Antioxidative effects of quercetin-glycosides isolated from the flower buds of Tussilago farfara L

Food Chem Toxicol. 2006 Aug;44(8):1299-307. doi: 10.1016/j.fct.2006.02.007. Epub 2006 Mar 6.

Abstract

A bioassay-guided fractionation of the ethylacetate soluble fraction from the flower buds of Tussilago farfara L. (Compositae) yielded two flavonoids, quercetin 3-O-beta-L-arabinopyranoside and quercetin 3-O-beta-D-glucopyranoside. These two sugar conjugates of quercetin exhibited higher antioxidative activity than their aglycone, quercetin by NBT superoxide scavenging assay. Moreover, treatment with quercetin 3-O-beta-L-arabinopyranoside significantly increased the total glutathione (GSH) contents and the protein level of gamma-glutamylcysteine ligase (gamma-GCL), a key enzyme required for glutathione (GSH) synthesis in a rat hepatocyte cell line. Subcellular fractionation and reporter gene analysis using antioxidant response element (ARE) construct revealed that quercetin 3-O-beta-L-arabinopyranoside increased the level of nuclear Nrf2 and reporter activity, and that these were associated with the induction of the gamma-GCL gene. After 24 h incubation of cells with quercetin 3-O-beta-L-arabinopyranoside, 23% of the glycoside was converted to its aglycone, quercetin, but gamma-GCL was not induced by 7 microM (23%) quercetin. These results suggest that the two quercetin-glycosides isolated from T. farfara L. have direct antioxidative properties, and that quercetin 3-O-beta-L-arabinopyranoside increases the cellular GSH level by inducing the gamma-GCL gene. These novel effects of quercetin-glycosides are suggestive to underlie the potential putative chemopreventive effects of T. farfara L.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Enzyme Induction / physiology
  • Flavonoids / chemistry
  • Flavonoids / isolation & purification*
  • Flavonoids / pharmacology*
  • Flowers / chemistry
  • Free Radical Scavengers / chemistry
  • Free Radical Scavengers / isolation & purification
  • Free Radical Scavengers / pharmacology
  • Gene Expression Regulation, Enzymologic / drug effects
  • Glutamate-Cysteine Ligase / biosynthesis
  • Glutamate-Cysteine Ligase / genetics
  • Glutamate-Cysteine Ligase / metabolism
  • Glutathione / metabolism
  • Glutathione Transferase / biosynthesis
  • Glutathione Transferase / metabolism
  • Glycosides / chemistry
  • Glycosides / isolation & purification*
  • Glycosides / pharmacology*
  • Hepatocytes
  • Molecular Conformation
  • NF-E2-Related Factor 2 / metabolism
  • Nitroblue Tetrazolium / chemistry
  • Nuclear Magnetic Resonance, Biomolecular
  • Rats
  • Superoxides / metabolism
  • Transcriptional Activation / drug effects
  • Tussilago / chemistry*

Substances

  • Flavonoids
  • Free Radical Scavengers
  • Glycosides
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • Superoxides
  • Nitroblue Tetrazolium
  • Glutathione Transferase
  • Glutamate-Cysteine Ligase
  • Glutathione