Suppr超能文献

从威灵仙根及根茎中分离得到的酚苷和吲哚生物碱及其抗炎活性。

Phenolic glycosides and indole alkaloids isolated from the roots and rhizomes of Clematis chinensis and their anti-inflammatory activity.

作者信息

Jiang Hai-Bing, Shao Si-Yuan, Wei Ya-Zi, Lin Ming-Bao, Li Shuai

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, 100050, People's Republic of China.

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, 100050, People's Republic of China.

出版信息

Phytochemistry. 2023 Nov;215:113832. doi: 10.1016/j.phytochem.2023.113832. Epub 2023 Aug 19.

Abstract

Six undescribed compounds, including three phenolic glycosides (1-3) and three indole alkaloids (4-6), together with ten known alkaloids (7-16) and three known phenolic glycosides (17-19), were isolated from 70% EtOH aqueous extracts of the roots and rhizomes of Clematis chinensis Osbeck. The structures were elucidated by NMR, HRESIMS and X-ray diffraction spectroscopies. The anti-inflammatory activity of these compounds was evaluated, and twelve compounds showed significant inhibitory activity against TNF-α with an inhibition ratio from 47.87% to 94.70% at a dose of 10 μM. Compound 7 exhibited significant inhibitory activity against TNF-α and IL-6 with IC values of 3.99 μM and 2.24 μM, respectively. Compound 8 displayed potent anti-inflammatory activity against mouse ear edema induced by croton oil. A mechanistic study suggested that compounds 7 and 8 decreased the activation of the NF-κB signaling pathway to reduce the secretion of inflammatory factors in LPS-induced RAW 264.7 cells.

摘要

从威灵仙根及根茎的70%乙醇水提取物中分离得到6个未描述的化合物,包括3个酚苷(1 - 3)和3个吲哚生物碱(4 - 6),以及10个已知生物碱(7 - 16)和3个已知酚苷(17 - 19)。通过核磁共振(NMR)、高分辨电喷雾电离质谱(HRESIMS)和X射线衍射光谱对其结构进行了鉴定。对这些化合物的抗炎活性进行了评估, 12个化合物在10 μM剂量下对肿瘤坏死因子-α(TNF-α)显示出显著的抑制活性,抑制率为47.87%至94.70%。化合物7对TNF-α和白细胞介素-6(IL-6)均表现出显著的抑制活性,其半数抑制浓度(IC)值分别为3.99 μM和2.24 μM。化合物8对巴豆油诱导的小鼠耳肿胀显示出较强的抗炎活性。机制研究表明,化合物7和8可降低核因子-κB(NF-κB)信号通路的激活,从而减少脂多糖(LPS)诱导的RAW 264.7细胞中炎症因子的分泌。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验