4.4 Article

Glucagon-like peptide-1 response to whey protein is less diminished by dipeptidyl peptidase-4 in comparison with responses to dextrin, a lipid and casein in rats

期刊

BRITISH JOURNAL OF NUTRITION
卷 125, 期 4, 页码 398-407

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114520002834

关键词

Glucagon-like peptide-1 responses; Dextrin; Whey protein; Casein; Dipeptidyl peptidase-4

资金

  1. JSPS KAKENHI [18K19158]
  2. Tojuro Iijima Foundation for Food Science and Technology
  3. Grants-in-Aid for Scientific Research [18K19158] Funding Source: KAKEN

向作者/读者索取更多资源

Although glucose is the most well-known nutrient to stimulate GLP-1 secretion, dietary peptides also play a significant role in stimulating GLP-1 secretion and inhibiting DPP-4 activity. Whey protein administration resulted in less degradation of GLP-1 compared to other nutrients, indicating a potential protective effect of dietary peptides on GLP-1.
Although glucose is the best-known nutrient to stimulate glucagon-like peptide-1 (GLP-1) secretion, dietary peptides also potently stimulate GLP-1 secretion. Certain peptide fragments derived from dietary proteins possess dipeptidyl peptidase-4 (DPP-4) inhibitory activity in vitro. Hence, we hypothesised that dietary peptides protect GLP-1 from degradation through attenuating DPP-4 activity in vivo. Here, we compared GLP-1 responses with dietary proteins, a carbohydrate and a lipid (Intralipos) in rats having or not having plasma DPP-4 activity. Plasma GLP-1 concentrations clearly increased by oral administration of whey protein (2-4 g/kg), but not by that of dextrin (2-4 g/kg), in control rats (untreated Sprague-Dawley rats and F344/Jcl rats), having DPP-4 activity. In contrast, dextrin administration increased the plasma GLP-1 concentrations as the whey protein administration did, in rats having reduced or no DPP-4 activity (a DPP-4 inhibitor, sitagliptin-treated Sprague-Dawley rats or DPP-4-deficient F344/DuCrl/Crlj rats). DPP-4 inhibition by sitagliptin treatment also enhanced GLP-1 response to Intralipos, and casein, but the treatment did not further enhance GLP-1 response to whey protein. Intestinal GLP-1 content and gastric emptying rate were not associated with differences in GLP-1 responses to test nutrients. The luminal contents from rats administered whey protein decreased DPP-4 activity in vitro. These results suggest that GLP-1 released by dextrin, Intralipos and casein was immediately degraded by DPP-4, while GLP-1 released by whey protein was less degraded. Our study provides novel in vivo evidence supporting the hypothesis that dietary peptides not only stimulate GLP-1 secretion but also inhibit DPP-4 activity to potentiate GLP-1 response.

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