Effect of maqui berry extract consumption on postprandial responses in mice: actions on digestive enzymes and relevance of DPP-IV inhibition

Abstract

Obesity remains a major global public health concern. Existent strategies to cope with obesity include inhibiting key digestive enzymes. This study evaluated the inhibitory potential of a maqui berry extract (MBE) to inhibit the digestive enzymes pancreatic lipase, α-glucosidase, and dipeptidyl-peptidase-4 (DPP-IV) which are involved in lipid and glucose absorption and homeostasis. We characterized MBE composition using UPLC-ESI-QqQ-MS/MS, identifying 30 (poly)phenols, 86% of which were anthocyanins derived from delphinidin and cyanidin. Results showed that MBE inhibited lipase, α-glucosidase, and DPP-IV in vitro with half-maximal inhibitory concentration (IC50) of 3.3 ± 0.1; 38 ± 5; and 3.1 ± 0.4 µg/mL respectively. In vivo evaluation of enzyme inhibition was performed in male mice orally challenged with olive oil, maltose, or glucose, measuring postprandial lipemia or glycemia. MBE treatment only affected the postprandial glycemia induced by the glucose challenge. This suggests DPP-IV inhibition, which is supported by the lower activity of DPP-IV in intestine and plasma of mice treated with MBE. Given the composition of MBE, it is feasible that the postprandial effects were mediated by the anthocyanidins present in the fruit. In summary, this study shows that MBE can modulate key metabolic enzymes, particularly DPP-IV, with promising implications for the dietary management of postprandial glycemia in metabolic disorders.

Supplementary files

Article information

Article type
Paper
Submitted
30 Oct 2025
Accepted
12 Jan 2026
First published
12 Jan 2026

Food Funct., 2026, Accepted Manuscript

Effect of maqui berry extract consumption on postprandial responses in mice: actions on digestive enzymes and relevance of DPP-IV inhibition

A. Lucini Mas, J. I. Mosele, C. Carrieri, C. Favari, L. Bresciani, P. Mena, C. Fraga and M. Galleano, Food Funct., 2026, Accepted Manuscript , DOI: 10.1039/D5FO04669F

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