Flavonoids and sesquiterpenes from Tecurium ramosissimum promote antiproliferation of human cancer cells and enhance antioxidant activity: A structure-activity relationship study

被引:89
作者
Ben Sghaier, Mohamed [2 ]
Skandrani, Ines [2 ]
Nasr, Nouha [2 ]
Franca, Marie-Genuieve Dijoux [3 ]
Chekir-Ghedira, Leila [1 ,2 ]
Ghedira, Kamel [2 ]
机构
[1] Fac Med Dent, Dept Cellular & Mol Biol, Lab Biol Cellulaire & Mol, Monastir 5000, Tunisia
[2] Fac Pharm, Unite Pharmacognosie Biol Mol 99 UR 07 03, Monastir 5000, Tunisia
[3] Univ Claude Bernard, Lab Botan Pharmacognosie & Phytotherapie, UMR Ecol Microbienne 5557, CNRS,Fac Pharm,Inst Sci Pharmaceut & Biol, F-69373 Lyon 08, France
关键词
Teucrium ramosissimum; Flavonoids; Sesquiterpene; Antioxidant activity; Antiproliferative effect; SCAVENGING ACTIVITY RELATIONSHIPS; LIPID-PEROXIDATION; TYROSINE KINASE; DIETARY POLYPHENOLS; NATURAL FLAVONOIDS; PHENOLIC-COMPOUNDS; QUERCETIN; APOPTOSIS; CAPACITY; INHIBITION;
D O I
10.1016/j.etap.2011.07.003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Fractionation of the chloroformic extracts from Teucrium ramosissimum leaves resulted in the isolation of three flavonoids: genkwanin (1), cirsimaritin (2) and 4',7-dimethoxy apigenin (4) and one sesquiterpene: beta-eudesmol (3). The structures were determined using data obtained from H-1 and C-13 NMR spectra, as well as by various correlation experiments (COSY, HMQC and HMBC). The antioxidant activities of the isolated flavonoids from T. ramosissimum leaves were evaluated by measuring their ability to scavenge the radical ABTS(+center dot) and through chemical assays: cupric reducing antioxidant capacity (CUPRAC), reducing power (RP) and ferric reducing antioxidant power (FRAP). Furthermore, the effects of T. ramosissimum isolated molecules, on inhibition of cell proliferation and induction of apoptosis in human leukemia cells, were also examined. Cirsimaritin showed the best activity in the ABTS assay with TEAC value 2.04 mu M, whereas apigenin and 4',7-dimethoxy apigenin exhibited the highest antioxidant activity using the CUPRAC, RP and FRAP assays with TEAC values 10.5, 1.39 and 0.71 mu M respectively. The cytotoxic activity revealed that the beta-eudesmol inhibited significantly the proliferation of K562 cells (IC50 = 20 mu g/ml). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:336 / 348
页数:13
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