Novel Insights into the Inhibitory Effect and Mechanism of Proanthocyanidins from Pyracantha fortuneana Fruit on α-Glucosidase

J Food Sci. 2017 Oct;82(10):2260-2268. doi: 10.1111/1750-3841.13816. Epub 2017 Sep 14.

Abstract

Proanthocyanidins were extracted from Pyracantha fortuneana fruit (PFF), and their structures were investigated through 13 C nuclear magnetic resonance (13 C NMR), high performance liquid chromatography (HPLC) and high resolution mass spectrometry (HRMS). The results showed that these compounds were predominantly constituted of procyanidin with A-type and B-type linkage and coexistence of procyanidins glucoside. Spectroscopy methods were used to analyze the inhibitory activity of proanthocyanidins on α-glucosidase. The results demonstrated that these compounds exhibited excellent inhibitory effect on α-glucosidase with the IC50 value of 0.15 ± 0.01 μg/mL, and they reversibly inhibited α-glucosidase in a non-competitive type. The fluorescence quenching analysis revealed that proanthocyanidins statically quenched the fluorescence spectra by forming an inhibitor-α-glucosidase complex. Molecular docking results further indicated that the driving powers of the interaction between proanthocyanidins and α-glucosidase were hydrogen bonds and hydrophobic force. The main inhibitory mechanism of proanthocyanidins on α-glucosidase may be due to the insertion of proanthocyanidins into the pocket of the enzyme altering the catalytic configuration of the active site in a manner, thus reducing substrate binding affinity. The findings of this work provided a new perspective that proanthocyanidins from PFF with a possibility to be used as novel natural anti-diabetic agents in functional food industries.

Practical application: In this study, Pyracantha fortuneana fruit proanthocyanidins with a yield of 3.05% were identified for the first time as predominantly constituted of procyanidin with A-type and B-type linkage and coexistence of procyanidins glucoside. Proanthocyanidins from P. fortuneana fruit had higher anti-α-glucosidase activity value compared with positive control acarbose, which indicated that P. fortuneana fruit proanthocyanidins with a possibility to be used as novel natural antidiabetic agents in functional food industries.

Keywords: Pyracantha fortuneana; proanthocyanidins; α-glucosidase.

MeSH terms

  • Biflavonoids
  • Catalytic Domain
  • Catechin
  • Chromatography, High Pressure Liquid
  • Fruit / chemistry*
  • Glycoside Hydrolase Inhibitors / pharmacology*
  • Hypoglycemic Agents
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Molecular Docking Simulation
  • Molecular Structure
  • Proanthocyanidins / isolation & purification
  • Proanthocyanidins / pharmacology*
  • Pyracantha / chemistry*
  • Spectrometry, Fluorescence
  • alpha-Glucosidases / metabolism*

Substances

  • Biflavonoids
  • Glycoside Hydrolase Inhibitors
  • Hypoglycemic Agents
  • Proanthocyanidins
  • procyanidin
  • Catechin
  • alpha-Glucosidases