Glucose tolerance, lipids, and GLP-1 secretion in JCR:LA-cp rats fed a high protein fiber diet

Obesity (Silver Spring). 2008 Jan;16(1):40-6. doi: 10.1038/oby.2007.16.

Abstract

Background: We have shown that individually, dietary fiber and protein increase secretion of the anorexigenic and insulinotropic hormone, glucagon-like peptide-1 (GLP-1).

Objective: Our objective was to combine, in one diet, high levels of fiber and protein to maximize GLP-1 secretion, improve glucose tolerance, and reduce weight gain.

Methods and procedures: Lean (+/?) and obese (cp/cp) male James C Russell corpulent (JCR:LA-cp) rats lacking a functional leptin receptor were fed one of four experimental diets (control, high protein (HP), high fiber (HF, prebiotic fiber inulin), or combination (CB)) for 3 weeks. An oral glucose tolerance test (OGTT) was performed to evaluate plasma GLP-1, insulin and glucose. Plasma lipids and intestinal proglucagon mRNA expression were determined.

Results: Energy intake was lower with the HF diet in lean and obese rats. Weight gain did not differ between diets. Higher colonic proglucagon mRNA in lean rats fed a CB diet was associated with higher GLP-1 secretion during OGTT. The HP diet significantly reduced plasma glucose area under the curve (AUC) during OGTT in obese rats, which reflected both an increased GLP-1 AUC and higher fasting insulin. Diets containing inulin resulted in the lowest plasma triglyceride and total cholesterol levels.

Discussion: Overall, combining HP with HF in the diet increased GLP-1 secretion in response to oral glucose, but did not improve glucose tolerance or lipid profiles more than the HF diet alone did. We also suggest that glycemic and insulinemic response to prebiotics differ among rat models and future research work should examine their role in improving glucose tolerance in diet-induced vs. genetic obesity with overt hyperleptinemia.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Glucose / metabolism*
  • Body Weight / drug effects
  • Body Weight / physiology
  • Dietary Fiber / pharmacology*
  • Dietary Proteins / pharmacology*
  • Disease Models, Animal
  • Duodenum / drug effects
  • Duodenum / metabolism
  • Duodenum / pathology
  • Glucagon-Like Peptide 1 / blood*
  • Glucose Tolerance Test
  • Insulin Resistance / physiology
  • Inulin / pharmacology*
  • Jejunum / drug effects
  • Jejunum / metabolism
  • Jejunum / pathology
  • Lipids / blood*
  • Male
  • Obesity / metabolism*
  • Proglucagon / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred Strains
  • Weight Gain / drug effects
  • Weight Gain / physiology

Substances

  • Blood Glucose
  • Dietary Fiber
  • Dietary Proteins
  • Lipids
  • RNA, Messenger
  • Proglucagon
  • Glucagon-Like Peptide 1
  • Inulin

Grants and funding