Steroidal saponins with anti-inflammatory activity from Tribulus terrestris L.

Miao-Miao Yang, M. Oppong, Jin Di, Qing Yuan, Yan-Xx Chang, Miaomiao Jiang, Shijie Cao, Pengzhi Dong, Lin Li, Yan Xie, Xia-gang Luan, Li-min Hu, Lijuan Chai, P. Zhang
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引用次数: 4

Abstract

Abstract Objective: Tribulus terrestris L. (T. terrestris) is a highly valuable traditional Chinese medicine used to treat stroke, inflammation, pulmonary fibrosis, liver cancer, and urolithiasis. To identify the basic substance responsible for the anti-inflammatory effect of TST (total saponins of Tribulus), its chemical composition was systematically studied, and its effect of inhibiting nitric oxide generation and the expression of related inflammatory factors were determined. Methods: To separate chemical constituents from T. terrestris by column chromatography. Spectroscopic methods, including 1D and 2D nuclear magnetic resonance spectroscopy (NMR) and mass spectrometry (MS) techniques, were used to elucidate the isolated compounds. The anti-inflammatory activities of TST and several compounds were evaluated in vitro. Results: Fifteen steroidal saponins, including 9 furostanol steroidal saponins (1, 2, 3, 4, 5, 6, 7, 8, and 15) and 6 isospirostanol steroidal saponins (9, 10, 11, 12, 13, and 14), were isolated from T. terrestris. TST significantly decreased the expression of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) in RAW 264.7 cells stimulated by lipopolysaccharides. Compounds 13 and 15 evidently reduced TNF-α expression. Compounds 6, 10, 12, 13, and 15 markedly reduced IL-6 expression. Conclusions: Compounds 1 was a novel furostanol steroidal saponin, named 26-O-β-D-glucopyranosyl-(25R)-5α-furostan-12-carbonyl-20(22)-en-3β, 26-diol-3-O-{β-D-xylopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-glucopyranosyl-(1→4)-[α-L-rhamnopyranosyl-(1→2)]-β-D-galactopyranoside}. Compounds 2 was isolated from the family Zygophyllaceae for the first time, and 5 and 6 were isolated from the Tribulus genus. TST and compounds 6, 10, 12, 13, and 15 exerts anti-inflammatory activity.
刺蒺藜甾体皂苷类抗炎活性研究。
摘要目的:蒺藜是一种治疗中风、炎症、肺纤维化、肝癌、尿石症的中药材。为确定蒺藜总皂苷(TST)抗炎作用的基础物质,系统研究其化学成分,并测定其抑制一氧化氮生成及相关炎症因子表达的作用。方法:采用柱层析法分离地皮的化学成分。利用一维和二维核磁共振波谱(NMR)和质谱(MS)等光谱方法对分离得到的化合物进行了鉴定。体外研究了TST及几种化合物的抗炎活性。结果:从地参中分离得到15种甾体皂苷,包括9种糠甾醇甾体皂苷(1、2、3、4、5、6、7、8、15)和6种异螺甾醇甾体皂苷(9、10、11、12、13、14)。TST可显著降低脂多糖刺激的RAW 264.7细胞中肿瘤坏死因子-α (TNF-α)和白细胞介素-6 (IL-6)的表达。化合物13和15明显降低TNF-α的表达。化合物6、10、12、13和15显著降低IL-6的表达。结论:化合物1为新型糠甾醇甾体皂苷,命名为26-O-β- d -葡萄糖吡喃基-(25R)-5α-糠甾醇-12-羰基-20(22)-en-3β, 26-二醇-3- o -{β- d -木糖吡喃基-(1→2)-[β- d -木糖吡喃基-(1→3)]-β- d -葡萄糖吡喃基-(1→4)-[α- l-鼠李糖吡喃基-(1→2)]-β- d -半乳糖吡喃苷}。其中化合物2为首次从蒺藜科植物中分离得到,化合物5和6为从蒺藜属植物中分离得到。TST和化合物6、10、12、13和15具有抗炎活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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