| Literature DB >> 31927321 |
Nunzio Cardullo1, Vera Muccilli2, Luana Pulvirenti3, Anaëlle Cornu4, Laurent Pouységu5, Denis Deffieux6, Stéphane Quideau7, Corrado Tringali8.
Abstract
Diabetes mellitus is a metabolic disorder characterized by hyperglycemia, which can be counteracted by inhibition of α-glucosidase and α-amylase, both involved in the carbohydrate metabolism. Fourteen C-glucosidic ellagitannins and three galloylated glucoses were studied as potential α-glucosidase and α-amylase inhibitors. Most of the compounds were found to be moderate inhibitors of α-amylase, but potent inhibitors of α-glucosidase, showing low-micromolar IC50 values, far lower than that of the antidiabetic drug acarbose. This selectivity can be an advantage for their possible application as functional food ingredients with anti-diabetic properties because strong α-amylase inhibition generally causes undesired side effects. The best inhibitors were selected for further studies. Intrinsic fluorescence measurements confirmed their high affinity towards α-glucosidase, highlighting a static quenching mechanism. Circular dichroism measurements and kinetics of inhibition indicated that the most active C-glucosidic ellagitannin roburin D (RobD) is a competitive inhibitor, whereas α-pentagalloylglucose (α-PGG) acts as a mixed-type inhibitor.Entities:
Keywords: Hydrolyzable tannins; Hypoglycemic activity; Inhibition kinetics; Intrinsic fluorescence; α-Amylase inhibition; α-Glucosidase inhibition
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Year: 2019 PMID: 31927321 DOI: 10.1016/j.foodchem.2019.126099
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514