Inhibition of Kupffer cell functions as an explanation for the hepatoprotective properties of silibinin

Hepatology. 1996 Apr;23(4):749-54. doi: 10.1053/jhep.1996.v23.pm0008666328.


The flavonoid silibinin, the main compound extracted from the milk thistle Silybum marianum, displays hepatoprotective properties in acute and chronic liver injury. To further elucidate the mechanisms by which it acts, we studied the effects of silibinin on different functions of isolated rat Kupffer cells, namely the formation of superoxide anion radical (02-), nitric oxide (NO), tumor necrosis factor alpha (TNF-alpha), prostaglandin E(2) (PGE(2)), and leukotriene B(4) (LTB(4)). Production of 02- and NO were inhibited in a dose-dependent manner, with an 50 percent inhibitory concentration (IC(50)) value around 80 micro mol/L. No effect on TNF-alpha formation was detected. Opposite effects were found on the cyclooxygenase and 5-lipoxygenase pathway of arachidonic acid metabolism. Whereas no influence on PGE(2) formation was observed with silibinin concentrations up to 100 micro mol/L, a strong inhibitory effect on LTB(4) formation became evident. The IC(50)-value for inhibiting the formation of this eicosanoid was determined to be 15 micro mol/L silibinin. The strong inhibition of LTB(4), formation by silibinin was confirmed in experiments with phagocytic cells isolated from human liver. Hence, while rather high concentrations of silibinin are necessary to diminish free radical formation by activated Kupffer cells, significant inhibition of the 5-lipoxygenase pathway already occurs at silibinin concentrations which are achieved in vivo. Selective inhibition of leukotriene formation by Kupffer cells can at least partly account for the hepatoprotective properties of silibinin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dinoprostone / biosynthesis
  • Humans
  • Kupffer Cells / drug effects*
  • Kupffer Cells / physiology
  • Leukotriene B4 / biosynthesis
  • Liver / drug effects*
  • Male
  • Nitric Oxide / biosynthesis
  • Rats
  • Rats, Wistar
  • Silymarin / pharmacology*
  • Superoxides / metabolism
  • Tumor Necrosis Factor-alpha / biosynthesis


  • Silymarin
  • Tumor Necrosis Factor-alpha
  • Superoxides
  • Leukotriene B4
  • Nitric Oxide
  • Dinoprostone