Protective effect of polysaccharides from Sargassum horneri against oxidative stress in RAW264.7 cells

Int J Biol Macromol. 2014 Jul:68:98-106. doi: 10.1016/j.ijbiomac.2014.04.037. Epub 2014 Apr 24.

Abstract

This study was designed to investigate chemical composition and the protective effects of polysaccharides isolated from Sargassum horneri against hydrogen peroxide (H2O2)-induced oxidative injury in RAW264.7 cells. Results showed that isolated polysaccharides (SHSc) and the major fractions (SHS1, SHS0.5) contained sulfate ester, and SHS1 was high fucose-containing sulfated polysaccharide. After preincubation with three isolated polysaccharides, RAW264.7 cells viability were significantly restored and decreased in cellular LDH release (P<0.05). SHS1 and SHS0.5 decreased intracellular ROS level, intracellular NO and malonic dialdehyde (MDA) level (P<0.05), restoring activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) (P<0.05), decreasing inducible nitric oxide synthase (iNOS) (P<0.05). Moreover, preincubation of SHS1 with RAW264.7 cells resulted in the increase of the gene expression level of endogenous antioxidant enzymes such as MnSOD and GSH-Px (P<0.05). These results clearly showed that SHSc and its fractions could attenuate H2O2-induced stress injury in RAW264.7 cells, and a similar efficiency in protecting RAW264.7 cells against H2O2-induced oxidative injury between SHS1 and Vitamin C. Taken together, our findings suggested that SHS1 can effectively protect RAW264.7 cells against oxidative stress by H2O2, which might be used as a potential natural antioxidant in the functional food and pharmaceutical industries.

Keywords: Antioxidant activity; RAW264.7 cells; Sargassum horneri polysaccharides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Ascorbic Acid / pharmacology
  • Cell Line
  • Cell Survival / drug effects
  • Culture Media
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism
  • Hydrogen Peroxide / toxicity
  • Intracellular Space / drug effects
  • Intracellular Space / metabolism
  • Macrophages / drug effects
  • Macrophages / enzymology
  • Macrophages / pathology*
  • Malondialdehyde / metabolism
  • Mice
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Oxidative Stress / drug effects*
  • Polysaccharides / isolation & purification
  • Polysaccharides / pharmacology*
  • Protective Agents / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Real-Time Polymerase Chain Reaction
  • Sargassum / chemistry*
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Time Factors

Substances

  • Antioxidants
  • Culture Media
  • Polysaccharides
  • Protective Agents
  • RNA, Messenger
  • Nitric Oxide
  • Malondialdehyde
  • Hydrogen Peroxide
  • Glutathione Peroxidase
  • Nitric Oxide Synthase Type II
  • Superoxide Dismutase
  • Ascorbic Acid