4.7 Article

Inhibitory effect of raspberries on starch digestive enzyme and their antioxidant properties and phenolic composition

Journal

FOOD CHEMISTRY
Volume 119, Issue 2, Pages 592-599

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2009.06.063

Keywords

Raspberry; Digestive enzymes; alpha-Glucosidase; ORAC; Anthocyanins; Phenolic acids

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Seven primocane fall-bearing raspberry (Rubus idaeus L.) cultivars, Nova (red), Dinkum (red), Heritage (red), Autumn Britten (red), Josephine, Anne (yellow), Fall Gold (yellow) were analysed for potential health promoting properties including their inhibitory effect on starch and fat digestive enzymes, antioxidant activities, and phenolic composition. The tested raspberry extracts showed no detectable inhibition of pancreatic alpha-amylase and lipase. However, all the extracts exhibited potent inhibition of alpha-glucosidase with IC50 from 16.8 to 34.2 mu g/mL. Four phenolic compounds, ellagic acid, cyanidin-diglucoside, pelargonidin-3-rutinoside, and catechin were identified as the active alpha-glucosidase inhibitors. The raspberry extracts also possessed significant antioxidant activities with oxygen radical absorbance capacities (ORAC) ranging from 136,7 to 205.2 mu mol Trolox equivalents (TE)/g dry weight fruit and DPPH radical scavenging activities from 305 to 351 mu mol TE/g. The total phenolic content of raspberry cultivars; varied significantly from 40.9 to 98.5 mg of gallic acid equivalents/g dry weight. The anthocyanin content varied widely from 0.1 to 9.5 mg cyanidin 3-glucoside equivalents/g. Nine phenolic acids were quantified in raspberries and their total amounts varied from 157.3 to 713.5 mu g/g. The enzyme inhibition and antioxidant properties of raspberry cultivars were not correlated with their total phenolic, anthocyanin, and phenolic acid content. Overall, 'Dinkum' and 'Josephine' raspberry varieties possess higher total phenolic content, ORAC, DPPH radical scavenging activity, and alpha-glucosidase inhibitory activity than other five cultivars. (C) 2009 Elsevier Ltd. All rights reserved.

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