Dieckol isolated from Ecklonia cava inhibits α-glucosidase and α-amylase in vitro and alleviates postprandial hyperglycemia in streptozotocin-induced diabetic mice

被引:160
作者
Lee, Seung-Hong [1 ]
Park, Mi-Hwa [2 ]
Heo, Soo-Jin [3 ]
Kang, Sung-Myung [1 ]
Ko, Seok-Chun [1 ]
Han, Ji-Sook [2 ]
Jeon, You-Jin [1 ,4 ]
机构
[1] Jeju Natl Univ, Dept Marine life Sci, Cheju 690756, South Korea
[2] Pusan Natl Univ, Dept Food Sci & Nutr, Pusan 609735, South Korea
[3] Korea Ocean Res & Dev Inst, Marine Living Resources Res Dept, Ansan 426774, South Korea
[4] Jeju Natl Univ, Marine & Environm Res Inst, Cheju 695814, South Korea
关键词
Ecklonia cava; Dieckol; alpha-Glucosidase; alpha-Amylase; Postprandial hyperglycemia; Diabetic mice; ANTIOXIDANT ACTIVITIES; OXIDATIVE STRESS; LUNG FIBROBLAST; ACARBOSE; ALGAE;
D O I
10.1016/j.fct.2010.06.032
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
This study was designed to investigate whether dieckol may inhibit alpha-glucosidase and alpha-amylase activities, and alleviate postprandial hyperglycemia in streptozotocin-induced diabetic mice. Dieckol isolated from Ecklonia cava, brown algae, evidenced prominent inhibitory effect against alpha-glucosidase and alpha-amylase. The IC50 values of dieckol against a-glucosidase and alpha-amylase were 0.24 and 0.66 mM, respectively, which evidenced the higher activities than that of acarbose. Dieckol did not exert any cytotoxic effect in human umbilical vein endothelial cells (HUVECs) at various concentrations (from 0.33 to 2.69 mM). The increase of postprandial blood glucose levels were significantly suppressed in the dieckol administered group than those in the streptozotocin-induced diabetic or normal mice. Moreover, the area under curve (AUC) was significantly reduced via dieckol administration (259 versus 483 mmol min/l) in the diabetic mice as well as it delays absorption of dietary carbohydrates. Therefore, these result indicated that dieckol might be a potent inhibitor for a-glucosidase and alpha-amylase. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2633 / 2637
页数:5
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