天然产物研究与开发 ›› 2024, Vol. 36 ›› Issue (8): 1357-1367.doi: 10.16333/j.1001-6880.2024.8.009

• 研究简报 • 上一篇    下一篇

杏叶防风的化学成分及抗炎活性研究(Ⅱ)

汪   洋1,薛靖怡3,4,雷   艳3,5,潘   洁1,杨   畅1,李勇军1,2,3,马   雪1*   

  1. 1贵州医科大学民族药与中药开发应用教育部工程研究中心 贵州省药物制剂重点实验室;2国家苗药工程技术研究中心;3贵州医科大学药学院,贵阳 550004;4贵州省毕节市七星关区妇幼保健院;5毕节市第二人民医院,毕节 551700
  • 出版日期:2024-08-28 发布日期:2024-08-29
  • 基金资助:
    国家自然科学基金(U1812403);贵州省高层次创新人才培养计划(20165677);贵州省科技计划(黔科合中引地[2023]006)

Chemical constituents and anti-inflammatory activity of Pimpinella candolleana (Ⅱ)

WANG Yang1,XUE Jing-yi3,4,LEI Yan3,5,PAN Jie1,YANG Chang1,LI Yong-jun1,2,3,MA Xue1*   

  1. 1Guizhou Medical University Engineering Research Center for the Developmentand Application of Ethnic Medicine and TCM (Ministry of Education) /Guizhou Medical University Guizhou Provincial Key Laboratory of Pharmaceutics;2National Engineering Research Center of Miao′s Medicines;3Guizhou Medical University College of Pharmacy,Guiyang 550004,China;4Bijie City Qixingguan District Maternal and Child Health Hospital;5The 2nd People′s Hospital of Bijie,Bijie 551700,China

  • Online:2024-08-28 Published:2024-08-29
  • Supported by:

摘要:

为了研究杏叶防风(Pimpinella candolleana)的化学成分及其抗炎活性,采用正相硅胶、ODS反相硅胶、D101大孔吸附树脂及MCI树脂等多种色谱方法对杏叶防风70%乙醇提取物部位进行了分离,并通过与文献对比波谱数据鉴定化合物结构。体外培养小鼠单核巨噬细胞白血病细胞(RAW 264.7)细胞,脂多糖(lipopolysaccharide,LPS)诱导RAW 264.7细胞建立氧化损伤模型,利用一氧化氮(NO)试剂盒检测NO浓度,评价各化合物的抗炎活性。从该植物中分离得到25个黄酮类化合物,分别鉴定为1-hydroxy-2,3,4,7-tetramethoxyxanthone(1)、1-hydroxy-2,3,4,6-tetramethoxyxanthone(2)、bellidifolin(3)、desmethylbellidifolin(4)、当药醇苷(5)、日本当药黄素(6)、异日本獐牙菜素(7)、木犀草素-7-O-β-D-芸香糖苷(8)、luteolin-7-O-β-D-glucopyranosyl-(1→6)-[6′′′-O-caffeoyl]-β-D-glucopyranoside(9)、木犀草素-4′-O-β-D-葡萄糖苷(10)、木犀草素-6-C-β-L-岩藻糖苷(11)、荭草素(12)、异荭草素(13)、槲皮素-3-O-β-D-半乳糖苷(14)、芹菜素(15)、quercetin-3-O-β-D-(6″-caffeoylgalactoside)(16)、小麦黄素-7-O-β-D-葡萄糖苷(17)、葛根素(18)、牡荆素(19)、商陆素-3-O-β-D-葡萄糖苷(20)、商陆素-3-O-β-D-半乳糖苷(21)、鼠李素-3-O-β-D-半乳糖苷(22)、鼠李素-3-O-β-D-葡萄糖苷(23)、异鼠李素-3O-β-D-葡萄糖苷(24)、柯伊利素-7-O-β-D-葡萄糖苷(25)。其中,化合物13~15首次从杏叶防风中分离得到,化合物1~1216~25首次从茴芹属植物中分离得到;生物活性测定结果表明,化合物1~36~1012~1517~202325能抑制LPS诱导的RAW 264.7细胞的NO释放,显示出一定的抗炎活性。

关键词: 杏叶防风, 化学成分, 结构鉴定, 抗炎

Abstract:

This study aims to explore the chemical constituents and anti-inflammatory activities of extracts from Pimpinella candolleana.The 70% ethanol extract from P. candolleana were isolated by different chromatographic procedures including silica gel,ODS gel,D101 macroporous resin and MCI resin column.The structures of the compounds were identified by comparing the spectral data with the literature.Their potential anti-inflammatory effects were evaluated on murine macrophage cell line (RAW 264.7) stimulated by lipopolysaccharide (LPS).Twenty-five compounds were isolated and identified as 1-hydroxy-2,3,4,7-tetramethoxyxanthone(1),1-hydroxy-2,3,4,6-tetramethoxyxanthone(2), bellidifolin(3), desmethylbellidifolin(4), swertianolin(5), swertiajaponin(6),isoswertiajaponin(7),luteolin-7-O-β-D-rutinoside(8),luteolin-7-O-β-D-glucopyranosyl-(1→6)-[6′′′-O-caffeoyl]-β-D-glucopyranoside(9),luteolin-4′-O-β-D-glucopyranoside(10),luteolin-6-C-β-L-fucoside(11),orientin(12),isoorientin(13),quercetin-3-O-β-D-glucopyranoside(14),apigenin(15),quercetin-3-O-β-D-(6″-caffeoylgalactoside)(16), tricin-7-O-β-D-glucopyranoside(17),puerarin(18),vitexin(19),ombuin-3-O-β-D-glucopyranoside(20), ombuin-3-O-β-D-galacopyranoside(21), rhamnetin-3-O-β-D-galactopyranoside(22),rhamnetin-3-O-β-D-glucopyranoside(23),isorhamnetin-3-O-β-D-glucopyranoside(24),chrysoeriol-7-O-β-D-glucopyranoside(25).Compounds 13-15 were firstly isolated from this plant.Furthermore,compounds 1-12,16-25 were isolated from the genus Pimpinella for the first time.The results of bioassay showed that compounds 1-3,6-10,12-15,17-20,23,25 exhibited different degrees of inhibitory effect against NO production in LPS-stimulated RAW 264.7 cells and displayed potential anti-inflammatory activity.

Key words: Pimpinella candolleana, chemical constituents, structural identification, anti-inflammatory

中图分类号:  R284.1