Skip to main content
Article
Endogenous Levels of Echinacea Alkylamides and Ketones Are Important Contributors to the Inhibition of Prostaglandin E2 and Nitric Oxide Production in Cultured Macrophages
Journal of Agricultural and Food Chemistry
  • Carlie A. LaLone, Iowa State University
  • Ludmila Rizshsky, Iowa State University
  • Kimberly D.P. Hammer, Iowa State University
  • Lankun Wu, Iowa State University
  • Avery K.S. Solco, Iowa State University
  • Man-Yu Yum, Iowa State University
  • Basil J. Nikolau, Iowa State University
  • Eve S. Wurtele, Iowa State University
  • Patricia A. Murphy, Iowa State University
  • Meehye Kim, Korea Food and Drug Administration
  • Diane F. Birt, Iowa State University
Document Type
Article
Publication Date
1-1-2009
DOI
10.1021/jf901202y
Abstract

Because of the popularity of Echinacea as a dietary supplement, researchers have been actively investigating which Echinacea constituent or groups of constituents are necessary for immunemodulating bioactivities. Our prior studies indicate that alkylamides may play an important role in the inhibition of prostaglandin E2 (PGE2) production. High-performance liquid chromatography fractionation, employed to elucidate interacting anti-inflammatory constituents from ethanol extracts of Echinacea purpurea, Echinacea angustifolia, Echinacea pallida, and Echinacea tennesseensis, identified fractions containing alkylamides and ketones as key anti-inflammatory contributors using lipopolysaccharideinduced PGE2 production in RAW264.7 mouse macrophage cells. Nitric oxide (NO) production and parallel cytotoxicity screens were also employed to substantiate an anti-inflammatory response. E. pallida showed significant inhibition of PGE2 with a first round fraction, containing gas chromatography-mass spectrometry (GC-MS) peaks for Bauer ketones 20, 21, 22, 23, and 24, with 23 and 24 identified as significant contributors to this PGE2 inhibition. Chemically synthesized Bauer ketones 21 and 23 at 1 μM each significantly inhibited both PGE2 and NO production. Three rounds of fractionation were produced from an E. angustifolia extract. GC-MS analysis identified the presence of Bauer ketone 23 in third round fraction 3D32 and Bauer alkylamide 11 making up 96% of third round fraction 3E40. Synthetic Bauer ketone 23 inhibited PGE2 production to 83% of control, and synthetic Bauer alkylamide 11 significantly inhibited PGE2 and NO production at the endogenous concentrations determined to be present in their respective fraction; thus, each constituent partially explained the in vitro anti-inflammatory activity of their respective fraction. From this study, two key contributors to the anti-inflammatory properties of E. angustifolia were identified as Bauer alkylamide 11 and Bauer ketone 23.

Comments

Posted with permission from Journal of Agricultural and Food Chemistry 57, no. 19 (2009): 8820–8830, doi:10.1021/jf901202y. Copyright 2009 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
Date Available
January 16, 2013
File Format
application/pdf
Citation Information
Carlie A. LaLone, Ludmila Rizshsky, Kimberly D.P. Hammer, Lankun Wu, et al.. "Endogenous Levels of Echinacea Alkylamides and Ketones Are Important Contributors to the Inhibition of Prostaglandin E2 and Nitric Oxide Production in Cultured Macrophages" Journal of Agricultural and Food Chemistry Vol. 57 Iss. 19 (2009) p. 8820 - 8830
Available at: http://works.bepress.com/basil-nikolau/18/