Combinatorial usage of fungal polysaccharides from Cordyceps sinensis and Ganoderma atrum ameliorate drug-induced liver injury in mice

Food Chem Toxicol. 2018 Sep:119:66-72. doi: 10.1016/j.fct.2018.05.027. Epub 2018 May 16.

Abstract

This study investigated the possible protective effect of combined fungal polysaccharides (CFP), consisting of Cordyceps sinensis polysaccharides (CSP) and Ganoderma atrum polysaccharides (PSG) with well-defined structural characteristics, against cyclophosphamide (CTX)-induced hepatotoxicity in mice. Our results indicated CFP effectively prevented the liver injury by decreasing toxicity markers (aspartate transaminase, alanine aminotransferase and alkaline phosphatase). Further biochemical and molecular analysis indicated CSP particularly inhibited the activation of Toll-like receptor 9 (TLR9) and its related inflammatory signals, including pro-inflammatory cytokines, inducible nitric oxide synthase, and cyclooxygenase-2 to modulate hepatic inflammation response. Relatively, through activation of peroxisome proliferator-activated receptor α (PPARα), PSG increased hepatic glutathione peroxidase and glutathione content depleted by CTX, as well as prevented mitochondria-dependent apoptosis with regulation on Bcl-2 family proteins (Bad, Bax and Bcl-2). In addition, protective effect of CFP was associated with enhanced modulations on cellular oxidant/antioxidant imbalance, mitochondrial apoptotic pathway and pro-inflammatory factors via PPARα upregulation and TLR9 downregulation. Taking together, the combinatorial approach based on CSP and PSG presented a practical option for the management of drug-induced liver injury.

Keywords: Combinatorial usage; Cordyceps sinensis; Ganoderma atrum; Hepatoprotective; Oxidative stress.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Apoptosis / drug effects
  • Biomarkers
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Cordyceps / chemistry*
  • Cyclophosphamide / toxicity*
  • Female
  • Fungal Polysaccharides / chemistry
  • Fungal Polysaccharides / pharmacology*
  • Ganoderma / chemistry*
  • Gene Expression Regulation / drug effects
  • Liver / drug effects
  • Liver / metabolism
  • Mice
  • Mice, Inbred BALB C
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • Specific Pathogen-Free Organisms
  • Toll-Like Receptor 9 / genetics
  • Toll-Like Receptor 9 / metabolism

Substances

  • Antioxidants
  • Biomarkers
  • Fungal Polysaccharides
  • PPAR alpha
  • Tlr9 protein, mouse
  • Toll-Like Receptor 9
  • Cyclophosphamide