Silymarin inhibits TNF-alpha-induced expression of adhesion molecules in human umbilical vein endothelial cells

FEBS Lett. 2003 Aug 28;550(1-3):89-93. doi: 10.1016/s0014-5793(03)00827-5.

Abstract

Silymarin is known to have an anti-atherosclerotic activity, but the mechanism responsible for it remains unclear. Here, we demonstrate a possible mechanism involved in the anti-atherosclerotic activity of silymarin. Silymarin inhibited THP-1 cell adhesion to human umbilical vein endothelial cells (HUVECs). Silymarin also suppressed the TNF-alpha-induced protein and mRNA expression of adhesion molecules, such as VCAM-1, ICAM-1 and E-selectin, in HUVECs. Moreover, silymarin suppressed the TNF-alpha-induced DNA binding of NF-kappaB/Rel in HUVECs. Taken together, these results demonstrate that silymarin exerts an anti-atherosclerotic activity, at least in part, by inhibiting the expression of adhesion molecules.

MeSH terms

  • Cell Adhesion / drug effects
  • Cell Adhesion / genetics
  • Cell Adhesion Molecules / biosynthesis
  • Cell Adhesion Molecules / drug effects
  • Cell Adhesion Molecules / genetics*
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cells, Cultured
  • DNA / metabolism
  • E-Selectin / drug effects
  • E-Selectin / genetics
  • E-Selectin / metabolism
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / drug effects*
  • Gene Expression / drug effects
  • Humans
  • Intercellular Adhesion Molecule-1 / drug effects
  • Intercellular Adhesion Molecule-1 / genetics
  • Intercellular Adhesion Molecule-1 / metabolism
  • Monocytes / cytology
  • Monocytes / drug effects
  • NF-kappa B / drug effects
  • NF-kappa B / metabolism
  • Silymarin / pharmacology*
  • Tumor Necrosis Factor-alpha / pharmacology*
  • Umbilical Veins / cytology
  • Umbilical Veins / drug effects*
  • Vascular Cell Adhesion Molecule-1 / drug effects
  • Vascular Cell Adhesion Molecule-1 / genetics
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • Cell Adhesion Molecules
  • E-Selectin
  • NF-kappa B
  • Silymarin
  • Tumor Necrosis Factor-alpha
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • DNA