Schisandrin A protects intestinal epithelial cells from deoxynivalenol-induced cytotoxicity, oxidative damage and inflammation

Sci Rep. 2019 Dec 16;9(1):19173. doi: 10.1038/s41598-019-55821-4.

Abstract

Extensive research has revealed the association of continued oxidative stress with chronic inflammation, which could subsequently affect many different chronic diseases. The mycotoxin deoxynivalenol (DON) frequently contaminates cereals crops worldwide, and are a public health concern since DON ingestion may result in persistent intestinal inflammation. There has also been considerable attention over the potential of DON to provoke oxidative stress. In this study, the cytoprotective effect of Schisandrin A (Sch A), one of the most abundant active dibenzocyclooctadiene lignans in the fruit of Schisandra chinensis (Turcz.) Baill (also known as Chinese magnolia-vine), was investigated in HT-29 cells against DON-induced cytotoxicity, oxidative stress and inflammation. Sch A appeared to protect against DON-induced cytotoxicity in HT-29 cells, and significantly lessened the DON-stimulated intracellular reactive oxygen species and nitrogen oxidative species production. Furthermore, Sch A lowered DON-induced catalase, superoxide dismutase and glutathione peroxidase antioxidant enzyme activities but maintains glutathione S transferase activity and glutathione levels. Mechanistic studies suggest that Sch A reduced DON-induced oxidative stress by down-regulating heme oxygenase-1 expression via nuclear factor (erythroid-derived 2)-like 2 signalling pathway. In addition, Sch A decreased the DON-induced cyclooxygenase-2 expression and prostaglandin E2 production and pro-inflammatory cytokine interleukin 8 expression and secretion. This may be mediated by preventing DON-induced translocation of nuclear factor-κB, as well as activation of mitogen-activated protein kinases pathways. In the light of these findings, we concluded that Sch A exerted a cytoprotective role in DON-induced toxicity in vitro, and it would be valuable to examine in vivo effects.

MeSH terms

  • Catalase / metabolism
  • Cell Cycle Checkpoints / drug effects
  • Cell Cycle Checkpoints / genetics
  • Cell Death / drug effects
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Cyclooctanes / pharmacology*
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Cytoprotection* / drug effects
  • Dinoprostone / biosynthesis
  • Enterocytes / drug effects
  • Enterocytes / metabolism
  • Enterocytes / pathology*
  • Gene Expression Regulation / drug effects
  • Glutathione Peroxidase / metabolism
  • HT29 Cells
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / metabolism
  • Humans
  • Inflammation / genetics
  • Inflammation / pathology*
  • Inflammation Mediators / metabolism
  • Interleukin-8 / biosynthesis
  • Lignans / pharmacology*
  • Lipid Peroxidation / drug effects
  • MAP Kinase Signaling System / drug effects
  • Models, Biological
  • NF-E2-Related Factor 2 / metabolism
  • NF-kappa B / metabolism
  • Nitrites / metabolism
  • Oxidative Stress / drug effects*
  • Oxidative Stress / genetics
  • Polycyclic Compounds / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species / metabolism
  • Superoxide Dismutase / metabolism
  • Trichothecenes / toxicity*

Substances

  • Cyclooctanes
  • Inflammation Mediators
  • Interleukin-8
  • Lignans
  • NF-E2-Related Factor 2
  • NF-kappa B
  • Nitrites
  • Polycyclic Compounds
  • RNA, Messenger
  • Reactive Oxygen Species
  • Trichothecenes
  • schizandrin A
  • Catalase
  • Glutathione Peroxidase
  • Heme Oxygenase-1
  • Cyclooxygenase 2
  • Superoxide Dismutase
  • deoxynivalenol
  • Dinoprostone