Anti-Inflammatory Activity of Labdane and Norlabdane Diterpenoids from Leonurus sibiricus Related to Modulation of MAPKs Signaling Pathway

被引:0
作者
Trang, Nguyen Minh [1 ]
Vinh, Le Ba [2 ]
Phong, Nguyen Viet [3 ,4 ]
Yang, Seo Young [3 ,4 ]
机构
[1] Chungnam Natl Univ, Coll Pharm, Daejeon, South Korea
[2] Vietnam Acad Sci & Technol, Inst Marine Biochem IMBC, Hanoi, Vietnam
[3] Kyungpook Natl Univ, Teachers Coll, Dept Biol Educ, 80 Daehak Ro, Daegu 41566, South Korea
[4] Kyungpook Natl Univ, Inst Phylogen & Evolut, 80 Daehak Ro, Daegu 41566, South Korea
基金
新加坡国家研究基金会;
关键词
Leonurus sibiricus; labdane diterpenoid; anti-inflammation; MAPKs; NF-KAPPA-B; EXTRACTS; CELLS; PHYTOCHEMISTRY; JAPONICUS;
D O I
10.1055/a-2440-5166
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Leonurus sibiricus, a widely cultivated herbaceous plant in Asian countries, exhibits diverse medicinal applications. Recent studies emphasize its pharmacological properties and efficacy in promoting bone health. In addition to the known compounds and their pharmacological activities, in this study, we isolated and elucidated two new labdane-type diterpenoids, (3R,5R,6S,10S)-3,6-dihydroxy-15-ethoxy-7-oxolab- den-8(9),13(14)-dien-15,16-olide (1) and (4R,5R,10S)-18-hy- droxy-14,15-bisnorlabda-8-en-7,13-dione (2), a new natural phenolic compound, and a known compound from L. sibiricus using advanced spectroscopic techniques, including circular dichroism spectroscopy, high-resolution mass spectrometry, and 1- and 2-dimensional NMR. Among these, compound 1 demonstrated potent inhibition of nitric oxide (NO) production and inducible nitric oxide synthase (iNOS) mRNA expression levels, followed by compound 2. Whereas compounds 3 and 4 did not exhibit effectiveness in RAW264.7 macrophages. Moreover, compound 1 suppressed pro-inflammatory markers induced by lipopolysaccharide (LPS) stimulation. Compound 1 also suppressed iNOS and cyclooxygenase-2 (COX-2) protein levels and downregulated pro-inflammatory cytokines. Additionally, compound 1 showed inhibition of the phosphorylation of p38, JNK, and ERK, key mediators of the MAPK signaling pathway. These findings indicate that a natural-derived product, compound 1, might be a potential candidate as an anti-inflammation mediator.
引用
收藏
页码:29 / 39
页数:11
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