Stellera chamaejasme Methanolic Extract Attenuates Nitric Oxide Production and Enhances Heme Oxygenase 1 Expression in Murine Macrophages

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...

Full description

Saved in:
Bibliographic Details
Main Authors: Yayeh Taddesse, Eun Ju Im, Dongmi Kwak, Young Chul Lee, Eujin Hyun, Mei Hong, Ping Jiao, Qi Jia, Youn-Kyoung Goo, Seung-Bok Hong, Suk Kim, Man Hee Rhee
Format: บทความวารสาร
Language:English
Published: Science Faculty of Chiang Mai University 2019
Online Access:http://it.science.cmu.ac.th/ejournal/dl.php?journal_id=8274
http://cmuir.cmu.ac.th/jspui/handle/6653943832/63906
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
Description
Summary: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 mg/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 IkB-a. 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-kB (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.