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A germacranolide sesquiterpene lactone suppressed inducible nitric oxide synthase by downregulating NF-kappa B activity

Authors
Lee, Hwa JinJung, HyeyounKwon, JunhyeLi, HuaLee, Da YeonLim, Hyo JinKim, Mi-RanMoon, Dong-CheulRyu, Jae-Ha
Issue Date
Mar-2011
Publisher
CANADIAN SCIENCE PUBLISHING, NRC RESEARCH PRESS
Keywords
nitric oxide; germacranolide sesquiterpene lactone; Carpesium triste var. manshuricum; nuclear factor kappa B; macrophage; inflammation; inducible nitric oxide synthase
Citation
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, v.89, no.3, pp 232 - 237
Pages
6
Journal Title
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY
Volume
89
Number
3
Start Page
232
End Page
237
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/12642
DOI
10.1139/Y11-004
ISSN
0008-4212
1205-7541
Abstract
A germacranolide sesquiterpene lactone, 2 alpha,5-epoxy-5,10-dihydroxy-6 alpha-angeloyloxy-9 beta-(3-methylbutyloxy)-germacran-8 alpha,12-olide (EDAG), isolated from Carpesium triste var. manshuricum, showed inhibitory activity in the production of nitric oxide (NO) and the expression of inducible nitric oxide synthase (iNOS) mRNA and protein in LPS-activated macrophage cells. Molecular analysis reveals that these suppressive effects are correlated with the inhibition of NF-kappa B activation by EDAG. Immunoblotting showed that EDAG suppressed the LPS-induced degradation of I-kappa B alpha and decreased nuclear translocation of p65. Futhermore, EDAG showed reduced phosphorylation of ERK1/2 and p38 MAPK, whereas activation of JNK was not changed. These data suggest, at least in part, that EDAG utilizes the signal cascades of ERK1/2, p38 MAPK, and NF-kappa B for the suppression of iNOS gene expression.
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