New chromones from the roots of Saposhnikovia divaricata (Turcz.) Schischk with anti-inflammatory activity

被引:13
|
作者
Sun, Yan [1 ]
Jiang, Peng [1 ]
Jiang, Yi-Kai [1 ]
Pan, Juan [1 ]
Wu, Jia-Tong [1 ]
Li, Xiao-Mao [1 ]
Guan, Wei [1 ]
Min, Xin-Yu [1 ]
Wang, Yu-Xuan [1 ]
Kuang, Hai-Xue [1 ]
Liu, Yan [1 ]
Yang, Bing-You [1 ]
机构
[1] Heilongjiang Univ Chinese Med, Key Lab Basic & Applicat Res Beiyao, Minist Educ, Harbin, Peoples R China
基金
中国国家自然科学基金;
关键词
Saposhnikovia divaricata; Chromone; Anti-inflammatory; RAW264; 7; cells; CHEMICAL-CONSTITUENTS; GLYCOSIDES; INHIBITION;
D O I
10.1016/j.bioorg.2023.106447
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fifteen new chromones, sadivamones A-E (1-5), cimifugin monoacetate (6), sadivamones F-N (7-15), together with fifteen known chromones (16-30), were isolated from the ethyl acetate portions of 70% ethanol extract of Saposhnikovia divaricata (Turcz.) Schischk roots. The structures of the isolates were determined using 1D/2D NMR data and electron circular dichroism (ECD) calculations. Meanwhile, LPS induced RAW264.7 inflammatory cell model was used to determine the potential anti-inflammatory activity of all the isolated compounds in vitro. The results showed that compounds 2, 8, 12-13, 18, 20-22, 24, and 27 significantly inhibited the production of lipopolysaccharide (LPS)-induced NO in macrophages. To determine the signaling pathways involved in the suppression of NO production by compounds 8, 12 and 13, we investigated ERK and c-Jun N-terminal protein kinase (JNK) expression by western blot analysis. Further mechanistic studies demonstrated that compounds 12 and 13 inhibited the phosphorylation of ERK and the activation of ERK and JNK signaling in RAW264.7 cells via MAPK signaling pathways. Taken together, compounds 12 and 13 may be valuable candidates for the treatment of inflammatory diseases.
引用
收藏
页数:12
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