In vitro studies on mangiferin protection against cadmium-induced human renal endothelial damage and cell death via the MAP kinase and NF-κB pathways

J Recept Signal Transduct Res. 2016;36(1):57-66. doi: 10.3109/10799893.2015.1019137. Epub 2015 Mar 23.

Abstract

The therapeutic effects of the natural antioxidant mangiferin (a xanthonoid and potent oxygen free radical scavenger), which is widely distributed in mango fruit, against CdCl(2)-induced toxicity in human renal glomerulus endothelial cells (HRGEC) were investigated. The viability of HREGCs that were treated with CdCl(2) (25 µ mol) and co-treated with mangiferin (75 µ mol) for 24 h was measured by crystal violet dye. The exposure of human glomerulus renal endothelial cells to cadmium promotes a polarized apical secretion of IL-6 and IL-8, two pivotal proinflammatory cytokines known to play a significant role in renal inflammation. Proinflammatory cytokine secretion by human renal glomerulus endothelial cells could be the result of cadmium-induced IL-6 secretion via an NF-κB-dependent pathway. However, IL-8 secretion involves the phosphor-JNK phospho-p38 signaling pathway. The results of the current study reveal that mangiferin could prevent both cadmium-induced IL-6 and IL-8 secretion by human glomerulus endothelial cells and be used to prevent renal inflammation.

Keywords: Cadmium; NF-κB; interleukins; mangiferin; renal inflammation.

MeSH terms

  • Apoptosis / drug effects*
  • Blotting, Western
  • Cadmium / adverse effects*
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / pathology
  • Humans
  • In Vitro Techniques
  • Kidney Glomerulus / drug effects*
  • Kidney Glomerulus / metabolism
  • Kidney Glomerulus / pathology
  • Mitogen-Activated Protein Kinases / metabolism*
  • NF-kappa B / metabolism*
  • Signal Transduction / drug effects
  • Xanthones / pharmacology*

Substances

  • NF-kappa B
  • Xanthones
  • Cadmium
  • mangiferin
  • Mitogen-Activated Protein Kinases