In vitro antioxidant, immunomodulatory and anticancer activities of two fractions of aqueous extract from Helicteres angustifolia L. root

被引:11
作者
Li, Kejuan [1 ]
Yang, Xi [1 ]
Hu, Xuansheng [1 ]
Han, Chao [1 ]
Lei, Zhongfang [1 ]
Zhang, Zhenya [1 ]
机构
[1] Univ Tsukuba, Grad Sch Life & Environm Sci, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058572, Japan
关键词
Immunomodulatory; Macrophages; Cytotoxic; Anticancer; Antioxidant; SOYBEAN CURD RESIDUE; GANODERMA-LUCIDUM; POLYSACCHARIDES; STERCULIACEAE; CONSTITUENTS; MACROPHAGES; DERIVATIVES; EXPRESSION; MECHANISM; APOPTOSIS;
D O I
10.1016/j.jtice.2015.12.022
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Helicteres angustifolia L. (H. angustifolia) has been widely used in traditional Chinese medicine system to treat a variety of diseases including cancer. In order to characterize the bioactivities of H. angustifolia, we first obtained the aqueous root extract (ARE) which was then further partitioned into two fractions, namely ethanol fraction (EF) and water fraction (WF), and their antioxidant, immunomodulatory and anticancer activities were evaluated respectively. Results indicated that both EF and WF possessed strong antioxidant activities, and EF was the major component to exhibit the cytotoxic activity in ARE with IC50 values of (33.98 +/- 1.58) and (35.56 +/- 0.42) mu g/ml against human lung cancer cell lines A549 and H1299 for 72 h treatment, respectively. As for immunomodulatory activities, WF was shown to stimulate the proliferation of macrophages (292.76 +/- 31.42%) and phagocytic activity at 12.5 mu g/ml, and increase the production of nitric oxide. Furthermore, WF was also observed to significantly mitigate doxorubicin (DOX) induced toxicity (from 18.42% to 63.63%) and apoptosis (from 90.8% to 57.5%) at 100 mu g/ml, respectively. The above findings highlight the functional characteristics of WF and EF in their contribution to the anticancer activities of ARE, which also provides important scientific evidence for developing ARE as a potent anticancer reagent. (C) 2015 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 82
页数:8
相关论文
共 29 条
[1]   Iron-chelation properties of phenolic acids bearing catechol and galloyl groups [J].
Andjelkovic, M ;
Van Camp, J ;
De Meulenaer, B ;
Depaemelaere, G ;
Socaciu, C ;
Verloo, M ;
Verhe, R .
FOOD CHEMISTRY, 2006, 98 (01) :23-31
[2]  
Aziz MH, 2003, INT J ONCOL, V23, P17
[3]   IFN-γ primes macrophages for enhanced TNF-α expression in response to stimulatory and non-stimulatory amounts of microparticulate β-glucan [J].
Berner, MD ;
Sura, ME ;
Alves, BN ;
Hunter, KW .
IMMUNOLOGY LETTERS, 2005, 98 (01) :115-122
[4]   CONSTITUENTS OF FORMOSAN ANTITUMOR FOLK MEDICINE .3. A MANSONONE FROM HELICTERES-ANGUSTIFOLIA [J].
CHEN, CM ;
CHEN, ZT ;
HONG, YL .
PHYTOCHEMISTRY, 1990, 29 (03) :980-982
[5]   The isolation and identification of two compounds with predominant radical scavenging activity in hempseed (seed of Cannabis sativa L.) [J].
Chen, Tianpeng ;
He, Jinfeng ;
Zhang, Jianchun ;
Li, Xiaohui ;
Zhang, Hua ;
Hao, Jianxiong ;
Li, Lite .
FOOD CHEMISTRY, 2012, 134 (02) :1030-1037
[6]   Pregnane, coumarin and lupane derivatives and cytotoxic constituents from Helicteres angustifolia [J].
Chen, Wenliang ;
Tang, Weidong ;
Lou, Liguang ;
Zhao, Weimin .
PHYTOCHEMISTRY, 2006, 67 (10) :1041-1047
[7]   Cucurbitacin B 2-sulfate and cucurbitacin glucosides from the root bark of Helicteres angustifolia [J].
Chen, Zong-Tsi ;
Lee, Shwu-Woan ;
Chen, Chiu-Ming .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2006, 54 (11) :1605-1607
[8]   NEW FLAVOID GLYCOSIDES OF HELICTERES-ANGUSTIFOLIA [J].
CHEN, ZT ;
LEE, SW ;
CHEN, CM .
HETEROCYCLES, 1994, 38 (06) :1399-1406
[9]   Macrophage immunomodulatory activity of polysaccharides isolated from Glycyrrhiza uralensis fish [J].
Cheng, Anwei ;
Wan, Fachun ;
Wang, Jiaqi ;
Jin, Zhengyu ;
Xu, Xueming .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2008, 8 (01) :43-50
[10]   Cytotoxic lignans from the stems of Helicteres hirsuta collected in Indonesia [J].
Chin, YW ;
Jones, WP ;
Rachman, I ;
Riswan, S ;
Kardono, LBS ;
Chai, HB ;
Farnsworth, NR ;
Cordell, GA ;
Swanson, SM ;
Cassady, JM ;
Kinghorn, AD .
PHYTOTHERAPY RESEARCH, 2006, 20 (01) :62-65