α-Glucosidase inhibitory effect by the flower buds of Tussilago farfara L.

被引:125
作者
Gao, Hong
Huang, Yi-Na
Gao, Bo
Xu, Pei-Yu
Inagaki, Chika
Kawabata, Jun [1 ]
机构
[1] Hokkaido Univ, Grad Sch Agr, Div Appl Biosci, Kita Ku, Sapporo, Hokkaido 0608589, Japan
[2] Sichuan Univ, Hua Xi Med Ctr, Dept Publ Hlth, Chengdu 610064, Peoples R China
基金
日本学术振兴会;
关键词
alpha-glucosidase; maltase inhibitor; postprandial hyperglycemia; Tussilago farfara; BAICALEIN; 5,6,7-TRIHYDROXYFLAVONE; SUBSTITUTION; COMPOSITAE; LEAVES; PLANTS; RING;
D O I
10.1016/j.foodchem.2007.07.064
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
Methanolic extracts from the medicinal parts of 50 traditional Chinese herbs were tested in screening experiments for rat intestinal alpha-glucosidase. The methanolic extract from flower buds of Tussilago farfara L. (Compositae) showed the highest maltase inhibitory activity, with maltose as a substrate. Enzyme assay-guided fractionation of this extract afforded. 3,4-dicaffeoylquinic acid (1), 3,5-dicaffeoyl-quinic acid (2), 4,5-dicaffeoylquinic acid (3) and rutin (4), and the structures of these compounds were elucidated on the basis of MS and NMR data analyses. Compounds 1, 2 and 3 showed comparative maltase inhibitory activities, and the IC50 values were 0.91 mM, 0.90 mM and 0.89 mM, respectively. Comparison of the activities of 1-3, chlorogenic acid (5), quinic acid (6) and caffeic acid (7) suggested that the number of caffeoyl groups attached to a quinic acid core were important for the potency. Rutin (4) showed moderate activity and inhibited 41 % of maltase activity at a concentration of 1 mM. This is the first report on mammalian alpha-glucosidase inhibition of T farfara and the isolation of 1, 2 and 3 from this herb species. These results suggest a use of the extract of T farfara for antidiabetes. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1195 / 1201
页数:7
相关论文
共 26 条
[1]
[Anonymous], [No title captured]
[2]
BASNET P, 1996, BIOL PHARM BULL, V11, P1479
[3]
Targeting postprandial hyperglycemia: A comparative study of insulinotropic agents in type 2 diabetes [J].
Carroll, MF ;
Gutierrez, A ;
Castro, M ;
Tsewang, D ;
Schade, DS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (11) :5248-5254
[5]
α-glucosidase inhibition of 6-hydroxyflavones.: Part 3:: Synthesis and evaluation of 2,3,4-trihydroxybenzoyl-containing flavonoid analogs and 6-aminoflavones as α-glucosidase inhibitors [J].
Gao, H ;
Kawabata, J .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (05) :1661-1671
[6]
Importance of the B ring and its substitution on the α-glucosidase inhibitory activity of baicalein, 5,6,7-trihydroxyflavone [J].
Gao, H ;
Kawabata, J .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2004, 68 (09) :1858-1864
[7]
Structure-activity relationships for α-glucosidase inhibition of baicalein, 5,6,7-trihydroxyflavone:: The effect of A-ring substitution [J].
Gao, H ;
Nishioka, T ;
Kawabata, J ;
Kasai, T .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2004, 68 (02) :369-375
[8]
In vitro antioxidative effects and tyrosinase inhibitory activities of seven hydroxycinnamoyl derivatives in green coffee beans [J].
Iwai, K ;
Kishimoto, N ;
Kakino, Y ;
Mochida, K ;
Fujita, T .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (15) :4893-4898
[9]
Advantages of α-glucosidase inhibition as monotherapy in elderly type 2 diabetic patients [J].
Johnston, PS ;
Lebovitz, HE ;
Coniff, RF ;
Simonson, DC ;
Raskin, P ;
Munera, CL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (05) :1515-1522
[10]
6-hydroxyflavonoids as α-glucosidase inhibitors from marjoram (Origanum majorana) leaves [J].
Kawabata, J ;
Mizuhata, K ;
Sato, E ;
Nishioka, T ;
Aoyama, Y ;
Kasai, T .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2003, 67 (02) :445-447