用户名: 密码: 验证码:
中药蒲葵子有效部位化学成分及药材质量控制的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
蒲葵子为棕榈科植物蒲葵Livistona chinensis R.Br.的干燥成熟果实。性味甘、淡、涩,平,具有软坚散结、收敛止血之功效,适用于癥瘕结气,崩漏,跌打损伤,眼底出血等症。现代研究表明,蒲葵子具有抗癌之功效,民间广泛用于治疗各种癌症,如食道癌、鼻咽癌、恶性葡萄胎、白血病、绒毛膜上皮癌、肺癌。但对蒲葵子有效部位药理研究及化学成分研究未见有公开的报道。为了进一步合理开发利用蒲葵子药材,寻找其有效成分,揭示其抗肿瘤作用物质基础,并为药材质量标准的制定提供科学依据,本课题以蒲葵子为研究对象,对其药效物质基础进行了系统研究。
     化学成分预试验结果表明蒲葵子中可能含有酚类、蒽醌类、香豆素、甾体三萜类、皂苷类、氨基酸类等成分。
     本课题针对蒲葵子的功效及临床应用,选择适宜的肿瘤细胞株对蒲葵子进行了体外抗肿瘤活性部位初步筛选。首先对蒲葵子进行部位分离,对其石油醚提取物、乙酸乙酯提取物、正丁醇提取物和水提取物,采用MTT法测定了它们各自对人慢性粒细胞白血病细胞株K562、人卵巢癌细胞株SKOV3、人结肠癌细胞株HT-29、人膀胱癌细胞株T24等四种瘤株的生长抑制情况;采用ELISA法检测了它们各自对肿瘤细胞分泌血管内皮生长因子(VEGF)水平的影响;以活性部位作用于VEGF诱导后的人脐静脉内皮细胞株(HUVEC),采用RT-PCR和Western blot方法分析内皮细胞Flk-1 mRNA和蛋白的表达变化。结果表明,蒲葵子乙酸乙酯提取物可选择性地抑制结肠癌细胞株HT-29和膀胱癌细胞株T24肿瘤细胞的生长,其抑制率可分别达74.66%和86.52%,并可显著降低各肿瘤细胞株分泌VEGF的水平。石油醚提取物对HT-29和T24生长也有一定的抑制作用,其最高抑制率分别为43.80%和38.67%,并可降低各肿瘤细胞分泌VEGF水平,但作用强度均不及乙酸乙酯部位。水和正丁醇提取物未表现抗肿瘤活性。对VEGF诱导内皮细胞表达Flk-1 mRNA和蛋白,乙酸乙酯提取物表现出明显的抑制作用。药理研究结果表明蒲葵子乙酸乙酯提取物有较好的抗肿瘤作用,是抗肿瘤作用的主要活性部位,石油醚提取物也显示一定的活性。
     对体外抗肿瘤试验筛选出的活性部位,采用柱色谱方法进一步进行系统的化学成分分离和纯化,运用熔点测定、UV、IR、MS、~1H-NMR、~(13)C-NMR等方法进行结构鉴定。从蒲葵子乙酸乙酯部位分离得到10个化合物,鉴定了其中5个化合物,分别为:(-)表缅茄儿茶精((-)-epiafzelechin,Ⅰ)、β-胡萝卜苷(daucosterol,Ⅱ)、β-谷甾醇(β-sitosterol,Ⅲ)、1,6,8-三羟基-3-甲基蒽醌(emodin,Ⅵ)、5,7,4'三羟基-3',5'-二甲氧基黄酮(tricin,Ⅶ),其中1,6,8-三羟基-3-甲基蒽醌为首次从该植物中分得。
     采用GC-MS分析鉴定蒲葵子的石油醚提取部位脂肪酸成分,鉴定出其中11个化合物,占总脂肪酸的94.54%,其中棕榈酸(37.10%)、亚油酸(27.90%)、油酸(20.96%)相对含量较高,不饱和脂肪酸相对含量达到52.28%,并含有ω-3多不饱和脂肪酸:α-亚麻酸、二十碳五烯酸。
     本课题首次对蒲葵子药材进行了质量控制的研究。建立了小麦黄素对照品的标准;采用高效液相色谱法测定了蒲葵子药材中小麦黄素的含量;并对蒲葵子药材进行了指纹图谱的研究,研究结果表明,该方法稳定、可靠、重现性好,10批药材得到的色谱指纹图谱共标定了31个共有峰,其共有峰的相对保留时间基本一致,不同产地批次蒲葵子药材化学组成相似,其相对比例较稳定。
     综上所述,本课题首次确定了蒲葵子的乙酸乙酯提取物是其体外抗肿瘤作用的主要活性部位,石油醚提取物也有一定的活性。从乙酸乙酯提取物中分离鉴定了5个化合物,从石油醚提取物中鉴定了11个化合物。同时对蒲葵子药材进行了指纹图谱研究。本课题为最终揭示蒲葵子抗肿瘤作用及其物质基础,建立药材质量的科学评价方法,实现药材可持续开发利用及抗肿瘤中药新药开发提供了科学依据。
Fructus Livistonae Chinensis is the dried ripe fruit of Livistona chinensis R.Br.It is sweet,tasteless,astringent in flavour and mild in nature.Its actions include softening and dissolving hard masses,stopping bleeding by astringency.It can be used for abdominal lumps,stagnation of qi,metrorrhagia,Traumatic injury,subhyaloid hemorrhage et al. Modern research had delicated that Fructus Livistonae Chinensis possessed the effect of anti-tumor,and widely used for the treatment of cancer in the folk,such as esophagus cancer,nasopharyngeal cancer,chorioadenoma,leukaemia,choriocarcinoma,lung cancer. But researches on the effective part about chemical constituents and pharmacology haven't been reported.In order to obtain a more comprehensive understanding of its effective physiological constituents,reveal the substantial foundation of anti-tumor effect and provide scientific basis of producing medicine reasonably,a phytochemical study has been carried out.
     The fore-experiments of its chemical components showed that it contained phenols, anthraquinones,coumarin,steroids,triterpenoids,saponin,amino acids,et al.
     The 70%alcoholic extracts obtained from the dried fruits were divided into four portions including petroleum ether extracts,ethyl acetate extracts,n-Butyl alcohel extracts and water extracts for the first time.MTT assay and ELISA were used to detect the proliferation and the secretion of vascular endothelial growth factor(VEGF) of chronic myelogenous leukemia K562,ovarian neoplasm SKOV3,colon carcinoma HT-29 and bladder cancer T24 cell lines respectively.The expression of fetal liver kinase(Flk-1) protein and mRNA in endothelial cells induced by VEGF was analyzed by Western blotting and RT-PCR.The results showed that the ethyl acetate part could selectively inhibit the proliferation of HT-29 and T24 cell lines in a dose-dependent manner(the maximum inhibitory rate were 74.66%and 86.52%),and could significantly inhibit the secretion of VEGF protein of the four tumor cell lines.The petroleum ether part had similar inhibitory effect as well as the ethyl acetate part,but its potency is inferior to the ethyl acetate part(the maximum inhibitory rate were 43.80%and 38.67%),The water-soluble and n-butanol parts had no effect on different tumor cell lines.The ethyl acetate part could inhibit significantly the expression of Flk-1 protein and mRNA of HUVEC induced by VEGF.The ethyl acetate part has fine anti-tumor activity,and its mechanism might be associated with reducing VEGF protein secretion and inhibiting the expression of Flk-1 mRNA and protein.
     Effective parts were seperated and purified by chromatographic methods. Compounds were identified by determining melting point,UV,IR,MS,~1H-NMR, ~(13)C-NMR,et al.10 compounds had been isolated from ethyl acetate extract of Fructus Livistonae Chinensis,and 5 compounds were identified:(-) -epiafzelechin(Ⅰ), daucosterol(Ⅱ),β-sitosterol(Ⅲ),emodin(Ⅵ),tricin(Ⅶ).The compoundⅥwere obtained from the plant for the first time.
     For the first time,we analyzed the chemical constituents of petroleum ether extracts of Fructus Livistonae Chinensis and the constituents were separated and identified by GC-MS.The results showed that 11 compounds were identified. Unsaturated fatty acids constituted 52.28%of the total fatty acids,which includeω-3 Polyunsaturated fatty acid:α-linolenic acid,EPA.
     For the first time,the content of tricin in Fructus Livistonae Chinensis was determined by HPLC.The results showed the HPLC method was sentives and specifive. Finger printing research on Fructus Livistonae Chinensis was conducted.The results showed that 31 peaks could denote the fundamental substance of Fructus Livistonae Chinensis,the research method was advanced and feasible,which indicated the finger printing is somehow meanmingful as a measure of quality control when the chemical components are unknown.
     The research provided the scientific fundation to reveal the substantial foundation of anti-tumor effect,establish scientific evaluating method of quality control,achieve medicine material continuously reasonable exploitation,exploit antitumor new medicine of Chinese herbal medicine.
引文
[1]梁蓓蓓,刘华钢.天然药物抗肿瘤作用的研究进展[J].中国肿瘤,2007,16(9):705-708.
    [2]甄永苏.抗肿瘤药物研究与开发[M].北京:化学工业出版社,2004,9:10.
    [3]广西中药材标准:271-272.
    [4]程剑华,李以镔主编.抗癌植物药及其验方[J].江西:江西科学技术出版社,1998:752.
    [5]赵守训,黄泰康,丁志遵等主编.中药辞海(第三卷)[J].北京:中国医药科技出版社,1997:1107-1108.
    [6]刘志平,崔建国,黄初升,等.蒲葵籽中有效化学成分的研究[J].中草药,2007,38(2):178-180.
    [7]陈屏,杨峻山.蒲葵籽化学成分研究[J].中草药,2007,38(5):665-668.
    [8]Zhong,Zhenguo;Cui,Jianguo;Zhang,Fengfen;et al.Anti-tumor extractive of livistona chinensis,preparation and application thereof[J].Faming Zhuanli Shenqing Gongkai Shuomingshu,2006,19 pp.
    [9]Delle Monache,F.;Ferrari,F.;Poce-Tucci,A.;et al.Catechins with(+)-epi-configuration in nature[J].Phytochemistry(Elsevier),1972,11(7):2333-2335.
    [10]Mala,Vajanti;Dahot,M.Umar.Chemical constituents of Livistona chinensis seeds[J].Science International(Lahore),1994,6(3):231-233.
    [11]Javed,M.Akhtar;Ahmad,Manzoor;Raie,M.Yaqub.Studies of Livistona chinensis oil[J].Pakistan Journal of Scientific and Industrial Research,1993,36(10):435-436.
    [12]Dahot,M.Umar;Mala,Vajanti.Chemical analysis of Livistona chinensis seed pulp[J].Journal of the Chemical Society of Pakistan,1997,19(4):320-323.
    [13]He,Xiao-yu;Cui,Jian-guo;Huang,Chu-sheng;et al.Analysis of fatty oil from the root of Chinese fan-palm by GC-MS[J].Huagong Jishu Yu Kaifa,2003,32(2):31-32.
    [14]Maurer-Menestrina,J uliana;Sassaki,Guilherme L.;Simas,Fernanda F.;et al.Structure of a highly substitute -ed -xylan of the gum exudate of the palm Livistona chinensis(Chinese fan)[J].Carbohydrate Research,2003,338(18):1843-1850.
    [15]秦盛莹,刘雯,陈晓辉,等.4种中药抗肿瘤活性的初步研究[J].西北药学杂志,2007,22(1):16-18.
    [16]曾春晖,杨柯,郑作文.蒲葵子的含药血清体外抗肿瘤作用的实验研究[J].广西中医药,2007,30(1):58.
    [17]黄才,覃燕梅,梁念慈.石上柏和蒲葵子对蛋白激酶C活性的影响[J].中草药,1995,26(8):414-418.
    [18]Liu,Su Ying;Hsu,Chao Chin;Ho,I Ching.Antitumor metastatic components in Trapa taiwanensis Nakai and Livistona chinensis R.Br.Bulletin of the Institute of Zoology[J].Academia Sinica,1987,26(2):143-50.
    [19]Cheung Susan;Tai Joseph.In vitro studies of the dry fruit of Chinese fan palm Livistona chinensis.Department of Pathology and Pediatrics,Center for Complementary Medicine Research,BC's Research Institute for Children's and Women's Health[J].University of British Columbia,4480.
    [20]Sartippour M R;Liu C;Shao Z M;et al.Livistona extract inhibits angiogenesis and cancer growth[J].Oncology reports,2001,8(6):1355-7.
    [21]Wen-Chuang Huang,Rae-Mann Hsu,Lang-Ming Chi,et al.Selective downregulation of EGF receptor and downstream MAPK pathway in human cancer cell lines by active components partially purified from the seeds of Livistona chinensis R.Brown[J].Cancer Letters,2007,248:137-146.
    [22]Nakatani,Nobuji.Antioxidants in herbs of Okinawa islands[J].ACS Symposium Series,2003,859(Oriental Foods and Herbs):166-175.
    [23]吴英德,宋向群,胡晓桦,等.复方金蒲片临床研究概述[J].广西医学,2007,29(11):1722-1724.
    [24]刘颖新,黎福祥.金蒲抑瘤片在鼻咽癌的临床应用研究[J].广东微量元素科学,2002,9(2):33-36.
    [25]HarmeyJ H,Bouchier-Hayes D.Vascutar endothelial growth factor(VEGF),a survival factor for turnout cells:implications for anti-angiogenic therapy[J].BioEssays,2002,24:280-283.
    [26]Ferrara N,Henzel W J.Pituitary follicular cells secrete a novel heparin-binding growth factor specific for vascular endthelial cells.Biochem Biophys Res Commun[J],1989,161(2):851-858.
    [27]Dvorak HE,Brown IE,Delmar M,et al.Vascular permeability factor/vascular endothelial growth factor,microvascular hyperpermeability,and angiogenesis[J].Am J Patbol,1995,146:1029-1039.
    [28]楼凤吕,丁林生,李玲玲,等.北马兜铃的化学成分研究[J].中草药,1986,17(9):6.
    [29]杨云,冯卫生.中药化学成分提取分离手册[M].北京:中国中医药出版社,1998:3.
    [30]毕志明,王峥涛,张勉,等.流苏石斛化学成分的研究[J].中国药科大学学报,2001,32(6):421-422.
    [31]XU Chuan he.Information of the Chinese Pharmacological Society[J],1984,3:101.
    [32]刘本君,郭宏军,葛佳瑞.多不饱和脂肪酸与肿瘤关系的研究进展[J].畜牧兽医科技信息,2007:7-8.
    [33]国家医药管理局中草药情报中心.植物药有效成分手册[M].北京:人民卫生出版社,1986:1073.
    [34]董南,王海燕,陈良龙,等.HPLC测定毛茛属几种植物中小麦黄素的含量[J].中国中药杂志,2007,32(22):2427-2428.
    [35]李兰芳,郝冬生,张文彦,等.小麦黄素水剂中小麦黄素含量的反相高效液相色谱法测定[J].分析测试学报,2001,20(3):56-58.
    [1]贾敏如.防治恶性肿瘤的天然药物[J].成都中医药大学学报,2002,25(2):25-31.
    [2]孟繁浩,巩丽颖,佟馨.抗癌药物—喜树碱类衍生物研究进展[J].生命的化学,2002,22(3):265-267.
    [3]CHENG Lei,ZHOU xiu-jia.Review on anficancer mechanism of some plant alkaloids[J].中草药,2004,35(2):216-221.
    [4]林云,张灿,华维一.原小檗碱类化合物的构效关系研究进展[J].药学进展,2002,26(2):76-80.
    [5]Frei E,Bieler C A,Arlt V M,et al.Covalent binding of the anticancer drug ellipticine to DNA in V79 cells transfected with human cytochrome P450 enzymes[J].Biochem Pharmacol,2002,64(2):289-295.
    [6]许相儒,蒋纪恺.苦参及其生物碱抗肿瘤活性研究进展[J].中国中西医结合杂志,1998,18(5):314-316.
    [7]焦霞,沈其昀.苦参生物碱的临床及药理研究进展[J].中药新药与临床药理,2002,13(3):192-194.
    [8]卢大用,曹静懿,胥彬.三尖杉酯和高三尖杉酯碱的生物活性及临床应用[J].天然产物研究与开发,1999,12(5)::70-73.
    [9]kaye SB.pregress in the treatment of Ovarina cancer[J].Anti Cancer Drags,1999,9:2731.
    [10]SINGER WD.Ceilular uptake and tubulin binding properties of four vinca alkaloids[J].Biochem Pharmacol,1992,43:545.
    [11]丁健.抗肿瘤药物的研究新进展[J].中国新药杂志,2000,(3):150.
    [12]Armand JP,CunnindlairD,Cutesm E,et al.Clincal advnces with topoisom erase I inhibitors in gastrointes tinal mali-gnancies[J].Anti Cancer Drugs,1999,10:5.
    [13]李贵海,潘成业,孙付军,等.中药生物碱逆转小鼠S180肉瘤细胞获得性多药耐药相关生物因子的过度表达[J].中国中药杂志,2005,30(23):1844-1848.
    [14]董宁征,顾振纶.一叶秋碱的抗肿瘤作用及其机制研究[J].中成药,1999,(4):193.
    [15]李达,刘瑞芹.中医药诱导肿瘤细胞凋亡的可行性探讨[J].中国中西医结合杂志,1996,16(7):433.
    [16]迟德彪,雷林生,金宏,等.钩吻素子体外诱导人结肠癌Lovo细胞凋亡的实验研究[J].第一军医大学学报,2003,23(9):911-913.
    [17]王寅,方云峰,林文,等.钩吻总碱对肝癌细胞HepG2的体外抑制作用[J].中药材,2001,24(8):579.
    [18]张兰兰,林敬明,吴忠.钩吻化学成分与药理研究进展[J].中药材,2003,26(6):451-453.
    [19]张彦,蒋纪恺.苦参碱诱导K562白血病细胞分化和凋亡的实验研究[J].癌症,2000,21(4):193.
    [20]张燕军,夏天,赵建斌.苦参碱对SMMC-7721细胞系的诱导分化作用[J].第四军医大学学报,1998,19(3):340-342.
    [21]赵凤鸣,许冬青,王明艳,等.巴豆生物碱对人胃癌细胞SGC-7901的诱导分化作用研究[J].中医药学刊,2005,23(1):134.
    [22]司维柯,尚桃元,康格非.苦参碱对人肝癌细胞HepG2的细胞形态影响和相关增殖因素的变化[J].第三军医大学学报,2000,22(6):553-556.
    [23]金艳书,吴学敏,娄金丽.苦参碱对人肝癌细胞增殖、细胞周期及细胞凋亡的影响[J].中国临床康复,2006,10(3):107-109.
    [24]陈伟忠,曾欣,林勇,等.苦参碱对肝癌细胞HepG2增殖的影响及端粒酶活性调控的体外研究[J].肿瘤学杂志,2002,8(3):168-170.
    [25]黄建,张鸣杰.苦参碱抑制大肠癌HT-29细胞环氧化酶-2表达的研究[J].中国中西医结合杂志,2005,25(3):240-243.
    [26]何於娟,蒋纪恺,欧一衡,等.苦参碱对K562细胞早期原癌基因表达的影响[J].癌症,2002,21(4):369-372.
    [27]朱宁希,吕庆华.苦参碱对白血病细胞诱导分化作用和机理研究[J].上海中医药大学学报,2001,15(1):43-44.
    [28]冯骥良,黄高开,张永清,等.苦参碱抑制JM细胞株增殖和诱导凋亡的研究[J].中国中药杂志,2003,28(5):437-442.
    [29]田晓丽,孙殿甲,堵年生.新疆骆驼蓬种子抗肿瘤活性成分的研究[J].新疆医科大学学报,2003,26(2):113-116.
    [30]彭海燕,章永红,韩英,等.槲寄生碱对乳腺癌细胞抑制作用的实验研究[J].吉林中医药,2003,9:50-51.
    [31]彭海燕,章永红,韩英,等.槲寄生碱抗肝癌作用实验研究[J].实用中医药杂志,2004, 20(5):227.
    [32]余建强,蒋袁絮.槐定碱,氧化槐定碱的药理学研究进展[J].宁夏医学院学报,2005,27(1):78-80.
    [33]杨秀伟,冉福香,吴军,等.马钱子生物碱成分的体外抗肿瘤活性筛选[J].中国现代中药,2006,8(9):11-13.
    [34]徐立生,曲长芝.抗癌药巴豆生物碱、顺铂对红细胞膜的作用[J].中华肿瘤杂志,1995,17(2):115.
    [35]陶上乘,王静珍.苦豆子生物碱的药理作用[J].中国药学杂志,1992,27(4):201.
    [36]路岐祥,谭焕然.苦参碱等五种单体生物碱影响免疫功能的探讨[J].上海免疫学杂志,1987,7(6):335.
    [37]杨秀伟,冉福香,王瑞卿,等.44种生物碱类化合物对人胃癌细胞株BGC和人肝癌细胞株BEL-7402细胞增殖抑制活性的筛选[J].中国现代中药,2007,9(2):6-9.
    [38]杨秀伟,冉福香,王瑞卿,等.44种生物碱类化合物对人鼻咽癌细胞株KB和人白血病细胞株HL-60细胞增殖抑制活性的筛选[J].中国现代中药,2007,9(1):8-13.
    [39]杨秀伟,王瑞卿,冉福香,等.26种生物碱类化合物对人乳腺癌细胞系BCAP细胞株增殖抑制活性的筛选[J].中国现代中药,2007,9(3):9-11.
    [40]毛雪石.黄酮类化合物的抗肿瘤活性[J].国外医学药学分册,1995,22(2):92-96.
    [41]Chang L C,Gerhauser C,Song L,et al.Activity-guide isolation of constituents ofTephrosia purpureawith thpotential to induce the phase Ⅱ enzyme,quinone,reductas[J].J Nat Prod,1997,60(9):869-873.
    [42]Snait Tamira,Mark Eizenberg.Estrogen-like Activity of Glabrene and other Constituents Isolated from Licorice Root[J].Journal of Steroid Biochemistry & Molecular Biology,2001,78:291.
    [43]Kimberly M Jackson,Marisela DeLeon.Dibenzoylmethane induces Cell Cycle Deregulation in Human Prostate Cancer Cells[J].Cancer Letters.2002,178-161.
    [44]Bianca Fuhrman,Nina Volkova.Antiatherosclerotic Effects of Licorice Extracts Supplementation on Hypercholesterolemic Patients;Increased Resistance of LDL to Atherogenic Modifications,Reduced Plasma Lipid Levels,and Decreased Systolic Blood Pressure[J].Nutrition,2002,18:268.
    [45]钱士辉,王价先,杨念云,等.陈皮提取物体内抗肿瘤作用及其对癌细胞增殖周期的影响[J].中国中药杂志,2003,28(12):167-170.
    [46]李兰英,彭蕴汝,钱士辉,等.陈皮多甲氧基黄酮类成分对人肝癌SMMC-7721、HepG2细胞株增殖的影响[J].中药材,2007,30(3):324-326.
    [47]Sonoda M,Nishiyama T,Matsukwa Y.Cytotoxic activities of flavonoids from two Scutellaria plants in Chinese medicine[J].J Ethnopharmc -ol,2004,91(1):65-8.
    [48]王婷,张金超,陈瑶,等.6种淫羊藿黄酮抗氧化和抗肿瘤活性的比较[J].中国中药杂志,2007,32(8):8-11.
    [49]Shen SC,Chen YC,Hsu FL,et a.l Differential apoptosis-inducing effect of quercetin and itsglycosidesin human promyeloleukemic HL-60 cells by alternative activation of the caspase 3cascade[J].Journal of Cellular Biochemistry,2003,89(5):1044-55.
    [50]Miyata Y,Sato T,Yano M,et a.l Activation of protein kinase C betall/epsilon-c-Jun NH 2-term in alkinase pathway and inhibition Of mitogen-activated protein/extracellular signal-regulated kinasel/2 phosphoryla-tion in antitumor invasive activity induced by the polymethoxy fl[J].Molecular Cancer Therapeutics,2004,3(7):839-47.
    [51]Fu Y,Hsieh TC,Guo J,et a.l Licochalcone-A,a novel flavonoid isolated from licorice root (Glycyrrhiza glabra),causes G2 and late-G1 arrests in androgen-independentPC-3 prostate cancer cells[J].Biochemical& Biophysical Research Communications,2004,322(1):263-70.
    [52]Liu JJ,Huang TS,ChengWF,et a.l Baicalein and baicalin are potent inhibitors of angiogenesis:Inhibition of endothelial cell proliferation,migration and differentiation[J].International Journal ofCancer,2003,106(4):559-65.
    [53]ImaiY,Tsukahara S,Asada S,eta.l Phytoestrogens/flavonoids re-verse breast cancer resistance protein/ABCG2-mediated multi-drug resistance[J].CancerResearch,2004,64(12):4346-52.
    [54]黄云虹,甄永苏.大黄酸诱导肿瘤细胞凋亡及丝裂霉素的协同作用[J].药学学报,2001,36(5):334-338.
    [55]Lee HZ,Hsu S L,Liu M C,et al.Effects and mechanisms of aioe-emodin on cell death in human lung squamous cell carcinoma[J].European Journal of Pharmacology,2001,431(3):287-295.
    [56]Lee HZ.Protein Kinase C in aloe-emodin and emodin-iduced apoptisis in lung carcinoma cell[J].British Journal of Pharmacology,2001,134(5):1093-1103.
    [57]Lee HZ.Effects and mechanism of emodin on cell death in human lung sqamous cell[J].British Journal of Pharmacology,2001,134(1):11-20.
    [58]Chen Y C,Shen S C,Lee E R,et al.Emodin induces apoptosis in human promyeloeukemicHL-60 cells accompanied by aclivation of caspase 3cascade but independent of reactive oxygen species producion[J].Biochemical Pharmacology,2002,64(12):1713-1724.
    [59]Jing X B,Ueki N,Cheng J D,et al.Induction of apoptosis in hepatocellular carcinoma cell lines by emdion[J].Japanese Journal of Cancer Research,2002,93(8):874-882.
    [60]Po-liu Kuo,Ta-Chen Liu,Chun-Ching Liu.The antiproliferative activity of aloe-emodin is through p53dependent and p21-dependent apoptptic patheay in human hepatoma cell lines[J].Japanese Journal of Cancer Research,2002,71(16):1879-1892.
    [61]Srinivas G,Anto RJ,Srinivas P,et al..Emodin induces apoptosis of human cervical cancer cells though poly(APD-ribose) polymerase cleavage and activation of caspase-9[J].Eur JPharmacol,2003,473:117.
    [62]Po-liu Kuo,Ta-Chen Liu,Chun-ehing Liu,et al.lnduction of cytochromes P450|A| and |B| by emodin in human lung adenocarcinoma cell line CLS[J].DrugMetabolism and Disposition,2001,29(9):1 229-1 235.
    [63]Wurm G,Grimm H,Geres U.Plumbagin:reactivity,toxicity,and antimicrobial activity of aDrosera and Plumbagonatural substances[J].Dtsch Apoth Ztg,1984,124(43):2128-2132.
    [64]Srinivas P,Gopinath G,Banerji A.Plumbagin induces reactive oxygen species which mediate apoptosis in human cervical cancer cells[J].Mol Carcinog,2004,40:201-211.
    [65]姜晓峰,甄永苏.大黄素抑制人高转移巨大细胞肺癌PG细胞的肿瘤转移相关性质[J].癌症,2001,20(8):789.
    [66]Chang CJ,Ashendel CL,Geahlen RL,et al..Oncogene signal transduction inhibitions from medical plants[J].InVivo,1996,10(2):185.
    [67]Jayasuriya H,Koonchanok NM,Geahlen RL,et al.Emodin,a protein tyrosine kinase inhibitor from polygonum cuspidatum[J].JNat Prod,1992,55:696.
    [68]Zhang L,Lau YK,Xi L,et al..Tyrosine kinase inhbitiors emodin and its derivative repress HER-2/neu-induced cellular transformation and metastasis- associate properties[J].Oncogene,1998,16(22):2855.
    [69]Zhang L,Lau YK,Xia W,et al..Tyrosine kinase inhibitiors emodin suppresses growth of HER-2/neu-over expressing breast cancer cells in athymic mice and senstizes these cells to the inhibitory effect of paclitaxel[J].Oncogene,1998,16(22):2855.
    [70]Chan TCK,Chang CJ,Koonchanok NM,et al..Selective inhibition of the growth of ras-transformed humabronchial epithelial cells by emodin,a protein-tyrosine knase inhibitor[J].Biochem Biophys Res Commun,1993193(3):1152.
    [71]Kabsroski NK,Gibbons DL.BCR-ABL kinase activation confers increased resistance to genotoxic damage via cecycle block[J].Oncogene,1996,13:2 225.
    [72]王新华,甄永苏.大黄素抑制人高转移巨细胞肺癌PG细胞的肿瘤转移相关性质[J].癌症,2001,20(8):789.
    [73]徐丽敏,陈学荣,毛舒和.大黄素和大黄酸对Cdo-1细胞株的影响[J].中华皮肤科杂志,2000,33(1):47.
    [74]徐丽敏,陈学荣,毛舒和.大黄素和大黄酸对角质形成细胞体外培养细胞周期的影响[J].临床皮肤科杂志,2000,29(3):153.
    [75]刘睿,顾谦群,崔承彬,等.密脉鹅掌柴的化学成分及其抗肿瘤活性[J].中草药,2005,36(3):328-332.
    [76]韩洁,翁新楚,毕开顺.紫草中活性成分的体外抗癌作用[J].精细化工,2007,24(5):473-477.
    [77]Kagedal K,Bironaite D,Dllinegor K,et al.Anthraguinone cytotoxicity and apoptosis in primary calture of rat heputocytes[J].Free Radic Res,1999,31(5):419.
    [78]徐丽敏,毛舒和.大黄酸对Cdo-16细胞线粒体的作用[J].天津医科大学学报,1996,5(4):109.
    [79]苏云明,吴波,王莉.芦荟抗肿瘤作用研究[J].黑龙江中医药大学学报,2002,15(3):181.
    [80]Jae SC,Hee JL,Kun YP,et al.In vivoantimuta genic etlectss of anthraquinone aglycones and naphthopyrone glycosides from Cassia tora[J].Planta Medica 1997,63:11.
    [81]李继成,林则田,张启堂,等.内折香茶菜素和内折香茶菜素D抗肿瘤作用的实验研究[J].中草药,2001,32(11):49.
    [82]李继成,杨丽嘉,刘兰琦,等.内折香茶菜乙素抗肿瘤作用的研究[J].中草药,2000,31(9):681.
    [83]李继成,袁宝梅,苏金玲,等.内折香茶菜抗癌成分的研究[J].河南医科大学学报,1996,31(1):64.
    [84]刘桂芳,娄政钢,乌淑香.狼毒大戟的化学成分研究[J].中草药,1989,20(7):2-4.
    [85]Jia Z J,Ding Y L,Wang Q G,et al.Advance in the research of pharmacological actions of Euphorbiaceae[J].Phytochemistry,1990,29(2):343.
    [86]Wan J Z,Dao F C,Ai J H.Two novel myrinsol diterpenes from euphorhiaprolifer[J].Chinese Chemical Letters,2002,13(8):744-747.
    [87]Bloch S,Stevigny C,Depauw GMC,et al.Enttrachyuloban-3 β-ol,a new cytotoxic diterpene from croton zambesicus[J].Planta.Med.,2002,68(7):647-649.
    [88]Ei-Mokkawy S,Meselhy M R,Nakamura N,et al.12-Oacetylphorhol-13-decan-oate potently inhibitors cytopathic effects of hunman immunodeficiency virus type 1(HIV-1),with activation of protein kinase C[J].Chem.Pharm.Bull.1999,47(9):1346-1347.
    [89]Toth JO,Luu Bang et Guy Orisson,Les acides ganoderiques T Z:triterpenes cytotoxiques de Ganoderma lucidum(Polyporacee)[J].Tetrahedron Lett,1983,24(10):1081.
    [90]Lin CN,Tome WP.Novel cytotoxic principles of Formosan Ganoderma lucidum[J].Chem Pharm Bull,1989,37(2):531-533.
    [91]Huang SM,Yang XL,Wang BW,et al.Antitumor activity of ethanol -soluble and acidic components from Ganoderma lucidum[J].Nat Pro Res Dev,2004,16(2):146-148.
    [92]Zhao W Z,Frank E,Liu H Y,et al.Boswellic acid acetateInduces differentiation and apoptosis in highly metastatic Melanoma and fibrosarcoma cells[J].CancerDe -tectPrev,2003,27:67-75.
    [93]李铁军,邱彦,芮耀诚,等.糙叶败酱中新的环烯醚萜苷元成分体外抗肿瘤作用研究[J].解放军药学学报,2004,20(2):101-102.
    [94]毛俊琴,李铁军,邱彦,等.糙叶败酱中环烯醚萜苷元成分抗结肠癌作用的实验研究[J].药学实践杂志,2007,25(1):10-12.
    [95]何萍,李帅,王素娟,等.半夏化学成分的研究[J].中国中药杂志,2005,30(9):671-674.
    [96]杨光忠,李援朝.雷公藤抗肿瘤三萜成分的研究[J].林产化学与工业,2006,26(4):19-22.
    [97]杨燕军,陈慧云,林洁红,等.枫香槲寄生化学成分及抗肿瘤活性研究[J].广州中医药大学学报,2007,24(2):158-161.
    [98]姜彬慧,杨万春,赵余庆.绞股蓝抗肿瘤作用研究现状[J].中药材,2003,26(9):683-686.
    [99]张晓,李金华,何承伟,等.半边旗二萜类化合物的植化及抗肿瘤活性初步研究[J].中国药学杂志,1999,34(8):512.
    [100]崔燎,张晓,梁念慈,等.一种新二萜类化合物的体外抗肿瘤作用研究[J].中国药理学通报,1998,14(1):50.
    [101]何太平,严卫红,莫丽儿,等.半边旗提取物5F对高转移卵巢癌细胞HO-8910PM细胞增殖的影响及作用机制的实验研究[J].海南医学院学报,2006,12(1):20.
    [102]兰柳波,梁念慈,莫立几,等.半边旗抗肿瘤有效成分5F的纯化及其体外增效作用[J].中国药理学通报,2003,19(7):804.
    [103]何承伟,梁念慈,莫丽几,等.半边旗抗肿瘤有效成分6F对HL-60细胞周期的影响及体外增效作用[J].癌症,1998,17(3):191.
    [104]Cheung HY,Cheung SH,Li J,et al.Andrographolide isolated from Andrographis paniculata induces cell cycle arrest and mitochondrial-mediated apoptosis in human leukemic HL-60cells[J].Planta Med,2005,71(12):1106-1111.
    [105]Kumar RA,Sridevi K,Kumar NV,et al.Anticancer and immunostimulatory compounds from Andrographis paniculata[J].J Ethnopharmacol,2004,92(2-3):291-295.
    [106]Rajagopal S,Kumar RA,Deevi DS,et al.Andrographolide,apotential cancer therapeutic agent isolated from Andrographis paniculata[J].J Exp Ther Oncol,2003,3(3):147-158.
    [107]张富赓,胡人杰,张韶瑜,等.轮叶婆婆纳中二萜类化学成分的体外抗癌活性研究[J].中草药,2005,36(10):1520-1523.
    [108]Hideyuki Ito,Eri Kobayashi,YoshieTakamatsu.Polyphenols from Eriobotrya japonicaand their cytotoxicity against human oral tumor cell lines[J].ChemPharm -Bull,2000,48(5):687-693.
    [109]薛存宽,何学斌,张书勤,等.缬草环烯醚萜抗肿瘤作用的实验研究[J].实用中西医结合杂志,2005,14(15):1969-1972.
    [110]Tang W,Liu JW,Zhao WM,et al.Ganoderic acid T from Ganoderma lucidum mycelia induces mitochondda mediated apoptosis in lung cancer cells[J].Life Sci,2006,6[epubahead of print]
    [111]黄龙,张如松,王彩芳,等.白花败酱化学成分研究[J].中药材,2007,30(4):415-417.
    [112]张维文,黎银燕,张贵平,等.熊果酸诱导人乳腺癌细胞MCF-7凋亡的实验研究[J].中药材,2005,28(4):297-301.
    [113]JingYK,NakajoS,XiaLJ,etal.Boswellic acid acetate induces differentiation and apoptosis in leukemia cell lines[J].Leuk Res,1999,23:43-50.
    [114]Smith-Kielland I,Dornish J M,Malterud K E,et alCytotoxic triterpenoids from the leaves ofEuphorbi pulcherrima[J].Plant Med,1996,62(4):322-325.
    [115]林忠宁,林育纯,SHEN Han-ming,等.菊花倍半萜烯内酯诱导人鼻咽癌细胞毒性和凋亡的研究[J].中草药,2002,33(10):909-912.
    [116]高小平,李伯刚,周建,等.W雷公藤内酯醇体外抗肿瘤作用和诱导细胞凋亡的研究[J].天然产物研究与开发,2000,12(1):18.
    [117]范云双,姚智,腾杰,等.绿升麻中具有抗肿瘤活性的三萜类化合物[J].中草药,2007,38(2):167-170.
    [118]张曼颖,等.刺五加叶皂甙诱导肺癌细胞凋亡的研究[J].吉林大学学报(医学版),2002,28(1):37.
    [119]叶红军,等.刺五加叶皂甙诱发肝癌细胞凋亡的研究[J].临床肝胆病杂志,2002,18(3):162.
    [120]徐从立,陈海生,谭兴起,等.中药天冬的化学成分研究[J].天然产物研究与开发,2005,17(2):128-130.
    [121]张乃哲,等.抑凋谢基因bcl-2蛋白在大鼠实验性肝癌发病过程中的表达[J].实用肿瘤杂志,1999,14(1):11.
    [122]张乃哲,等.N-乙酰氨基葡萄糖转移酶Ⅲ在大鼠实验性肝癌发病中表达[J].中国实验动物学报,1997,5(2):120.
    [123]朱慧明,吴铁,崔燎,等.半边旗多糖对肺腺癌SPCA-1细胞的诱导凋亡作用[J].中国新医药,2003,2(12):1.
    [124]范玉琳,邢增涛,卫功庆,等.鹿茸蛋白的提取分离及其抗肿瘤活性[J].经济动物学报,1998,2(1):27-31.
    [125]刘睿,顾谦群,崔承彬,等.长叶水麻的三个酚酸类化学成分及其抗肿瘤活性[J].中国药物化学杂志,2004,14(4):193-196.
    [126]怡悦.关于肿瘤细胞增殖抑制成分的研究(15):臭梧桐及臭牡丹叶的活性成分[J].国外医药(中医中药分册),2002,24(4):247.
    [127]SCHEMPP C M,KIRKIN V,SIMONHAARHAUS B,et al.Inhibition of tumor cell growth by hyperforin,a novel anticancerdrug from St.John's wort that acts by induction of apoptosis[J].Oncogene,2002,21(8):1242-1250.
    [128]KATARINAHOSTANOKA,JUERGENREICHLING,SILVIABOMMER,etal.Hyperforin a constitu -ent of St.John's wort(hypericumperforatum L.)extract induces apoptosis by triggering activation of caspases and with hypericin synergisticaly exerts cytotoxicity towards human malignant cell lines[J].European Journal of Pharmaceutics and Biopharma -ceutics,2003,56:121-132.
    [129]陈铁晖,严国鸿,陈华.姜黄的化学成分及抗肿瘤作用研究进展[J].海峡预防医学杂志,2004,10(6):23-25.
    [130]刘睿,顾谦群,崔承彬,等.密脉鹅掌柴的化学成分及其抗肿瘤活性[J].中草药,2005, 36(3):328-332.
    [131]范玉琳,邢增涛,卫功庆,等.鹿茸蛋白的提取分离及其抗肿瘤活性[J].经济动物学报,1998,2(1):27-31.
    [132]孔景临,杜秀宝,范崇旭,等.一种槲寄生多肽的一级结构分析和抗肿瘤活[J].药学学报,2004,39(10):813-817.
    [133]吕萍,陈兴勇,赵宗阁,等.蛇毒抗肿瘤蛋白化学成分的研究[J].药物生物技术,2007,14(4):287-290.
    [134]魏少荫,李敏.大蒜活性成分阿藿烯的抗肿瘤作用研究进展[J].中草药,2006,37(9):1430-1433.

© 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