用户名: 密码: 验证码:
柴胡属植物化学成分和质量控制研究及天目藜芦化学成分研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
柴胡属植物化学成分和质量控制研究及天目藜芦化学成分研究本文研究了伞形科柴胡属植物北柴胡(Bupleurum chinense DC.)中的活性成分及有毒植物大叶柴胡(B. longiradiatum)中的毒性成分。从两种柴胡植物中共分离鉴定了34个化合物,其中10个为新化合物,从而阐明了柴胡属植物有效成分和毒性成分物质基础。并进一步进行了中药柴胡的质量控制研究,考察并建立了基于药效成分和毒性成分的相应的定性、定量分析方法和中药化学指纹图谱分析方法。此外,研究了百合科藜芦属植物天目藜芦(Veratrum schindleri Loes. f.)中的化学成分,从中共分离鉴定了36个化合物,其中2个为新化合物,34个为首次从该植物中分得。
In this study, attempts have been made to isolate and define the bioactive and toxic constituents from plants of Bupleurum chinense and B. longiradiatum, to explore chemical components in Bupleurum and clarify the bioactive and toxic material foundation in this genue. From the two plants, 34 compounds in total have been obtained, including 10 new compounds. Furthermore, different kinds of analical methods, including qualitative and quantitative analysis and chemical fingerprint method, have been developed for the comprehensive quality control of Bupleurum, which will ensure the the safety and effective of Chaihu in clinical usage. In addition, another plant, Veratrum schindleri, was also investigated for chemical constituents. From the entire parts of this plant, 36 compounds were isolated and identified including 2 new compounds and 34 compounds isolated from the plant for the first time.
引文
[1] Pan, S.L. Bupleurum Species—Scientific Evaluation and Clinical Application, Taylor and Trancis Group: Boca Raton, FL, 2006; pp 1–6.
    [2] China Pharmacopoeia Committee. Pharmacopoeia of the People’s Republic of China; Chemical Industry Press: Beijing, 2005, p 198.
    [3] Chang, H.M., But, P.P.H., Pharmacology and Applications of Chinese Materia Medica, World Scientific Publishing, Singapore 1987, Vol. II, pp. 967–974.
    [4]赵吉福,郭允珍,孟宪纤.大叶柴胡的毒性成分.药学学报. 1987, 22, 507–511.
    [5] Abe, H., Sakaguchi, M., Odashima, S., Arichi, S. Protective effect of saikosaponin-d isolated from Bupleurum falcatum L. on CCl4-induced liver injury in the rat. Naunyn Schmiedebergs Arch. Pharmacol. 1982, 320, 266–271.
    [6] Benito, P.B., Martinez,M.J.A., Sen, A.M.S., Gomez, A.S., Matellano, L.F., Contreras, S.S., Lanza, A.M.D. In vivo and in vitro anti-inflammatory activity of saikosaponins. Life Sci. 1998, 63, 1147–1156.
    [7] Tsai, Y.J., Chen, I.L., Horng, L.Y., Wu, R.T. Induction of differentiation in rat C6 glioma cells with saikosaponins. Phytother. Res. 16, 2002, 117–121.
    [8] Motoo, Y., Sawabu, N. Antitumor effects of saikosaponins, baicalin and baicalien on human hepatoma cell lines. Cancer Lett. 1994, 86, 91–95.
    [9] Kato, M., Pu, M.Y., Isobe, K., Iwamoto, T., Nagase, F., Lwin, T., Zhang, Y.H., Hattori, T., Yanagita, N., Nakashima, I. Characterization of the immunoregulatory action of saikosaponin-d. Cell. Immunol. 1994, 159, 15–25.
    [10]贾琦,张如意.柴胡属植物中皂甙化学研究进展.药学学报. I989, 24, 961–971.
    [11]刘沁舡,谭利,白焱晶,梁鸿,赵玉英.柴胡属植物皂苷近10年研究概况.中国中药杂志. 2002, 27, 7-11.
    [12] Morita, M., Nakajima, K., Ikeya, Y., Mitsuhashi, H. Polyacetylenes from roots of Bupleurum falcatum. Phytochemistry 1991, 30, 1543–1545.
    [13] Barrero, A.F., Herrador, M.M., Akssira, M., Arteaga, P., Romera, J.L., Lignans and polyacetylenes from Bupleurum acutifolium. J. Nat. Prod. 1999, 62, 946–948.
    [14] Barrero, A.F., Haidour, A., Munoz-Dorado, M., Akssira, M., Sedqui, A., Mansour, I. Polyacetylenes, terpenoids and flavonoids from Bupleurum spinosum. Phytochemistry 1998, 48, 1237–1240.
    [15] Bohlmann, F., Rode, K.M. Polyacetylenverbindungen, CXLIII. Die Polyine ausOpopanax chironium Kch. Chem. Ber. 1968, 101, 525-531.
    [16] Bohlmann, F., Zdero, C., Thefeld, W. Polyacetylenverbindungen, 200. Notizüber die Inhaltsstoffe von Bupleurum-Arten. Chem. Ber. 1971, 104, 2030-2032.
    [17] Bohlmann, F., Burkhardt, T., Zdero, C., Naturally Occurring Acetylenes; London Academic Press: London, 1973, pp 3–26.
    [18] The Editorial Committee on the Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Chinese Materia Medica, vol. 5, Shanghai Science and Technology Press, Shanghai, 1996 (Zhonghua Bencao, in Chinese), p. 909.
    [19] Yen, M.H., Lin, C.C., Chuang, C.H., Liu, S.Y. Evaluation of root quality of Bupleurum species by TLC scanner and the liver protective effects of 'Xiao-chai-hu-tang' prepared using three different Bupleurum species. J. Ethnopharmacol. 1991, 34, 155–165.
    [20] Li, X.Q., Gao, Q.T., Chen, X.H., Bi, K.S. High Performance Liquid Chromatographic Assay of Saikosaponins from Radix Bupleuri in China. Biol. Pharm. Bull. 2005, 28, 1736–1742.
    [21] Kanazawa, H., Nagata, Y., Matsushima, Y., Tomoda, M., Takai, N. Simultaneous determination of Ginsenosides and saikosaponins by high-performance liquid chromatography. J. Chromatogr. 1990, 507, 327–332.
    [22] Shimizu, K., Amagaya, S., Ogihara, Y. Quantitative analysis of the metabolites of saikosaponin a using high-performance liquid chromatography. J. Chromatogr. 1984, 307,488–492.
    [23] Liau, B.C., Hsiao, S.S., Lee, M.R., Jong, T.T., Chiang, S.T. Quality control of Chinese medicinal preparations LC/ ESI(+)/MS/MS analyses of saikosaponin-a and -c as markers of Bupleuri redix samples. J. Pharm. Biomed. Anal. 2007, 43, 1174–1178.
    [24] Hsieh, Y.Z., and Huang, H.Y. Determination of saikosaponins by micellar electrokinetic capillary chromatography. J. Chromatogr. A 1997, 759, 193–201.
    [25] Shon, T.K., Zhu, S., Lee, S.C., Shoyama, Y., Tanaka, H. Pharmacologically Active Saikosaponin in Bupleurum falcatum Detected by Competitive ELISA and Eastern Blotting Using Monoclonal Antibodies. Plant Prod. Sci. 2008, 11, 192–197.
    [26] Zhu, S., Shimokawa, S., Shoyama,Y., Tanaka, H. A novel analytical ELISA-based methodology for pharmacologically active saikosaponins. Fitoterapia 2006, 77, 100–108.
    [27] Tian, R.T., Xie, P.S, Liu, H.P. Evaluation of traditional Chinese herbal medicine:Chaihu (Bupleuri Radix) by both high-performance liquid chromatographic and high-performance thin-layer chromatographic fingerprint and chemometric analysis. J. Chromatogr. A 2009,1216, 2150–2155.
    [28]张宏娜,赵玉英,梁鸿,黄璐琦,张庆英,张志翔. HPLC-ELSD法同时测定柴胡中柴胡皂苷a, c, d, f的含量.药物分析杂志. 2007, 27, 1150-1153.
    [29] Bao, Y.W., Li, C., Shen, H.W., Nan, F.J. Determination of saikosaponin derivatives in Radix bupleuri and in pharmaceuticals of the Chinese multiherb remedy Xiaochaihu-tang using liquid chromatographic tandem mass spectrometry. Anal. Chem. 2004, 76, 4208–4216.
    [30] Hsieh, Y.Z., Huang, H.Y. Determination of saikosaponins by micellar electrokinetic capillary chromatography. J. Chromatogr. A 1997, 759, 193-201.
    [1] Pan, S.L. Bupleurum Species—Scientific Evaluation and Clinical Application, Taylor and Trancis Group: Boca Raton, FL, 2006; pp 1–6.
    [2] Abe, H., Sakaguchi, M., Odashima, S., Arichi, S. Protective effect of saikosaponin-d isolated from Bupleurum falcatum L. on CCl4-induced liver injury in the rat. Naunyn Schmiedebergs Arch. Pharmacol. 1982, 320, 266–271.
    [3] Benito, P.B., Martinez,M.J.A., Sen, A.M.S., Gomez, A.S., Matellano, L.F., Contreras, S.S., Lanza, A.M.D. In vivo and in vitro anti-inflammatory activity of saikosaponins. Life Sci. 1998, 63, 1147–1156.
    [4] Tsai, Y.J., Chen, I.L., Horng, L.Y., Wu, R.T. Induction of differentiation in rat C6 glioma cells with saikosaponins. Phytother. Res. 16, 2002, 117–121.
    [5] Motoo, Y., Sawabu, N. Antitumor effects of saikosaponins, baicalin and baicalien on human hepatoma cell lines. Cancer Lett. 1994, 86, 91–95.
    [6] Kato, M., Pu, M.Y., Isobe, K., Iwamoto, T., Nagase, F., Lwin, T., Zhang, Y.H., Hattori, T., Yanagita, N., Nakashima, I. Characterization of the immunoregulatory action of saikosaponin-d. Cell. Immunol. 1994, 159, 15–25.
    [7]金惠芳,蒋毅,罗思齐.空心柴胡和柴首根部的化学成分研究.中国中药杂志. 1996, 21, 739-741.
    [8]王英华,邢世瑞,羽野芳生.小叶黑柴胡中皂甙成分的研究. 1998, 23, 96-98.
    [9] Ding, J. K., Fujino, H., Kasai, R., Fujimoto, N., Tanaka, O., Zhou, J., Matsuura, H, Fuwa. Chemical evaluation of Bupleurum species collected in Yunnan. Chem. Pharm. Bull. 1986, 50, 1158-1162.
    [10] Seto, H., Otake, N., Luo, S. Q., Qian, F. G., Xu, G. Y., Pan, S. L. Isolation of Triterpenoid Glycosides (Saikosaponins) from Bupleurum kunmingense and Their Chemical Structures. Agric. Biol. Chem. 1986, 50, 943-948.
    [11] Ishii, H., Seo, S., Tori, K., Tozyo, T., Yoshimura, Y. The structures of saikosaponin-e and acetylsaikosaponins, minor components isolated from Bupleurum falcatum L., determined by C-13 NMR spectroscopy. Tetrahedron Lett. 1977, 1227-1230.
    [1] Pan, S.L. Bupleurum Species—Scientific Evaluation and Clinical Application, Taylor and Trancis Group: Boca Raton, FL, 2006, pp 1–6.
    [2]陈学韶.大叶柴胡毒性的初步研究.药学通报, 1981, 16, 318.
    [3]赵吉福,郭允珍,孟宪纤.大叶柴胡的毒性成分.药学学报. 1987, 22, 507–511.
    [4] Morita, M., Nakajima, K., Ikeya, Y., Mitsuhashi, H. Polyacetylenes from roots of Bupleurum falcatum. Phytochemistry 1991, 30, 1543–1545.
    [5] Barrero, A.F., Herrador, M.M., Akssira, M., Arteaga, P., Romera, J.L., Lignans and polyacetylenes from Bupleurum acutifolium. J. Nat. Prod. 1999, 62, 946–948.
    [6] Barrero, A.F., Haidour, A., Munoz-Dorado, M., Akssira, M., Sedqui, A., Mansour, I. Polyacetylenes, terpenoids and flavonoids from Bupleurum spinosum. Phytochemistry 1998, 48, 1237–1240.
    [7] Bohlmann, F., Rode, K.M. Polyacetylenverbindungen, CXLIII. Die Polyine aus Opopanax chironium Kch. Chem. Ber. 1968, 101, 525-531.
    [8] Bohlmann, F., Zdero, C., Thefeld, W. Polyacetylenverbindungen, 200. Notizüber die Inhaltsstoffe von Bupleurum-Arten. Chem. Ber. 1971, 104, 2030-2032.
    [9] Schulte, K.E., Potter, B. Polyacetylenes from Pituranthus tortuosus (Desf.) Bnth. and Hook. Arch. Pharm. (Weinheim) 1977, 310, 945–963.
    [10] Schulte, K.E., Wulfhorst, G. Polyacetylene compounds from Aegopodium podagraria L.. Arch. Pharm. (Weinheim) 1977, 310, 285–298.
    [11] Bohlmann, F., Rode, K.M. Polyacetylenverbindungen, CXLIII. Die Polyine aus Opopanax chironium Kch. Chem. Ber. 1968, 101, 525-531.
    [12] Bohlmann, F., Burkhardt, T., Zdero, C., Naturally occurring acetylenes; London Academic Press: London, 1973, pp 3–26.
    [13] Ohtani, I., Kusumi, T., Kashman, Y., Kakisawa, H. NMR application of Mosher's method. J. Am. Chem. Soc. 1991, 113, 4092–4096.
    [14] Siddiq, A., Dembitsky, V. Acetylenic anticancer agents. Anticancer Agents Med. Chem 2008, 8, 132–170.
    [15] Dembitsky, V.M. Anticancer activity of natural and synthetic acetylenic lipids. Lipids 2006, 41, 883–924.
    [16] Mosmman, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65, 55–63.
    [1]刘沁舡,谭利,白焱晶,梁鸿,赵玉英.柴胡属植物皂苷近10年研究概况.中国中药杂志. 2002, 27, 7-11.
    [2] Pan, S.L., Bupleurum Species—Scientific Evaluation and Clinical Application, Taylor and Trancis Group, Boca Raton, FL, USA 2006.
    [3] Oleszek, W., Bialy, Z. Chromatographic determination of plant saponins—An update (2002–2005). J. Chromatogr. A 2006, 1112, 78-91.
    [4] Liau, B.C., Hsiao, S.S., Lee, M.R., Jong, T.T., Chiang, S.T. Quality control of Chinese medicinal preparations LC/ ESI(+)/MS/MS analyses of saikosaponin-a and -c as markers of Bupleuri redix samples. J. Pharm. Biomed. Anal. 2007, 43, 1174–1178.
    [5] Bao, Y.W., Li, C., Shen, H.W., Nan, F.J. Determination of saikosaponin derivatives in Radix bupleuri and in pharmaceuticals of the Chinese multiherb remedy Xiaochaihu-tang using liquid chromatographic tandem mass spectrometry. Anal. Chem. 2004, 76, 4208–4216.
    [6] Kimata, M., Kasai, R., Tanaka, O. Saponin of juksiho and roots Bupleurum longeradiatum Turcz L. Chem. Pharm. Bull. 1982, 30, 4373-4377.
    [7] Ishii, H., Seo, S., Tori, K., Tozyo, T., Yoshimura, Y. The structures of saikosaponin-e and acetylsaikosaponins, minor components isolated from Bupleurum falcatum L., determined by C-13 NMR spectroscopy. Tetrahedron Lett. 1977, 1227-1230.
    [8] Seto, H., Otake, N., Luo, S. Q., Qian, F. G., Xu, G. Y., Pan, S. L. Isolation of Triterpenoid Glycosides (Saikosaponins) from Bupleurum kunmingense and Their Chemical Structures. Agric. Biol. Chem. 1986, 50, 943-948.
    [9] Kubota, T., Hinoh, H. The constitution of saponins isolated from Bupreurum faleatum L. Tetrahedron Lett. 1968, 303–306.
    [10] Zhao, Y.Y., Luo, H.S., Wang, B., Ma, L.B., Tu, G. Z., Zhang, R. Y. Triterpenoid saponins from Bupleurum smithii var. parvifolium. Phytochemistry 1996, 42, 1673-1675.
    [11] Domon, B., Costello, C. E. A systematic nomenclature for carbohydrate fragmentations in FAB-MS/MS spectra of glycoconjugates. Glycoconj. J. 1988, 5, 397-409.
    [12] Liu, S.Y., Cui, M., Liu, Z.Q., Song, F.R., Mo, W.J. Structural analysis of saponins from medicinal herbs using electrospray ionization tandem mass spectrometry. J. Am. Soc. Mass Spectrom. 2004, 15, 133-141.
    [13] Li, L., Tsao, R., Dou, J.P., Song, F.R., Liu, Z.Q., Liu, S.Y. Detection of saponins in extract of Panax notoginseng by liquid chromatography–electrospray ionisation-mass spectrometry. Anal. Chim. Acta 2005, 536, 21–28.
    [14] Cuyckens, F., Claeys, M. Mass spectrometry in the structural analysis of flavonoids. J. Mass Spectrom. 2004, 39, 1-15.
    [15] Kobayashi, Y., Ogihara, Y. New triterpenoid glycosides from the leaves of Bupleurem rotundifolium L. Chem. Pharm. Bull. 1981, 29, 2230-2236.
    [16] Ebata, N., Nakajima, K., Hayashi, K., Okada, M., Maruno, M. Saponins from the root of Bupleurum falcatum. Phytochemistry 1996, 41, 895-901.
    [17] Madl, T., Sterk, H., Mittelbach, M., Rechberger, G.N. Tandem Mass Spectrometric Analysis of a Complex Triterpene Saponin Mixture of Chenopodium quinoa. J. Am. Soc. Mass Spectrom. 2006, 17, 795-806.
    [14] Cuyckens, F., Claeys, M. Mass spectrometry in the structural analysis of flavonoids. J. Mass Spectrom. 2004, 39, 1-15.
    [9] Ding, J. K., Fujino, H., Kasai, R., Fujimoto, N., Tanaka, O., Zhou, J., Matsuura, H, Fuwa. Chemical evaluation of Bupleurum species collected in Yunnan. Chem. Pharm. Bull. 1986, 50, 1158-1162.
    [20] Funayama, S., Hikino, H. Hypotensive principles of Diospyros kaki leaves. Chem. Pharm. Bull. 1979, 27, 2865-2868.
    [1] Wang, Y.S., in Chang, H.M., But, P.P.H., (Ed.), Pharmacology and Applications of Chinese Materia Medica, World Scientific Publishing, Singapore, 1987, pp. 978–988.
    [2] Pan, S.L., Bupleurum Species—Scientific Evaluation and Clinical Application, Taylor and Trancis Group, Boca Raton, FL, USA 2006.
    [3] Abe, H., Sakaguchi, M., Odashima, S., Arichi, S. Protective effect of saikosaponin-d isolated from Bupleurum falcatum L. on CCl4-induced liver injury in the rat. Naunyn Schmiedebergs Arch. Pharmacol. 1982, 320, 266–271.
    [4] Benito, P.B., Martinez,M.J.A., Sen, A.M.S., Gomez, A.S., Matellano, L.F., Contreras, S.S., Lanza, A.M.D. In vivo and in vitro anti-inflammatory activity of saikosaponins. Life Sci. 1998, 63, 1147–1156.
    [5] Tsai, Y.J., Chen, I.L., Horng, L.Y., Wu, R.T. Induction of differentiation in rat C6 glioma cells with saikosaponins. Phytother. Res. 16, 2002, 117–121.
    [6] Motoo, Y., Sawabu, N. Antitumor effects of saikosaponins, baicalin and baicalien on human hepatoma cell lines. Cancer Lett. 1994, 86, 91–95.
    [7] Kato, M., Pu, M.Y., Isobe, K., Iwamoto, T., Nagase, F., Lwin, T., Zhang, Y.H., Hattori, T., Yanagita, N., Nakashima, I. Characterization of the immunoregulatory action of saikosaponin-d. Cell. Immunol. 1994, 159, 15–25.
    [8] Yen, M.H., Lin, C.C., Chuang, C.H., Liu, S.Y. Evaluation of root quality of Bupleurum species by TLC scanner and the liver protective effects of 'Xiao-chai-hu-tang' prepared using three different Bupleurum species. J. Ethnopharmacol. 1991, 34, 155–165.
    [9] Li, X.Q., Gao, Q.T., Chen, X.H., Bi, K.S. High Performance Liquid Chromatographic Assay of Saikosaponins from Radix Bupleuri in China. Biol. Pharm. Bull. 2005, 28, 1736–1742.
    [10] Kanazawa, H., Nagata, Y., Matsushima, Y., Tomoda, M., Takai, N. Simultaneous determination of Ginsenosides and saikosaponins by high-performance liquid chromatography. J. Chromatogr. 1990, 507, 327–332.
    [11] Shimizu, K., Amagaya, S., Ogihara, Y. Quantitative analysis of the metabolites of saikosaponin a using high-performance liquid chromatography. J. Chromatogr. 1984, 307,488–492.
    [12] Liau, B.C., Hsiao, S.S., Lee, M.R., Jong, T.T., Chiang, S.T. Quality control of Chinese medicinal preparations LC/ ESI(+)/MS/MS analyses of saikosaponin-a and -c asmarkers of Bupleuri redix samples. J. Pharm. Biomed. Anal. 2007, 43, 1174–1178.
    [13] Hsieh, Y.Z., and Huang, H.Y. Determination of saikosaponins by micellar electrokinetic capillary chromatography. J. Chromatogr. A 1997, 759, 193–201.
    [14] Shon, T.K., Zhu, S., Lee, S.C., Shoyama, Y., Tanaka, H. Pharmacologically Active Saikosaponin in Bupleurum falcatum Detected by Competitive ELISA and Eastern Blotting Using Monoclonal Antibodies. Plant Prod. Sci. 2008, 11, 192–197.
    [15] Zhu, S., Shimokawa, S., Shoyama,Y., Tanaka, H. A novel analytical ELISA-based methodology for pharmacologically active saikosaponins. Fitoterapia 2006, 77, 100–108.
    [16] Bao, Y.W., Li, C., Shen, H.W., Nan, F.J. Determination of saikosaponin derivatives in Radix bupleuri and in pharmaceuticals of the Chinese multiherb remedy Xiaochaihu-tang using liquid chromatographic tandem mass spectrometry. Anal. Chem. 2004, 76, 4208–4216.
    [17] H.Q. Huang, X. Zhang, M. Lin, Y.H. Shen, S.K. Yan, W.D. Zhang, Characterization and identification of saikosaponins in crude extracts from three Bupleurum species using LC-ESI-MS. J. Sep. Sci. 2008, 31, 3190–3201.
    [18] Chai, X.Y., Li, S.L., Li, P. Quality evaluation of Flos Lonicerae through a simultaneous determination of seven saponins by HPLC with ELSD. J. Chromatogr. A 1070, 2005, 43–48.
    [19] Qi, L.W., Yu, Q.T., Li, P., Li, S.L., Wang, Y.X., Sheng, L.H., Yi, L. Quality evaluation of Radix Astragali through a simultaneous determination of six major active isoflavonoids and four main saponins by high-performance liquid chromatography coupled with diode array and evaporative light scattering detectors. J. Chromatogr. A 1134, 2006, 162–169.
    [20] Kim, S.N., Ha, Y.W., Shin, H., Son, S.H., Wu, S.J., Kim, Y.S., Simultaneous quantification of 14 ginsenosides in Panax ginseng C.A. Meyer (Korean red ginseng) by HPLC-ELSD and its application to quality control. J. Pharm. Biomed. Anal. 2007, 45, 164–170.
    [21] Yoshida T. and Majors, R.E. High-speed analyses using rapid resolution liquid chromatography on 1.8-m porous particles. J. Sep. Sci. 2006, 29, 2421–2432.
    [22] Seto, H., Otake, N., Luo, S. Q., Qian, F. G., Xu, G. Y., Pan, S. L. Isolation of Triterpenoid Glycosides (Saikosaponins) from Bupleurum kunmingense and Their Chemical Structures. Agric. Biol. Chem. 1986, 50, 943-948.
    [23] Kimata, M., Kasai, R., Tanaka, O., Chem. Pharm. Bull. 1982, 30, 4373–4377.
    [24] Ishii, H., Seo, S., Tori, K., Tozyo, T., Yoshimura, Y. The structures of saikosaponin-e and acetylsaikosaponins, minor components isolated from Bupleurum falcatum L., determined by C-13 NMR spectroscopy. Tetrahedron Lett. 1977, 1227-1230.
    [25] Kubota, T. and Hinoh, H. The constitution of saponins isolated from Bupleurum falcatum L. Tetrahedron Lett. 1968, 3, 303–306.
    [26] Ebata, N., Nakajima, K., Hayashi, K., Okada, M., Maruno, M. Saponins from the root of Bupleurum falcatum. Phytochemistry 1996, 41, 895-901.
    [27] Zhao, Y.Y., Luo, H.S., Wang, B., Ma, L.B., Tu, G. Z., Zhang, R. Y. Triterpenoid saponins from Bupleurum smithii var. parvifolium. Phytochemistry 1996, 42, 1673-1675.
    [28]林东昊,茅仁刚,王智华,洪筱坤,潘胜利. 23种国产柴胡属植物中柴胡皂苷a, c, d含量的RP-HPLC测定.药物分析杂志. 2004, 24, 479–483.
    [29] Kitagawa, I., Taniyama, T., Yoshikawa, M., Ikenishi, Y., Nakagawa, Y. Chemical structures of malonyl-ginsenosides Rbi, Rb2, Re, and Rd isolated from the root of Panax ginsengСA. Meyer. Chem. Pharm. Bull., 1989, 37, 2961–2970.
    [30] Oleszek, W., Bialy, Z. Chromatographic determination of plant saponins—An update (2002–2005). J. Chromatogr. A 2006, 1112, 78-91.
    [31] Qi, L.W., Yu, Q.T., Yi, L., Ren, M.T., Wen, X. D., Wang, Y. X., Li, P. Simultaneous determination of 15 marker constituents in various Radix Astragali preparations by solid-phase extraction and high-performance liquid chromatography. J. Sep. Sci. 2008, 31, 97–106.
    [32]刘和平,谢培山,田润涛.柴胡属药材皂苷高效薄层色谱指纹图谱的研究中药新药与临床药理. 2008, 19, 38–42.
    [1] Chan, K. Some aspects of toxic contaminants in herbal remedies. Chemosphere 2003, 52, 1361–1371.
    [2] Jordan, S.A., Cunningham, D.G., Marles, R.J. Assessment of herbal medicinal products: Challenges, and opportunities to increase the knowledge base for safety assessment. Toxicol. Appl. Pharmacol., 2010, 243, 108-210.
    [3] Schaneberg, B. T., Khan, I. A. Analysis of products suspected of containing Aristolochia or Asarum species. J Ethnopharmacol, 2004, 94, 245-249.
    [4] Pan, S.L., Bupleurum Species—Scientific Evaluation and Clinical Application, Taylor and Trancis Group, Boca Raton, FL, USA, 2006.
    [5]赵吉福,郭允珍,孟宪纤.大叶柴胡的毒性成分.药学学报. 1987, 22, 507–511.
    [6] You, Y.J., Lee, I.S., Kim, Y., Bae, K.H., Ahn, B.Z. Antiangiogenic Activity of Bupleurum Iongiradiatum on human umbilical venous endothelial cells. Arch. Pharm. Res. 2002, 25, 600–640.
    [7] Bohlmann, F., Burkhardt, T., Zdero, C., Naturally occurring acetylenes, London Academic Press, London, 1973, pp 3–26.
    [8] Anet, E.F.L.J., Lythgoe, B., Silk, M.H., Trippet, S., J. Chem. Soc 1953, 62, 309–322.
    [9] Minto,R.E., Blacklock, B.J. Biosynthesis and function of polyacetylenes and allied natural products. Prog. Lipid Res. 2008, 47, 233–306.
    [10] Huang, H.Q., Zhang, X., Shen, Y.H., Su, J., Liu, X.H., Tian, J.M., Lin, S., Zhang, W.D. Fast determination of saikosaponins in Bupleurum by rapid resolution liquid chromatography with evaporative light scattering detection. J. Pharm. Biomed. Anal. 2009, 49, 1048–1055.
    [11] Morita, M., Nakajima, K., Ikeya, Y., Mitsuhashi, H. Polyacetylenes from roots of Bupleurum falcatum. Phytochemistry 1991, 30, 1543–1545.
    [12] Barrero, A.F., Herrador, M.M., Akssira, M., Arteaga, P., Romera, J.L., Lignans and polyacetylenes from Bupleurum acutifolium. J. Nat. Prod. 1999, 62, 946–948.
    [13] Estevez-Braun, A., Estevez-Reyes, R., Moujir, L.M., Ravelo, A.G., Gonzalez, A.G.. Antibiotic Activity and Absolute Configuration of 8S-Heptadeca-2(Z),9(Z)-diene-4,6-diyne-1,8-diol from Bupleurum salicifolium. J. Nat. Prod. 1994, 57, 1178–1182.
    [14] Barrero, A.F., Haidour, A., Munoz-Dorado, M., Akssira, M., Sedqui, A., Mansour, I. Polyacetylenes, terpenoids and flavonoids from Bupleurum spinosum.Phytochemistry 1998, 48, 1237–1240.
    [1] WHO, Guidelines for the Assessment of Herbal Medicine, World Health Organization, Munich, 1991.
    [2] Yang, L.W., Wu, D.H., Tang, X., Peng, W., Wang, X.R., Ma, Y., Su, W.W. Fingerprint quality control of Tianjihuang by high-performance liquid chromatography–photodiode array detection. J. Chromatogr. A 2005, 1070, 35-42.
    [3] Gong, F., Liang, Y.Z., Xie, P.S., Chau, F. Information theory applied to chromatographic fingerprint of herbal medicine for quality control. J. Chromatogr. A 2003, 1002, 25-40.
    [4] Faghihi, J., Jiang, X., Vierling, R., Goldman, S., Sharfstein, S., Sarver, J., Erhardt. P., J. Chromatogr. A, 2001, 915, 61-74.
    [5] Katalinic, V. High-performance liquid chromatographic determination of flavan fingerprints in plant extracts. J. Chromatogr. A, 1997, 775, 359-367.
    [6] Pan, S.L., Bupleurum Species—Scientific Evaluation and Clinical Application, Taylor and Trancis Group, Boca Raton, FL, USA, 2006.
    [7]王有志,张亚云.中药柴胡的物种调查和鉴定.中国药学杂志. 1994, 29, 16-18.
    [8] Abe, H., Sakaguchi, M., Odashima, S., Arichi, S. Protective effect of saikosaponin-d isolated from Bupleurum falcatum L. on CCl4-induced liver injury in the rat. Naunyn Schmiedebergs Arch. Pharmacol. 1982, 320, 266–271.
    [9] Kubota, T., and Hinoh, H. The constitution of saponins isolated from Bupleurum falcatum L. Tetrahedron Lett. 1968, 3, 303–306.
    [10] Ebata, N., Nakajima, K., Hayashi, K., Okada, M., Maruno, M. Saponins from the root of Bupleurum falcatum. Phytochemistry 1996, 41, 895-901.
    [11] Zhao, Y.Y., Luo, H.S., Wang, B., Ma, L.B., Tu, G. Z., Zhang, R. Y. Triterpenoid saponins from Bupleurum smithii var. parvifolium. Phytochemistry 1996, 42, 1673-1675.
    [12]林东昊,茅仁刚,王智华,洪筱坤,潘胜利. 23种国产柴胡属植物中柴胡皂苷a, c, d含量的RP-HPLC测定.药物分析杂志. 2004, 24, 479–483.
    [1]陈世忠,徐国钧,徐珞珊等.藜芦属药用植物两新种.中国药科大学学报, 1991, 22 (6): 338-340.
    [2]任毅.秦岭种子植物补遗――裸子植物门和被子植物门的单子叶植物[J].西北植物学报, 2000, 20(4): 658-660.
    [3]杜贵友,方文贤.有毒中药现代化研究与合理应用[M].人民卫生出版社, 2003.
    [4]中国科学院中国植物志编辑委员会.中国植物志[M].北京:科学出版社, 1999.
    [5]刘慎谔.东北植物检索表[M].科学出版社, 1959.
    [6]吴寿金,赵泰,秦永祺.现代中草药成分化学[M].中国医药科技出版社, 2004.
    [7] Zhao,W.J., Tezuka, Y., Kikuchi , T., Studies on constituents of veratrum plants.I. Constituents of Veratrum maackii reg.:isolation and structure determination of a new alkaloid,maackinine. Chem. Pharm. Bull., 1989, 37, 2920-2928.
    [8] Kadota, S., Chen, S.Z., Li, J.X., Xu, G.J., Namba, T. A steroidal alkaloid from Veratrum oblongum. Phytochemistry, 1995, 38, 777-781.
    [9] Chung, M., Teng, C., Cheng, K. An antiplatelet principle of Veratrum formosanum. Planta Medica,1992, 58, 274-275.
    [10]赵伟杰,孟庆伟,王世盛.天目藜芦生物碱的化学研究.中国中药杂志,2003, 28, 985-986.
    [11]毛晓峰,史志诚,王亚洲.我国藜芦属植物研究进展.动物毒物学, 2003, 18, 17-21.
    [12]梁广义,孙南君.狭叶藜芦中活性成分的化学研究I.狭叶藜芦乙的结构以及其它成分的鉴定.药学学报, 1984,19, 131-136.
    [13]杨崇仁,刘润民,周俊.蒙自藜芦的甾体生物碱研究.云南植物研究, 1987, 9, 359-364.
    [14] Mizuo, M.Z., Tan, R.X., Zhen, P., Two steroidal alkaloid glucosides from Veratrum taliense. Phytochemistry, 1990, 29, 359-361.
    [15] Zhou, C.X., Liu, J.L., Ye., W.C., Neoverataline A and B, two antifungal alkaloids with a novel carbon skeleton from Veratrum taliense. Tetrahedron,2003, 59, 5743-5747.
    [16] Zhao, W.J., Tezuka, Y., Kikuchi, T. studies on constituents of veratrum plants.Ⅱ. constituentsof veratrum nigrum L.var.ussuriense.(1).Structure and 1H- and 13C-Nuclear Magnetic.Resonance Spectra ofa new alkaloid,verussurinine,and related alkaloids .Chem. Pharm.Bull.,1991, 39, 549-554.
    [17] Tezuka, Y., Kikuchi, T., Zhao, W.J. (+)-Verussurine, a New Steroidal Alkaloid fromthe Roots and Rhizomes of Veratrum nigrum var. ussuriense and Structure Revision of (+)-Verabenzoamine. J.Nat.Prod.,1998, 61,1397-1399.
    [18]全香花,朴惠善,孙向红,等.兴安藜芦的化学成分研究.中国药学杂志, 2003, 38, 914-916.
    [19] Tezuka, Y., Kikuchi, T.,. Two new steroidal alkaloids, 20-isoveratramine and verapatuline, from the roots and rhizomes of Veratrum patulum. J. Nat. Prod. 1987, 61, 1078- 1081.
    [20]徐暾海,徐雅红.藜芦属植物化学成分和药理作用.国外医药·植物药分册, 2004, 17, 185-189.
    [21]赵伟杰,郭永沺.乌苏里藜芦中氐类化合物的化学研究.中国药物化学杂志, 1998, 8, 35-37.
    [22]赵伟杰,郭永沺.毛穗藜芦中氐类化合物的化学研究.中国中药杂志. 1998, 23, 619.
    [23]赵伟杰,郭永沺.藜芦生物碱中刺孢麴霉碱的分离与鉴定.中国中药杂志. 1991,16, 425-426.
    [24]赵伟杰,郭永沺.乌苏里藜芦中橙黄胡椒酰胺的分离鉴定.中国中药杂志. 1998, 23,41.
    [25]赵录英,赵画晨,吴博威.藜芦混碱对离体心泵功能的效应及其与洋地黄类药物的对比.山西医科大学学报. 2004, 33, 231-232.
    [26]康毅,王国祥.牛磺酸抗藜芦碱实验性心律失常作用.天津医药. 1989, 4, 199-201
    [27]郭春花.甘草酸钾和阿托品抗藜芦碱实验性心率失常作用.长治医学院学报. 1998, 12, 251-252.
    [28]王建民,魏苑,钟慈声.乌苏里藜芦生物碱对豚鼠心肌细胞动作电位及钙电流的影响.第三军医大学学报. 2003, 23, 1403-1405.
    [29]李淑媛,李卫平,李传勋.盐酸乌苏里藜芦碱对麻醉犬血流动力学的研究.中国药学杂志. 1997, 32, 407-409.
    [30]刘燕,高广猷,叶丽虹.光脉黎芦碱的降压作用.大连医学院学报. 1991,13, 68-71.
    [31]马丽焱,周远鹏,江京俐.狭叶藜芦碱甲对犬血流动力学的影响.中草药. 1998, 29, 105-107.
    [32]韩国柱,李欣燕,吕莉.乌苏里藜芦碱抗血栓作用的研究.中草药. 2003, 34, 1107-1110.
    [33]韩国柱,李欣燕,吕莉.乌苏里藜芦碱对大鼠血小板聚集以及小鼠全血凝血时间及尾出血时间的影响.中国药理学会通讯. 2004,19, 8-10.
    [34]由广旭,周琴,李卫平.乌苏里藜芦碱对大鼠脑缺血一再灌注损伤的保护作用.中草药. 2004, 35, 908-911.
    [35]杨静娴,戴淑芳,韩国柱.乌苏里藜芦碱对家兔和大鼠血液流变学及小鼠出血时间的影响.中药药理与临床. 1998, 14, 22-24.
    [36]李欣燕,任洪灿,韩国柱.乌苏里藜芦碱在大鼠的血液流变学作用.大连医科大学学报.2004,26, 165-167.
    [37]李欣燕,韩国柱,张书文.乌苏里藜芦碱对血小板聚集及凝血与出血时间的影响.中草药. 2004, 35, 1269-1272.
    [38]卢步峰,鲁友明,黄诒森.藜芦碱对分离的大鼠神经细胞内游离钙的影响.中国药理学通报. 1994, 10, 214-216.
    [39]段建红,段玉斌,胡三觉.藜芦碱引起神经元放电峰峰间期慢波振荡.生物药理学报. 2004,18, 49-52.
    [40]段建红,段玉斌,邢俊玲,胡三觉.藜芦碱致使大鼠背根神经节A类神经元产生触发性振荡.生理学报. 2004, 54, 208-212.
    [41]谢勇,段玉斌,徐健学,等.在大鼠受损坐骨神经上由藜芦碱诱发的抛物线簇放电.生物化学与生物物理学报. 2003,35, 806-810.
    [42]郑善子,崔春权,刘永镇.藜芦乳膏对毛囊蠕形螨的体外杀虫作用.延边大学医学学报. 2004,27, 31-32.
    [43]杨素华,李东宁,孙健.藜芦乳膏治疗疥疮的疗效观察.辽宁中医杂志. 2004, 29, 664.
    [44]李太一,申成华,郑善子,等.藜芦乳膏的皮肤毒性实验研究.延边大学医学学报. 2004,27, 118-120.
    [45] Markham, K.R., Mabry, T.J.,1975. Ultraviolet–visible and proton magnetic resonance spectroscopy of flavonoids. In: Harborne, J.B., Mabry, T.J.,Mabry, H. (Eds.), The Flavonoids. Chapman and Hall, London, pp. 45–77.
    [46] Markham, K.R., Geiger, H., 1994. 1H nuclear magnetic resonance spectroscopy of flavonoids and their glycosides in hexadeuterodimethylsulfoxide. In: Harborne, J.B. (Ed.), The Flavonoids Advances in Research since 1986. Chapman and Hall, London, pp. 441–497.
    [47] Seabra, R.M., Moreira, M.M., Costa, M.A.C., Paul, M.I., 6,3’,4’-trihydroxy-4-methoxy-5-methylaurone from Cyperus capitatus.Phytochemistry 1995, 40, 1579–1580.
    [48] Seabra, R.M., Andrade, P.B., Ferebres, F., Moreira, M.M. Methoxylated aurones from cyperus capitatus. Phytochemistry 1997, 45, 839–840.
    [49] Pelter, A., Ward, R.S., Heller, H.G. Carbon-13 nuclear magnetic resonance spectra of (Z)-and (E)-aurones. J. Chem. Soc. [Perkin] 1979, 1, 328–329.
    [50] Zhao, W. J., Tezuka,Y., Kikuehi, T., Studies on constituents of Veratrum plants I Constituents of Veratrum maackii Regel Isolation and structure determination of a new alkaloid maackinine. Chem. Pharm. Bull., 1989, 37, 2920-2928.
    [51] Terry J. Gilbertson, Zygacine and zygadenine: The major alkaloids from Zygadenus gramineus. Phytochemistry 1973, 12, 2079-2080.
    [52] El Sayed K A, Mc Chesney J D, Halim A F, et al, A study of alkaloids in Veratrum virideation. Int. J. Pharm. 1996, 34, 161-173.
    [53]杨崇仁,刘润民,周俊,等.蒙自藜芦的甾体生物碱研究.云南植物研究, 1987, 9, 359-364.
    [54] Fried, J., White, H.L., Wintersteiner, O. Germidine and germitrine, two new ester alkaloids from Veratrum viride. J. Am. Chem. Soc., 1949, 71, 3260–3261.
    [55] Tezuka, Y., Kikuchi, T., Zhao, W.J., Chen, J., Guo, Y.T. (+)-Verussurine, a new steroidal alkaloid from the roots and rhizomes of Veratrum nigrum var. ussuriense and structure revision of (+)-verabenzoamine. J. Nat. Prod. 1998,6, 1397-1399.
    [56] Kupchan, S.M., Afonso, A. Veratrum alkaloids XXXVII. The structure of germanitrine, a hypotensive ester alkaloid. J Am Pharm Assoc. 1959, 48, 731–734.
    [57] Tang, J., Li, H.L., Shen, Y.H., Jin, H.Z., Yan, S.K., Liu, R.H., Zhang, W.D. Four new germine esters from Veratrum dahuricum. Helv. Chim. Acta 2007, 90, 769– 775.
    [58] Adam, G., Schreiber, K., Tomko, J., Vassova, A. Verazin, einneues veratrum-alkaloid mit 22,26-iminocholestan-gerüst. Tetrahedron 1967, 23, 167-171.
    [59] Taskhanova, E.M., Shakirov, R., Yunusov, S.Y. Alkaloids of Zygadenus sibiricus. The structure of verazinine. Chem. Nat. Compd. 1985, 21, 343-344.
    [60] Ripperger, H., Steroidal alkaloids from roots of Solanum spirale. Phytochemistry, 1996, 43, 705-707.
    [61]廖立平,李萍.四季青叶化学成分研究.中国药科大学学报, 2004, 35(3): 205-206
    [62]Masuda, T., Jitoe, A., Kato, S., Nakatani, N. Acetylated flavonol glycosides from Zingiber zerumbet. Phytochemistry 1991, 30, 2391-2392.
    [63] Nakatani, N., Jitoe, A., Masuda, T., Yonemori, S. Flavonoid constituents of Zingiberzerumbet Smith. Agric. Biol. Chem. 1991, 55, 455-462.
    [64] Usia, T., Iwata, H., Hiratsuka, A., Watabe, T., Kadota, S., Tezuka, Y. Sesquiterpenes and Flavonol Glycosides from Zingiber aromaticum and Their CYP3A4 and CYP2D6 Inhibitory Activities. J. Nat. Prod. 2004, 67, 1079-1083.
    [65]凌云,鲍燕燕,朱莉莉,郑俊华,蔡少青,肖越.蒲公英化学成分的研究.中国药学杂志. 1997, 32(10): 584-586.
    [66]程宇镳,张东明,庾石山,丁怡.穿鞘菝葜化学成分的研究,中国中药杂志. 2003, 28(3): 233-235.
    [67] Hanama, F., Tahara, S., Mizutani, J. Antifungal stress compounds from Veratrum grandiflorum leaves treated with cupric chloride. Phytochemistry 1992, 31, 3005-3007.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700