Intervention effects of sulfate glycosaminoglycan from swim bladder against arsenic-induced damage in IEC-6 cells

Int J Biol Macromol. 2023 Dec 1:252:126460. doi: 10.1016/j.ijbiomac.2023.126460. Epub 2023 Aug 22.

Abstract

In this study, a purified macromolecular sulfate glycosaminoglycan whose structural characterization is similar to chondroitin sulfate from the swim bladder of Aristichthys nobilis, named SBSG, was used to explore the intervention effects on arsenic-induced intestinal epithelial cells (IEC-6) damage. Arsenic exposure led to cell membrane rupture, mitochondrial dysfunction, oxidative damage, and down-regulation of tight junction proteins expression. Treatment with SBSG could alleviate arsenic exposure-induced cell damage by decreasing the extracellular lactate dehydrogenase activity and influencing mitochondrial membrane potential, reactive oxygen species level, malondialdehyde content, and anti-oxidative enzyme activity. On the other hand, SBSG could promote nitric oxide production to achieve potential immunoregulation. The Western blot showed that intervention of SBSG mainly could restrain the activation of the JNK signaling pathway and up-regulate the expression of ZO-1 against arsenic-induced cell damage. This study provides a new perspective for understanding the heavy metal detoxification of SBSG on the intestinal and indicates that SBSG could be used as natural antioxidant resistant to heavy metal toxicity.

Keywords: Glycosaminoglycan; Heavy metals; Intestinal epithelial cells.

MeSH terms

  • Arsenic* / toxicity
  • Epithelial Cells
  • Glycosaminoglycans / pharmacology
  • Metals, Heavy* / pharmacology
  • Oxidative Stress
  • Sulfates / pharmacology
  • Urinary Bladder

Substances

  • Arsenic
  • Glycosaminoglycans
  • Sulfates
  • Metals, Heavy