and transepithelial resistance and to evaluate the effect of glutamine (Gln) and its stable derivative, alanyl-glutamine (Ala-Gln), on TxA-induced damage. Migration was measured in rat intestinal epithelial cells (IEC-6) 6 and 24 hr after a razor scrape of the cell monolayer. Cell proliferation was indirectly measured utilizing the tetrazolium salt WST-1. The cells were incubated with TxA (1-100 ng/ml) in medium without Gln or medium containing Gln or Ala-Gln (1-30 mM). Apoptosis was quantified in IEC-6 cells using annexin V assay. Transepithelial resistance was measured using an epithelial voltohmmeter across T84 cells seeded on a transwell filter. TxA-induced a dose-dependent reduction of migration and also caused dose and time-dependent apoptosis in IEC-6 cells. Gln and Aln-Gln significantly enhanced IEC-6 cell migration and proliferation. Gln and Ala-Gln also prevented the inhibition of migration, apoptosis, and the initial drop in transepithelial resistance induced by TxA. In conclusion, both peptides reduced toxin-induced epithelial damage and thus might play an adjunctive role in C. difficile-induced colitis therapy.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Toxins,
http://linkedlifedata.com/resource/pubmed/chemical/Dipeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Enterotoxins,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamine,
http://linkedlifedata.com/resource/pubmed/chemical/alanylglutamine,
http://linkedlifedata.com/resource/pubmed/chemical/tcdA protein, Clostridium difficile
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0163-2116
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
50
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1271-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16047471-Animals,
pubmed-meshheading:16047471-Apoptosis,
pubmed-meshheading:16047471-Bacterial Toxins,
pubmed-meshheading:16047471-Cell Line,
pubmed-meshheading:16047471-Cell Movement,
pubmed-meshheading:16047471-Cell Proliferation,
pubmed-meshheading:16047471-Dipeptides,
pubmed-meshheading:16047471-Dose-Response Relationship, Drug,
pubmed-meshheading:16047471-Electric Impedance,
pubmed-meshheading:16047471-Enterotoxins,
pubmed-meshheading:16047471-Epithelial Cells,
pubmed-meshheading:16047471-Glutamine,
pubmed-meshheading:16047471-Intestines,
pubmed-meshheading:16047471-Necrosis,
pubmed-meshheading:16047471-Rats,
pubmed-meshheading:16047471-Time Factors
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pubmed:year |
2005
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pubmed:articleTitle |
Clostridium difficile toxin A induces intestinal epithelial cell apoptosis and damage: role of Gln and Ala-Gln in toxin A effects.
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pubmed:affiliation |
Center for Global Health, Department of Intemal Medicine, School of Medicine, University of Virginia, Charlottesville, Virginia, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, N.I.H., Extramural
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