Study on structure characterization of pectin from the steamed ginseng and the inhibition activity of lipid accumulation in oleic acid-induced HepG2 cells

Int J Biol Macromol. 2020 Sep 15:159:57-65. doi: 10.1016/j.ijbiomac.2020.04.167. Epub 2020 Apr 24.

Abstract

Two acid polysaccharides were obtained from steamed ginseng (GPS-1 and GPS-2) through water extraction, ion-exchange chromatography and gel chromatography. The structural features and ability of the polysaccharides to inhibit lipid accumulation in oleic acid-induced HepG2 cells were studied. GPS-1 consisted of type I arabinogalactans (AG-I), arabinogalactans-II (AG-II) and rhamnogalacturonan I (RG-I) domains. GPS-2 was a pectin-like polysaccharide consisting mainly of the homogalacturonan (HG) domain and a small amount of AG domain. Both GPS-1 and GPS-2 had branches attaching on O-3 of (1 → 6)-GalA or O-4 of (1 → 2)-Rha and terminated by either Ara or Gal. An in vitro experiment revealed that GPS-1 treatment at 50-400 μg/ml could dose-dependently decrease intracellular lipid accumulation and cholesterol (TC) and triglycerides (TG) levels. GPS-1 exerted a more serious hypolipidemic effect than GPS-2 did. Moreover, GPS-1 considerably increased the phosphorylation of AMP-activated protein kinase (AMPK) and affected the expression of AMPK downstream targets, including the inhibition of the protein expression of sterol regulatory element-binding protein 1c (SREBP-1c) and activation of Acetyl-CoA carboxylase (ACC). Results suggest that GPS-1 could inhibit lipid accumulation via the AMPK the signalling pathway.

Keywords: HepG2 cell; Lipid accumulation; Pectin; Steamed ginseng.

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • Arabinose / chemistry
  • Cholesterol / metabolism
  • Hep G2 Cells
  • Humans
  • Hypolipidemic Agents / chemistry*
  • Hypolipidemic Agents / pharmacology
  • Lipid Metabolism / drug effects
  • Oleic Acid / pharmacology
  • Panax / chemistry*
  • Pectins / chemistry*
  • Pectins / pharmacology
  • Protein Kinases / metabolism
  • Triglycerides / metabolism

Substances

  • Hypolipidemic Agents
  • Triglycerides
  • Oleic Acid
  • Pectins
  • Cholesterol
  • Arabinose
  • Protein Kinases
  • AMP-Activated Protein Kinase Kinases