Cited by 197Microbial Metabolites in Food BiotechnologyNatural Antidiabetic Agents StudiesDiabetes Treatment and Management

Involvement of endogenous glucagon-like peptide-1(7–36) amide on glycaemia-lowering effect of oligofructose in streptozotocin-treated rats

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Cani, Patrice D, Daubioul, Catherine A, Reusens, Brigitte, Remacle, Claude, Catillon, Grégory, Delzenne, Nathalie M·2005·Journal of Endocrinology

Abstract

We have evaluated the influence of oligofructose (OFS), a fermentable dietary fibre, on glucose homeostasis, insulin production and intestinal glucagon-like peptide-1 (GLP-1) in streptozotocin-treated diabetic rats. Male Wistar rats received either i.v. streptozotocin (STZ; 40 mg/kg) or vehicle (CT); one week later, they were fed for 6 weeks with either the standard diet (STZ-CT), or with a diet containing 10% oligofructose (STZ-OFS); both diets were available ad libitum. In a second set of experiments (duration 4 weeks), a supplemental group of food-restricted rats (STZ-Res) receiving a similar intake as CT rats, was added. OFS improved glucose tolerance and reduced food intake as compared with STZ-CT rats in both the post-prandial state and after an oral glucose tolerance test. After 6 weeks, portal and pancreatic insulin concentrations were doubled in STZ-OFS rats. Food restriction improved these parameters when compared with STZ-CT rats, but to a lesser extent than in the STZ-OFS group. We have shown that OFS treatment increased portal and colonic GLP-1(7–36) amide levels and doubled colonic proglucagon and prohormone convertase 1 mRNA levels; both OFS and food restriction lowered ileal GLP-1(7–36) amide levels as compared with levels in STZ-CT rats. We propose that OFS, through its fermentation in the colon, promotes the expression and secretion of colonic peptides, namely GLP-1(7–36) amide, with beneficial consequences on glycaemia, insulin secretion and hyperphagia in diabetic rats.

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  • Some prebiotics, including the polysaccharide inulin as well as FOS and GOS, increase production of both GLP-1 and PYY.

    “Some prebiotics, a polysaccharide inulin as well as FOS and GOS were shown to increase the production of both GLP-1 and PYY (Cani et al., 2005;Everard et al., 2011).”

    From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Cani et al., 2005

    The Results section reports that oligofructose increased portal GLP-1 levels in streptozotocin-treated rats, and the Introduction describes oligofructose as a fructan obtained from inulin. The paper does not establish that inulin, FOS, and GOS each increase both GLP-1 and PYY; the reported experiment concerns oligofructose and GLP-1, not PYY or GOS. (LLM, conf=0.88)

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Cites

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Research works printed but not linked: 20

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Authors
Cani, P. D., Daubioul, C. A., Reusens, B., Remacle, C., Catillon, G., & Delzenne, N. M.
Affiliations
  • UCLouvain (BE)
  • University College London (GB)
Venue
Journal of Endocrinology
Published
2005-06
Volume
185
Issue
3
Pages
457-465
ISSN
  • 0022-0795 (ISSN-L)
  • 1479-6805
OpenAlex
W2141739994
Cited by
197
References
0
Citations by year
2025: 3 · 2024: 5 · 2023: 6 · 2022: 5 · 2021: 7 · 2020: 14 · 2019: 8 · 2018: 10 · 2017: 11 · 2016: 11 · 2015: 10 · 2014: 13 · 2013: 13 · 2012: 6
FWCI
9.78
Type
journal article
Language
en
Open access
Locations
  • Journal of Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
  • DIAL (Catholic University of Leuven) (submittedVersion, other-oa)
Funders
  • Danone
  • Instituto Danone
Topics
  • Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Natural Antidiabetic Agents Studies
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
Keywords
fructooligosaccharides, glucagon-like peptide-1(7-36)amide, type 2 diabetes, streptozotocin-induced diabetes, glucose homeostasis, insulin secretion, dietary restriction, dietary fiber fermentation, proglucagon, prohormone convertase 1, hyperphagia
MeSH terms
Actins, Animals, Blood Glucose, Colon, Diabetes Mellitus, Experimental, Eating, Glucagon-Like Peptides, Fermentation, Food Deprivation, Glucagon, Glucose Tolerance Test, Insulin, Islets of Langerhans, Male, Oligosaccharides, Peptide Fragments, Protein Precursors, RNA, Messenger, Rats, Wistar, Reverse Transcriptase Polymerase Chain Reaction, Proprotein Convertase 1, Rats, Glucagon-Like Peptide 1, Proglucagon

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