Anti-inflammatory constituents from the root of Litsea cubeba in LPS-induced RAW 264.7 macrophages. (1st September 2016)

• Record Type: Journal Article
• Authors: Lin, Bing; Sun, Lian-Na; Xin, Hai-Liang; Nian, Hua; Song, Hong-Tao; Jiang, Yi-Ping; Wei, Zhen-Qiao; Qin, Lu-Ping; Han, Ting
• Is Part Of: Pharmaceutical biology. Volume 54:Number 9(2016:Sep.)
• Page Start: 1741
• Page End: 1747
• Publication Date: 2016-09-01
• Subjects: Anti-arthritic -- IκBα -- IKKβ -- rheumatoid arthritis -- RT-PCR -- Traditional Chinese Medicine; Pharmacognosy -- Periodicals; Materia medica, Vegetable -- Periodicals; 615.321
• DOI: 10.3109/13880209.2015.1126619
• Languages: English
• ISSNs: 1388-0209

Abstract

Abstract: Context Litsea cubeba (Lour.) Pers. (Lauraceae) has long been used as a folk remedy in Traditional Chinese Medicine (TCM) for the treatment of rheumatic diseases. Previous studies from our laboratory indicated that L. cubeba extract showed anti-arthritic activity in rats. Objective To study L. cubeba chemically and biologically and to find the potential constituents responsible for its anti-arthritic effect. Materials and methods The compounds were isolated from the root of L. cubeba by column chromatography which eluted with PE:EtOAc gradient system, and the structures were elucidated by detailed spectroscopic data analysis; the anti-inflammatory activity of the isolated compounds was evaluated by lipopolysaccharide (LPS)-induced RAW 264.7 cells and the TNF-α and NO level were measured by ELISA (commercial kit); The iNOS and COX-2 mRNA expression were measured by RT-PCR and the phosphorylation of IκBα, IKKβ, P38 and Akt were determined by western blots. Results A novel 9-fluorenone, 1-ethoxy-3, 7-dihydroxy-4, 6-dimethoxy-9-fluorenone (1 ), together with 4 known compounds, namely pinoresinol (2 ), syringaresinol (3 ), 9, 9′- O -di-( E )-feruloyl-meso-5, 5′-dimethoxysecoisolariciresinol (4 ) and lyoniresinol (5 ) were isolated from the root of L. cubeba for the first time. The IC50 for NO inhibition on compounds1 and4 were 56.1 ± 1.2 and 32.8 ± 2.3 μM, respectively. The IC50 for TNF-α inhibition were 28.2 ± 0.9 and 15.0 ± 1.0 μM, respectively. Both1 and4 suppress mRNA expression of iNOS, COX-2 and protein phosphorylation of IκBα, IKKβ in LPS-induced RAW 264.7 cells. Discussion and conclusion Compounds1 and4 isolated from L. cubeba exhibited potent anti-inflammatory activity through the NF-κB signal pathway.