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Cited 3 time in webofscience Cited 4 time in scopus
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Stellera chamaejasme Methanolic Extract Attenuates Nitric Oxide Production and Enhances Heme Oxygenase 1 Expression in Murine Macrophages

Authors
Taddesse, YayehIm, Eun JuKwak, DongmiLee, Young ChulHyun, EujinHong, MeiJiao, PingJia, QiGoo, Youn-KyoungHong, Seung-BokKim, SukRhee, Man Hee
Issue Date
Jul-2017
Publisher
CHIANG MAI UNIV, FAC SCIENCE
Keywords
Stellera chamaejasme; hemoxyginase 1; nitric oxide; murine macrophages
Citation
CHIANG MAI JOURNAL OF SCIENCE, v.44, no.3, pp 858 - 868
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
CHIANG MAI JOURNAL OF SCIENCE
Volume
44
Number
3
Start Page
858
End Page
868
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/13619
ISSN
0125-2526
Abstract
Stellera chamaejasme has been used in Chinese folk medicine against skin diseases, chronic tracheitis, and tuberculosis. However, the medicinal value of this plant has not been verified experimentally and there exists paucity of data as to the anti-inflammatory and anti-oxidant properties. Therefore, we explored that Stellera chamaejasme methanolic extract (SCME) potently inhibited nitric oxide (NO) release in LPS stimulated RAW264.7 cells. SCME (1-10 mu g/ml) also down-regulated inducible nitric oxide synthase (iNOS) mRNA and protein expressions, while it markedly enhanced HO-1 expression. Moreover, SCME alone induced the phosphorylations of ERK1/2, JNK, p38(MAPK), Akt, and I kappa B-alpha. Likewise, SCME increased the nuclear levels of phosphorylated Nrf-2, c-Fos, c-Jun and ATF-2 transcription factors. On the other hand, inhibitors of ERK1/2 (PD98059), PI-3K/Akt (LY294002), protein kinase (PK)-A (H-89), PKC (H-7) and NF-kappa B (BAY117082) attenuated SCME induced HO-1 expression, suggesting the involvement of these pathways. Taken together, we reported for the first time that SCME potently inhibited NO production whereas it up-regulated HO-1 expression at low concentrations. Thus, this extract could be a potential source of natural compounds that may reduce the overwhelming inflammation and cellular oxidation.
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