Antihypertensive Effects of Corn Silk Extract and Its Novel Bioactive Constituent in Spontaneously Hypertensive Rats: The Involvement of Angiotensin-Converting Enzyme Inhibition

Molecules. 2019 May 16;24(10):1886. doi: 10.3390/molecules24101886.

Abstract

Corn silk tea has been used in folk medicine for anti-hypertensive healthcare. Angiotensin-converting enzyme (ACE) plays a crucial role on the homeostasis of blood pressure. However, effects of corn silk tea on ACE activity and the presence of ACE inhibitory constituents in corn silk are still unknown. Here we applied proteomics and bioinformatics approaches to identify corn silk bioactive peptides (CSBps) that target ACE from the boiling water extract of corn silk (CSE). CSE significantly reduced systolic blood pressure (SBP) levels in spontaneously hypertensive rats and inhibited the ACE activity. By proteomics coupled with bioinformatics analyses, we identified a novel ACE inhibitory peptide CSBp5 in CSE. CSBp5 significantly inhibited the ACE activity and decreased SBP levels in a dose-dependent manner. Docking analysis showed that CSBp5 occupied the substrate-binding channel of ACE and interacted with ACE via hydrogen bonds. In conclusion, we identified that CSE exhibited anti-hypertensive effects in SHRs via the inhibition of ACE, the target of most anti-hypertensive drugs. In addition, an ACE inhibitory phytopeptide CSBp5 that decreased SBP levels in rats was newly identified. Our findings supported the ethnomedical use of corn silk tea on hypertension. Moreover, the identification of ACE inhibitory phytopeptide in corn silk further strengthened our findings.

Keywords: angiotensin-converting enzyme; bioactive phytopeptide; corn silk; hypertension.

MeSH terms

  • Amino Acid Sequence
  • Angiotensin-Converting Enzyme Inhibitors / chemistry*
  • Angiotensin-Converting Enzyme Inhibitors / pharmacology*
  • Animals
  • Antihypertensive Agents / chemistry*
  • Antihypertensive Agents / pharmacology*
  • Blood Pressure / drug effects
  • Chromatography, Liquid
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Hydrogen Bonding
  • Hypertension / drug therapy
  • Hypertension / physiopathology
  • Male
  • Models, Molecular
  • Peptides / chemistry
  • Peptides / pharmacology
  • Plant Extracts / chemistry*
  • Plant Extracts / pharmacology*
  • Protein Conformation
  • Rats
  • Rats, Inbred SHR
  • Structure-Activity Relationship
  • Tandem Mass Spectrometry
  • Zea mays / chemistry*

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Antihypertensive Agents
  • Peptides
  • Plant Extracts