Immunoenhancement Effects of Glycosaminoglycan from Apostichopus japonicus: In Vitro and In Cyclophosphamide-Induced Immunosuppressed Mice Studies

Mar Drugs. 2017 Nov 7;15(11):347. doi: 10.3390/md15110347.

Abstract

In this study, the immunomodulatory activities of Apostichopus japonicus glycosaminoglycan (AHG) on the nature killer (NK) cells, cytotoxic T lymphocytes (CTLs) and cyclophosphamide (CY)-treated mice were investigated. After stimulation with multiple concentrations of AHG (0-100 μg/mL), NK cells and CTLs displayed outperformance against YAC-1 and B16 cells, respectively. Furthermore, the mitogen-induced splenic lymphocyte proliferation in CY-induced immunosuppressed mice was significantly promoted by AHG. In addition, the administration of AHG dramatically increased the splenocytes Ca2+ concentration and the delayed-type hypersensitivity (DTH) reaction in a dose-dependent manner. Besides, AHG could strongly increase the total antioxidant capacity (T-AOC), the activities of superoxidase dismutase (SOD), catalase (CAT) as well as glutathione peroxidase (GSH-PX), and could decrease the malondialdehyde (MDA) level in the heart, kidney and liver. These findings indicated that AHG played an important role in the immune enhancement and protection against CY-induced immunosuppression and oxidative damage. Our findings provide experimental evidence for further research and possible immunostimulatory applications of AHG in clinical practice.

Keywords: cyclophosphamide; glycosaminoglycan; immunomodulation; sea cucumber.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Antioxidants / pharmacology
  • Calcium
  • Catalase / metabolism
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Cyclophosphamide / toxicity*
  • Cytokines
  • Glutathione Peroxidase / metabolism
  • Glycosaminoglycans / chemistry
  • Glycosaminoglycans / pharmacology*
  • Immunocompromised Host
  • Killer Cells, Natural / drug effects*
  • Malondialdehyde / metabolism
  • Mice
  • Spleen / cytology
  • Stichopus / chemistry*
  • Superoxide Dismutase / metabolism
  • T-Lymphocytes, Cytotoxic / drug effects*

Substances

  • Antioxidants
  • Cytokines
  • Glycosaminoglycans
  • Malondialdehyde
  • Cyclophosphamide
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Calcium