Effect of ultrasonic degradation of hyaluronic acid extracted from rooster comb on antioxidant and antiglycation activities

Pharm Biol. 2017 Dec;55(1):156-163. doi: 10.1080/13880209.2016.1232740. Epub 2016 Sep 21.

Abstract

Content: Recently, low-molecular-weight hyaluronic acid (LMWHA) has been reported to have novel features, such as free radical scavenging activities, antioxidant activities and dietary supplements.

Objective: In this study, hyaluronic acid (HA) was extracted from rooster comb and LMWHA was obtained by ultrasonic degradation in order to assess their antioxidant and antiglycation activities.

Materials and methods: Molecular weight (Mw) and the content of glucuronic acid (GlcA) were used as the index for comparison of the effect of ultrasonic treatment. The effects on the structure were determined by ultraviolet (UV) spectra and Fourier transform infrared spectra (FTIR). The antioxidant activity was determined by three analytical assays (DPPH, NO and TBARS), and the inhibitory effect against glycated-BSA was also assessed.

Results: The GlcA content of HA and LMWHA was estimated at about 48.6% and 47.3%, respectively. The results demonstrate that ultrasonic irradiation decreases the Mw (1090-181 kDa) and intrinsic viscosity (1550-473 mL/g), which indicate the cleavage of the glycosidic bonds. The FTIR and UV spectra did not significantly change before and after degradation. The IC50 value of HA and LWMHA was 1.43, 0.76 and 0.36 mg/mL and 1.20, 0.89 and 0.17 mg/mL toward DPPH, NO and TBARS, respectively. Likewise LMWHA exhibited significant inhibitory effects on the AGEs formation than HA.

Discussion and conclusion: The results demonstrated that the ultrasonic irradiation did not damage and change the chemical structure of HA after degradation; furthermore, decreasing Mw and viscosity of LMWHA after degradation may enhance the antioxidant and antiglycation activity.

Keywords: FTIR; Polysaccharide; SEC-MALLS; advanced glycation end products; free radical; lipid peroxidation.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Antioxidants / chemistry
  • Antioxidants / isolation & purification
  • Antioxidants / pharmacology*
  • Biphenyl Compounds / chemistry
  • Chickens / metabolism*
  • Comb and Wattles / metabolism*
  • Drug Stability
  • Glucuronic Acid / isolation & purification
  • Glycation End Products, Advanced / metabolism*
  • Glycosylation
  • Hyaluronic Acid / chemistry
  • Hyaluronic Acid / isolation & purification
  • Hyaluronic Acid / pharmacology*
  • Hypoglycemic Agents / chemistry
  • Hypoglycemic Agents / isolation & purification
  • Hypoglycemic Agents / pharmacology*
  • Lipid Peroxidation / drug effects
  • Male
  • Molecular Structure
  • Molecular Weight
  • Nitric Oxide / chemistry
  • Picrates / chemistry
  • Protein Processing, Post-Translational / drug effects*
  • Serum Albumin, Bovine / metabolism*
  • Spectrophotometry, Ultraviolet
  • Spectroscopy, Fourier Transform Infrared
  • Thiobarbituric Acid Reactive Substances / chemistry
  • Tissue Extracts / chemistry
  • Tissue Extracts / isolation & purification
  • Tissue Extracts / pharmacology*
  • Ultrasonics*
  • Viscosity

Substances

  • Antioxidants
  • Biphenyl Compounds
  • Glycation End Products, Advanced
  • Hypoglycemic Agents
  • Picrates
  • Thiobarbituric Acid Reactive Substances
  • Tissue Extracts
  • advanced glycation end products-bovine serum albumin
  • Serum Albumin, Bovine
  • Nitric Oxide
  • Glucuronic Acid
  • Hyaluronic Acid
  • 1,1-diphenyl-2-picrylhydrazyl