阿卡波糖
磺胺
化学
淀粉酶
IC50型
药理学
生物化学
非竞争性抑制
酶
功能性食品
体外
医学
食品科学
有机化学
作者
Nunzio Cardullo,Vera Muccilli,Luana Pulvirenti,Anaëlle Cornu,Laurent Pouységu,Denis Deffieux,Stéphane Quideau,Corrado Tringali
出处
期刊:Food Chemistry
[Elsevier BV]
日期:2019-12-28
卷期号:313: 126099-126099
被引量:148
标识
DOI:10.1016/j.foodchem.2019.126099
摘要
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.
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