Anti-inflammatory iridoid glycosides from Paederia scandens (Lour.) Merrill

被引:11
|
作者
Xu, Yanxiang [1 ,2 ]
Zeng, Jia [3 ]
Wang, Lin [1 ,2 ]
Xu, Jingwen [1 ,2 ]
He, Xiangjiu [1 ,2 ]
Wang, Yihai [1 ,2 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
[2] Guangdong Engn Res Ctr Lead Cpds & Drug Discovery, Guangzhou 510006, Peoples R China
[3] Beijing Univ Chinese Med, Sch Life Sci, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Paederia scandens (Lour; ) Merrill; Rubiaceae; Iridoid glycosides; Anti-inflammatory; NO inhibition; NF-KB; CHEMICAL-CONSTITUENTS; PAEDEROSIDIC ACID; ANTINOCICEPTIVE ACTIVITY; AERIAL PARTS; GLUCOSIDES; RUBIACEAE; EXTRACTS; FRACTION; LEAVES; MODEL;
D O I
10.1016/j.phytochem.2023.113705
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
Eight previously undescribed iridoid glycosides together with 20 known congeners were isolated from the aerial parts of Paederia scandens (Lour.) Merrill (Rubiaceae). Their structures incorporating absolute configurations were elucidated based on the comprehensive analyses of NMR data, HR-ESI-MS spectrometry, and ECD data. The potential anti-inflammatory activities of the isolated iridoids were evaluated in lipopolysaccharide-stimulated RAW 264.7 macrophages. Compound 6 significantly inhibited the production of nitric oxide with an IC50 value of 15.30 mu M. The results of immunoblotting, qPCR, and immunofluorescence staining assays revealed that compound 6 exhibited anti-inflammatory activity by suppressing nuclear translocation of NF -KB and reducing the expression of COX-2, iNOS, IL-1 beta, and IL-6. These results provide a basis for further development and utilization of P. scandens as a natural source of potential anti-inflammatory agents.
引用
收藏
页数:12
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