High-fat-induced intestinal permeability dysfunction associated with altered fecal bile acids
AIM: To investigate whether high-fat-feeding is associ- ated with increased intestinal permeability via altera- tions in bile acid metabolism. METHODS: Male C57BI/6J mice were fed on a high-fat (n = 26) or low-fat diet (n = 24) for 15 wk. Intestinal permeability was measured from duodenum, jejunum,...
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Published in | World journal of gastroenterology : WJG Vol. 18; no. 9; pp. 923 - 929 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
United States
Baishideng Publishing Group Co., Limited
07.03.2012
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Subjects | |
Online Access | Get full text |
ISSN | 1007-9327 2219-2840 2219-2840 |
DOI | 10.3748/wjg.v18.i9.923 |
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Summary: | AIM: To investigate whether high-fat-feeding is associ- ated with increased intestinal permeability via altera- tions in bile acid metabolism.
METHODS: Male C57BI/6J mice were fed on a high-fat (n = 26) or low-fat diet (n = 24) for 15 wk. Intestinal permeability was measured from duodenum, jejunum, ileum and colon in an Ussing chamber system using 4 kDa FITC-labeled dextran as an indicator. Fecal bile ac- ids were analyzed with gas chromatography. Segments of jejunum and colon were analyzed for the expression of farnesoid X receptor (FXR) and tumor necrosis factor |
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Bibliography: | 14-1219/R Bile acids; Bile salts; Diet-induced obesity;Farnesoid X-activated receptor; Intestinal permeability;Ursodeoxycholic acid AIM: To investigate whether high-fat-feeding is associ- ated with increased intestinal permeability via altera- tions in bile acid metabolism. METHODS: Male C57BI/6J mice were fed on a high-fat (n = 26) or low-fat diet (n = 24) for 15 wk. Intestinal permeability was measured from duodenum, jejunum, ileum and colon in an Ussing chamber system using 4 kDa FITC-labeled dextran as an indicator. Fecal bile ac- ids were analyzed with gas chromatography. Segments of jejunum and colon were analyzed for the expression of farnesoid X receptor (FXR) and tumor necrosis factor ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Correspondence to: Lotta Stenman, MSc, Institute of Biomedicine, Pharmacology, P.O.Box 63, FI-00014 University of Helsinki, Helsinki 00280, Finland. lotta.stenman@helsinki.fi Author contributions: Stenman LK designed the study, performed the experiments, analyzed the data, and wrote the manuscript; Holma R and Korpela R were involved in designing the study and editing the manuscript. Telephone: +358-9-19125354 Fax: +358-9-19125364 |
ISSN: | 1007-9327 2219-2840 2219-2840 |
DOI: | 10.3748/wjg.v18.i9.923 |