Related Experiment Video
Updated: Feb 12, 2026

Author Spotlight: Sieving Fruit Pulp to Detect Immature Tephritid Fruit Flies in the Field
Published on: July 28, 2023
Fruit Wines Inhibitory Activity Against α-Glucosidase
Uros Cakar1, Nada Grozdanic2, Aleksandar Petrovic3
1University of Belgrade,Faculty of Pharmacy, Vojvode Stepe 450, 11000 Belgrade, Serbia.
Blueberry wine shows significant potential for managing type 2 diabetes by inhibiting alpha-glucosidase. This fruit wine may help control postprandial hyperglycemia, offering a natural approach to diabetes management.
Area of Science:
- Food Science
- Biochemistry
- Pharmacology
Background:
- Fruit wines possess health-promoting properties, including enzyme modulation.
- Potential preventive role in diabetes mellitus and other chronic diseases.
Purpose of the Study:
- Evaluate the alpha-glucosidase inhibitory activity of various fruit wines.
- Investigate blueberry, black chokeberry, blackberry, raspberry, and sour cherry wines.
Main Methods:
- Fruit wines were prepared, with some samples having sugar added to pomace to increase alcohol and phenolic extraction.
- Alpha-glucosidase inhibitory activity was assessed and compared to acarbose.
- Molecular docking was used to study the binding energy of key compounds.
Main Results:
- All fruit wines demonstrated higher alpha-glucosidase inhibition than acarbose.
- Blueberry wine exhibited the most potent inhibition (IC50 = 24.14 µg/mL with sugar, 46.39 µg/mL without).
- Chlorogenic acid was the primary contributor to inhibition; ellagic acid had a lesser effect.
Conclusions:
- Blueberry wine is a promising candidate for medicinal food targeting early-stage type 2 diabetes.
- Further research is needed to confirm its therapeutic potential for controlling postprandial hyperglycemia.
Related Concept Videos
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
Acarbose and miglitol are...
Fruit Development, Structure, and Function
Excitatory and Inhibitory Effects of Neurotransmitters
α-Alkylation of Ketones via Enolate Ions
Factors Affecting α-Alkylation of Ketones: Choice of Base
The reaction involving bases like EtO− whose conjugate acid EtOH (pKa = 15.9) is stronger than the ketone (pKa = 19.2) results in an equilibrium mixture with higher ketone concentration. As a consequence,...
Reactions of α-Halocarbonyl Compounds: Nucleophilic Substitution

