Identification of Novel Peptides in Distillers' Grains as Antioxidants, α-Glucosidase Inhibitors, and Insulin Sensitizers: In Silico and In Vitro Evaluation

Nutrients. 2024 Apr 25;16(9):1279. doi: 10.3390/nu16091279.

Abstract

Distillers' grains are rich in protein and constitute a high-quality source of various bioactive peptides. The purpose of this study is to identify novel bioactive peptides with α-glucosidase inhibitory, antioxidant, and insulin resistance-ameliorating effects from distiller's grains protein hydrolysate. Three novel peptides (YPLPR, AFEPLR, and NDPF) showed good potential bioactivities, and the YPLPR peptide had the strongest bioactivities, whose IC50 values towards α-glucosidase inhibition, radical scavenging rates of 2,2'-azino-bis (3-ethylbenzothiazoline-6- sulfonic acid) (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) were about 5.31 mmol/L, 6.05 mmol/L, and 7.94 mmol/L, respectively. The glucose consumption of HepG2 cells treated with YPLPR increased significantly under insulin resistance condition. Moreover, the YPLPR peptide also had a good scavenging effect on intracellular reactive oxygen species (ROS) induced by H2O2 (the relative contents: 102.35% vs. 100%). Molecular docking results showed that these peptides could stably combine with α-glucosidase, ABTS, and DPPH free radicals, as well as related targets of the insulin signaling pathway through hydrogen bonding and van der Waals forces. This research presents a potentially valuable natural resource for reducing oxidative stress damage and regulating blood glucose in diabetes, thereby increasing the usage of distillers' grains peptides and boosting their economic worth.

Keywords: UHPLC-ESI-HRMS/MS; bioactive peptides; insulin resistance; molecular docking; reactive oxygen species.

MeSH terms

  • Antioxidants* / pharmacology
  • Benzothiazoles
  • Biphenyl Compounds
  • Computer Simulation
  • Edible Grain
  • Glycoside Hydrolase Inhibitors* / pharmacology
  • Hep G2 Cells
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Insulin
  • Insulin Resistance*
  • Molecular Docking Simulation*
  • Peptides* / chemistry
  • Peptides* / pharmacology
  • Picrates
  • Protein Hydrolysates / pharmacology
  • Reactive Oxygen Species / metabolism
  • Sulfonic Acids
  • alpha-Glucosidases / metabolism

Substances

  • Glycoside Hydrolase Inhibitors
  • Antioxidants
  • Peptides
  • alpha-Glucosidases
  • Protein Hydrolysates
  • Reactive Oxygen Species
  • Hypoglycemic Agents
  • 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid
  • Insulin
  • Sulfonic Acids
  • 1,1-diphenyl-2-picrylhydrazyl
  • Biphenyl Compounds
  • Picrates
  • Benzothiazoles