The traditional medical uses and cytotoxic activities of sixty-one Egyptian plants: Discovery of an active cardiac glycoside from Urginea maritima

被引:95
作者
El-Seedi, Hesham R. [1 ,2 ]
Burman, Robert [1 ]
Mansour, Ahmed [3 ]
Turki, Zaki [4 ]
Boulos, Loutfy [5 ]
Gullbo, Joachim [6 ]
Goransson, Ulf [1 ]
机构
[1] Uppsala Univ, Biomed Ctr, Dept Med Chem, Div Pharmacognosy, S-75123 Uppsala, Sweden
[2] Menoufia Univ, Fac Sci, Dept Chem, Shibin Al Kawm 32512, Egypt
[3] St Catherine, Sinai, Egypt
[4] Menoufia Univ, Fac Sci, Dept Bot, Shibin Al Kawm 32512, Egypt
[5] Univ Alexandria, Fac Sci, Dept Bot, Alexandria 21561, Egypt
[6] Uppsala Univ, Dept Med Sci, Div Clin Pharmacol, S-75185 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
Egyptian medicinal plants; Anticancer screening; Cardiac glycoside; Urginea maritima; FMCA assay; MEDICINAL-PLANTS; NATURAL-PRODUCTS; ETHNOPHARMACOLOGICAL SURVEY; TOPOISOMERASE-I; DRUG DISCOVERY; BUFADIENOLIDES; VITRO; CAMPTOTHECIN; STRATEGIES; ALKALOIDS;
D O I
10.1016/j.jep.2012.12.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Medicinal plants from the Sinai desert are widely used in traditional Bedouin medicine to treat a range of conditions including, cancers, and may thus be useful sources of novel anti-tumor compounds. Information on plants used in this way was obtained through collaboration with Bedouin herbalists. Aim of the study: To document the traditional uses of 61 species from 29 families of Egyptian medicinal plants and to investigate their biological activity using a cytotoxicity assay. Material and methods: MeOH extracts of the 61 plant species investigated were dissolved in 10% DMSO and their cytotoxic activity was evaluated. The extracts were tested in duplicate on three separate occasions at three different concentrations (1, 10 and 100 mu g/ml) against human lymphoma U-937 GTB. The most active extract was subjected to bioassay-guided fractionation using HPLC and LC/ESI-MS to isolate and identify its active components. Results and discussion: The most potent extracts were those from Asclepias sinaica, Urginea maritima, Nerium oleander and Catharanthus roseus, followed by those from Cichorium endivia, Pulicaria undulate and Melia azedarach. Literature reports indicate that several of these plants produce cardiac glycosides. Bioassay-guided fractionation of alcoholic U. maritima extracts led to the isolation of a bioactive bufadienolide that was subsequently shown to be proscillaridin A, as determined by 1D and 2D NMR spectroscopy. This result demonstrates the value of plants used in traditional medicine as sources of medicinally interesting cytotoxic compounds. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:746 / 757
页数:12
相关论文
共 89 条
[1]   A cardenolide glycoside from Gomphocarpus sinaicus [J].
Abdel-Azim, NS .
PHYTOCHEMISTRY, 1998, 49 (01) :273-275
[2]   Potential antimalarials from Nigerian plants: A review [J].
Adebayo, J. O. ;
Krettli, A. U. .
JOURNAL OF ETHNOPHARMACOLOGY, 2011, 133 (02) :289-302
[3]  
Ahmad SS, 2007, PAK J BOT, V39, P355
[4]   Ethnopharmacological survey of wild medicinal plants in Showbak, Jordan [J].
Al-Qura'n, S. .
JOURNAL OF ETHNOPHARMACOLOGY, 2009, 123 (01) :45-50
[5]   Screening of vincristine yield in ex vitro and in vitro somatic embryos derived plantlets of Catharanthus roseus L. (G) Don. [J].
Aslam, Junaid ;
Mujib, Abdul ;
Nasim, Seikh A. ;
Sharma, Maheshwar Prasad .
SCIENTIA HORTICULTURAE, 2009, 119 (03) :325-329
[6]   The state of the art of traditional Arab herbal medicine in the eastern region of the Mediterranean: A review [J].
Azaizeh, Hassan ;
Saad, Bashar ;
Khalil, Khalid ;
Said, Omar .
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2006, 3 (02) :229-235
[7]   Drug discovery from medicinal plants [J].
Balunas, MJ ;
Kinghorn, AD .
LIFE SCIENCES, 2005, 78 (05) :431-441
[8]  
Batanouny K.H., 1999, WILD MED PLANTS EGYP, P173
[9]   Inhibition of DNA topoisomerases I and II, and growth inhibition of breast cancer MCF-7 cells by ouabain, digoxin and proscillaridin A [J].
Bielawski, Krzysztof ;
Winnicka, Katarzyna ;
Bielawska, Anna .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (07) :1493-1497
[10]  
Bnouham M., 2002, Dubai Diabetes Endocrinol J, V10, P33, DOI [10.1159/000497550, DOI 10.1159/000497550]