Suppr超能文献

从白蝴蝶中分离得到的几种二萜类化合物的抗炎活性。

Anti-inflammatory activities of several diterpenoids isolated from Hemionitis albofusca.

机构信息

College of Life Science, Shanghai Normal University, Shanghai, 201418, People's Republic of China.

Maanshan Institute for Food and Drug Control and Adverse Drug Reaction, Ma'anshan, 243000, People's Republic of China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2024 Jan;397(1):437-449. doi: 10.1007/s00210-023-02626-y. Epub 2023 Jul 18.

Abstract

Hemionitis albofusca (Baker) Christenh is a plant that grows in various regions of China. Although it is not recognized as a traditional medicine, it is often mistakenly labelled and used as Aleuritopteris argentea (S. G. Gmél.) Fée to alleviate menstruation-related issues. Recently, several diterpenoids such as ent-16-oxo-17-norkauran-19-oic acid (Compound A), 14-oxy-7β,20-dihydroxycyath-12,18-diene (Compound B), ent-8(14),15-pimaradiene-2β,19-diol (Compound C), ent-kaurane-16-ene-2β,18α-diol (Compound D), ent-kaurane-2β,16α,18α-triol (Compound E), and onychiol B have been extracted from H. albofusca. In this study, we investigated the anti-inflammatory activity of these diterpenes. We confirmed that compounds A ~ D suppressed the amount of cellular NO production by inhibiting the expression and transcription of iNOS protein. They also significantly inhibited the expression and transcription of inflammatory factors TNF-α and IL-6. Additionally, Compounds A and C suppressed the activation of the NF-κB signaling pathway and inhibited the phosphorylation level of p38, ultimately down-regulating inflammation. Compound B suppressed the activation of the NF-κB signaling pathway, while Compound D inhibited the phosphorylation level of p38 and down-regulated the activation of the p38 MAPK signaling pathway. In a word, our investigation supports the potential application of natural diterpenes as lead compounds for developing anti-inflammatory agents.

摘要

白玉凤尾蕨(Baker)Christenh 是一种生长在中国多个地区的植物。尽管它不是传统药物,但常被错误地标记并用作海金沙(Aleuritopteris argentea(S. G. Gmél.)Fée)来缓解与月经相关的问题。最近,从白玉凤尾蕨中提取到了几种二萜类化合物,如 ent-16-氧代-17-去甲贝壳杉烷-19-酸(化合物 A)、14-氧-7β,20-二羟基贝壳杉-12,18-二烯(化合物 B)、ent-8(14),15-松脂二烯-2β,19-二醇(化合物 C)、ent-贝壳杉烷-16-烯-2β,18α-二醇(化合物 D)、ent-贝壳杉烷-2β,16α,18α-三醇(化合物 E)和onychiol B。在本研究中,我们研究了这些二萜的抗炎活性。我们证实化合物 A-D 通过抑制 iNOS 蛋白的表达和转录来抑制细胞中 NO 产物的产生。它们还显著抑制了炎症因子 TNF-α 和 IL-6 的表达和转录。此外,化合物 A 和 C 抑制了 NF-κB 信号通路的激活,并抑制了 p38 的磷酸化水平,最终下调了炎症。化合物 B 抑制了 NF-κB 信号通路的激活,而化合物 D 抑制了 p38 的磷酸化水平并下调了 p38 MAPK 信号通路的激活。总之,我们的研究支持将天然二萜作为开发抗炎药物的先导化合物的潜在应用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验