西比露中的拉布丹和诺拉布丹二萜类化合物的抗炎活性与调节 MAPKs 信号通路有关

IF 2.1 4区 医学 Q3 CHEMISTRY, MEDICINAL
Planta medica Pub Date : 2024-11-04 DOI:10.1055/a-2440-5166
Nguyen Minh Trang, Le Ba Vinh, Nguyen Viet Phong, Seo Young Yang
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引用次数: 0

摘要

西比露草是一种在亚洲国家广泛种植的草本植物,具有多种药用价值。最近的研究强调了它在促进骨骼健康方面的药理特性和功效。除了已知的化合物及其药理活性外,本研究还分离并阐明了两种新的唇形科二萜类化合物:(3R,5R,6S,10S)-3、(3R,5R,6S,10S)-3, 6-dihydroxy-15-ethoxy-7-oxolabden-8(9),13(14)-dien-15,16-olide (1) 和 (4R,5R,10S)-18-hydroxy-14,15-bisnorlabda-8-en-7,13-dione (2)。利用先进的光谱技术,包括圆二色性光谱、高分辨率质谱以及一维和二维核磁共振技术,研究了一种新的天然酚类化合物--18-羟基-14,15-bisnorlabda-8-en-7,13-二酮(2)和一种已知的西比露藻化合物。其中,化合物 1 能有效抑制一氧化氮(NO)的产生和诱导型一氧化氮合酶(iNOS)mRNA 的表达水平,其次是化合物 2。而化合物 3 和 4 对 RAW264.7 巨噬细胞没有效果。此外,化合物 1 还能抑制脂多糖(LPS)刺激诱导的促炎标记物。化合物 1 还抑制了 iNOS 和环氧化酶-2(COX-2)蛋白水平,并下调了促炎细胞因子。此外,化合物 1 还抑制了 MAPK 信号通路的关键介质 p38、JNK 和 ERK 的磷酸化。这些研究结果表明,天然提取物化合物 1 可能是一种潜在的抗炎介质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Inflammatory Activity of Labdane and Norlabdane Diterpenoids from Leonurus sibiricus Related to Modulation of MAPKs Signaling Pathway.

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-oxolabden-8(9),13(14)-dien-15,16-olide (1: ) and (4R,5R,10S)-18-hydroxy-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.

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来源期刊
Planta medica
Planta medica 医学-药学
CiteScore
5.10
自引率
3.70%
发文量
101
审稿时长
1.8 months
期刊介绍: Planta Medica is one of the leading international journals in the field of natural products – including marine organisms, fungi as well as micro-organisms – and medicinal plants. Planta Medica accepts original research papers, reviews, minireviews and perspectives from researchers worldwide. The journal publishes 18 issues per year. The following areas of medicinal plants and natural product research are covered: -Biological and Pharmacological Activities -Natural Product Chemistry & Analytical Studies -Pharmacokinetic Investigations -Formulation and Delivery Systems of Natural Products. The journal explicitly encourages the submission of chemically characterized extracts.
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