4.6 Article

Dietary Fructooligosaccharides and Wheat Bran Elicit Specific and Dose-Dependent Gene Expression Profiles in the Proximal Colon Epithelia of Healthy Fischer 344 Rats

Journal

JOURNAL OF NUTRITION
Volume 141, Issue 5, Pages 790-797

Publisher

OXFORD UNIV PRESS
DOI: 10.3945/jn.110.133421

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Funding

  1. Health Canada operating fund
  2. Health Canada Genomics Initiative
  3. Natural Sciences and Engineering Research Council of Canada
  4. Genomics grant

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Proximal colon epithelial gene responses to diets containing increasing levels of dietary fermentable material (FM) from 2 different sources were measured to determine whether gene expression patterns were independent of the source of FM. Male Fischer 344 rats (10/group) were fed for 6 wk a control diet containing 10% (g/g) cellulose (0% FM); or a 2, 5, or 10% wheat bran (WB) diet (1, 2, 5% FM); or a 2, 5, or 8% fructooligosaccharides (FOS) diet (2, 5, 8% FM). WB and FOS were substituted for cellulose to give a final 10% nondigestible material content including FM. Gene responses were relative to expression in rats fed the control diet. The gene response patterns associated with feeding similar to 2% FM (5% WB and 2% FOS) were similar (similar to 10 gene changes >= 1.6-fold; P <= 0.01) and involved genes associated with transport (Scnn1g, Mt1a), transcription (Zbtb16, Egr1), immunity (Fkbp5), a gut hormone (Retn1 beta), and lipid metabolism (Scd2, Instg1). These changes were also similar to those associated with 5% FM but only in rats fed the 10% WB diet. In contrast, the 5% FOS diet (similar to 5% FM) was associated with 68 gene expression changes 1.6-fold (P <= 0.01). The diet with the highest level of fermentation (8% FOS, similar to 8% FM) was associated with 132 changes >= 1.6-fold (P <= 0.01), including genes associated with transport, cellular proliferation, oncogene and tumor metastasis, the cell cycle, apoptosis, signal transduction, transcript regulation, immunity, gut hormones, and lipid metabolic processes. These results show that both the amount and source of FM determine proximal colon epithelial gene response patterns in rats. J. Nutr. 141: 790-797, 2011.

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