高等学校化学学报 ›› 2002, Vol. 23 ›› Issue (1): 63.

• 研究论文 • 上一篇    下一篇

黄花倒水莲皂甙Reinioside C在大鼠体内代谢产物的鉴定

张东明1, 宫濑敏男2, 野口博司2, 谷泽久之2, 马万云1, 陈瓞延1   

  1. 1. 清华大学物理系单原子分子测控教育部重点实验室, 北京 100084;
    2. 静冈县立大学药学院, 静冈 422, 日本
  • 收稿日期:2000-09-11 出版日期:2002-01-24 发布日期:2002-01-24
  • 通讯作者: 张东明(1963年出生),男,博士,助理研究员,主要从事药物分析研究.
  • 基金资助:

    国家自然科学基金(批准号:30070209)资助

Identification of Metabolites of Reinioside C, A Triterpene Saponin from the Roots of Polygala fallax Hemsl

ZHANG Dong-Ming1, Miyase Toshio2, Noguchi Hiroshi2, Tanizawa Hisayuki2, MA Wan-Yun1, CHEN Die-Yan1   

  1. 1. Key Laboratory of or Single Atomicand Molecular Detectionof Educational Ministry, Department of Physics, Tsinghua University, Beijing 100084, China;
    2. School of Pharmaceutical Sciences, Universityof Shizuoka, 5221, Yada Shizuoka 422, Japan
  • Received:2000-09-11 Online:2002-01-24 Published:2002-01-24

摘要: 为了探讨五环三萜皂甙ReiniosideC在大鼠体内代谢产物的结构,单剂量口服ReiniosideC,5h后放血处死,用制备型高效液相色谱方法对血液和各脏器进行提取分离,从大肠内容物和粪中,分离得到了7种代谢产物.用FAB-MS,1H NMR和13C NMR方法鉴定了它们的结构.

关键词: Reinioside C, 皂甙, 黄花倒水莲, 代谢物

Abstract: Triterpene saponins were widely distributed in the oriental traditional crude drugs, which play important roles as anti-inflammatory, anticancer and antihepatitis agent. For example, from Ginseng Radix, Bupleuri Radix, Polygalae Radix, Platycodi Radix etc, many bioactive and available triterpene saponins were obtained and they could explain the effect of the crude drug. However metabolic transformation of triterpene saponin in vivo have not been reported. We studied the metabolism of reinioside C, a triterpene saponin from the roots of Polygala fallax Hemsl in rats. After oral administration of reinioside C, seven metabolites(RA-RG) of reinioside Cwere obtained from the content of large intestin and feces. The structures of metabolites were elucidated as 28-O-α Lrhamnopyranosyl-(1→2)-(3,4 diacetyl)-β-Dfucopyranosyl presenegin, 28-O-β-Dxylopyranosyl-(1→4)-α-Lrhamnopyranosyl-(1→2)-(3,4 diacetyl)-β-Dfucopyranosyl presenegin, 28-O-α-Lrhamnopyranosyl-(1→2) (3,4-diacetyl)-β-Dfucopyranosyl presenegin3 O-β-Dglucopyranosyl-(1→2)-β-Dglucopy ranoside, 28-O-β-Dxylopyranosyl-(1→4)-α-Lrhamnopyranosyl-(1→2)-β-D-fucopyranosyl presenegin 3-O-β-Dglucopyranosyl-(1→2)-β-Dglucopyranoside, 28-O-β-Dxylopyranosyl-(1→4)-α-Lrhamnopy ranosyl-(1→2)-(3 acetyl)-β-D-fucopyranosyl presenegin-3-O-β-D-glu copyranosyl-(1→2)-β-D-glucopyranoside, 28-O-β-D-xylopyranosyl-(1→4)-α-Lrhamnopyranosyl-(1→2)-(4 acetyl)-β-D-fucopyranosyl pre senegin3 O-β-D-glucopyranosyl-(1→2)-β-Dglucopyranoside, 28-O-β-D-fucopyranosyl presenegin, respectively, on the basis of spectroscopic data.

Key words: Reinioside C, Triterpene saponin, Polygala fallax, Metabolite

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