4.7 Article

l-Glutamine and Whole Protein Restore First-Phase Insulin Response and Increase Glucagon-Like Peptide-1 in Type 2 Diabetes Patients

Journal

NUTRIENTS
Volume 7, Issue 4, Pages 2101-2108

Publisher

MDPI
DOI: 10.3390/nu7042101

Keywords

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Funding

  1. National Health and Medical Research Council (NHMRC) of Australia [535949]
  2. Diabetes Australia Research Trust
  3. Neil Hamilton Fairley Fellowship from NHMRC
  4. Don Chisholm Fellowship
  5. Australian Diabetes Society
  6. Sachdev Foundation (the Garvan Research Foundation)
  7. NNF Center for Basic Metabolic Research [Holst Group] Funding Source: researchfish

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l-glutamine triggers glucagon-like peptide-1 (GLP-1) release from L cells in vitro and when ingested pre-meal, decreases postprandial glycaemia and increases circulating insulin and GLP-1 in type 2 diabetes (T2D) patients. We aimed to evaluate the effect of oral l-glutamine, compared with whole protein low in glutamine, on insulin response in well-controlled T2D patients. In a randomized study with a crossover design, T2D patients (n = 10, 6 men) aged 65.1 +/- 5.8, with glycosylated hemoglobin (HbA1c) 6.6% +/- 0.7% (48 +/- 8 mmol/mol), received oral l-glutamine (25 g), protein (25 g) or water, followed by an intravenous glucose bolus (0.3 g/kg) and hyperglycemic glucose clamp for 2 h. Blood was frequently collected for analyses of glucose, serum insulin and plasma total and active GLP-1 and area under the curve of glucose, insulin, total and active GLP-1 excursions calculated. Treatments were tested 1-2 weeks apart. Both l-glutamine and protein increased first-phase insulin response (p <= 0.02). Protein (p = 0.05), but not l-glutamine (p = 0.2), increased second-phase insulin response. Total GLP-1 was increased by both l-glutamine and protein (p <= 0.02). We conclude that oral l-glutamine and whole protein are similarly effective in restoring first-phase insulin response in T2D patients. Larger studies are required to further investigate the utility of similar approaches in improving insulin response in diabetes.

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