AJP - GI Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Gastrointest Liver Physiol 296: G1140-G1149, 2009. First published February 12, 2009; doi:10.1152/ajpgi.90534.2008
0193-1857/09 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
296/5/G1140    most recent
90534.2008v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mennigen, R.
Right arrow Articles by Bruewer, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mennigen, R.
Right arrow Articles by Bruewer, M.

MUCOSAL BIOLOGY

Probiotic mixture VSL#3 protects the epithelial barrier by maintaining tight junction protein expression and preventing apoptosis in a murine model of colitis

Rudolf Mennigen,1 Kerstin Nolte,1 Emile Rijcken,1 Markus Utech,1 Bettina Loeffler,2 Norbert Senninger,1 and Matthias Bruewer1

1University Hospital Muenster, Department of General and Visceral Surgery; and 2University Hospital Muenster, Department of Microbiology, Muenster, Germany

Submitted 8 September 2008 ; accepted in final form 11 February 2009

Changes in epithelial tight junction protein expression and apoptosis increase epithelial permeability in inflammatory bowel diseases. The effect of the probiotic mixture VSL#3 on the epithelial barrier was studied in dextran sodium sulfate (DSS)-induced colitis in mice. Acute colitis was induced in BALB/c mice (3.5% DSS for 7 days). Mice were treated with either 15 mg VSL#3 or placebo via gastric tube once daily during induction of colitis. Inflammation was assessed by clinical and histological scores. Colonic permeability to Evans blue was measured in vivo. Tight junction protein expression and epithelial apoptotic ratio were studied by immunofluorescence and Western blot. VSL#3 treatment reduced inflammation (histological colitis scores: healthy control 0.94 ± 0.28, DSS + placebo 14.64 ± 2.55, DSS + VSL#3 8.43 ± 1.82; P = 0.011). A pronounced increase in epithelial permeability in acute colitis was completely prevented by VSL#3 therapy [healthy control 0.4 ± 0.07 (extinction/g), DSS + placebo 5.75 ± 1.67, DSS + VSL#3 0.26 ± 0.08; P = 0.003]. In acute colitis, decreased expression and redistribution of the tight junction proteins occludin, zonula occludens-1, and claudin-1, -3, -4, and -5 were observed, whereas VSL#3 therapy prevented these changes. VSL#3 completely prevented the increase of epithelial apoptotic ratio in acute colitis [healthy control 1.58 ± 0.01 (apoptotic cells/1,000 epithelial cells), DSS + placebo 13.33 ± 1.29, DSS + VSL#3 1.72 ± 0.1; P = 0.012]. Probiotic therapy protects the epithelial barrier in acute colitis by preventing 1) decreased tight junction protein expression and 2) increased apoptotic ratio.

inflammatory bowel disease; probiotics; dextran sodium sulfate colitis; intestinal barrier



Address for reprint requests and other correspondence: R. Mennigen, Univ. Hospital Muenster, Dept. of General and Visceral Surgery, Waldeyerstr. 1, D-48149 Muenster, Germany (e-mail: rudolf.mennigen{at}uni-muenster.de)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2009 by the American Physiological Society.