Bioguided chemical characterization of pequi (Caryocar brasiliense) fruit peels towards an anti-diabetic activity
•The antidiabetic potential of Caryocar brasiliense fruit peel extract was assessed.•Bioactive fractions were identified by cytokines and digestive enzymes inhibition.•UPLC-PDA-ESI-MS/MS analyses disclosed hydrolysable tannins in the active fractions.•A corilagin and geraniin rich fraction reduced g...
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Published in | Food chemistry Vol. 345; p. 128734 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
30.05.2021
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Subjects | |
Online Access | Get full text |
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Summary: | •The antidiabetic potential of Caryocar brasiliense fruit peel extract was assessed.•Bioactive fractions were identified by cytokines and digestive enzymes inhibition.•UPLC-PDA-ESI-MS/MS analyses disclosed hydrolysable tannins in the active fractions.•A corilagin and geraniin rich fraction reduced glycaemia in starch tolerance test.•Fruit peels have potential for developing functional foods to manage type-2 diabetes.
Pequi fruit peels are an underexploited source of polyphenols. The anti-diabetic potential of an extract and fractions from the peels were evaluated in a panel of assays. The extract and fractions thereof inhibited the release of cytokines involved in insulin resistance – TNF, IL-1β, and CCL2 – by lipopolysaccharide-stimulated THP-1 cells. The ethyl acetate fraction inhibited in vitro α-glucosidase (pIC50 = 4.8 ± 0.1), an enzyme involved in the metabolization of starch and disaccharides to glucose, whereas a fraction enriched in tannins (16C) induced a more potent α-glucosidase inhibition (pIC50 = 5.3 ± 0.1). In the starch tolerance test in mice, fraction 16C reduced blood glucose level (181 ± 10 mg/dL) in comparison to the vehicle-treated group (238 ± 11 mg/dL). UPLC-DAD-ESI-MS/MS analyses disclosed phenolic acids and tannins as constituents, including corilagin and geraniin. These results highlight the potential of pequi fruit peels for developing functional foods to manage type-2 diabetes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0308-8146 1873-7072 |
DOI: | 10.1016/j.foodchem.2020.128734 |