枇杷花化学成分及生物活性的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
枇杷花系蔷薇科植物枇杷Eiobotrya.japonica(Thumb.)Lindl.之花。枇杷叶是一种常用中药,关于其化学成分及生物活性研究较多,但对于枇杷花的研究甚少,有关成分的抑菌及抗肿瘤生物活性的研究尚未报道。因此本文对枇杷花的化学成分及生物活性进行了初步研究。
     对枇杷花采用溶剂系统提取法,分为乙酸乙酯部分、95%乙醇部分、50%乙醇部分和水层四个部分,对这四个部分进行黄酮显色鉴别及含量测定,发现黄酮主要集中于50%乙醇部分,各部分的黄酮类别有所差异,但主要有黄酮类、黄酮醇类及二氢黄酮类化合物。
     本实验对枇杷花的乙酸乙酯提取部分采用硅胶柱层析、反相柱层析、Sephadex LH-20凝胶柱层析,结合薄层色谱、半制备色谱进行多次分离纯化与重结晶,从中分离得到了7个化合物,其中化合物7为两种单一化合物组成的混合物;利用核磁共振(NMR)、质谱(MS)等现代化分析测试手段测定其化学结构,经过波谱分析、理化常数及文献检索,鉴定了这些化合物的结构,分别为:β-谷甾醇(1)、齐墩果酸(2)、熊果酸(3)、3β,19α-二羟基-4-醛基-乌索-12-烯-28-酸(4)、β-胡萝卜苷(5)、槲皮素-3-O-β-D-半乳糖苷(6)、2α-羟基乌索酸与2α-羟基齐墩果酸(7)。其中化合物1、4、5、6、7为首次从枇杷花中分离得到。
     在生物活性方面,采用纸片扩散法和MTT法对枇杷花乙酸乙酯层分离得到的片段以及单一化合物进行了抑菌、抗肿瘤细胞的生物活性实验。实验表明,乙酸乙酯层分离的片段及化合物对大肠杆菌、金黄色葡萄球菌的抑菌作用很弱;除化合物6外,对白色念珠菌均具有不同程度的抑制作用,其中化合物2、4、5、7的抑菌效果优于阳性对照组。MTT实验中,片段E2-2-1及化合物2、3、7对白血病细胞K562有较好的抑制效果,且为浓度依赖性抑制作用,抑制癌细胞K562生长作用最强的化合物3,剂量为20μg/ml时,抑制率达91.96%。根据单一化合物对抗肿瘤K562活性的研究,初步确定该植物抗肿瘤K562的主要活性成分是三萜类化合物。
Loquat flower is the flower of Eriobotrya japonica which belongs to Rosaseae category. Loquat leaf is a widely used Chinese medicine which has been much studied about its chemical components and biological activities. However, the reports of loquat flower are scarce and there is no report about its components and biological activities. Therefore,the dissertation preliminary study on the chemical components and biological activities of loquat flower.
     The loquat flower was extracted with systematic solvents, such as ethyl acetate, 95% ethanol, 50% ethanol and water. Flavonoids were identified and their contents determined in those extractives. Flovonoids were mainly contained in the 50% ethanol extractive. They are mainly flavones, flavanols, and flavonvones.
     In our experiment, the compounds in ethyl acetate extractive of loquat flower were separated and purified with column chromatography on silica gel, C18 and sephadex LH-20 gel, TLC, semipreparative chromatography and recrystallization. Seven components were separated and their structures were identified using NMR and MS and their physical &chemical constants were determined. They areβ-sitostero (l), Oleanic acid (2), Ursolic acid (3), 3β,19α-dihydroxyursolic-4-aldehyde-12-en-28-acid (4),β-daucosteriol (5), quercetin-3-O-α-L-galactoside(6), 2α-hydroxyursolic acid and 2α- maslinic acid (7). Among them, compound 1, 4, 5, 6 and 7 are first time separated from this plant.
     The antibacterial and antineoplastic effects of the compounds and extractive fractions were measured by Kirby-Bauer and MTT method. Our experiment indicated that the ethyl acetate extractive had poor antibiotic activities on Escherichiacoli and Staphylococcus aureus; compounds and extractive fractions except compound 6 had different antibiotic activities on Candidaabbicans. Compound 2, 4, 5 and 7 were better than the positive comparison. Section E2-2-1 and compound 2, 3, 7 were fairly effective to prohibit leukemia cell K562, the effect depending on their concentration. Compound 3 has an inhibitive rate of 91.96% to leukemia cell K562 in a 20μg/ml concentration. Triperpenoids were discovered as the main anti-tumor active component on K562 in this plant.
引文
[1]张婷婷,令桢民,赵旺生.枇杷的研究现状和研究前景[J].农产品加工·学刊,2006,(7):50-51
    [2]全国中草药汇编编写组.全国中草药汇编[M].北京:人民卫生出版社,1996,504
    [3]陆林博.枇杷叶的化学成分研究[D].南京师范大学,2006
    [4] LINDLEY J.Description as Eriobotrya japonica[J].Trans Linn Soc,1822,991:102.
    [5]杨向晖,林顺权,何小龙.枇杷属植物性状的补充描述与商榷[J].果树学报,2007,24(2):151-156
    [6]国家中医药管理局《中华本草》编委会.中华本草,第4册[M].上海:上海科学技术出版社, 1999: 140
    [7]阴健.中药现代研究与临床应用.北京:中国古籍出版社,1995:219
    [8]沙娜,梁敬钰.枇杷叶研究进展[J].海峡药学, 2006, 18(1): 6-10
    [9]郭宇,吴松吉,朴惠善.枇杷叶的化学成分及药理活性研究进展[J].时珍国医国药, 2006, 17(6): 928-930
    [10]成丽,刘燕,陈凌亚,等.枇杷花三萜皂甙成分的研究[J].华西医大学报,2001:32(2):283-285
    [11] De Tommasi N, De Simone F, C Cirino G,etal.Hypoglycemic effects of sesquiterpene glycosides and polyhydroxylated triterpenoids of Eriobotrya japonica [J]. Planta Med,1991,57(5): 414
    [12] Shimizu M,Fukurmura H,Tanaarni S,et al.Anti-inflammatory constituents of topically applied crude drugs.I.constituents and anti-inflammatory effect 0f Eriobotrya japonica Lind1.[J].chem Pharm Bull,1986,34(6).2614.
    [13] N.De Tommasi, R,Aquino, F.De Simone,and C.Pizza, New sesquiterpene and ionone glycosides from Eriobotrya japonica [J].J Nat Prod,1992,35:1025
    [14] HyunAh Jung,Jong Cheol Park,HaeYoung Chung,et al.An一tioxidant flavonides and chlorogenicacid from the leaves of Eri-oPotryajaponica[J]. Arch.PharmacalRes,1999,22(2):213-218.
    [15] Nobuo Kawahara,Motoyoshi Satake,Yukihiro Goda.A Newacy-lated flavonolgly coside from the leaves of Eriobotryajaponica[J].Chem.Pharm.Bull, 2002,50(12): 1619-1620
    [16] S.Louati,M.S.J.Simmonds,R.J.Grayer,etal.Flavonoids from Eriobotrya japonica (Rosaceae) growing in Tunisia[J].Biochemi-cal Systematics and Ecology,2003,31(1):99-101
    [17] Chen,C.P., Wang,H.Y. The effects of oleanolic acid and dimethyl dicarbonate biphenyls on acute liver injury[J]. Chem. Pharm.Bull ,1989,34(3):326-329
    [18]川原信夫(日).枇杷叶成分的研究[J].国外医学中医中药分册,2003,25(5):316.
    [19] Hideyuki Ito, Eri Kobayashi, YoshieTakamatsu. Polyphenols from Eriobotrya japonicaand their cytotoxicity against human oral tumor cell lines[J].Chem.Pharm.Bull,2000,48(5):687-693.
    [20] WuQing-Li.Studies on the Chemical constituents of loqua leaves[J]. AcsSeries, 2003,859:292-306
    [21] Hideyuki Ito,Eri Kobayashi,Shu-HanLi,etal.Antitumoractivity of compounds isolated from leaves of Eriobotry ajaponic[J].Journal of Agricultural and Food Chemistry, 2003,50(8):2400-2403.
    [22] Masakazu Miyakado,Keisuka Watanabe.A New dibenzo furanphytoalex in from the leaves of loquat,E.japonical.Nippon Noyaku Gakkaishi,1985,10(1):101-106
    [23]中国医学科学院药物研究所.中药志(第2册)[M].北京:人民卫生出版社,1984,72
    [24]余世春.常用中药枇杷叶生物活性成分研究-鞭柱唐松草与长柄唐松草化学成分及毛莨科次生代谢产物的化学系统学意义[D].中国协和医科大学,1999
    [25] de Tommasi N,de Simone F,Pizza C,et al.Consitituelrlts 0f Eriobotrya japonica .A study 0f their antiviral properties[J].J Nat Prod,1992,55(8):1067.
    [26] LangZZ,AquinoR,de Feo V,et a1.Polyhydroxylated triterpenes from Eriobotrya japonica[J].Planta Med,1990,56:330.
    [27]鞠建华,周亮,林耕,等.枇杷叶中三萜类成分及其抗炎,镇咳活性研究.中国药学杂志,2003,38(10):752-757
    [28]王立为,刘新明,余世春,等.枇杷叶抗炎和止咳作用研究.中草药,2004,35(2):174-176
    [29]邓晶晶,卢先明,蒋桂华,等.枇杷花镇咳祛痰和抗炎的药效学研究.时珍国医国药,2006,17(12):2469-2470
    [30] Mineo Shimizu,Hideki Fukumura,Hideki Tsuji,et,al.Anti-in-flammatory Constituents of Topically Applied Crude Drugs.I.Constituents and Anti-inflammatory effect of Eriobotry ajaponicaLindl.Chem.Pharm.Bull,1986,34(6):2614-2617
    [31]葛金芳,李俊姚,宏伟,等.枇杷叶提取物对佐剂性关节炎的作用及部分机制研究[J].中国药理通讯,2003,20(3):48
    [32]葛金芳.枇杷叶三萜酸的抗炎免疫作用及对慢性支气管炎的治疗作用与机制研究[D].合肥:安徽医科大学,2004
    [33]王柏康.枇杷叶煎治疗小儿急性肾小球炎80例[J].河北中医,1998,20(6):325-326
    [34] NoreenW.,WaddodA.,Hidayat H.K.,WahidS.A.,etal.Effect of Eriobotry ajaponicaon Blood Glucose Levels of Normal and Al-loxan-Diabetic Rabits[J].Planta Med.,1988,54:196-199
    [35] J.Chen,W.L.Li,J.L.Wu,etal. Hypoglycemic effects of a sesquiterpene glycoside isolated from leaves of loquat (Eriobotrya japonica (Thunb.) Lindl.)[J].Phytomedicine,2008,15:98-102
    [36] Nunziatina De Tommasi, Rita Aquino, Francesco De Simone,etal.Plant Metabolites new sesquiterpene and iononeglycosides from Eriobotryajaponic[J]. Nat.Prod, 1992,55(8):1025-1032
    [37] Shoko Taniguchi,Yoko Imayoshi, Eri Kobayashi, etal.Production of bioactive triterpenes by Eriobotryajaponica[J].Phytochemistry,2002,59(3):315-323.
    [38]中国药典委员会.中国药典2000年版(一部)[S].北京:化学工业出版社,2000.163.
    [39] Ito Hideyuki, Kobayashi E,Li SH,etal. Antitumor or activity of compounds isolated from leaves of Eriobotry ajaponic[J].Ac. Food Chem,2003,50(8):2400
    [40]杨庆新,黄建安,刘仲华,等.枇杷叶中三萜酸的研究进展[J].食品工业科技,2008,29(8):282-284
    [41] Takashi Yoshida, Hideyuki Ito, Tsutomu Hatano, etal.Anti-tu-morconstituents from the leaves of Eriobotry ajaponica.BioIndustry,2003,20(2):27-33
    [42] Martin-Aragon S, de las Heras B, Sanchez-Reus MI, etal.Pharmacological modification of endogenous antioxidant enzymes by ursolic acid on tetrachloride induced liver damage in rats and primary cultures of rat hepatocytes[J].Exp Toxicol Pathol,2001,53(2/3):199-206
    [43] Saraswat B, Visen PK, Agarwal DP. Ursolic acid isolated from Eucalyptus tereticornis protects against ethanol toxicity in isolated rat hepatocytes[J].Phytother Res, 2000,14(3):163-166
    [44]韩德伟.齐墩果酸防治实验性肝硬变发生的研究[J].中医杂志,1981,22(3):217
    [45]任骏.齐墩果酸对前列腺素及环核苷酸的影响[J].中国药理学报,1991,7(3):179
    [46]王立新,韩广轩,刘文庸,等.齐墩果酸的化学与药理研究[J].药学实践杂志,200l,19(2):105
    [47] Chiang LC, Chiang W, Chang MY,etal.Antileukemic activity of selected natural products in Taiwan[J]. Am J Chin Med,2003,31(1):37-46
    [48] Takashi Komiya, Yumiko Achiwa, Hirotake Katsuzaki, et al. Effect of Oleanolicand Ursolicacids isolated from loquaton the growth of human lymphoid Leukemia Cells[J].FoodSci,Tech-nol.Int.Tokyo,1998,4(4):282-284
    [49]匡海学,董小萍,石任兵.中药化学[M].中国中医药出版社,2003,1:21~25
    [50]姚新生主编.天然药物化学[M].人民卫生出版社.2002,18-20
    [51]尹佩辉.桐粕活性成分的提取、分离纯化及抗病毒作用研究[D].湖南农业大学,2006
    [52]张静泽,颜艳.吸附树脂分离技术在中药研究中的应用[J].中国中药杂志,2004,29(7):28-30
    [53]王凯,岳宣峰.中药有效成分分离纯化技术应用进展[J].榆林学院院报,2005,15(3):21-23
    [54]耿家玲,沈勇,宋兴武.三七叶甙的开发与利用[J].云南中医学院学报,2001,24 (3):7-8
    [55]孟祥颖,李向高.西洋参不同部位中黄酮的含量测定[J].长春中医学院学报,2002,14(2) :29-30
    [56]吕晓玲,姚中铭,姜平平.凝胶层析法精制栀子黄色素的研究[J ].食品与发酵工业,2001,27(4) :39 -42
    [57] Cato F. Combination of chromatographic techniques for thepreparative isolation of anthocyanins applied on blackcurrant(Ribes nigrum) fruits[J]. J Chromatogr A, 1998, 825 (1): 89-95.
    [58] Abreu P, Pereira A, Relva A. Characterisation of a sugar fraction from Sarcocephalus latifolius stem bark extract [J].Carbohydr Polym, 2001, 45(2): 155-160.
    [59]王凤美,陈军辉,李磊,等.高速逆流色谱法分离制备丹酚酸B[J].天然产物研究与开发,2006,18(1):100-104
    [60]冯顺卿,李药兰,邱玉明,等.高速逆流色谱分离长瓣金莲花中的黄酮类物质[J].色谱,2003,21(6):627
    [61]王凯,岳宣峰.中药有效成分分离纯化技术应用进展[J].榆林学院院报,2005,15(3):21-23
    [62]徐志红,肖泽仪,李磊,等.超滤深度提纯银杏黄酮[J].精细化工,2004,21(2):112-115
    [63]刘洪谦,屈凌波.生脉饮口服液超滤技术研究[J].中草药,1996,27(4):209-211
    [64]季梅,季华.天然产物有效成分分离纯化新技术及应用[J].食品与药品,2007,9(9):62-64
    [65]贺湘凌,谭天伟,Jan S,等.利用β-环糊精键合固定相分离纯化葛根素[J].色谱,2003,21(6):610-613
    [66]张春秀,胡小玲,卢锦花,等.双水相萃取法富集分离银杏叶浸取液的探讨[J].化学研究与应用,2001,13 (6):686-688
    [67]霍清,林强.利用双水相体系的温度诱导效应萃取甘草酸[J].化学通报,2002, (5):349- 352
    [68]王发松,黄世亮.柠檬醛分子蒸馏新工艺与毛叶木姜子果油成分分析[J].天然产物研究与开发,2002,14(2):55-57
    [69]孙学斌,程明,李娜,等.卫矛不同有效部位总黄酮含量及抗氧化性的研究[J].植物研究,2007,27(5):619-621
    [70]范维刚,解成喜,李锋,等.罗布麻叶中总黄酮含量的测定[J].光谱实验室,2005,22(3):464-466
    [71]姚新生主编.天然药物化学[M].人民卫生出版社.2002,181-184
    [72]叶善蓉,唐茜,杜晓.四川粗壮女贞苦丁茶中的黄酮的提取、分离与初步鉴定[J].四川农业大学报,2004,22(2):157-160
    [73]陈业高主编.植物化学成分[M].化工工业出版社.2004,269-273
    [74]郭宇.枇杷叶化学对照品的研究[D].延边大学,2007
    [75]徐成坤,王建中.北京石韦的化学成分研究[J].广东药学院学报,1999,15(1):21-22
    [76]尹峰,胡立宏,楼凤昌.罗勒化学成分的研究[J].中国天然药物,2004,2(1):20-23
    [77]刘戎,丁立生,王明奎,等.灰毛泡根部的化学成分[J].中草药,2003,34(5):394-396
    [78]钟瑞建.青钱柳中的五环三萜成分的研究[J].中草药,1996,27(7):387-388
    [79]林万隆,李定国,陈强,等.奥沙利铂综合治疗胃癌的疗效及机制[J].世界华人消化杂志,2003,11(10):1535-1539.
    [80]姚如永,初晓,张玉江,等.泥蚶提取物-海生素抗肿瘤作用的实验研究[J].中国海洋药物杂志,2005,24(1):33-36.
    [81] Chiang LC,Chiang W,chang MY,et al.Antileukemic activity of selected natural products in Taiwan[J].Am J Chin Med,2003,31(1):37-46

© 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