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Bioactive Compounds Extracted from Gamtae (Ecklonia cava) by Using Enzymatic Hydrolysis, a Potent ${alpha}$-Glucosidase and ${alpha}$-Amylase Inhibitor, Alleviates Postprandial Hyperglycemia in Diabetic Mice
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  • Bioactive Compounds Extracted from Gamtae (Ecklonia cava) by Using Enzymatic Hydrolysis, a Potent ${alpha}$-Glucosidase and ${alpha}$-Amylase Inhibitor, Alleviates Postprandial Hyperglycemia in Diabetic Mice
  • Bioactive Compounds Extracted from Gamtae (Ecklonia cava) by Using Enzymatic Hydrolysis, a Potent ${alpha}$-Glucosidase and ${alpha}$-Amylase Inhibitor, Alleviates Postprandial Hyperglycemia in Diabetic Mice
저자명
Lee. Seung-Hong,Park. Mi-Hwa,Han. Ji-Sook,Jeong. Yoonhwa,Kim. Misook,Jeon. You-Jin
간행물명
Food science and biotechnology
권/호정보
2012년|21권 4호|pp.1149-1155 (7 pages)
발행정보
한국식품과학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

This study was designed to investigate whether the brown alga gamtae (Ecklonia cava) may inhibit ${alpha}$-glucosidase and ${alpha}$-amylase activities, and alleviate postprandial hyperglycemia in streptozotocin-induced diabetic mice. For that purpose, we prepared an enzymatic hydrolysate from gamtae (EHG) by using the carbohydrase, Celluclast. EHG evidenced prominent inhibitory effect against ${alpha}$-glucosidase and ${alpha}$-amylase. The $IC_{50}$ values of EHG against ${alpha}$-glucosidase and ${alpha}$-amylase were 0.62 and 0.59 mg/mL, respectively, which evidenced the higher activities than that of acarbose. EHG did not exert any cytotoxic effect in human umbilical vein endothelial cells (HUVECs) at various concentrations (from 0.25 to 2 mg/mL). The increase of postprandial blood glucose levels were significantly suppressed in the EHG administered group than those in the streptozotocin-induced diabetic or normal mice. Moreover, the area under curve (AUC) was significantly reduced via EHG administration (6,102 vs. 10,425 $mg{cdot}min$/dL) in the diabetic mice as well as it delays absorption of dietary carbohydrates. These result indicated that EHG might be a potent inhibitor for ${alpha}$-glucosidase and ${alpha}$-amylase.