Limonoids from the roots of Melia azedarach and their anti-inflammatory activity

被引:4
|
作者
Song, Min [1 ,2 ,3 ,4 ]
Luo, Hui-Juan [1 ,2 ]
Li, Zi-Wei [3 ,4 ]
Qiu, Ling [1 ,2 ]
Zhao, Yu-Xin [1 ,2 ]
He, Cheng-Wei [1 ,2 ]
Zhang, Xiao-Qi [3 ,4 ]
Ye, Wen-Cai [3 ,4 ]
Lin, Li-Gen [1 ,2 ]
Zhang, Qing-Wen [1 ,2 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Univ Macau, Inst Chinese Med Sci, Macau, Peoples R China
[3] Jinan Univ, Coll Pharm, NMPA Key Lab Qual Evaluat TCM, Guangzhou 510632, Peoples R China
[4] Jinan Univ, Coll Pharm, Guangdong Prov Engn Res Ctr Modernizat TCM, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Melia azedarach L; Limonoids; Anti-inflammatory activity; 1L-1; beta; NLRP3; TRITERPENOIDS;
D O I
10.1016/j.phytochem.2023.113869
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
Twelve undescribed limonoids, meliazedarines J-U (1-12), along with a known one, were isolated from the roots of Melia azedarach. Their structures were elucidated by extensive spectroscopic investigations, X-ray diffraction analyses, and ECD calculations. Compounds 1-8 were identified as ring intact limonoids, while compounds 9-12 were established as ring C-seco ones. The anti-inflammatory potential of compounds 1-4, 6, 8, 9, and 11-13 was evaluated on macrophages. Compounds 1, 3, 4, 6, and 9 significantly suppressed nitric oxide production in lipopolysaccharide (LPS)-induced RAW 264.7 macrophages, among them compound 3 showed the best inhibitory effect with an IC50 value of 7.07 +/- 0.48 mu Mu. Furthermore, compound 3 effectively reduced interleukin-1 beta secretion in LPS plus nigericin-induced THP-1 macrophages by inhibiting NLRP3 inflammasome activation. The results strongly suggested that limonoids from the roots of M. azedarach might be candidates for treating inflammation-related diseases.
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页数:13
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