Rosmarinic acid failed to suppress hydrogen peroxide-mediated apoptosis but induced apoptosis of Jurkat cells which was suppressed by Bcl-2

Mol Cell Biochem. 2006 Apr;285(1-2):111-20. doi: 10.1007/s11010-005-9064-8. Epub 2006 Mar 14.

Abstract

Rosmarinic acid (RosA), frequently found as a secondary metabolite in herbs and medicinal plants, has exhibited antioxidative and anti-inflammatory activities. RosA was shown to inhibit the proliferation and induce apoptosis of Jurkat T cells but the mechanism of action of RosA in apoptosis remains elusive. RosA inhibited the proliferation of Jurkat cells in a dose-dependent manner by suppressing the expression of cyclin D3 and p21(Cip1/Waf1) and up-regulating p27(Kip1). RosA induced apoptosis of Jurkat cells in a dose-dependent manner and failed to protect them from hydrogen peroxide (H2O2)-mediated apoptosis. Induction of apoptosis by RosA correlated with suppression of Bcl-2 but not of Bak or PUMA. Overexpression of Bcl-2 protected Jurkat cells from both H2O2- and RosA-induced apoptosis by altering the ratio of anti- to pro-apoptotic members of the Bcl-2 family. In conclusion, RosA inhibited Jurkat cell proliferation by altering the expression of cyclins and cyclin-dependent kinase inhibitors and induced apoptosis most likely acting through the mitochondrial pathway and possessed no anti-oxidant properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / pharmacology
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins / metabolism
  • Cell Proliferation / drug effects
  • Cinnamates / pharmacology*
  • Depsides
  • Dose-Response Relationship, Drug
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Jurkat Cells / drug effects*
  • Proto-Oncogene Proteins c-bcl-2 / physiology*
  • Rosmarinic Acid

Substances

  • Antioxidants
  • Apoptosis Regulatory Proteins
  • Cinnamates
  • Depsides
  • Proto-Oncogene Proteins c-bcl-2
  • Hydrogen Peroxide