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龙胆根中的抗炎裂环烯醚萜苷类成分:龙胆的根及根茎。

The anti-inflammatory secoiridoid glycosides from gentianae scabrae radix: the root and rhizome of Gentiana scabra.

作者信息

He Yu-Min, Zhu Shu, Ge Yue-Wei, Kazuma Kohei, Zou Kun, Cai Shao-Qing, Komatsu Katsuko

机构信息

Division of Pharmacognosy, Department of Medicinal Resources, Institute of Natural Medicine, University of Toyama, 2630, Sugitani, Toyama, 930-0194, Japan.

出版信息

J Nat Med. 2015 Jul;69(3):303-12. doi: 10.1007/s11418-015-0894-8. Epub 2015 Mar 8.

DOI:10.1007/s11418-015-0894-8
PMID:25750086
Abstract

Gentianae Scabrae Radix is a well-known traditional medicine that is used for the treatment of hepatitis, cholecystitis and inflammatory diseases. It consists mainly of secoiridoid glycosides, with representatives of gentiopicroside, sweroside and swertiamarin. In the present study, a chemical investigation of the CHCl3 extract of Gentianae Scabrae Radix derived from Gentiana scabra Bunge yielded seven new (1-7) and ten known (8-17) secoiridoid glycosides. Their structures were elucidated by extensive spectroscopic analyses and comparison with literature data. All 17 compounds were evaluated for their inhibitory effects against NO, IL-6 and TNF-α productions induced by lipopolysaccharide (LPS) in RAW264 cells. Among them, 8-epi-kingiside derivatives 1-3; kingiside derivatives 4, 5 and 10; and a sweroside derivative 6 showed inhibition activity against IL-6 production with IC50 values of 51.70-61.10 μM, whereas sweroside derivatives 12 and 15-17 and a swertiamarin derivative 13 showed inhibition effects on both NO and IL-6 productions with IC50 values of 64.74-94.95 and 48.91-75.45 μM, respectively. All the compounds exhibited weak inhibitory activity (IC50 > 100 μM) in a TNF-α bioassay. Finally, a primary structure-activity relationship of these secoiridoid glycosides is discussed.

摘要

龙胆是一种著名的传统药物,用于治疗肝炎、胆囊炎和炎症性疾病。它主要由裂环烯醚萜苷组成,代表物有龙胆苦苷、獐牙菜苷和獐牙菜苦苷。在本研究中,对来源于龙胆的龙胆根的氯仿提取物进行化学研究,得到了7个新的(1 - 7)和10个已知的(8 - 17)裂环烯醚萜苷。通过广泛的光谱分析并与文献数据进行比较,阐明了它们的结构。对所有17种化合物进行了评价,考察其对脂多糖(LPS)诱导的RAW264细胞中NO、IL - 6和TNF -α产生的抑制作用。其中,8 -表 - 獐牙菜苦苷衍生物1 - 3;獐牙菜苦苷衍生物4、5和10;以及一个獐牙菜苷衍生物6对IL - 6的产生表现出抑制活性,IC50值为51.70 - 61.10 μM,而獐牙菜苷衍生物12和15 - 17以及一个獐牙菜苦苷衍生物13对NO和IL - 6的产生均有抑制作用,IC50值分别为64.74 - 94.95和48.91 - 75.45 μM。在TNF -α生物测定中,所有化合物均表现出较弱的抑制活性(IC50 > 100 μM)。最后,讨论了这些裂环烯醚萜苷的初步构效关系。

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