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Volume 16, Issue 5, Pages 406-415 (May 2009)


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Hypoglycemic activity of a novel anthocyanin-rich formulation from lowbush blueberry, Vaccinium angustifolium Aiton

Mary H. Gracea1, David M. Ribnickyb1, Peter Kuhnb, Alexander Poulevb, Sithes Logendrab, Gad G. Yousefa, Ilya Raskinb, Mary Ann LilaaCorresponding Author Informationemail address

Abstract 

Blueberry fruits are known as a rich source of anthocyanin components. In this study we demonstrate that anthocyanins from blueberry have the potency to alleviate symptoms of hyperglycemia in diabetic C57b1/6J mice. The anti-diabetic activity of different anthocyanin-related extracts was evaluated using the pharmaceutically acceptable self-microemulsifying drug delivery system: Labrasol. Treatment by gavage (500mg/kg body wt) with a phenolic-rich extract and an anthocyanin-enriched fraction formulated with Labrasol lowered elevated blood glucose levels by 33 and 51%, respectively. The hypoglycemic activities of these formulae were comparable to that of the known anti-diabetic drug metformin (27% at 300mg/kg). The extracts were not significantly hypoglycemic when administered without Labrasol, demonstrating its bio-enhancing effect, most likely due to increasing the bioavailability of the administered preparations. The phenolic-rich extract contained 287.0±9.7mg/g anthocyanins, while the anthocyanin-enriched fraction contained 595±20.0mg/g (cyanidin-3-glucoside equivalents), as measured by HPLC and pH differential analysis methods. The greater hypoglycemic activity of the anthocyanin-enriched fraction compared to the initial phenolic-rich extract suggested that the activity was due to the anthocyanin components. Treatment by gavage (300mg/kg) with the pure anthocyanins, delphinidin-3-O-glucoside and malvidin-3-O-glucoside, formulated with Labrasol, showed that malvidin-3-O-glucoside was significantly hypoglycemic while delphinidin-3-O-glucoside was not.

a University of Illinois, Department of Natural Resources and Environmental Sciences, 1201 S. Dorner Drive, Urbana, IL 61801, USA

b Rutgers University, SEBS, Foran Hall, 59 Dudley Road, New Brunswick, NJ 08901, USA

Corresponding Author InformationCorresponding author. Tel.: +12173335154; fax: +12172443469.

1 These authors contributed equally to this work.

PII: S0944-7113(09)00053-1

doi:10.1016/j.phymed.2009.02.018


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