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PMID: 19387591 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Two enone fatty acids isolated from Gracilaria verrucosa suppress the production of inflammatory mediators by down-regulating NF-kappaB and STAT1 activity in lipopolysaccharide-stimulated RAW 264.7 cells.

Archives of pharmacal research ·Vol. 32 ·No. 3 ·2009-03-00 ·Pages 453-62

Lee HJ, Dang HT, Kang GJ, Yang EJ, Park SS, Yoon WJ, Jung JH, Kang HK, Yoo ES

Abstract

Gracilaria verrucosa is a common marine red alga that has anti-oxidant and anti-cancer properties. Recently, we reported that anti-inflammatory constituents of G. verrucosa operate through an unknown mechanism. For this reason, we isolated two enone fatty acids from G. verrucosa and investigated their molecular mechanism in LPS-stimulated RAW264.7 cells. We found that the two compounds inhibited the production of inflammatory markers (nitric oxide, TNF-alpha, and IL-6) in a dose-dependent manner. We next studied the effects of G. verrucosa compounds on LPS-induced signaling pathways. The two compounds suppressed NF-kappaB reporter activity by interfering with nuclear translocation of NF-kappaB and suppressed JAK/STAT (p-STAT1) signaling. These results suggest that G. verrucosa inhibits the production of inflammatory mediators (NO, TNF-alpha, and IL-6) by suppressing the activation of NF-kappaB and the phosphorylation of STAT1.

MeSH Terms
Animals Anti-Inflammatory Agents/isolation & purification,pharmacology Cell Line Dose-Response Relationship, Drug Down-Regulation Fatty Acids/isolation & purification,pharmacology Gracilaria/chemistry Inflammation Mediators/metabolism Interleukin-6/metabolism Janus Kinases/metabolism Lipopolysaccharides/pharmacology Macrophages/drug effects,immunology,metabolism Mice Nitric Oxide/metabolism Nitric Oxide Synthase Type II/metabolism Phosphorylation Promoter Regions, Genetic/drug effects STAT1 Transcription Factor/metabolism Signal Transduction/drug effects Transcription Factor RelA/genetics,metabolism Tumor Necrosis Factor-alpha/metabolism
Chemicals
Anti-Inflammatory Agents Fatty Acids Inflammation Mediators Interleukin-6 Lipopolysaccharides Rela protein, mouse STAT1 Transcription Factor Stat1 protein, mouse Transcription Factor RelA Tumor Necrosis Factor-alpha lipopolysaccharide, Escherichia coli O111 B4 Nitric Oxide Nitric Oxide Synthase Type II Janus Kinases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Lee Hye-Ja
Department of Pharmacology, College of Medicine, Jeju National University, Jeju, 690-756, Korea.
Dang Hung-The
Kang Gyeoung-Jin
Yang Eun-Jin
Park Sun-Soon
Yoon Weon-Jong
Jung Jee H
Kang Hee-Kyoung
Yoo Eun-Sook
Article Info
Journal
Archives of pharmacal research
Abbr.
Arch Pharm Res
ISSN
0253-6269
Published
2009-03-00
Epub
2009-00-23
Pages
453-62
Language
English
Region
Korea (South)
NLM ID
8000036
Subset
IM
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