Insulin, glucagon-like peptide 1, glucose-dependent insulinotropic polypeptide and insulin-like growth factor I as putative mediators of the hypolipidemic effect of oligofructose in rats

J Nutr. 1998 Jul;128(7):1099-103. doi: 10.1093/jn/128.7.1099.

Abstract

The addition of oligofructose as a dietary fiber decreases the serum concentration and the hepatic release of VLDL-triglycerides in rats. Because glucose, insulin, insulin-like growth factor I (IGF-I) and gut peptides [i.e., glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1)]) are factors involved in the metabolic response to nutrients, this paper analyzes their putative role in the hypolipidemic effect of oligofructose. Male Wistar rats were fed a nonpurified diet with or without 10% oligofructose for 30 d. Glucose, insulin, IGF-I and GIP concentrations were measured in the serum of rats after eating. GIP and GLP-1 contents were also assayed in small intestine and cecal extracts, respectively. A glucose tolerance test was performed in food-deprived rats. Serum insulin level was significantly lower in oligofructose-fed rats both after eating and in the glucose tolerance test, whereas glycemia was lower only in the postprandial state. IGF-I serum level did not differ between groups. GIP concentration was significantly higher in the serum of oligofructose-fed rats. The GLP-1 cecal pool was also significantly higher. In this study, we have shown that cecal proliferation induced by oligofructose leads to an increase in GLP-1 concentration. This latter incretin could be involved in the maintenance of glycemia despite a lower insulinemia in the glucose tolerance test in oligofructose-fed rats. We discuss also the role of hormonal changes in the antilipogenic effect of oligofructose.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Cecum / metabolism
  • Eating
  • Fructose / administration & dosage
  • Fructose / pharmacology*
  • Gastric Inhibitory Polypeptide / blood*
  • Gastric Inhibitory Polypeptide / metabolism
  • Glucagon / blood*
  • Glucagon / metabolism
  • Glucagon-Like Peptide 1
  • Glucose Tolerance Test
  • Hypolipidemic Agents*
  • Insulin / blood*
  • Insulin-Like Growth Factor I / metabolism*
  • Intestine, Small / metabolism
  • Male
  • Peptide Fragments / blood*
  • Peptide Fragments / metabolism
  • Protein Precursors / blood*
  • Protein Precursors / metabolism
  • Rats
  • Rats, Wistar
  • Weight Gain

Substances

  • Blood Glucose
  • Hypolipidemic Agents
  • Insulin
  • Peptide Fragments
  • Protein Precursors
  • Fructose
  • Gastric Inhibitory Polypeptide
  • Insulin-Like Growth Factor I
  • Glucagon-Like Peptide 1
  • Glucagon