Document Type
Article
Publication Date
2007
Journal or Book Title
Journal of Agricultural and Food Chemistry
Volume
55
Issue
18
First Page
7314
Last Page
7322
DOI
10.1021/jf063711a
Abstract
Inhibition of prostaglandin E2 (PGE2) production in lipopolysaccharide-stimulated RAW264.7 mouse macrophage cells was assessed with an enzyme immunoassay following treatments with Echinacea extracts or synthesized alkamides. Results indicated that ethanol extracts diluted in media to a concentration of 15 μg/mL from E. angustifolia, E. pallida, E. simulata, and E. sanguinea significantly inhibited PGE2 production. In further studies, PGE2 production was significantly reduced by all synthesized alkamides assayed at 50 μM, by Bauer alkamides 8, 12A analogue, and 14, Chen alkamide 2, and Chen alkamide 2 analogue at 25 μM and by Bauer alkamide 14 at 10 μM. Cytotoxicity did not play a role in the noted reduction of PGE2production in either the Echinacea extracts or synthesized alkamides. High-performance liquid chromatography analysis identified individual alkamides present at concentrations below 2.8 μM in the extracts from the six Echinacea species (15 μg/mL crude extract). Because active extracts contained 2, it is likely that alkamides may contribute toward the anti-inflammatory activity of Echinacea in a synergistic or additive manner.
Copyright Owner
American Chemical Society
Copyright Date
2007
Language
en
File Format
application/pdf
Recommended Citation
LaLone, Carlie A.; Hammer, Kimberly D.P.; Wu, Lankun; Bae, Jaehood; Leyva, Norma; Liu, Yi; Solco, Avery K.S.; Kraus, George A.; Murphy, Patricia A.; Wurtele, Eve S.; Kim, Ok-Kyung; Seo, Kwon II; Widrlechner, Mark P.; and Birt, Diane F., "Echinacea Species and Alkamides Inhibit Prostaglandin E2 Production in RAW264.7 Mouse Macrophage Cells" (2007). Food Science and Human Nutrition Publications. 21.
https://lib.dr.iastate.edu/fshn_ag_pubs/21
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Comments
Posted with permission from Journal of Agricultural and Food Chemistry 55, no. 18 (2007): 7314–7322, doi:10.1021/jf063711a. Copyright 2007 American Chemical Society.