Literature DB >> 28393287

Starch-enriched diet modulates the glucidic profile in the rat colonic mucosa.

Maria Gabriella Gabrielli1, Daniele Tomassoni2.   

Abstract

PURPOSE: The protective function of the intestinal mucosa largely depends on carbohydrate moieties that as a part of glycoproteins and glycolipids form the epithelial glycocalyx or are secreted as mucins. Modifications of their expression can be induced by an altered intestinal microenvironment and have been associated with inflammatory disorders and colorectal cancer. Given the influence of dietary factors on the gut ecosystem, here we have investigated whether a long term feeding on a starch-rich diet can modulate the glucidic profile in the colonic mucosa of rats.
METHODS: Animals were divided into two groups and maintained for 9 months at different diets: one group was fed a standard diet, the second was fed a starch-enriched diet. Samples of colonic mucosa, divided in proximal and distal portions, were processed for microscopic analysis. Conventional stainings and lectin histochemistry were applied to identify acidic glycoconjugates and specific sugar residues in oligosaccharide chains, respectively. Some lectins were applied on adjacent sections after sialidase/fucosidase digestion, deacetylation, and oxidation to characterize either terminal dimers or sialic acid acetylation.
RESULTS: An increase in sulfomucins was found to be associated with the starch-enriched diet that affected also the expression of several sugar residues as well as fucosylated and sialylated sequences in both proximal and distal colon.
CONCLUSIONS: Although the mechanisms leading to such a modulation are at present unknown, either an altered intestinal microbiota or a dysregulation of glycosylation patterns might be responsible for the types and distribution of changes in the glucidic profile here observed.

Entities:  

Keywords:  Colon; Glycosylation; Lectin histochemistry; Sialic acid; Starch-rich diet

Mesh:

Substances:

Year:  2017        PMID: 28393287     DOI: 10.1007/s00394-017-1393-3

Source DB:  PubMed          Journal:  Eur J Nutr        ISSN: 1436-6207            Impact factor:   5.614


  43 in total

1.  DIAMINE METHODS FOR DIFFERENTIALING MUCOSUBSTANCES HISTOCHEMICALLY.

Authors:  S S SPICER
Journal:  J Histochem Cytochem       Date:  1965-03       Impact factor: 2.479

2.  Genome analysis of Bifidobacterium bifidum PRL2010 reveals metabolic pathways for host-derived glycan foraging.

Authors:  Francesca Turroni; Francesca Bottacini; Elena Foroni; Imke Mulder; Jae-Han Kim; Aldert Zomer; Borja Sánchez; Alessandro Bidossi; Alberto Ferrarini; Vanessa Giubellini; Massimo Delledonne; Bernard Henrissat; Pedro Coutinho; Marco Oggioni; Gerald F Fitzgerald; David Mills; Abelardo Margolles; Denise Kelly; Douwe van Sinderen; Marco Ventura
Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-25       Impact factor: 11.205

Review 3.  Mucin function in inflammatory bowel disease: an update.

Authors:  Doron Boltin; Tsachi T Perets; Alex Vilkin; Yaron Niv
Journal:  J Clin Gastroenterol       Date:  2013-02       Impact factor: 3.062

4.  Genetic strategies for mucin metabolism in Bifidobacterium bifidum PRL2010: an example of possible human-microbe co-evolution.

Authors:  Francesca Turroni; Christian Milani; Douwe van Sinderen; Marco Ventura
Journal:  Gut Microbes       Date:  2011-05-01

5.  Differential glycosylation of MUC1 and CEACAM5 between normal mucosa and tumour tissue of colon cancer patients.

Authors:  Eirikur Saeland; Ana I Belo; Sandra Mongera; Irma van Die; Gerrit A Meijer; Yvette van Kooyk
Journal:  Int J Cancer       Date:  2011-11-28       Impact factor: 7.396

Review 6.  Intestinal goblet cells and mucins in health and disease: recent insights and progress.

Authors:  Young S Kim; Samuel B Ho
Journal:  Curr Gastroenterol Rep       Date:  2010-10

7.  Effect of high amylose maize starches on colonic fermentation and apoptotic response to DNA-damage in the colon of rats.

Authors:  Richard K Le Leu; Ying Hu; Ian L Brown; Graeme P Young
Journal:  Nutr Metab (Lond)       Date:  2009-03-07       Impact factor: 4.169

Review 8.  Increasing the α 2, 6 sialylation of glycoproteins may contribute to metastatic spread and therapeutic resistance in colorectal cancer.

Authors:  Jung-Jin Park; Minyoung Lee
Journal:  Gut Liver       Date:  2013-11-11       Impact factor: 4.519

9.  Rapid fucosylation of intestinal epithelium sustains host-commensal symbiosis in sickness.

Authors:  Joseph M Pickard; Corinne F Maurice; Melissa A Kinnebrew; Michael C Abt; Dominik Schenten; Tatyana V Golovkina; Said R Bogatyrev; Rustem F Ismagilov; Eric G Pamer; Peter J Turnbaugh; Alexander V Chervonsky
Journal:  Nature       Date:  2014-10-01       Impact factor: 49.962

10.  Increased susceptibility to colitis and colorectal tumors in mice lacking core 3-derived O-glycans.

Authors:  Guangyu An; Bo Wei; Baoyun Xia; J Michael McDaniel; Tongzhong Ju; Richard D Cummings; Jonathan Braun; Lijun Xia
Journal:  J Exp Med       Date:  2007-05-21       Impact factor: 14.307

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