Quantification of Multifunctional Dipeptide YA from Oyster Hydrolysate for Quality Control and Efficacy Evaluation

Biomed Res Int. 2018 Sep 24:2018:8437379. doi: 10.1155/2018/8437379. eCollection 2018.

Abstract

YA is an angiotensin-I-converting enzyme- (ACE-) inhibitory peptide from oyster hydrolysate with antihypertensive activity. Its antioxidant and anti-inflammatory activity were investigated in this study. YA can dose-dependently quench DPPH and ABTS radical and inhibit lipopolysaccharide-induced nitric oxide in RAW 264.7 cells. YA is a multifunctional peptide and was selected as an indicator for quality control and efficacy evaluation of oyster hydrolysate. A practical HPLC/UV assay for YA quantification was developed and validated. It was proved to be accurate and reliable, according to parameters such as specificity, linearity, precision, and accuracy. The quantity results of YA showed that the stage of enzymatic hydrolysis was a critical control point for quality control; the efficacy of oyster hydrolysate can be enhanced after digested in the gastrointestinal tract due to the release of YA by brush border peptidases. Therefore, YA from oyster hydrolysate is a potential bioactive ingredient for functional foods to combat hypertension.

MeSH terms

  • Angiotensin-Converting Enzyme Inhibitors* / analysis
  • Angiotensin-Converting Enzyme Inhibitors* / chemistry
  • Animals
  • Dipeptides* / analysis
  • Dipeptides* / chemistry
  • Mice
  • Ostreidae / chemistry*
  • Protein Hydrolysates* / analysis
  • Protein Hydrolysates* / chemistry
  • Quality Control*
  • RAW 264.7 Cells

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Dipeptides
  • Protein Hydrolysates