Glycosidase inhibitory phenolic compounds from the seed of Psoralea corylifolia

被引:73
作者
Oh, Kyeong Yeol [1 ]
Lee, Jin Hwan [2 ]
Curtis-Long, Marcus J.
Cho, Jung Keun [1 ]
Kim, Jun Young [1 ]
Lee, Woo Song [3 ]
Park, Ki Hun [1 ]
机构
[1] GyeongSang Natl Univ, Grad Sch, Inst Agr & Life Sci, EB NCRC,Div Appl Life Sci,Program BK21, Jinju 660701, South Korea
[2] Minist Environm, NAKDONG River Basin Environm Off, Dept Monitoring & Anal, Chang Won 641722, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Bioind Res Ctr, Jeoungeup 580185, South Korea
基金
新加坡国家研究基金会;
关键词
Glycosidase; alpha-Glucosidase inhibitor; alpha-Mannosidase inhibitor; Psoralea corylifolia; GLYCOSYLATION;
D O I
10.1016/j.foodchem.2010.01.022
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The seeds of Psoralea corylifolia were extracted into five different polar solvents: chloroform, 50% ethanol in water, ethanol, methanol and water. All extracts were evaluated for glycosidase inhibitory activity. The chloroform extract (CE) showed the lowest IC50 values against alpha-glucosidase (82.9 mu g/ml) and alpha-mannosidase (132 mu g/ml). Chromatography of CE yielded nine phenolic compounds which were identified as isovabachalcone (1), 4'-O-methylbavachalcone (2), isobavachromene (3), corylifolin (4), bavachinin (5), psoralidin (6). neobavaisoflavone (7), corylifol A (8), and bakuchiol (9). All isolated compounds, apart from compound 5, possessed alpha-glucosidase inhibitory activities. Among them, compounds 6-8 exhibited potent inhibition with IC(50)s of 13.7, 27.7 and 11.3 mu M, respectively. Furthermore, compounds 2 and 6 showed alpha-mannosidase inhibitory activity. Mechanistic analysis of their inhibition modes against alpha-glucosidase showed that compounds (6 and 7) were noncompetitive, whereas compound 8 was mixed. Furthermore, the most active glycosidase inhibitors (2,6-8) were proven to be present in the native seed in high quantities by an HPLC chromatogram. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:940 / 945
页数:6
相关论文
共 23 条
[1]   Inhibitory activity of cyanidin-3-rutinoside on α-glucosidase [J].
Adisakwattana, S ;
Ngamrojanavanich, N ;
Kalampakorn, K ;
Tiravanit, W ;
Roengsumran, S ;
Yibchok-Anun, S .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2004, 19 (04) :313-316
[2]   Glycosidase inhibitors: update and perspectives on practical use [J].
Asano, N .
GLYCOBIOLOGY, 2003, 13 (10) :93R-104R
[3]   Preparation and in vitro evaluation of radioiodinated bakuchiol as an anti tumor agent [J].
Bapat, K ;
Chintalwar, GJ ;
Pandey, U ;
Thakur, VS ;
Sarma, HD ;
Samuel, G ;
Pillai, MRA ;
Chattopadhyay, S ;
Venkatesh, M .
APPLIED RADIATION AND ISOTOPES, 2005, 62 (03) :389-393
[4]   GLYCOSIDASES IN CANCER AND INVASION [J].
BERNACKI, RJ ;
NIEDBALA, MJ ;
KORYTNYK, W .
CANCER AND METASTASIS REVIEWS, 1985, 4 (01) :81-101
[5]  
BHALLA VK, 1968, TETRAHEDRON LETT, P2401
[6]  
CHANG HM, 1986, PHARM APPL CHINESE M, P636
[7]   Targeting glycosylation as a therapeutic approach [J].
Dwek, RA ;
Butters, TD ;
Platt, FM ;
Zitzmann, N .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (01) :65-75
[8]  
FERNANDES B, 1991, CANCER RES, V51, P718
[9]   Antioxidants from a Chinese medicinal herb -: Psoralea corylifolia L. [J].
Guo, JM ;
Weng, XC ;
Wu, H ;
Li, QH ;
Bi, KS .
FOOD CHEMISTRY, 2005, 91 (02) :287-292
[10]   GLYCOSYLATION INHIBITORS IN BIOLOGY AND MEDICINE [J].
JACOB, GS .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1995, 5 (05) :605-611