| Literature DB >> 28554870 |
Myoung-Sook Shin1, Jun Yeon Park2, Jaemin Lee3, Hye Hyun Yoo4, Dae-Hyun Hahm5, Sang Cheon Lee6, Sanghyun Lee3, Gwi Seo Hwang2, Kiwon Jung7, Ki Sung Kang8.
Abstract
In this study, we investigated the anti-inflammatory effects and mechanisms of cirsimaritin isolated from an ethanol extract of the aerial parts of Cirsium japonicum var. maackii Maxim. using RAW264.7 cells. The extract and its flavonoid cirsimaritin inhibited nitric oxide (NO) production and inducible nitric oxide synthase expression in RAW264.7 cells. Cirsimaritin inhibited interleukin-6, tumor necrosis factor-α, and NO production in a concentration-dependent manner in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. From a western blot study, pretreatment with cirsimaritin inhibited phosphorylation/degradation of IκBα and phosphorylation of Akt in LPS-stimulated RAW264.7 cells. Moreover, cirsimaritin suppressed activation of LPS-induced transcription factors, such as c-fos and signal transducer and activator of transcription 3 (STAT3), in RAW264.7 cells. Collectively, these results show that cirsimaritin possesses anti-inflammatory activity, which is regulated by inhibition of c-fos and STAT3 phosphorylation in RAW264.7 cells.Entities:
Keywords: Cirsimaritin; Cirsium japonicum; Inflammation
Mesh:
Substances:
Year: 2017 PMID: 28554870 DOI: 10.1016/j.bmcl.2017.05.051
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823