期刊论文详细信息
BMC Complementary and Alternative Medicine
Antiangiogenesis and antioxidant activity of ethanol extracts of Pithecellobium jiringa
Zhari Ismail3  AminMalikShahAbdul Majid1  Norshirin Idris1  Armaghan Shafaei3  Abdalrahim FA Aisha3  Zeyad D Nassar2  Nahdzatul Syima Muslim1 
[1] EMAN Testing & Research Laboratory, Department of Pharmacology, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Minden, Penang 11800, Malaysia;School of Pharmacy, University of Queensland, Brisbane, QLD, Australia;Department of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Minden, Penang 11800, Malaysia
关键词: Phytochemical analysis;    Antioxidant;    Antiangiogenesis;    Pithecellobium jiringa;   
Others  :  1231510
DOI  :  10.1186/1472-6882-12-210
 received in 2012-04-16, accepted in 2012-10-31,  发布年份 2012
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【 摘 要 】

Background

Angiogenesis plays a critical role in embryonic development and various physiological processes. However, excessive angiogenesis is associated with several pathological conditions including cancer. Pithecellobium jiringa (Jack) Prain is a traditional medicinal plant from the family Leguminosae. It is native to the Southeast Asia, where it has been used traditionally for treatment of various ailments such as hypertension and diabetes. The present work is aimed to study antioxidant and antiangiogenesis activities of P. jiringa ethanol extracts.

Methods

P. jiringa fruit rinds were extracted with ethanol and 50% ethanol. The antioxidant property was analysed using, 1,1-diphenyl-2-picryl-hydrazyl free radical scavenging assay. Phytochemical analysis was performed using thin layer chromatography and colorimetric methods. Then, cell growth inhibition was studied against a panel of human cell lines by MTT test. In vitro inhibition of angiogenesis was studied by the following assays: isolated rat aortic rings cell viability, colony formation, endothelial cell migration, endothelial tube formation on matrigel, and expression of vascular endothelial growth factor by endothelial cells. In vivo antiangiogenesis effect was studied by utilising fertilised chick embryos assay. The results were statistically analysed by analysis of variance.

Results

Ethanolic and 50% hydro-ethanolic extracts showed relatively high concentration of total phenolics associated with potent antioxidant activity. The rat aortic rings study conducted showed potent inhibition of the microvessels outgrowth with IC50s 5.27 ± 0.81 μg/ml (ethanolic) and 4.45 ± 0.63 μg/ml (50% hydro-ethanolic). Both extracts arrested the growth of human endothelial cells via down-regulation of VEGF expression, leading to inhibition of other angiogenesis cascades including migration of endothelial cells, and formation of capillary network on matrigel matrix. The extracts also inhibited the neovascularisation of chick embryo chorioallantoic membrane.

Conclusions

P. jiringa extracts inhibit angiogenesis by blocking the VEGF expression thus inhibiting endothelial cells proliferation, migration and differentiation most likely due to presence of the antioxidant phenolics.

【 授权许可】

   
2012 Muslim et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Folkman J: What is the evidence that tumors are angiogenesis dependent? J Natl Cancer Inst 1990, 82(1):4.
  • [2]Folkman J: Tumor Angiogenesis: Therapeutic Implications. N Engl J Med 1971, 285(21):1182-1186.
  • [3]Folkman J: Angiogenesis and apoptosis. Semin Cancer Biol 2003, 13(2):159-167.
  • [4]Fernández-Pachón M, Villano D, García-Parrilla M, Troncoso A: Antioxidant activity of wines and relation with their polyphenolic composition. Anal Chim Acta 2004, 513(1):113-118.
  • [5]Hc-C C, Lo Y-J, Lu F-J: Xanthine Oxidase Inhibitors from the Leaves of Alsophila Spinulosa (HOOK) Tryon. J Enzyme Inhib Med Chem 1994, 8(1):61-71.
  • [6]Cos P, Ying L, Calomme M, Hu JP, Cimanga K, Van Poel B, Pieters L, Vlietinck AJ, Berghe DV: Structure-Activity Relationship and Classification of Flavonoids as Inhibitors of Xanthine Oxidase and Superoxide Scavengers. J Nat Prod 1998, 61(1):71-76.
  • [7]Cao Y, Cao R: Angiogenesis inhibited by drinking tea. Nature 1999, 398(6726):381-381.
  • [8]Lamy S, Blanchette M, Michaud-Levesque J, Lafleur R, Durocher Y, Moghrabi A, Barrette S, Gingras D, Béliveau R: Delphinidin, a dietary anthocyanidin, inhibits vascular endothelial growth factor receptor-2 phosphorylation. Carcinogenesis 2006, 27(5):989.
  • [9]Sartippour MR, Shao ZM, Heber D, Beatty P, Zhang L, Liu C, Ellis L, Liu W, Go VL, Brooks MN: Green tea inhibits vascular endothelial growth factor (VEGF) induction in human breast cancer cells. J Nutr 2002, 132(8):2307.
  • [10]Lamy S, Gingras D, Béliveau R: Green tea catechins inhibit vascular endothelial growth factor receptor phosphorylation. Cancer Res 2002, 62(2):381.
  • [11]Barceloux DG: Djenkol Bean [Archidendron jiringa (Jack) I. C. Nielsen]. In Medical Toxicology of Natural Substances: Foods, Fungi, Medicinal Herbs, Toxic Plants, and Venomous Animals. John Wiley & Sons, Inc, Hoboken, New Jersey; 2008:59-61.
  • [12]Zakaria M, Ali Mohd M: Traditional Malay Medicinal Plants. Institut Terjemahan Negara Malaysia Berhad, Kuala Lumpur; 2010.
  • [13]Mohd Azizi CY, Nik Norulaini NA, Wahyu BS, Mohd Omar AK: Supercritical carbon dioxide extraction of constituents of pithecellobium jiringan seeds and their identification using time of flight gas spectrometry. 2006.
  • [14]Norulaini NANIK, Zaidul ISM, Azizi CYM, Zhari I, Noramin MN, Sahena F, Omar AKM: Supercritical carbon dioxide fractionation of pithecellobium jiringan jack seed compositions using fast gas chromatography time of flight mass spectrometry. J Food Process Eng 2010, 34(5):1746-1758.
  • [15]Brown KJ, Maynes SF, Bezos A, Maguire DJ, Ford MD, Parish CR: A novel in vitro assay for human angiogenesis. Lab Investig 1996, 75(4):539-555.
  • [16]Nicosia RF, Lin YJ, Hazelton D, Qian X: Endogenous regulation of angiogenesis in the rat aorta model. Role of vascular endothelial growth factor. Am J Pathol 1997, 151(5):1379.
  • [17]Mosmann T: Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J Immunol Methods 1983, 65(1–2):55-63.
  • [18]Franken NAP, Rodermond HM, Stap J, Haveman J, van Bree C: Clonogenic assay of cells in vitro. Nat Protocols 2006, 1(5):2315-2319.
  • [19]Liang CC, Park AY, Guan JL: In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro. Nat Protoc 2007, 2(2):329-333.
  • [20]Bandyopadhyay A, YONG Z, Malik SN, Kreisberg J, Brattain MG, Sprague EA, JIAN L, Lopez-Casillas F, Sun LZ: Extracellular domain of TGFÎ2 type III receptor inhibits angiogenesis and tumor growth in human cancer cells. Oncogene 2002, 21(22):3541-3551.
  • [21]West DC, Thompson WD, Sells PG, Burbridge MF: Angiogenesis assays using chick chorioallantoic membrane. Methods Mol Med 2001, 46:107-130.
  • [22]Nassar ZD, Aisha AFA, Ahamed MBK, Ismail Z, Abu-Salah KM, Alrokayan SA, Majid AMSA: Antiangiogenic properties of Koetjapic acid, a natural triterpene isolated from Sandoricum koetjaoe Merr. Cancer Cell International 2011, 11(1):12. BioMed Central Full Text
  • [23]Sharma OP, Bhat TK: DPPH antioxidant assay revisited. Food Chem 2009, 113(4):1202-1205.
  • [24]Trease G, Evans W: Pharmacognosy, 12* edition. English Language Book Society/Bailliere Tindall 1983., 1
  • [25]Lizcano LJ, Bakkali F, Begoña Ruiz-Larrea M, Ignacio Ruiz-Sanz J: Antioxidant activity and polyphenol content of aqueous extracts from Colombian Amazonian plants with medicinal use. Food Chem 2010, 119(4):1566-1570.
  • [26]Kosalec I, Bakmaz M, Pepeljnjak S, Vladimir-Knezevic S: Quantitative analysis of the flavonoids in raw propolis from northern Croatia. Acta Pharm 2004, 54(1):65-72.
  • [27]Houghton P, Howes MJ, Lee C, Steventon G: Uses and abuses of in vitro tests in ethnopharmacology: visualizing an elephant. J Ethnopharmacol 2007, 110(3):391-400.
  • [28]Olsson ME, Gustavsson KE, Andersson S, Nilsson Ã, Duan RD: Inhibition of cancer cell proliferation in vitro by fruit and berry extracts and correlations with antioxidant levels. J Agric Food Chem 2004, 52(24):7264-7271.
  • [29]Cai Y, Luo Q, Sun M, Corke H: Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer. Life Sci 2004, 74(17):2157-2184.
  • [30]Yang CS, Landau JM, Huang MT, Newmark HL: Inhibition of carcinogenesis by dietary polyphenolic compounds. Annu Rev Nutr 2001, 21(1):381-406.
  • [31]Tapiero H, Tew K, Nguyen Ba G, Mathe G: Polyphenols: do they play a role in the prevention of human pathologies? Biomed Pharmacother 2002, 56(4):200-207.
  • [32]Murakami A, Ali AM, Mat-Salleh K, Koshimizu K, Ohigashi H: Screening for the in vitro anti-tumor-promoting activities of edible plants from Malaysia. Biosci Biotechnol Biochem 2000, 64(1):9-16.
  • [33]Eccles SA, Court W, Patterson L, Sanderson S: In Vitro Assays for Endothelial Cell Functions Related to Angiogenesis: Proliferation, Motility, Tubular Differentiation, and Proteolysis. In Methods in Molecular Biology, Angiogenesis Protocols. 467th edition. Edited by Martin S, Murray C. Humana Press, Clifton, New Jersey; 2009:159-181.
  • [34]Kondo T, Ohta T, Igura K, Hara Y, Kaji K: Tea catechins inhibit angiogenesis in vitro, measured by human endothelial cell growth, migration and tube formation, through inhibition of VEGF receptor binding. Cancer Lett 2002, 180(2):139-144.
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