Oenothera paradoxa defatted seeds extract and its bioactive component penta-O-galloyl-β-D-glucose decreased production of reactive oxygen species and inhibited release of leukotriene B4, interleukin-8, elastase, and myeloperoxidase in human neutrophils

J Agric Food Chem. 2010 Sep 22;58(18):9960-6. doi: 10.1021/jf101740y.

Abstract

In this study, we analyzed ex vivo the effect of an aqueous extract of Oenothera paradoxa defatted seeds on the formation of neutrophil-derived oxidants. For defining active compounds, we also tested lypophilic extract constituents such as gallic acid, (+)-catechin, ellagic acid, and penta-O-galloyl-β-D-glucose and a hydrophilic fraction containing polymeric procyanidins. The anti-inflammatory potential of the extract and compounds was tested by determining the release from activated neutrophils of elastase, myeloperoxidase, interleukin-8 (IL-8), and leukotriene B4 (LTB4), which are considered relevant for the pathogenesis of cardiovascular diseases. The extract of O. paradoxa defatted seeds displays potent antioxidant effects against both 4β-phorbol-12β-myristate-α13-acetate- and formyl-met-leu-phenylalanine-induced reactive oxygen species production in neutrophils with IC50 values around 0.2 μg/mL. All types of polyphenolics present in the extract contributed to the extract antioxidant activity. According to their IC50 values, penta-O-galloyl-β-D-glucose was the more potent constituent of the extract. In cell-free assays, we demonstrated that this effect is partially due to the scavenging of O2- and H2O2 oxygen species. The extract and especially penta-O-galloyl-β-D-glucose significantly inhibit elastase, myeloperoxidase IL-8, and LTB4 release with an IC50 for penta-O-galloyl-β-D-glucose of 17±1, 15±1, 6.5±2.5, and around 20 μM, respectively. The inhibition of penta-O-galloyl-β-D-glucose on reactive oxygen species and especially on O2- production, myeloperoxidase, and chemoattractant release may reduce the interaction of polymorphonuclear leukocyte with the vascular endothelium and by that potentially diminish the risk of progression of atherosclerosis development.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / toxicity
  • Antioxidants / chemistry
  • Antioxidants / pharmacology*
  • Antioxidants / toxicity
  • Cells, Cultured
  • Humans
  • Hydrolyzable Tannins / pharmacology*
  • Hydrolyzable Tannins / toxicity
  • Interleukin-8 / metabolism
  • Leukotriene B4 / metabolism
  • Neutrophils / drug effects*
  • Neutrophils / enzymology
  • Neutrophils / metabolism
  • Oenothera / chemistry*
  • Pancreatic Elastase / metabolism
  • Peroxidase / metabolism
  • Plant Extracts / chemistry
  • Plant Extracts / pharmacology*
  • Plant Extracts / toxicity
  • Reactive Oxygen Species / metabolism*
  • Seeds / chemistry*
  • Young Adult

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antioxidants
  • CXCL8 protein, human
  • Hydrolyzable Tannins
  • Interleukin-8
  • Plant Extracts
  • Reactive Oxygen Species
  • Leukotriene B4
  • pentagalloylglucose
  • Peroxidase
  • Pancreatic Elastase